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.
rs199628606
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr2:241195795 (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>A / C>G / C>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
A=0.000000 (0/163104, ALFA)T=0.000000 (0/163104, ALFA)T=0.00015 (12/78698, PAGE_STUDY) (+ 4 more)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- ANO7 : Missense 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.
Release Version: 20230706150541
| Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|
| Total | Global | 163226 | C=1.000000 | A=0.000000, T=0.000000 |
| European | Sub | 146882 | C=1.000000 | A=0.000000, T=0.000000 |
| African | Sub | 3868 | C=1.0000 | A=0.0000, T=0.0000 |
| African Others | Sub | 168 | C=1.000 | A=0.000, T=0.000 |
| African American | Sub | 3700 | C=1.0000 | A=0.0000, T=0.0000 |
| Asian | Sub | 3304 | C=1.0000 | A=0.0000, T=0.0000 |
| East Asian | Sub | 2652 | C=1.0000 | A=0.0000, T=0.0000 |
| Other Asian | Sub | 652 | C=1.000 | A=0.000, T=0.000 |
| Latin American 1 | Sub | 442 | C=1.000 | A=0.000, T=0.000 |
| Latin American 2 | Sub | 950 | C=1.000 | A=0.000, T=0.000 |
| South Asian | Sub | 274 | C=1.000 | A=0.000, T=0.000 |
| Other | Sub | 7506 | C=1.0000 | A=0.0000, T=0.0000 |
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").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| Allele Frequency Aggregator | Total | Global | 163104 | C=1.000000 | A=0.000000, T=0.000000 |
| Allele Frequency Aggregator | European | Sub | 146778 | C=1.000000 | A=0.000000, T=0.000000 |
| Allele Frequency Aggregator | Other | Sub | 7502 | C=1.0000 | A=0.0000, T=0.0000 |
| Allele Frequency Aggregator | African | Sub | 3854 | C=1.0000 | A=0.0000, T=0.0000 |
| Allele Frequency Aggregator | Asian | Sub | 3304 | C=1.0000 | A=0.0000, T=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 950 | C=1.000 | A=0.000, T=0.000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 442 | C=1.000 | A=0.000, T=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 274 | C=1.000 | A=0.000, T=0.000 |
| The PAGE Study | Global | Study-wide | 78698 | C=0.99985 | T=0.00015 |
| The PAGE Study | AfricanAmerican | Sub | 32516 | C=0.99972 | T=0.00028 |
| The PAGE Study | Mexican | Sub | 10810 | C=1.00000 | T=0.00000 |
| The PAGE Study | Asian | Sub | 8316 | C=1.0000 | T=0.0000 |
| The PAGE Study | PuertoRican | Sub | 7916 | C=1.0000 | T=0.0000 |
| The PAGE Study | NativeHawaiian | Sub | 4534 | C=1.0000 | T=0.0000 |
| The PAGE Study | Cuban | Sub | 4230 | C=0.9993 | T=0.0007 |
| The PAGE Study | Dominican | Sub | 3828 | C=1.0000 | T=0.0000 |
| The PAGE Study | CentralAmerican | Sub | 2450 | C=1.0000 | T=0.0000 |
| The PAGE Study | SouthAmerican | Sub | 1982 | C=1.0000 | T=0.0000 |
| The PAGE Study | NativeAmerican | Sub | 1260 | C=1.0000 | T=0.0000 |
| The PAGE Study | SouthAsian | Sub | 856 | C=1.000 | T=0.000 |
| 14KJPN | JAPANESE | Study-wide | 28256 | C=0.99996 | T=0.00004 |
| GO Exome Sequencing Project | Global | Study-wide | 13006 | C=0.99985 | T=0.00015 |
| GO Exome Sequencing Project | European American | Sub | 8600 | C=1.0000 | T=0.0000 |
| GO Exome Sequencing Project | African American | Sub | 4406 | C=0.9995 | T=0.0005 |
| 1000Genomes_30x | Global | Study-wide | 6404 | C=0.9997 | T=0.0003 |
| 1000Genomes_30x | African | Sub | 1786 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | Europe | Sub | 1266 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | South Asian | Sub | 1202 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | East Asian | Sub | 1170 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | American | Sub | 980 | C=0.998 | T=0.002 |
| 1000Genomes | Global | Study-wide | 5008 | C=0.9998 | T=0.0002 |
| 1000Genomes | African | Sub | 1322 | C=1.0000 | T=0.0000 |
| 1000Genomes | East Asian | Sub | 1008 | C=1.0000 | T=0.0000 |
| 1000Genomes | Europe | Sub | 1006 | C=1.0000 | T=0.0000 |
| 1000Genomes | South Asian | Sub | 978 | C=1.000 | T=0.000 |
| 1000Genomes | American | Sub | 694 | C=0.999 | T=0.001 |
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 2 | NC_000002.12:g.241195795C>A |
| GRCh38.p14 chr 2 | NC_000002.12:g.241195795C>G |
| GRCh38.p14 chr 2 | NC_000002.12:g.241195795C>T |
| GRCh37.p13 chr 2 | NC_000002.11:g.242135210C>A |
| GRCh37.p13 chr 2 | NC_000002.11:g.242135210C>G |
| GRCh37.p13 chr 2 | NC_000002.11:g.242135210C>T |
| ANO7 RefSeqGene | NG_029845.2:g.12287C>A |
| ANO7 RefSeqGene | NG_029845.2:g.12287C>G |
| ANO7 RefSeqGene | NG_029845.2:g.12287C>T |
Gene: ANO7, anoctamin 7
(plus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| ANO7 transcript variant 2 | NM_001001666.4:c.256C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform 2 | NP_001001666.2:p.Arg86= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant 2 | NM_001001666.4:c.256C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform 2 | NP_001001666.2:p.Arg86Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant 2 | NM_001001666.4:c.256C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform 2 | NP_001001666.2:p.Arg86Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant 1 | NM_001370694.2:c.259C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform 1 | NP_001357623.1:p.Arg87= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant 1 | NM_001370694.2:c.259C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform 1 | NP_001357623.1:p.Arg87Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant 1 | NM_001370694.2:c.259C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform 1 | NP_001357623.1:p.Arg87Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X1 | XM_047444596.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X1 | XP_047300552.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X1 | XM_047444596.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X1 | XP_047300552.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X1 | XM_047444596.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X1 | XP_047300552.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X2 | XM_047444597.1:c.301C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X2 | XP_047300553.1:p.Arg101= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X2 | XM_047444597.1:c.301C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X2 | XP_047300553.1:p.Arg101Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X2 | XM_047444597.1:c.301C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X2 | XP_047300553.1:p.Arg101Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X3 | XM_047444598.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X3 | XP_047300554.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X3 | XM_047444598.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X3 | XP_047300554.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X3 | XM_047444598.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X3 | XP_047300554.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X4 | XM_047444599.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X4 | XP_047300555.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X4 | XM_047444599.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X4 | XP_047300555.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X4 | XM_047444599.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X4 | XP_047300555.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X5 | XM_047444600.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X5 | XP_047300556.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X5 | XM_047444600.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X5 | XP_047300556.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X5 | XM_047444600.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X5 | XP_047300556.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X6 | XM_047444601.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X6 | XP_047300557.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X6 | XM_047444601.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X6 | XP_047300557.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X6 | XM_047444601.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X6 | XP_047300557.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X7 | XM_047444602.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X7 | XP_047300558.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X7 | XM_047444602.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X7 | XP_047300558.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X7 | XM_047444602.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X7 | XP_047300558.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X8 | XM_011511263.3:c.301C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X8 | XP_011509565.2:p.Arg101= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X8 | XM_011511263.3:c.301C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X8 | XP_011509565.2:p.Arg101Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X8 | XM_011511263.3:c.301C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X8 | XP_011509565.2:p.Arg101Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X9 | XM_047444603.1:c.301C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X9 | XP_047300559.1:p.Arg101= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X9 | XM_047444603.1:c.301C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X9 | XP_047300559.1:p.Arg101Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X9 | XM_047444603.1:c.301C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X9 | XP_047300559.1:p.Arg101Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X10 | XM_047444604.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X10 | XP_047300560.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X10 | XM_047444604.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X10 | XP_047300560.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X10 | XM_047444604.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X10 | XP_047300560.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X11 | XM_047444606.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X11 | XP_047300562.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X11 | XM_047444606.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X11 | XP_047300562.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X11 | XM_047444606.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X11 | XP_047300562.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X12 | XM_011511267.3:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X12 | XP_011509569.2:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X12 | XM_011511267.3:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X12 | XP_011509569.2:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X12 | XM_011511267.3:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X12 | XP_011509569.2:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X13 | XM_047444607.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X13 | XP_047300563.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X13 | XM_047444607.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X13 | XP_047300563.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X13 | XM_047444607.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X13 | XP_047300563.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X14 | XM_047444608.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X14 | XP_047300564.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X14 | XM_047444608.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X14 | XP_047300564.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X14 | XM_047444608.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X14 | XP_047300564.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X15 | XM_047444609.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X15 | XP_047300565.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X15 | XM_047444609.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X15 | XP_047300565.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X15 | XM_047444609.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X15 | XP_047300565.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X16 | XM_047444610.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X15 | XP_047300566.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X16 | XM_047444610.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X15 | XP_047300566.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X16 | XM_047444610.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X15 | XP_047300566.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X17 | XM_047444611.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X16 | XP_047300567.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X17 | XM_047444611.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X16 | XP_047300567.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X17 | XM_047444611.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X16 | XP_047300567.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X18 | XM_017004229.2:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X17 | XP_016859718.2:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X18 | XM_017004229.2:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X17 | XP_016859718.2:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X18 | XM_017004229.2:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X17 | XP_016859718.2:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X19 | XM_017004230.2:c.16C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X18 | XP_016859719.1:p.Arg6= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X19 | XM_017004230.2:c.16C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X18 | XP_016859719.1:p.Arg6Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X19 | XM_017004230.2:c.16C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X18 | XP_016859719.1:p.Arg6Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X20 | XM_047444612.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X19 | XP_047300568.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X20 | XM_047444612.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X19 | XP_047300568.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X20 | XM_047444612.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X19 | XP_047300568.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X23 | XM_047444613.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X20 | XP_047300569.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X23 | XM_047444613.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X20 | XP_047300569.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X23 | XM_047444613.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X20 | XP_047300569.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X24 | XM_047444614.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X21 | XP_047300570.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X24 | XM_047444614.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X21 | XP_047300570.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X24 | XM_047444614.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X21 | XP_047300570.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X25 | XM_047444615.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X22 | XP_047300571.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X25 | XM_047444615.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X22 | XP_047300571.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X25 | XM_047444615.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X22 | XP_047300571.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X26 | XM_047444616.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X23 | XP_047300572.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X26 | XM_047444616.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X23 | XP_047300572.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X26 | XM_047444616.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X23 | XP_047300572.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X27 | XM_047444617.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X24 | XP_047300573.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X27 | XM_047444617.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X24 | XP_047300573.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X27 | XM_047444617.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X24 | XP_047300573.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X28 | XM_047444618.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X25 | XP_047300574.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X28 | XM_047444618.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X25 | XP_047300574.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X28 | XM_047444618.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X25 | XP_047300574.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X29 | XM_047444619.1:c.304C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| anoctamin-7 isoform X26 | XP_047300575.1:p.Arg102= | R (Arg) > R (Arg) | Synonymous Variant |
| ANO7 transcript variant X29 | XM_047444619.1:c.304C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| anoctamin-7 isoform X26 | XP_047300575.1:p.Arg102Gly | R (Arg) > G (Gly) | Missense Variant |
| ANO7 transcript variant X29 | XM_047444619.1:c.304C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| anoctamin-7 isoform X26 | XP_047300575.1:p.Arg102Trp | R (Arg) > W (Trp) | Missense Variant |
| ANO7 transcript variant X21 | XR_007076376.1:n.356C>A | N/A | Non Coding Transcript Variant |
| ANO7 transcript variant X21 | XR_007076376.1:n.356C>G | N/A | Non Coding Transcript Variant |
| ANO7 transcript variant X21 | XR_007076376.1:n.356C>T | N/A | Non Coding Transcript Variant |
| ANO7 transcript variant X22 | XR_007076377.1:n.356C>A | N/A | Non Coding Transcript Variant |
| ANO7 transcript variant X22 | XR_007076377.1:n.356C>G | N/A | Non Coding Transcript Variant |
| ANO7 transcript variant X22 | XR_007076377.1:n.356C>T | N/A | Non Coding Transcript 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 | C= | A | G | T |
|---|---|---|---|---|
| GRCh38.p14 chr 2 | NC_000002.12:g.241195795= | NC_000002.12:g.241195795C>A | NC_000002.12:g.241195795C>G | NC_000002.12:g.241195795C>T |
| GRCh37.p13 chr 2 | NC_000002.11:g.242135210= | NC_000002.11:g.242135210C>A | NC_000002.11:g.242135210C>G | NC_000002.11:g.242135210C>T |
| ANO7 RefSeqGene | NG_029845.2:g.12287= | NG_029845.2:g.12287C>A | NG_029845.2:g.12287C>G | NG_029845.2:g.12287C>T |
| ANO7 transcript variant 2 | NM_001001666.4:c.256= | NM_001001666.4:c.256C>A | NM_001001666.4:c.256C>G | NM_001001666.4:c.256C>T |
| ANO7 transcript variant NGEP-S | NM_001001666.3:c.418= | NM_001001666.3:c.418C>A | NM_001001666.3:c.418C>G | NM_001001666.3:c.418C>T |
| ANO7 transcript variant 1 | NM_001370694.2:c.259= | NM_001370694.2:c.259C>A | NM_001370694.2:c.259C>G | NM_001370694.2:c.259C>T |
| ANO7 transcript variant 1 | NM_001370694.1:c.259= | NM_001370694.1:c.259C>A | NM_001370694.1:c.259C>G | NM_001370694.1:c.259C>T |
| ANO7 transcript variant NGEP-L | NM_001001891.3:c.421= | NM_001001891.3:c.421C>A | NM_001001891.3:c.421C>G | NM_001001891.3:c.421C>T |
| ANO7 transcript variant X8 | XM_011511263.3:c.301= | XM_011511263.3:c.301C>A | XM_011511263.3:c.301C>G | XM_011511263.3:c.301C>T |
| ANO7 transcript variant X1 | XM_011511263.2:c.418= | XM_011511263.2:c.418C>A | XM_011511263.2:c.418C>G | XM_011511263.2:c.418C>T |
| ANO7 transcript variant X8 | XM_011511263.1:c.418= | XM_011511263.1:c.418C>A | XM_011511263.1:c.418C>G | XM_011511263.1:c.418C>T |
| ANO7 transcript variant X12 | XM_011511267.3:c.304= | XM_011511267.3:c.304C>A | XM_011511267.3:c.304C>G | XM_011511267.3:c.304C>T |
| ANO7 transcript variant X2 | XM_011511267.2:c.421= | XM_011511267.2:c.421C>A | XM_011511267.2:c.421C>G | XM_011511267.2:c.421C>T |
| ANO7 transcript variant X13 | XM_011511267.1:c.421= | XM_011511267.1:c.421C>A | XM_011511267.1:c.421C>G | XM_011511267.1:c.421C>T |
| ANO7 transcript variant X19 | XM_017004230.2:c.16= | XM_017004230.2:c.16C>A | XM_017004230.2:c.16C>G | XM_017004230.2:c.16C>T |
| ANO7 transcript variant X4 | XM_017004230.1:c.16= | XM_017004230.1:c.16C>A | XM_017004230.1:c.16C>G | XM_017004230.1:c.16C>T |
| ANO7 transcript variant X18 | XM_017004229.2:c.304= | XM_017004229.2:c.304C>A | XM_017004229.2:c.304C>G | XM_017004229.2:c.304C>T |
| ANO7 transcript variant X3 | XM_017004229.1:c.421= | XM_017004229.1:c.421C>A | XM_017004229.1:c.421C>G | XM_017004229.1:c.421C>T |
| ANO7 transcript variant X4 | XM_047444599.1:c.304= | XM_047444599.1:c.304C>A | XM_047444599.1:c.304C>G | XM_047444599.1:c.304C>T |
| ANO7 transcript variant X9 | XM_047444603.1:c.301= | XM_047444603.1:c.301C>A | XM_047444603.1:c.301C>G | XM_047444603.1:c.301C>T |
| ANO7 transcript variant X1 | XM_047444596.1:c.304= | XM_047444596.1:c.304C>A | XM_047444596.1:c.304C>G | XM_047444596.1:c.304C>T |
| ANO7 transcript variant X2 | XM_047444597.1:c.301= | XM_047444597.1:c.301C>A | XM_047444597.1:c.301C>G | XM_047444597.1:c.301C>T |
| ANO7 transcript variant X3 | XM_047444598.1:c.304= | XM_047444598.1:c.304C>A | XM_047444598.1:c.304C>G | XM_047444598.1:c.304C>T |
| ANO7 transcript variant X5 | XM_047444600.1:c.304= | XM_047444600.1:c.304C>A | XM_047444600.1:c.304C>G | XM_047444600.1:c.304C>T |
| ANO7 transcript variant X6 | XM_047444601.1:c.304= | XM_047444601.1:c.304C>A | XM_047444601.1:c.304C>G | XM_047444601.1:c.304C>T |
| ANO7 transcript variant X7 | XM_047444602.1:c.304= | XM_047444602.1:c.304C>A | XM_047444602.1:c.304C>G | XM_047444602.1:c.304C>T |
| ANO7 transcript variant X10 | XM_047444604.1:c.304= | XM_047444604.1:c.304C>A | XM_047444604.1:c.304C>G | XM_047444604.1:c.304C>T |
| ANO7 transcript variant X11 | XM_047444606.1:c.304= | XM_047444606.1:c.304C>A | XM_047444606.1:c.304C>G | XM_047444606.1:c.304C>T |
| ANO7 transcript variant X15 | XM_047444609.1:c.304= | XM_047444609.1:c.304C>A | XM_047444609.1:c.304C>G | XM_047444609.1:c.304C>T |
| ANO7 transcript variant X13 | XM_047444607.1:c.304= | XM_047444607.1:c.304C>A | XM_047444607.1:c.304C>G | XM_047444607.1:c.304C>T |
| ANO7 transcript variant X16 | XM_047444610.1:c.304= | XM_047444610.1:c.304C>A | XM_047444610.1:c.304C>G | XM_047444610.1:c.304C>T |
| ANO7 transcript variant X20 | XM_047444612.1:c.304= | XM_047444612.1:c.304C>A | XM_047444612.1:c.304C>G | XM_047444612.1:c.304C>T |
| ANO7 transcript variant X17 | XM_047444611.1:c.304= | XM_047444611.1:c.304C>A | XM_047444611.1:c.304C>G | XM_047444611.1:c.304C>T |
| ANO7 transcript variant X14 | XM_047444608.1:c.304= | XM_047444608.1:c.304C>A | XM_047444608.1:c.304C>G | XM_047444608.1:c.304C>T |
| ANO7 transcript variant X21 | XR_007076376.1:n.356= | XR_007076376.1:n.356C>A | XR_007076376.1:n.356C>G | XR_007076376.1:n.356C>T |
| ANO7 transcript variant X22 | XR_007076377.1:n.356= | XR_007076377.1:n.356C>A | XR_007076377.1:n.356C>G | XR_007076377.1:n.356C>T |
| ANO7 transcript variant X24 | XM_047444614.1:c.304= | XM_047444614.1:c.304C>A | XM_047444614.1:c.304C>G | XM_047444614.1:c.304C>T |
| ANO7 transcript variant X23 | XM_047444613.1:c.304= | XM_047444613.1:c.304C>A | XM_047444613.1:c.304C>G | XM_047444613.1:c.304C>T |
| ANO7 transcript variant X25 | XM_047444615.1:c.304= | XM_047444615.1:c.304C>A | XM_047444615.1:c.304C>G | XM_047444615.1:c.304C>T |
| ANO7 transcript variant X26 | XM_047444616.1:c.304= | XM_047444616.1:c.304C>A | XM_047444616.1:c.304C>G | XM_047444616.1:c.304C>T |
| ANO7 transcript variant X27 | XM_047444617.1:c.304= | XM_047444617.1:c.304C>A | XM_047444617.1:c.304C>G | XM_047444617.1:c.304C>T |
| ANO7 transcript variant X28 | XM_047444618.1:c.304= | XM_047444618.1:c.304C>A | XM_047444618.1:c.304C>G | XM_047444618.1:c.304C>T |
| ANO7 transcript variant X29 | XM_047444619.1:c.304= | XM_047444619.1:c.304C>A | XM_047444619.1:c.304C>G | XM_047444619.1:c.304C>T |
| anoctamin-7 isoform 2 | NP_001001666.2:p.Arg86= | NP_001001666.2:p.Arg86= | NP_001001666.2:p.Arg86Gly | NP_001001666.2:p.Arg86Trp |
| anoctamin-7 isoform 1 | NP_001357623.1:p.Arg87= | NP_001357623.1:p.Arg87= | NP_001357623.1:p.Arg87Gly | NP_001357623.1:p.Arg87Trp |
| anoctamin-7 isoform X8 | XP_011509565.2:p.Arg101= | XP_011509565.2:p.Arg101= | XP_011509565.2:p.Arg101Gly | XP_011509565.2:p.Arg101Trp |
| anoctamin-7 isoform X12 | XP_011509569.2:p.Arg102= | XP_011509569.2:p.Arg102= | XP_011509569.2:p.Arg102Gly | XP_011509569.2:p.Arg102Trp |
| anoctamin-7 isoform X18 | XP_016859719.1:p.Arg6= | XP_016859719.1:p.Arg6= | XP_016859719.1:p.Arg6Gly | XP_016859719.1:p.Arg6Trp |
| anoctamin-7 isoform X17 | XP_016859718.2:p.Arg102= | XP_016859718.2:p.Arg102= | XP_016859718.2:p.Arg102Gly | XP_016859718.2:p.Arg102Trp |
| anoctamin-7 isoform X4 | XP_047300555.1:p.Arg102= | XP_047300555.1:p.Arg102= | XP_047300555.1:p.Arg102Gly | XP_047300555.1:p.Arg102Trp |
| anoctamin-7 isoform X9 | XP_047300559.1:p.Arg101= | XP_047300559.1:p.Arg101= | XP_047300559.1:p.Arg101Gly | XP_047300559.1:p.Arg101Trp |
| anoctamin-7 isoform X1 | XP_047300552.1:p.Arg102= | XP_047300552.1:p.Arg102= | XP_047300552.1:p.Arg102Gly | XP_047300552.1:p.Arg102Trp |
| anoctamin-7 isoform X2 | XP_047300553.1:p.Arg101= | XP_047300553.1:p.Arg101= | XP_047300553.1:p.Arg101Gly | XP_047300553.1:p.Arg101Trp |
| anoctamin-7 isoform X3 | XP_047300554.1:p.Arg102= | XP_047300554.1:p.Arg102= | XP_047300554.1:p.Arg102Gly | XP_047300554.1:p.Arg102Trp |
| anoctamin-7 isoform X5 | XP_047300556.1:p.Arg102= | XP_047300556.1:p.Arg102= | XP_047300556.1:p.Arg102Gly | XP_047300556.1:p.Arg102Trp |
| anoctamin-7 isoform X6 | XP_047300557.1:p.Arg102= | XP_047300557.1:p.Arg102= | XP_047300557.1:p.Arg102Gly | XP_047300557.1:p.Arg102Trp |
| anoctamin-7 isoform X7 | XP_047300558.1:p.Arg102= | XP_047300558.1:p.Arg102= | XP_047300558.1:p.Arg102Gly | XP_047300558.1:p.Arg102Trp |
| anoctamin-7 isoform X10 | XP_047300560.1:p.Arg102= | XP_047300560.1:p.Arg102= | XP_047300560.1:p.Arg102Gly | XP_047300560.1:p.Arg102Trp |
| anoctamin-7 isoform X11 | XP_047300562.1:p.Arg102= | XP_047300562.1:p.Arg102= | XP_047300562.1:p.Arg102Gly | XP_047300562.1:p.Arg102Trp |
| anoctamin-7 isoform X15 | XP_047300565.1:p.Arg102= | XP_047300565.1:p.Arg102= | XP_047300565.1:p.Arg102Gly | XP_047300565.1:p.Arg102Trp |
| anoctamin-7 isoform X13 | XP_047300563.1:p.Arg102= | XP_047300563.1:p.Arg102= | XP_047300563.1:p.Arg102Gly | XP_047300563.1:p.Arg102Trp |
| anoctamin-7 isoform X15 | XP_047300566.1:p.Arg102= | XP_047300566.1:p.Arg102= | XP_047300566.1:p.Arg102Gly | XP_047300566.1:p.Arg102Trp |
| anoctamin-7 isoform X19 | XP_047300568.1:p.Arg102= | XP_047300568.1:p.Arg102= | XP_047300568.1:p.Arg102Gly | XP_047300568.1:p.Arg102Trp |
| anoctamin-7 isoform X16 | XP_047300567.1:p.Arg102= | XP_047300567.1:p.Arg102= | XP_047300567.1:p.Arg102Gly | XP_047300567.1:p.Arg102Trp |
| anoctamin-7 isoform X14 | XP_047300564.1:p.Arg102= | XP_047300564.1:p.Arg102= | XP_047300564.1:p.Arg102Gly | XP_047300564.1:p.Arg102Trp |
| anoctamin-7 isoform X21 | XP_047300570.1:p.Arg102= | XP_047300570.1:p.Arg102= | XP_047300570.1:p.Arg102Gly | XP_047300570.1:p.Arg102Trp |
| anoctamin-7 isoform X20 | XP_047300569.1:p.Arg102= | XP_047300569.1:p.Arg102= | XP_047300569.1:p.Arg102Gly | XP_047300569.1:p.Arg102Trp |
| anoctamin-7 isoform X22 | XP_047300571.1:p.Arg102= | XP_047300571.1:p.Arg102= | XP_047300571.1:p.Arg102Gly | XP_047300571.1:p.Arg102Trp |
| anoctamin-7 isoform X23 | XP_047300572.1:p.Arg102= | XP_047300572.1:p.Arg102= | XP_047300572.1:p.Arg102Gly | XP_047300572.1:p.Arg102Trp |
| anoctamin-7 isoform X24 | XP_047300573.1:p.Arg102= | XP_047300573.1:p.Arg102= | XP_047300573.1:p.Arg102Gly | XP_047300573.1:p.Arg102Trp |
| anoctamin-7 isoform X25 | XP_047300574.1:p.Arg102= | XP_047300574.1:p.Arg102= | XP_047300574.1:p.Arg102Gly | XP_047300574.1:p.Arg102Trp |
| anoctamin-7 isoform X26 | XP_047300575.1:p.Arg102= | XP_047300575.1:p.Arg102= | XP_047300575.1:p.Arg102Gly | XP_047300575.1:p.Arg102Trp |
| anoctamin-7 isoform NGEP-short | NP_001001666.1:p.Arg140= | NP_001001666.1:p.Arg140= | NP_001001666.1:p.Arg140Gly | NP_001001666.1:p.Arg140Trp |
| anoctamin-7 isoform NGEP-long | NP_001001891.2:p.Arg141= | NP_001001891.2:p.Arg141= | NP_001001891.2:p.Arg141Gly | NP_001001891.2:p.Arg141Trp |
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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#.
35 SubSNP,
15 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | 1000GENOMES | ss488744903 | May 04, 2012 (137) |
| 2 | EXOME_CHIP | ss491334576 | May 04, 2012 (137) |
| 3 | NHLBI-ESP | ss712495337 | Apr 25, 2013 (138) |
| 4 | ILLUMINA | ss780812671 | Sep 08, 2015 (146) |
| 5 | ILLUMINA | ss783494665 | Sep 08, 2015 (146) |
| 6 | 1000GENOMES | ss1302377646 | Aug 21, 2014 (142) |
| 7 | EVA_EXAC | ss1686832333 | Apr 01, 2015 (144) |
| 8 | EVA_EXAC | ss1686832334 | Apr 01, 2015 (144) |
| 9 | ILLUMINA | ss1752348692 | Sep 08, 2015 (146) |
| 10 | ILLUMINA | ss1917762419 | Feb 12, 2016 (147) |
| 11 | ILLUMINA | ss1946071953 | Feb 12, 2016 (147) |
| 12 | ILLUMINA | ss1958525923 | Feb 12, 2016 (147) |
| 13 | GNOMAD | ss2733484710 | Nov 08, 2017 (151) |
| 14 | GNOMAD | ss2746928542 | Nov 08, 2017 (151) |
| 15 | GNOMAD | ss2788370550 | Nov 08, 2017 (151) |
| 16 | AFFY | ss2985206259 | Nov 08, 2017 (151) |
| 17 | ILLUMINA | ss3628329337 | Oct 11, 2018 (152) |
| 18 | ILLUMINA | ss3634821475 | Oct 11, 2018 (152) |
| 19 | ILLUMINA | ss3640528773 | Oct 11, 2018 (152) |
| 20 | ILLUMINA | ss3644774651 | Oct 11, 2018 (152) |
| 21 | ILLUMINA | ss3653974421 | Oct 11, 2018 (152) |
| 22 | ILLUMINA | ss3744489851 | Jul 13, 2019 (153) |
| 23 | ILLUMINA | ss3745121373 | Jul 13, 2019 (153) |
| 24 | PAGE_CC | ss3771002210 | Jul 13, 2019 (153) |
| 25 | ILLUMINA | ss3772617700 | Jul 13, 2019 (153) |
| 26 | EVA | ss3823876112 | Apr 25, 2020 (154) |
| 27 | TOPMED | ss4550767954 | Apr 27, 2021 (155) |
| 28 | TOPMED | ss4550767955 | Apr 27, 2021 (155) |
| 29 | 1000G_HIGH_COVERAGE | ss5252676988 | Oct 17, 2022 (156) |
| 30 | EVA | ss5337218853 | Oct 17, 2022 (156) |
| 31 | 1000G_HIGH_COVERAGE | ss5530330045 | Oct 17, 2022 (156) |
| 32 | TOMMO_GENOMICS | ss5688464410 | Oct 17, 2022 (156) |
| 33 | EVA | ss5847910873 | Oct 17, 2022 (156) |
| 34 | EVA | ss5935449070 | Oct 17, 2022 (156) |
| 35 | EVA | ss5957591811 | Oct 17, 2022 (156) |
| 36 | 1000Genomes | NC_000002.11 - 242135210 | Oct 11, 2018 (152) |
| 37 | 1000Genomes_30x | NC_000002.12 - 241195795 | Oct 17, 2022 (156) |
| 38 |
ExAC
Submission ignored due to conflicting rows: |
- | Oct 11, 2018 (152) |
| 39 |
ExAC
Submission ignored due to conflicting rows: |
- | Oct 11, 2018 (152) |
| 40 |
gnomAD - Genomes
Submission ignored due to conflicting rows: |
- | Apr 27, 2021 (155) |
| 41 |
gnomAD - Genomes
Submission ignored due to conflicting rows: |
- | Apr 27, 2021 (155) |
| 42 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 43 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 44 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 45 | GO Exome Sequencing Project | NC_000002.11 - 242135210 | Oct 11, 2018 (152) |
| 46 | The PAGE Study | NC_000002.12 - 241195795 | Jul 13, 2019 (153) |
| 47 | 14KJPN | NC_000002.12 - 241195795 | Oct 17, 2022 (156) |
| 48 |
TopMed
Submission ignored due to conflicting rows: |
- | Apr 27, 2021 (155) |
| 49 |
TopMed
Submission ignored due to conflicting rows: |
- | Apr 27, 2021 (155) |
| 50 | ALFA | NC_000002.12 - 241195795 | Apr 27, 2021 (155) |
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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 |
|---|---|---|---|
| ss2733484710 | NC_000002.11:242135209:C:A | NC_000002.12:241195794:C:A | (self) |
| 3759796111, ss4550767954 | NC_000002.12:241195794:C:A | NC_000002.12:241195794:C:A | (self) |
| ss1686832334, ss2733484710 | NC_000002.11:242135209:C:G | NC_000002.12:241195794:C:G | (self) |
| 13508785, 334504, ss488744903, ss491334576, ss712495337, ss780812671, ss783494665, ss1302377646, ss1686832333, ss1752348692, ss1917762419, ss1946071953, ss1958525923, ss2733484710, ss2746928542, ss2788370550, ss2985206259, ss3628329337, ss3634821475, ss3640528773, ss3644774651, ss3653974421, ss3744489851, ss3745121373, ss3772617700, ss3823876112, ss5337218853, ss5847910873, ss5957591811 | NC_000002.11:242135209:C:T | NC_000002.12:241195794:C:T | (self) |
| 17855980, 223679, 22301514, 3759796111, ss3771002210, ss4550767955, ss5252676988, ss5530330045, ss5688464410, ss5935449070 | NC_000002.12:241195794:C:T | NC_000002.12:241195794:C:T | (self) |
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs199628606
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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
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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.