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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.

rs1328679985

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:93239874 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
None
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
WNK2 : Synonymous Variant
Publications
0 citations
Genomic View
See rs on genome
Help

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").

None
Help

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.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 9 NC_000009.12:g.93239874G>A
GRCh37.p13 chr 9 NC_000009.11:g.96002156G>A
Gene: WNK2, WNK lysine deficient protein kinase 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
WNK2 transcript variant 2 NM_006648.4:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform 2 NP_006639.3:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant 1 NM_001282394.3:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform 1 NP_001269323.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X1 XM_005252137.4:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X1 XP_005252194.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X2 XM_017015045.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X2 XP_016870534.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X3 XM_017015047.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X3 XP_016870536.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X4 XM_017015048.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X4 XP_016870537.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X5 XM_017015049.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X5 XP_016870538.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X6 XM_017015050.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X6 XP_016870539.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X7 XM_005252140.3:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X7 XP_005252197.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X8 XM_047423741.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X8 XP_047279697.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X9 XM_017015051.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X9 XP_016870540.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X10 XM_047423742.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X10 XP_047279698.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X11 XM_047423743.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X11 XP_047279699.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X12 XM_017015052.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X12 XP_016870541.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X13 XM_017015053.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X13 XP_016870542.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X14 XM_047423744.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X14 XP_047279700.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X15 XM_005252144.3:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X15 XP_005252201.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X16 XM_047423745.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X16 XP_047279701.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X17 XM_047423746.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X17 XP_047279702.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X18 XM_047423747.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X18 XP_047279703.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X19 XM_047423748.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X19 XP_047279704.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X20 XM_047423749.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X20 XP_047279705.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X21 XM_047423750.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X21 XP_047279706.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X22 XM_047423751.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X22 XP_047279707.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X23 XM_047423752.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X23 XP_047279708.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X24 XM_047423753.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X24 XP_047279709.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X25 XM_017015054.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X25 XP_016870543.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X26 XM_017015055.2:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X26 XP_016870544.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X27 XM_047423754.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X27 XP_047279710.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X28 XM_047423756.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X28 XP_047279712.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X29 XM_047423757.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X29 XP_047279713.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X30 XM_047423758.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X30 XP_047279714.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X31 XM_047423759.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X31 XP_047279715.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X32 XM_047423760.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X32 XP_047279716.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X33 XM_047423761.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X33 XP_047279717.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X34 XM_047423762.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X34 XP_047279718.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X35 XM_047423763.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X35 XP_047279719.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X36 XM_047423764.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X36 XP_047279720.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X37 XM_047423765.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X37 XP_047279721.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X38 XM_047423767.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X38 XP_047279723.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X39 XM_047423768.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X39 XP_047279724.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X40 XM_047423769.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X40 XP_047279725.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X41 XM_047423770.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X41 XP_047279726.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X42 XM_047423771.1:c.1440G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X42 XP_047279727.1:p.Val480= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X43 XM_047423772.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X43 XP_047279728.1:p.Val265= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X44 XM_047423773.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X44 XP_047279729.1:p.Val265= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X45 XM_047423774.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X45 XP_047279730.1:p.Val265= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X46 XM_047423775.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X46 XP_047279731.1:p.Val265= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X47 XM_047423776.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X47 XP_047279732.1:p.Val265= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X48 XM_047423778.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X48 XP_047279734.1:p.Val265= V (Val) > V (Val) Synonymous Variant
WNK2 transcript variant X49 XM_047423779.1:c.795G>A V [GTG] > V [GTA] Coding Sequence Variant
serine/threonine-protein kinase WNK2 isoform X49 XP_047279735.1:p.Val265= V (Val) > V (Val) Synonymous Variant
Help

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.

Not Reported in ClinVar
Help

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 G= A
GRCh38.p14 chr 9 NC_000009.12:g.93239874= NC_000009.12:g.93239874G>A
GRCh37.p13 chr 9 NC_000009.11:g.96002156= NC_000009.11:g.96002156G>A
WNK2 transcript variant X1 XM_005252137.4:c.1440= XM_005252137.4:c.1440G>A
WNK2 transcript variant X5 XM_005252137.3:c.1440= XM_005252137.3:c.1440G>A
WNK2 transcript variant X5 XM_005252137.2:c.1440= XM_005252137.2:c.1440G>A
WNK2 transcript variant X2 XM_005252137.1:c.1440= XM_005252137.1:c.1440G>A
WNK2 transcript variant 2 NM_006648.4:c.1440= NM_006648.4:c.1440G>A
WNK2 transcript variant 2 NM_006648.3:c.1440= NM_006648.3:c.1440G>A
WNK2 transcript variant 1 NM_001282394.3:c.1440= NM_001282394.3:c.1440G>A
WNK2 transcript variant 1 NM_001282394.2:c.1440= NM_001282394.2:c.1440G>A
WNK2 transcript variant 1 NM_001282394.1:c.1440= NM_001282394.1:c.1440G>A
WNK2 transcript variant X7 XM_005252140.3:c.1440= XM_005252140.3:c.1440G>A
WNK2 transcript variant X16 XM_005252140.2:c.1440= XM_005252140.2:c.1440G>A
WNK2 transcript variant X11 XM_005252140.1:c.1440= XM_005252140.1:c.1440G>A
WNK2 transcript variant X15 XM_005252144.3:c.1440= XM_005252144.3:c.1440G>A
WNK2 transcript variant X23 XM_005252144.2:c.1440= XM_005252144.2:c.1440G>A
WNK2 transcript variant X15 XM_005252144.1:c.1440= XM_005252144.1:c.1440G>A
WNK2 transcript variant X2 XM_017015045.2:c.1440= XM_017015045.2:c.1440G>A
WNK2 transcript variant X6 XM_017015045.1:c.1440= XM_017015045.1:c.1440G>A
WNK2 transcript variant X3 XM_017015047.2:c.1440= XM_017015047.2:c.1440G>A
WNK2 transcript variant X11 XM_017015047.1:c.1440= XM_017015047.1:c.1440G>A
WNK2 transcript variant X4 XM_017015048.2:c.1440= XM_017015048.2:c.1440G>A
WNK2 transcript variant X12 XM_017015048.1:c.1440= XM_017015048.1:c.1440G>A
WNK2 transcript variant X5 XM_017015049.2:c.1440= XM_017015049.2:c.1440G>A
WNK2 transcript variant X14 XM_017015049.1:c.1440= XM_017015049.1:c.1440G>A
WNK2 transcript variant X6 XM_017015050.2:c.1440= XM_017015050.2:c.1440G>A
WNK2 transcript variant X15 XM_017015050.1:c.1440= XM_017015050.1:c.1440G>A
WNK2 transcript variant X9 XM_017015051.2:c.1440= XM_017015051.2:c.1440G>A
WNK2 transcript variant X18 XM_017015051.1:c.1440= XM_017015051.1:c.1440G>A
WNK2 transcript variant X12 XM_017015052.2:c.1440= XM_017015052.2:c.1440G>A
WNK2 transcript variant X19 XM_017015052.1:c.1440= XM_017015052.1:c.1440G>A
WNK2 transcript variant X13 XM_017015053.2:c.1440= XM_017015053.2:c.1440G>A
WNK2 transcript variant X20 XM_017015053.1:c.1440= XM_017015053.1:c.1440G>A
WNK2 transcript variant X25 XM_017015054.2:c.1440= XM_017015054.2:c.1440G>A
WNK2 transcript variant X26 XM_017015054.1:c.1440= XM_017015054.1:c.1440G>A
WNK2 transcript variant X26 XM_017015055.2:c.1440= XM_017015055.2:c.1440G>A
WNK2 transcript variant X27 XM_017015055.1:c.1440= XM_017015055.1:c.1440G>A
WNK2 transcript variant X10 XM_047423742.1:c.1440= XM_047423742.1:c.1440G>A
WNK2 transcript variant X11 XM_047423743.1:c.1440= XM_047423743.1:c.1440G>A
WNK2 transcript variant X14 XM_047423744.1:c.1440= XM_047423744.1:c.1440G>A
WNK2 transcript variant X19 XM_047423748.1:c.1440= XM_047423748.1:c.1440G>A
WNK2 transcript variant X20 XM_047423749.1:c.1440= XM_047423749.1:c.1440G>A
WNK2 transcript variant X21 XM_047423750.1:c.1440= XM_047423750.1:c.1440G>A
WNK2 transcript variant X29 XM_047423757.1:c.1440= XM_047423757.1:c.1440G>A
WNK2 transcript variant X30 XM_047423758.1:c.1440= XM_047423758.1:c.1440G>A
WNK2 transcript variant X36 XM_047423764.1:c.1440= XM_047423764.1:c.1440G>A
WNK2 transcript variant X37 XM_047423765.1:c.1440= XM_047423765.1:c.1440G>A
WNK2 transcript variant X17 XM_047423746.1:c.1440= XM_047423746.1:c.1440G>A
WNK2 transcript variant X46 XM_047423775.1:c.795= XM_047423775.1:c.795G>A
WNK2 transcript variant X31 XM_047423759.1:c.1440= XM_047423759.1:c.1440G>A
WNK2 transcript variant X32 XM_047423760.1:c.1440= XM_047423760.1:c.1440G>A
WNK2 transcript variant X8 XM_047423741.1:c.1440= XM_047423741.1:c.1440G>A
WNK2 transcript variant X35 XM_047423763.1:c.1440= XM_047423763.1:c.1440G>A
WNK2 transcript variant X16 XM_047423745.1:c.1440= XM_047423745.1:c.1440G>A
WNK2 transcript variant X18 XM_047423747.1:c.1440= XM_047423747.1:c.1440G>A
WNK2 transcript variant X40 XM_047423769.1:c.1440= XM_047423769.1:c.1440G>A
WNK2 transcript variant X22 XM_047423751.1:c.1440= XM_047423751.1:c.1440G>A
WNK2 transcript variant X23 XM_047423752.1:c.1440= XM_047423752.1:c.1440G>A
WNK2 transcript variant X24 XM_047423753.1:c.1440= XM_047423753.1:c.1440G>A
WNK2 transcript variant X27 XM_047423754.1:c.1440= XM_047423754.1:c.1440G>A
WNK2 transcript variant X28 XM_047423756.1:c.1440= XM_047423756.1:c.1440G>A
WNK2 transcript variant X33 XM_047423761.1:c.1440= XM_047423761.1:c.1440G>A
WNK2 transcript variant X34 XM_047423762.1:c.1440= XM_047423762.1:c.1440G>A
WNK2 transcript variant X38 XM_047423767.1:c.1440= XM_047423767.1:c.1440G>A
WNK2 transcript variant X39 XM_047423768.1:c.1440= XM_047423768.1:c.1440G>A
WNK2 transcript variant X41 XM_047423770.1:c.1440= XM_047423770.1:c.1440G>A
WNK2 transcript variant X42 XM_047423771.1:c.1440= XM_047423771.1:c.1440G>A
WNK2 transcript variant X43 XM_047423772.1:c.795= XM_047423772.1:c.795G>A
WNK2 transcript variant X47 XM_047423776.1:c.795= XM_047423776.1:c.795G>A
WNK2 transcript variant X44 XM_047423773.1:c.795= XM_047423773.1:c.795G>A
WNK2 transcript variant X45 XM_047423774.1:c.795= XM_047423774.1:c.795G>A
WNK2 transcript variant X49 XM_047423779.1:c.795= XM_047423779.1:c.795G>A
WNK2 transcript variant X48 XM_047423778.1:c.795= XM_047423778.1:c.795G>A
serine/threonine-protein kinase WNK2 isoform X1 XP_005252194.1:p.Val480= XP_005252194.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform 2 NP_006639.3:p.Val480= NP_006639.3:p.Val480=
serine/threonine-protein kinase WNK2 isoform 1 NP_001269323.1:p.Val480= NP_001269323.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X7 XP_005252197.1:p.Val480= XP_005252197.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X15 XP_005252201.1:p.Val480= XP_005252201.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X2 XP_016870534.1:p.Val480= XP_016870534.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X3 XP_016870536.1:p.Val480= XP_016870536.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X4 XP_016870537.1:p.Val480= XP_016870537.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X5 XP_016870538.1:p.Val480= XP_016870538.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X6 XP_016870539.1:p.Val480= XP_016870539.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X9 XP_016870540.1:p.Val480= XP_016870540.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X12 XP_016870541.1:p.Val480= XP_016870541.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X13 XP_016870542.1:p.Val480= XP_016870542.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X25 XP_016870543.1:p.Val480= XP_016870543.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X26 XP_016870544.1:p.Val480= XP_016870544.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X10 XP_047279698.1:p.Val480= XP_047279698.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X11 XP_047279699.1:p.Val480= XP_047279699.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X14 XP_047279700.1:p.Val480= XP_047279700.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X19 XP_047279704.1:p.Val480= XP_047279704.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X20 XP_047279705.1:p.Val480= XP_047279705.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X21 XP_047279706.1:p.Val480= XP_047279706.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X29 XP_047279713.1:p.Val480= XP_047279713.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X30 XP_047279714.1:p.Val480= XP_047279714.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X36 XP_047279720.1:p.Val480= XP_047279720.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X37 XP_047279721.1:p.Val480= XP_047279721.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X17 XP_047279702.1:p.Val480= XP_047279702.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X46 XP_047279731.1:p.Val265= XP_047279731.1:p.Val265=
serine/threonine-protein kinase WNK2 isoform X31 XP_047279715.1:p.Val480= XP_047279715.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X32 XP_047279716.1:p.Val480= XP_047279716.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X8 XP_047279697.1:p.Val480= XP_047279697.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X35 XP_047279719.1:p.Val480= XP_047279719.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X16 XP_047279701.1:p.Val480= XP_047279701.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X18 XP_047279703.1:p.Val480= XP_047279703.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X40 XP_047279725.1:p.Val480= XP_047279725.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X22 XP_047279707.1:p.Val480= XP_047279707.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X23 XP_047279708.1:p.Val480= XP_047279708.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X24 XP_047279709.1:p.Val480= XP_047279709.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X27 XP_047279710.1:p.Val480= XP_047279710.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X28 XP_047279712.1:p.Val480= XP_047279712.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X33 XP_047279717.1:p.Val480= XP_047279717.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X34 XP_047279718.1:p.Val480= XP_047279718.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X38 XP_047279723.1:p.Val480= XP_047279723.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X39 XP_047279724.1:p.Val480= XP_047279724.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X41 XP_047279726.1:p.Val480= XP_047279726.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X42 XP_047279727.1:p.Val480= XP_047279727.1:p.Val480=
serine/threonine-protein kinase WNK2 isoform X43 XP_047279728.1:p.Val265= XP_047279728.1:p.Val265=
serine/threonine-protein kinase WNK2 isoform X47 XP_047279732.1:p.Val265= XP_047279732.1:p.Val265=
serine/threonine-protein kinase WNK2 isoform X44 XP_047279729.1:p.Val265= XP_047279729.1:p.Val265=
serine/threonine-protein kinase WNK2 isoform X45 XP_047279730.1:p.Val265= XP_047279730.1:p.Val265=
serine/threonine-protein kinase WNK2 isoform X49 XP_047279735.1:p.Val265= XP_047279735.1:p.Val265=
serine/threonine-protein kinase WNK2 isoform X48 XP_047279734.1:p.Val265= XP_047279734.1:p.Val265=
Help

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#.

1 SubSNP submission
No Submitter Submission ID Date (Build)
1 GNOMAD ss2737711735 Nov 08, 2017 (151)
Help

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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss2737711735 NC_000009.11:96002155:G:A NC_000009.12:93239873:G:A (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1328679985

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top 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.

Software version is: 2.0.1.post761+d5e8e07