dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs150656857
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr9:93247611 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- C>G / C>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
G=0.000008 (2/264690, TOPMED)G=0.00007 (5/66700, ExAC)G=0.00017 (4/23038, ALFA) (+ 1 more)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- WNK2 : Synonymous Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
Population | Group | Sample Size | Ref Allele | Alt Allele |
---|---|---|---|---|
Total | Global | 23038 | C=0.99983 | G=0.00017 |
European | Sub | 15752 | C=0.99987 | G=0.00013 |
African | Sub | 3492 | C=1.0000 | G=0.0000 |
African Others | Sub | 122 | C=1.000 | G=0.000 |
African American | Sub | 3370 | C=1.0000 | G=0.0000 |
Asian | Sub | 168 | C=1.000 | G=0.000 |
East Asian | Sub | 112 | C=1.000 | G=0.000 |
Other Asian | Sub | 56 | C=1.00 | G=0.00 |
Latin American 1 | Sub | 146 | C=1.000 | G=0.000 |
Latin American 2 | Sub | 610 | C=1.000 | G=0.000 |
South Asian | Sub | 98 | C=1.00 | G=0.00 |
Other | Sub | 2772 | C=0.9993 | G=0.0007 |
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
DownloadStudy | Population | Group | Sample Size | Ref Allele | Alt Allele |
---|---|---|---|---|---|
TopMed | Global | Study-wide | 264690 | C=0.999992 | G=0.000008 |
ExAC | Global | Study-wide | 66700 | C=0.99993 | G=0.00007 |
ExAC | Europe | Sub | 40302 | C=0.99988 | G=0.00012 |
ExAC | Asian | Sub | 14834 | C=1.00000 | G=0.00000 |
ExAC | African | Sub | 5878 | C=1.0000 | G=0.0000 |
ExAC | American | Sub | 5158 | C=1.0000 | G=0.0000 |
ExAC | Other | Sub | 528 | C=1.000 | G=0.000 |
Allele Frequency Aggregator | Total | Global | 23038 | C=0.99983 | G=0.00017 |
Allele Frequency Aggregator | European | Sub | 15752 | C=0.99987 | G=0.00013 |
Allele Frequency Aggregator | African | Sub | 3492 | C=1.0000 | G=0.0000 |
Allele Frequency Aggregator | Other | Sub | 2772 | C=0.9993 | G=0.0007 |
Allele Frequency Aggregator | Latin American 2 | Sub | 610 | C=1.000 | G=0.000 |
Allele Frequency Aggregator | Asian | Sub | 168 | C=1.000 | G=0.000 |
Allele Frequency Aggregator | Latin American 1 | Sub | 146 | C=1.000 | G=0.000 |
Allele Frequency Aggregator | South Asian | Sub | 98 | C=1.00 | G=0.00 |
GO Exome Sequencing Project | Global | Study-wide | 13006 | C=0.99992 | G=0.00008 |
GO Exome Sequencing Project | European American | Sub | 8600 | C=0.9999 | G=0.0001 |
GO Exome Sequencing Project | African American | Sub | 4406 | C=1.0000 | G=0.0000 |
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Sequence name | Change |
---|---|
GRCh38.p14 chr 9 | NC_000009.12:g.93247611C>G |
GRCh38.p14 chr 9 | NC_000009.12:g.93247611C>T |
GRCh37.p13 chr 9 | NC_000009.11:g.96009893C>G |
GRCh37.p13 chr 9 | NC_000009.11:g.96009893C>T |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
WNK2 transcript variant 2 | NM_006648.4:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform 2 | NP_006639.3:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant 2 | NM_006648.4:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform 2 | NP_006639.3:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant 1 | NM_001282394.3:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform 1 | NP_001269323.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant 1 | NM_001282394.3:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform 1 | NP_001269323.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X1 | XM_005252137.4:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X1 | XP_005252194.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X1 | XM_005252137.4:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X1 | XP_005252194.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X2 | XM_017015045.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X2 | XP_016870534.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X2 | XM_017015045.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X2 | XP_016870534.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X3 | XM_017015047.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X3 | XP_016870536.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X3 | XM_017015047.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X3 | XP_016870536.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X4 | XM_017015048.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X4 | XP_016870537.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X4 | XM_017015048.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X4 | XP_016870537.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X5 | XM_017015049.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X5 | XP_016870538.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X5 | XM_017015049.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X5 | XP_016870538.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X6 | XM_017015050.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X6 | XP_016870539.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X6 | XM_017015050.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X6 | XP_016870539.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X7 | XM_005252140.3:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X7 | XP_005252197.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X7 | XM_005252140.3:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X7 | XP_005252197.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X8 | XM_047423741.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X8 | XP_047279697.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X8 | XM_047423741.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X8 | XP_047279697.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X9 | XM_017015051.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X9 | XP_016870540.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X9 | XM_017015051.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X9 | XP_016870540.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X10 | XM_047423742.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X10 | XP_047279698.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X10 | XM_047423742.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X10 | XP_047279698.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X11 | XM_047423743.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X11 | XP_047279699.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X11 | XM_047423743.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X11 | XP_047279699.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X12 | XM_017015052.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X12 | XP_016870541.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X12 | XM_017015052.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X12 | XP_016870541.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X13 | XM_017015053.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X13 | XP_016870542.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X13 | XM_017015053.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X13 | XP_016870542.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X14 | XM_047423744.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X14 | XP_047279700.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X14 | XM_047423744.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X14 | XP_047279700.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X15 | XM_005252144.3:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X15 | XP_005252201.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X15 | XM_005252144.3:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X15 | XP_005252201.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X16 | XM_047423745.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X16 | XP_047279701.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X16 | XM_047423745.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X16 | XP_047279701.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X17 | XM_047423746.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X17 | XP_047279702.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X17 | XM_047423746.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X17 | XP_047279702.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X18 | XM_047423747.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X18 | XP_047279703.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X18 | XM_047423747.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X18 | XP_047279703.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X19 | XM_047423748.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X19 | XP_047279704.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X19 | XM_047423748.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X19 | XP_047279704.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X20 | XM_047423749.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X20 | XP_047279705.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X20 | XM_047423749.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X20 | XP_047279705.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X21 | XM_047423750.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X21 | XP_047279706.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X21 | XM_047423750.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X21 | XP_047279706.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X22 | XM_047423751.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X22 | XP_047279707.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X22 | XM_047423751.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X22 | XP_047279707.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X23 | XM_047423752.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X23 | XP_047279708.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X23 | XM_047423752.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X23 | XP_047279708.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X24 | XM_047423753.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X24 | XP_047279709.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X24 | XM_047423753.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X24 | XP_047279709.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X25 | XM_017015054.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X25 | XP_016870543.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X25 | XM_017015054.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X25 | XP_016870543.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X26 | XM_017015055.2:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X26 | XP_016870544.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X26 | XM_017015055.2:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X26 | XP_016870544.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X27 | XM_047423754.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X27 | XP_047279710.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X27 | XM_047423754.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X27 | XP_047279710.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X28 | XM_047423756.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X28 | XP_047279712.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X28 | XM_047423756.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X28 | XP_047279712.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X29 | XM_047423757.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X29 | XP_047279713.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X29 | XM_047423757.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X29 | XP_047279713.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X30 | XM_047423758.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X30 | XP_047279714.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X30 | XM_047423758.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X30 | XP_047279714.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X31 | XM_047423759.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X31 | XP_047279715.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X31 | XM_047423759.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X31 | XP_047279715.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X32 | XM_047423760.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X32 | XP_047279716.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X32 | XM_047423760.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X32 | XP_047279716.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X33 | XM_047423761.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X33 | XP_047279717.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X33 | XM_047423761.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X33 | XP_047279717.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X34 | XM_047423762.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X34 | XP_047279718.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X34 | XM_047423762.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X34 | XP_047279718.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X35 | XM_047423763.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X35 | XP_047279719.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X35 | XM_047423763.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X35 | XP_047279719.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X36 | XM_047423764.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X36 | XP_047279720.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X36 | XM_047423764.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X36 | XP_047279720.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X37 | XM_047423765.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X37 | XP_047279721.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X37 | XM_047423765.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X37 | XP_047279721.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X38 | XM_047423767.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X38 | XP_047279723.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X38 | XM_047423767.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X38 | XP_047279723.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X39 | XM_047423768.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X39 | XP_047279724.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X39 | XM_047423768.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X39 | XP_047279724.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X40 | XM_047423769.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X40 | XP_047279725.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X40 | XM_047423769.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X40 | XP_047279725.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X41 | XM_047423770.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X41 | XP_047279726.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X41 | XM_047423770.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X41 | XP_047279726.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X42 | XM_047423771.1:c.1611C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X42 | XP_047279727.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X42 | XM_047423771.1:c.1611C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X42 | XP_047279727.1:p.Ala537= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X43 | XM_047423772.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X43 | XP_047279728.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X43 | XM_047423772.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X43 | XP_047279728.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X44 | XM_047423773.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X44 | XP_047279729.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X44 | XM_047423773.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X44 | XP_047279729.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X45 | XM_047423774.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X45 | XP_047279730.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X45 | XM_047423774.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X45 | XP_047279730.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X46 | XM_047423775.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X46 | XP_047279731.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X46 | XM_047423775.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X46 | XP_047279731.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X47 | XM_047423776.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X47 | XP_047279732.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X47 | XM_047423776.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X47 | XP_047279732.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X48 | XM_047423778.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X48 | XP_047279734.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X48 | XM_047423778.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X48 | XP_047279734.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X49 | XM_047423779.1:c.966C>G | A [GCC] > A [GCG] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X49 | XP_047279735.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
WNK2 transcript variant X49 | XM_047423779.1:c.966C>T | A [GCC] > A [GCT] | Coding Sequence Variant |
serine/threonine-protein kinase WNK2 isoform X49 | XP_047279735.1:p.Ala322= | A (Ala) > A (Ala) | Synonymous Variant |
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
Placement | C= | G | T |
---|---|---|---|
GRCh38.p14 chr 9 | NC_000009.12:g.93247611= | NC_000009.12:g.93247611C>G | NC_000009.12:g.93247611C>T |
GRCh37.p13 chr 9 | NC_000009.11:g.96009893= | NC_000009.11:g.96009893C>G | NC_000009.11:g.96009893C>T |
WNK2 transcript variant X1 | XM_005252137.4:c.1611= | XM_005252137.4:c.1611C>G | XM_005252137.4:c.1611C>T |
WNK2 transcript variant X5 | XM_005252137.3:c.1611= | XM_005252137.3:c.1611C>G | XM_005252137.3:c.1611C>T |
WNK2 transcript variant X5 | XM_005252137.2:c.1611= | XM_005252137.2:c.1611C>G | XM_005252137.2:c.1611C>T |
WNK2 transcript variant X2 | XM_005252137.1:c.1611= | XM_005252137.1:c.1611C>G | XM_005252137.1:c.1611C>T |
WNK2 transcript variant 2 | NM_006648.4:c.1611= | NM_006648.4:c.1611C>G | NM_006648.4:c.1611C>T |
WNK2 transcript variant 2 | NM_006648.3:c.1611= | NM_006648.3:c.1611C>G | NM_006648.3:c.1611C>T |
WNK2 transcript variant 1 | NM_001282394.3:c.1611= | NM_001282394.3:c.1611C>G | NM_001282394.3:c.1611C>T |
WNK2 transcript variant 1 | NM_001282394.2:c.1611= | NM_001282394.2:c.1611C>G | NM_001282394.2:c.1611C>T |
WNK2 transcript variant 1 | NM_001282394.1:c.1611= | NM_001282394.1:c.1611C>G | NM_001282394.1:c.1611C>T |
WNK2 transcript variant X7 | XM_005252140.3:c.1611= | XM_005252140.3:c.1611C>G | XM_005252140.3:c.1611C>T |
WNK2 transcript variant X16 | XM_005252140.2:c.1611= | XM_005252140.2:c.1611C>G | XM_005252140.2:c.1611C>T |
WNK2 transcript variant X11 | XM_005252140.1:c.1611= | XM_005252140.1:c.1611C>G | XM_005252140.1:c.1611C>T |
WNK2 transcript variant X15 | XM_005252144.3:c.1611= | XM_005252144.3:c.1611C>G | XM_005252144.3:c.1611C>T |
WNK2 transcript variant X23 | XM_005252144.2:c.1611= | XM_005252144.2:c.1611C>G | XM_005252144.2:c.1611C>T |
WNK2 transcript variant X15 | XM_005252144.1:c.1611= | XM_005252144.1:c.1611C>G | XM_005252144.1:c.1611C>T |
WNK2 transcript variant X2 | XM_017015045.2:c.1611= | XM_017015045.2:c.1611C>G | XM_017015045.2:c.1611C>T |
WNK2 transcript variant X6 | XM_017015045.1:c.1611= | XM_017015045.1:c.1611C>G | XM_017015045.1:c.1611C>T |
WNK2 transcript variant X3 | XM_017015047.2:c.1611= | XM_017015047.2:c.1611C>G | XM_017015047.2:c.1611C>T |
WNK2 transcript variant X11 | XM_017015047.1:c.1611= | XM_017015047.1:c.1611C>G | XM_017015047.1:c.1611C>T |
WNK2 transcript variant X4 | XM_017015048.2:c.1611= | XM_017015048.2:c.1611C>G | XM_017015048.2:c.1611C>T |
WNK2 transcript variant X12 | XM_017015048.1:c.1611= | XM_017015048.1:c.1611C>G | XM_017015048.1:c.1611C>T |
WNK2 transcript variant X5 | XM_017015049.2:c.1611= | XM_017015049.2:c.1611C>G | XM_017015049.2:c.1611C>T |
WNK2 transcript variant X14 | XM_017015049.1:c.1611= | XM_017015049.1:c.1611C>G | XM_017015049.1:c.1611C>T |
WNK2 transcript variant X6 | XM_017015050.2:c.1611= | XM_017015050.2:c.1611C>G | XM_017015050.2:c.1611C>T |
WNK2 transcript variant X15 | XM_017015050.1:c.1611= | XM_017015050.1:c.1611C>G | XM_017015050.1:c.1611C>T |
WNK2 transcript variant X9 | XM_017015051.2:c.1611= | XM_017015051.2:c.1611C>G | XM_017015051.2:c.1611C>T |
WNK2 transcript variant X18 | XM_017015051.1:c.1611= | XM_017015051.1:c.1611C>G | XM_017015051.1:c.1611C>T |
WNK2 transcript variant X12 | XM_017015052.2:c.1611= | XM_017015052.2:c.1611C>G | XM_017015052.2:c.1611C>T |
WNK2 transcript variant X19 | XM_017015052.1:c.1611= | XM_017015052.1:c.1611C>G | XM_017015052.1:c.1611C>T |
WNK2 transcript variant X13 | XM_017015053.2:c.1611= | XM_017015053.2:c.1611C>G | XM_017015053.2:c.1611C>T |
WNK2 transcript variant X20 | XM_017015053.1:c.1611= | XM_017015053.1:c.1611C>G | XM_017015053.1:c.1611C>T |
WNK2 transcript variant X25 | XM_017015054.2:c.1611= | XM_017015054.2:c.1611C>G | XM_017015054.2:c.1611C>T |
WNK2 transcript variant X26 | XM_017015054.1:c.1611= | XM_017015054.1:c.1611C>G | XM_017015054.1:c.1611C>T |
WNK2 transcript variant X26 | XM_017015055.2:c.1611= | XM_017015055.2:c.1611C>G | XM_017015055.2:c.1611C>T |
WNK2 transcript variant X27 | XM_017015055.1:c.1611= | XM_017015055.1:c.1611C>G | XM_017015055.1:c.1611C>T |
WNK2 transcript variant X10 | XM_047423742.1:c.1611= | XM_047423742.1:c.1611C>G | XM_047423742.1:c.1611C>T |
WNK2 transcript variant X11 | XM_047423743.1:c.1611= | XM_047423743.1:c.1611C>G | XM_047423743.1:c.1611C>T |
WNK2 transcript variant X14 | XM_047423744.1:c.1611= | XM_047423744.1:c.1611C>G | XM_047423744.1:c.1611C>T |
WNK2 transcript variant X19 | XM_047423748.1:c.1611= | XM_047423748.1:c.1611C>G | XM_047423748.1:c.1611C>T |
WNK2 transcript variant X20 | XM_047423749.1:c.1611= | XM_047423749.1:c.1611C>G | XM_047423749.1:c.1611C>T |
WNK2 transcript variant X21 | XM_047423750.1:c.1611= | XM_047423750.1:c.1611C>G | XM_047423750.1:c.1611C>T |
WNK2 transcript variant X29 | XM_047423757.1:c.1611= | XM_047423757.1:c.1611C>G | XM_047423757.1:c.1611C>T |
WNK2 transcript variant X30 | XM_047423758.1:c.1611= | XM_047423758.1:c.1611C>G | XM_047423758.1:c.1611C>T |
WNK2 transcript variant X36 | XM_047423764.1:c.1611= | XM_047423764.1:c.1611C>G | XM_047423764.1:c.1611C>T |
WNK2 transcript variant X37 | XM_047423765.1:c.1611= | XM_047423765.1:c.1611C>G | XM_047423765.1:c.1611C>T |
WNK2 transcript variant X17 | XM_047423746.1:c.1611= | XM_047423746.1:c.1611C>G | XM_047423746.1:c.1611C>T |
WNK2 transcript variant X46 | XM_047423775.1:c.966= | XM_047423775.1:c.966C>G | XM_047423775.1:c.966C>T |
WNK2 transcript variant X31 | XM_047423759.1:c.1611= | XM_047423759.1:c.1611C>G | XM_047423759.1:c.1611C>T |
WNK2 transcript variant X32 | XM_047423760.1:c.1611= | XM_047423760.1:c.1611C>G | XM_047423760.1:c.1611C>T |
WNK2 transcript variant X8 | XM_047423741.1:c.1611= | XM_047423741.1:c.1611C>G | XM_047423741.1:c.1611C>T |
WNK2 transcript variant X35 | XM_047423763.1:c.1611= | XM_047423763.1:c.1611C>G | XM_047423763.1:c.1611C>T |
WNK2 transcript variant X16 | XM_047423745.1:c.1611= | XM_047423745.1:c.1611C>G | XM_047423745.1:c.1611C>T |
WNK2 transcript variant X18 | XM_047423747.1:c.1611= | XM_047423747.1:c.1611C>G | XM_047423747.1:c.1611C>T |
WNK2 transcript variant X40 | XM_047423769.1:c.1611= | XM_047423769.1:c.1611C>G | XM_047423769.1:c.1611C>T |
WNK2 transcript variant X22 | XM_047423751.1:c.1611= | XM_047423751.1:c.1611C>G | XM_047423751.1:c.1611C>T |
WNK2 transcript variant X23 | XM_047423752.1:c.1611= | XM_047423752.1:c.1611C>G | XM_047423752.1:c.1611C>T |
WNK2 transcript variant X24 | XM_047423753.1:c.1611= | XM_047423753.1:c.1611C>G | XM_047423753.1:c.1611C>T |
WNK2 transcript variant X27 | XM_047423754.1:c.1611= | XM_047423754.1:c.1611C>G | XM_047423754.1:c.1611C>T |
WNK2 transcript variant X28 | XM_047423756.1:c.1611= | XM_047423756.1:c.1611C>G | XM_047423756.1:c.1611C>T |
WNK2 transcript variant X33 | XM_047423761.1:c.1611= | XM_047423761.1:c.1611C>G | XM_047423761.1:c.1611C>T |
WNK2 transcript variant X34 | XM_047423762.1:c.1611= | XM_047423762.1:c.1611C>G | XM_047423762.1:c.1611C>T |
WNK2 transcript variant X38 | XM_047423767.1:c.1611= | XM_047423767.1:c.1611C>G | XM_047423767.1:c.1611C>T |
WNK2 transcript variant X39 | XM_047423768.1:c.1611= | XM_047423768.1:c.1611C>G | XM_047423768.1:c.1611C>T |
WNK2 transcript variant X41 | XM_047423770.1:c.1611= | XM_047423770.1:c.1611C>G | XM_047423770.1:c.1611C>T |
WNK2 transcript variant X42 | XM_047423771.1:c.1611= | XM_047423771.1:c.1611C>G | XM_047423771.1:c.1611C>T |
WNK2 transcript variant X43 | XM_047423772.1:c.966= | XM_047423772.1:c.966C>G | XM_047423772.1:c.966C>T |
WNK2 transcript variant X47 | XM_047423776.1:c.966= | XM_047423776.1:c.966C>G | XM_047423776.1:c.966C>T |
WNK2 transcript variant X44 | XM_047423773.1:c.966= | XM_047423773.1:c.966C>G | XM_047423773.1:c.966C>T |
WNK2 transcript variant X45 | XM_047423774.1:c.966= | XM_047423774.1:c.966C>G | XM_047423774.1:c.966C>T |
WNK2 transcript variant X49 | XM_047423779.1:c.966= | XM_047423779.1:c.966C>G | XM_047423779.1:c.966C>T |
WNK2 transcript variant X48 | XM_047423778.1:c.966= | XM_047423778.1:c.966C>G | XM_047423778.1:c.966C>T |
serine/threonine-protein kinase WNK2 isoform X1 | XP_005252194.1:p.Ala537= | XP_005252194.1:p.Ala537= | XP_005252194.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform 2 | NP_006639.3:p.Ala537= | NP_006639.3:p.Ala537= | NP_006639.3:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform 1 | NP_001269323.1:p.Ala537= | NP_001269323.1:p.Ala537= | NP_001269323.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X7 | XP_005252197.1:p.Ala537= | XP_005252197.1:p.Ala537= | XP_005252197.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X15 | XP_005252201.1:p.Ala537= | XP_005252201.1:p.Ala537= | XP_005252201.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X2 | XP_016870534.1:p.Ala537= | XP_016870534.1:p.Ala537= | XP_016870534.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X3 | XP_016870536.1:p.Ala537= | XP_016870536.1:p.Ala537= | XP_016870536.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X4 | XP_016870537.1:p.Ala537= | XP_016870537.1:p.Ala537= | XP_016870537.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X5 | XP_016870538.1:p.Ala537= | XP_016870538.1:p.Ala537= | XP_016870538.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X6 | XP_016870539.1:p.Ala537= | XP_016870539.1:p.Ala537= | XP_016870539.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X9 | XP_016870540.1:p.Ala537= | XP_016870540.1:p.Ala537= | XP_016870540.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X12 | XP_016870541.1:p.Ala537= | XP_016870541.1:p.Ala537= | XP_016870541.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X13 | XP_016870542.1:p.Ala537= | XP_016870542.1:p.Ala537= | XP_016870542.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X25 | XP_016870543.1:p.Ala537= | XP_016870543.1:p.Ala537= | XP_016870543.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X26 | XP_016870544.1:p.Ala537= | XP_016870544.1:p.Ala537= | XP_016870544.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X10 | XP_047279698.1:p.Ala537= | XP_047279698.1:p.Ala537= | XP_047279698.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X11 | XP_047279699.1:p.Ala537= | XP_047279699.1:p.Ala537= | XP_047279699.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X14 | XP_047279700.1:p.Ala537= | XP_047279700.1:p.Ala537= | XP_047279700.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X19 | XP_047279704.1:p.Ala537= | XP_047279704.1:p.Ala537= | XP_047279704.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X20 | XP_047279705.1:p.Ala537= | XP_047279705.1:p.Ala537= | XP_047279705.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X21 | XP_047279706.1:p.Ala537= | XP_047279706.1:p.Ala537= | XP_047279706.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X29 | XP_047279713.1:p.Ala537= | XP_047279713.1:p.Ala537= | XP_047279713.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X30 | XP_047279714.1:p.Ala537= | XP_047279714.1:p.Ala537= | XP_047279714.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X36 | XP_047279720.1:p.Ala537= | XP_047279720.1:p.Ala537= | XP_047279720.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X37 | XP_047279721.1:p.Ala537= | XP_047279721.1:p.Ala537= | XP_047279721.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X17 | XP_047279702.1:p.Ala537= | XP_047279702.1:p.Ala537= | XP_047279702.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X46 | XP_047279731.1:p.Ala322= | XP_047279731.1:p.Ala322= | XP_047279731.1:p.Ala322= |
serine/threonine-protein kinase WNK2 isoform X31 | XP_047279715.1:p.Ala537= | XP_047279715.1:p.Ala537= | XP_047279715.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X32 | XP_047279716.1:p.Ala537= | XP_047279716.1:p.Ala537= | XP_047279716.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X8 | XP_047279697.1:p.Ala537= | XP_047279697.1:p.Ala537= | XP_047279697.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X35 | XP_047279719.1:p.Ala537= | XP_047279719.1:p.Ala537= | XP_047279719.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X16 | XP_047279701.1:p.Ala537= | XP_047279701.1:p.Ala537= | XP_047279701.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X18 | XP_047279703.1:p.Ala537= | XP_047279703.1:p.Ala537= | XP_047279703.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X40 | XP_047279725.1:p.Ala537= | XP_047279725.1:p.Ala537= | XP_047279725.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X22 | XP_047279707.1:p.Ala537= | XP_047279707.1:p.Ala537= | XP_047279707.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X23 | XP_047279708.1:p.Ala537= | XP_047279708.1:p.Ala537= | XP_047279708.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X24 | XP_047279709.1:p.Ala537= | XP_047279709.1:p.Ala537= | XP_047279709.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X27 | XP_047279710.1:p.Ala537= | XP_047279710.1:p.Ala537= | XP_047279710.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X28 | XP_047279712.1:p.Ala537= | XP_047279712.1:p.Ala537= | XP_047279712.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X33 | XP_047279717.1:p.Ala537= | XP_047279717.1:p.Ala537= | XP_047279717.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X34 | XP_047279718.1:p.Ala537= | XP_047279718.1:p.Ala537= | XP_047279718.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X38 | XP_047279723.1:p.Ala537= | XP_047279723.1:p.Ala537= | XP_047279723.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X39 | XP_047279724.1:p.Ala537= | XP_047279724.1:p.Ala537= | XP_047279724.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X41 | XP_047279726.1:p.Ala537= | XP_047279726.1:p.Ala537= | XP_047279726.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X42 | XP_047279727.1:p.Ala537= | XP_047279727.1:p.Ala537= | XP_047279727.1:p.Ala537= |
serine/threonine-protein kinase WNK2 isoform X43 | XP_047279728.1:p.Ala322= | XP_047279728.1:p.Ala322= | XP_047279728.1:p.Ala322= |
serine/threonine-protein kinase WNK2 isoform X47 | XP_047279732.1:p.Ala322= | XP_047279732.1:p.Ala322= | XP_047279732.1:p.Ala322= |
serine/threonine-protein kinase WNK2 isoform X44 | XP_047279729.1:p.Ala322= | XP_047279729.1:p.Ala322= | XP_047279729.1:p.Ala322= |
serine/threonine-protein kinase WNK2 isoform X45 | XP_047279730.1:p.Ala322= | XP_047279730.1:p.Ala322= | XP_047279730.1:p.Ala322= |
serine/threonine-protein kinase WNK2 isoform X49 | XP_047279735.1:p.Ala322= | XP_047279735.1:p.Ala322= | XP_047279735.1:p.Ala322= |
serine/threonine-protein kinase WNK2 isoform X48 | XP_047279734.1:p.Ala322= | XP_047279734.1:p.Ala322= | XP_047279734.1:p.Ala322= |
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
No | Submitter | Submission ID | Date (Build) |
---|---|---|---|
1 | NHLBI-ESP | ss342276872 | May 09, 2011 (134) |
2 | EVA_EXAC | ss1689553212 | Apr 01, 2015 (144) |
3 | GNOMAD | ss2737711804 | Nov 08, 2017 (151) |
4 | EVA | ss3824442746 | Apr 26, 2020 (154) |
5 | TOPMED | ss4828099167 | Apr 26, 2021 (155) |
6 | ExAC | NC_000009.11 - 96009893 | Oct 12, 2018 (152) |
7 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
8 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
9 | GO Exome Sequencing Project | NC_000009.11 - 96009893 | Oct 12, 2018 (152) |
10 | TopMed | NC_000009.12 - 93247611 | Apr 26, 2021 (155) |
11 | ALFA | NC_000009.12 - 93247611 | Apr 26, 2021 (155) |
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
---|---|---|---|
9681779, 900527, ss342276872, ss1689553212, ss2737711804, ss3824442746 | NC_000009.11:96009892:C:G | NC_000009.12:93247610:C:G | (self) |
665476728, 8451785980, ss4828099167 | NC_000009.12:93247610:C:G | NC_000009.12:93247610:C:G | (self) |
ss2737711804 | NC_000009.11:96009892:C:T | NC_000009.12:93247610:C:T | (self) |
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs150656857
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genomic regions, transcripts, and products
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Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.