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.
rs181121175
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr12:88087887 (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 / G>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
A=0.000291 (77/264690, TOPMED)A=0.000407 (68/166910, ALFA)A=0.00011 (9/78700, PAGE_STUDY) (+ 14 more)
- Clinical Significance
- Reported in ClinVar
- Gene : Consequence
- CEP290 : 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 | 183290 | G=0.999591 | A=0.000409, T=0.000000 |
| European | Sub | 155356 | G=0.999588 | A=0.000412, T=0.000000 |
| African | Sub | 9156 | G=0.9999 | A=0.0001, T=0.0000 |
| African Others | Sub | 352 | G=1.000 | A=0.000, T=0.000 |
| African American | Sub | 8804 | G=0.9999 | A=0.0001, T=0.0000 |
| Asian | Sub | 6294 | G=0.9990 | A=0.0010, T=0.0000 |
| East Asian | Sub | 4476 | G=0.9991 | A=0.0009, T=0.0000 |
| Other Asian | Sub | 1818 | G=0.9989 | A=0.0011, T=0.0000 |
| Latin American 1 | Sub | 442 | G=1.000 | A=0.000, T=0.000 |
| Latin American 2 | Sub | 950 | G=1.000 | A=0.000, T=0.000 |
| South Asian | Sub | 280 | G=1.000 | A=0.000, T=0.000 |
| Other | Sub | 10812 | G=0.99963 | A=0.00037, T=0.00000 |
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 |
|---|---|---|---|---|---|
| TopMed | Global | Study-wide | 264690 | G=0.999709 | A=0.000291 |
| Allele Frequency Aggregator | Total | Global | 166910 | G=0.999593 | A=0.000407, T=0.000000 |
| Allele Frequency Aggregator | European | Sub | 145224 | G=0.999601 | A=0.000399, T=0.000000 |
| Allele Frequency Aggregator | Other | Sub | 9380 | G=0.9996 | A=0.0004, T=0.0000 |
| Allele Frequency Aggregator | Asian | Sub | 6294 | G=0.9990 | A=0.0010, T=0.0000 |
| Allele Frequency Aggregator | African | Sub | 4340 | G=1.0000 | A=0.0000, T=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 950 | G=1.000 | A=0.000, T=0.000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 442 | G=1.000 | A=0.000, T=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 280 | G=1.000 | A=0.000, T=0.000 |
| The PAGE Study | Global | Study-wide | 78700 | G=0.99989 | A=0.00011 |
| The PAGE Study | AfricanAmerican | Sub | 32516 | G=0.99988 | A=0.00012 |
| The PAGE Study | Mexican | Sub | 10810 | G=1.00000 | A=0.00000 |
| The PAGE Study | Asian | Sub | 8318 | G=0.9995 | A=0.0005 |
| The PAGE Study | PuertoRican | Sub | 7916 | G=1.0000 | A=0.0000 |
| The PAGE Study | NativeHawaiian | Sub | 4534 | G=1.0000 | A=0.0000 |
| The PAGE Study | Cuban | Sub | 4230 | G=0.9998 | A=0.0002 |
| The PAGE Study | Dominican | Sub | 3828 | G=1.0000 | A=0.0000 |
| The PAGE Study | CentralAmerican | Sub | 2450 | G=1.0000 | A=0.0000 |
| The PAGE Study | SouthAmerican | Sub | 1982 | G=1.0000 | A=0.0000 |
| The PAGE Study | NativeAmerican | Sub | 1260 | G=1.0000 | A=0.0000 |
| The PAGE Study | SouthAsian | Sub | 856 | G=1.000 | A=0.000 |
| 14KJPN | JAPANESE | Study-wide | 28258 | G=0.99979 | A=0.00021 |
| 8.3KJPN | JAPANESE | Study-wide | 16760 | G=0.99982 | A=0.00018 |
| GO Exome Sequencing Project | Global | Study-wide | 11460 | G=0.99983 | A=0.00017 |
| GO Exome Sequencing Project | European American | Sub | 7956 | G=0.9997 | A=0.0003 |
| GO Exome Sequencing Project | African American | Sub | 3504 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | Global | Study-wide | 6404 | G=0.9994 | A=0.0006 |
| 1000Genomes_30x | African | Sub | 1786 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | Europe | Sub | 1266 | G=0.9968 | A=0.0032 |
| 1000Genomes_30x | South Asian | Sub | 1202 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | East Asian | Sub | 1170 | G=1.0000 | A=0.0000 |
| 1000Genomes_30x | American | Sub | 980 | G=1.000 | A=0.000 |
| 1000Genomes | Global | Study-wide | 5008 | G=0.9992 | A=0.0008 |
| 1000Genomes | African | Sub | 1322 | G=1.0000 | A=0.0000 |
| 1000Genomes | East Asian | Sub | 1008 | G=1.0000 | A=0.0000 |
| 1000Genomes | Europe | Sub | 1006 | G=0.9960 | A=0.0040 |
| 1000Genomes | South Asian | Sub | 978 | G=1.000 | A=0.000 |
| 1000Genomes | American | Sub | 694 | G=1.000 | A=0.000 |
| Genetic variation in the Estonian population | Estonian | Study-wide | 4480 | G=0.9984 | A=0.0016 |
| The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | G=0.9997 | A=0.0003 |
| UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | G=0.9997 | A=0.0003 |
| KOREAN population from KRGDB | KOREAN | Study-wide | 2922 | G=0.9997 | A=0.0003 |
| Northern Sweden | ACPOP | Study-wide | 600 | G=0.990 | A=0.010 |
| SGDP_PRJ | Global | Study-wide | 2 | G=0.5 | A=0.5 |
| Siberian | Global | Study-wide | 2 | G=0.5 | A=0.5 |
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 12 | NC_000012.12:g.88087887G>A |
| GRCh38.p14 chr 12 | NC_000012.12:g.88087887G>T |
| GRCh37.p13 chr 12 | NC_000012.11:g.88481664G>A |
| GRCh37.p13 chr 12 | NC_000012.11:g.88481664G>T |
| CEP290 RefSeqGene (LRG_694) | NG_008417.2:g.59330C>T |
| CEP290 RefSeqGene (LRG_694) | NG_008417.2:g.59330C>A |
Gene: CEP290, centrosomal protein 290
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| CEP290 transcript | NM_025114.4:c.4087C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa | NP_079390.3:p.Arg1363Trp | R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript | NM_025114.4:c.4087C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa | NP_079390.3:p.Arg1363= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X1 | XM_011538756.4:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X1 |
XP_011537058.1:p.Arg1650T… XP_011537058.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X1 | XM_011538756.4:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X1 | XP_011537058.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X2 | XM_011538757.4:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X1 |
XP_011537059.1:p.Arg1650T… XP_011537059.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X2 | XM_011538757.4:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X1 | XP_011537059.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X3 | XM_011538758.4:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X2 |
XP_011537060.1:p.Arg1650T… XP_011537060.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X3 | XM_011538758.4:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X2 | XP_011537060.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X4 | XM_011538759.3:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X3 |
XP_011537061.1:p.Arg1650T… XP_011537061.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X4 | XM_011538759.3:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X3 | XP_011537061.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X5 | XM_011538760.3:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X4 |
XP_011537062.1:p.Arg1650T… XP_011537062.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X5 | XM_011538760.3:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X4 | XP_011537062.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X6 | XM_017019980.3:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X5 |
XP_016875469.1:p.Arg1650T… XP_016875469.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X6 | XM_017019980.3:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X5 | XP_016875469.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X7 | XM_011538761.3:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X6 |
XP_011537063.1:p.Arg1650T… XP_011537063.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X7 | XM_011538761.3:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X6 | XP_011537063.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X8 | XM_017019981.3:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X7 |
XP_016875470.1:p.Arg1650T… XP_016875470.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X8 | XM_017019981.3:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X7 | XP_016875470.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X9 | XM_017019982.2:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X8 |
XP_016875471.1:p.Arg1650T… XP_016875471.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X9 | XM_017019982.2:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X8 | XP_016875471.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X10 | XM_047429558.1:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X9 |
XP_047285514.1:p.Arg1650T… XP_047285514.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X10 | XM_047429558.1:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X9 | XP_047285514.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X11 | XM_047429559.1:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X10 |
XP_047285515.1:p.Arg1650T… XP_047285515.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X11 | XM_047429559.1:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X10 | XP_047285515.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X12 | XM_011538762.4:c.4180C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X11 |
XP_011537064.1:p.Arg1394T… XP_011537064.1:p.Arg1394Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X12 | XM_011538762.4:c.4180C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X11 | XP_011537064.1:p.Arg1394= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X13 | XM_047429560.1:c.4180C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X11 |
XP_047285516.1:p.Arg1394T… XP_047285516.1:p.Arg1394Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X13 | XM_047429560.1:c.4180C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X11 | XP_047285516.1:p.Arg1394= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X14 | XM_047429561.1:c.4180C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X12 |
XP_047285517.1:p.Arg1394T… XP_047285517.1:p.Arg1394Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X14 | XM_047429561.1:c.4180C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X12 | XP_047285517.1:p.Arg1394= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X15 | XM_011538763.4:c.4087C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X13 |
XP_011537065.1:p.Arg1363T… XP_011537065.1:p.Arg1363Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X15 | XM_011538763.4:c.4087C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X13 | XP_011537065.1:p.Arg1363= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X16 | XM_047429562.1:c.4087C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X13 |
XP_047285518.1:p.Arg1363T… XP_047285518.1:p.Arg1363Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X16 | XM_047429562.1:c.4087C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X13 | XP_047285518.1:p.Arg1363= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X17 | XM_017019983.3:c.4066C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X14 |
XP_016875472.1:p.Arg1356T… XP_016875472.1:p.Arg1356Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X17 | XM_017019983.3:c.4066C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X14 | XP_016875472.1:p.Arg1356= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X18 | XM_047429563.1:c.4087C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X15 |
XP_047285519.1:p.Arg1363T… XP_047285519.1:p.Arg1363Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X18 | XM_047429563.1:c.4087C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X15 | XP_047285519.1:p.Arg1363= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X19 | XM_011538764.4:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X16 |
XP_011537066.1:p.Arg1650T… XP_011537066.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X19 | XM_011538764.4:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X16 | XP_011537066.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X20 | XM_011538765.4:c.4948C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X17 |
XP_011537067.1:p.Arg1650T… XP_011537067.1:p.Arg1650Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X20 | XM_011538765.4:c.4948C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X17 | XP_011537067.1:p.Arg1650= | R (Arg) > R (Arg) | Synonymous Variant |
| CEP290 transcript variant X21 | XM_011538766.4:c.3409C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X18 |
XP_011537068.1:p.Arg1137T… XP_011537068.1:p.Arg1137Trp |
R (Arg) > W (Trp) | Missense Variant |
| CEP290 transcript variant X21 | XM_011538766.4:c.3409C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| centrosomal protein of 290 kDa isoform X18 | XP_011537068.1:p.Arg1137= | R (Arg) > R (Arg) | 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.
Allele: A (allele ID:
318585
)
| ClinVar Accession | Disease Names | Clinical Significance |
|---|---|---|
| RCV000288370.3 | Joubert syndrome 5 | Uncertain-Significance |
| RCV000291084.3 | Bardet-Biedl syndrome 14 | Uncertain-Significance |
| RCV000345714.3 | Meckel syndrome, type 4 | Uncertain-Significance |
| RCV000389733.3 | Senior-Loken syndrome 6 | Uncertain-Significance |
| RCV000400374.3 | Leber congenital amaurosis 10 | Uncertain-Significance |
| RCV000548918.12 | not provided | Uncertain-Significance |
| RCV001085312.5 | Joubert syndrome,Meckel-Gruber syndrome,Nephronophthisis | Benign |
| RCV001273074.1 | Leber congenital amaurosis | Uncertain-Significance |
Allele: T (allele ID:
1079709
)
| ClinVar Accession | Disease Names | Clinical Significance |
|---|---|---|
| RCV001414879.4 | Joubert syndrome,Meckel-Gruber syndrome,Nephronophthisis | Likely-Benign |
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 | T |
|---|---|---|---|
| GRCh38.p14 chr 12 | NC_000012.12:g.88087887= | NC_000012.12:g.88087887G>A | NC_000012.12:g.88087887G>T |
| GRCh37.p13 chr 12 | NC_000012.11:g.88481664= | NC_000012.11:g.88481664G>A | NC_000012.11:g.88481664G>T |
| CEP290 RefSeqGene (LRG_694) | NG_008417.2:g.59330= | NG_008417.2:g.59330C>T | NG_008417.2:g.59330C>A |
| CEP290 transcript | NM_025114.4:c.4087= | NM_025114.4:c.4087C>T | NM_025114.4:c.4087C>A |
| CEP290 transcript | NM_025114.3:c.4087= | NM_025114.3:c.4087C>T | NM_025114.3:c.4087C>A |
| CEP290 transcript variant X1 | XM_011538756.4:c.4948= | XM_011538756.4:c.4948C>T | XM_011538756.4:c.4948C>A |
| CEP290 transcript variant X1 | XM_011538756.3:c.4948= | XM_011538756.3:c.4948C>T | XM_011538756.3:c.4948C>A |
| CEP290 transcript variant X1 | XM_011538756.2:c.4948= | XM_011538756.2:c.4948C>T | XM_011538756.2:c.4948C>A |
| CEP290 transcript variant X1 | XM_011538756.1:c.4948= | XM_011538756.1:c.4948C>T | XM_011538756.1:c.4948C>A |
| CEP290 transcript variant X3 | XM_011538758.4:c.4948= | XM_011538758.4:c.4948C>T | XM_011538758.4:c.4948C>A |
| CEP290 transcript variant X3 | XM_011538758.3:c.4948= | XM_011538758.3:c.4948C>T | XM_011538758.3:c.4948C>A |
| CEP290 transcript variant X3 | XM_011538758.2:c.4948= | XM_011538758.2:c.4948C>T | XM_011538758.2:c.4948C>A |
| CEP290 transcript variant X3 | XM_011538758.1:c.4948= | XM_011538758.1:c.4948C>T | XM_011538758.1:c.4948C>A |
| CEP290 transcript variant X2 | XM_011538757.4:c.4948= | XM_011538757.4:c.4948C>T | XM_011538757.4:c.4948C>A |
| CEP290 transcript variant X2 | XM_011538757.3:c.4948= | XM_011538757.3:c.4948C>T | XM_011538757.3:c.4948C>A |
| CEP290 transcript variant X2 | XM_011538757.2:c.4948= | XM_011538757.2:c.4948C>T | XM_011538757.2:c.4948C>A |
| CEP290 transcript variant X2 | XM_011538757.1:c.4948= | XM_011538757.1:c.4948C>T | XM_011538757.1:c.4948C>A |
| CEP290 transcript variant X12 | XM_011538762.4:c.4180= | XM_011538762.4:c.4180C>T | XM_011538762.4:c.4180C>A |
| CEP290 transcript variant X12 | XM_011538762.3:c.4180= | XM_011538762.3:c.4180C>T | XM_011538762.3:c.4180C>A |
| CEP290 transcript variant X12 | XM_011538762.2:c.4180= | XM_011538762.2:c.4180C>T | XM_011538762.2:c.4180C>A |
| CEP290 transcript variant X7 | XM_011538762.1:c.4180= | XM_011538762.1:c.4180C>T | XM_011538762.1:c.4180C>A |
| CEP290 transcript variant X15 | XM_011538763.4:c.4087= | XM_011538763.4:c.4087C>T | XM_011538763.4:c.4087C>A |
| CEP290 transcript variant X13 | XM_011538763.3:c.4087= | XM_011538763.3:c.4087C>T | XM_011538763.3:c.4087C>A |
| CEP290 transcript variant X13 | XM_011538763.2:c.4087= | XM_011538763.2:c.4087C>T | XM_011538763.2:c.4087C>A |
| CEP290 transcript variant X8 | XM_011538763.1:c.4087= | XM_011538763.1:c.4087C>T | XM_011538763.1:c.4087C>A |
| CEP290 transcript variant X19 | XM_011538764.4:c.4948= | XM_011538764.4:c.4948C>T | XM_011538764.4:c.4948C>A |
| CEP290 transcript variant X15 | XM_011538764.3:c.4948= | XM_011538764.3:c.4948C>T | XM_011538764.3:c.4948C>A |
| CEP290 transcript variant X15 | XM_011538764.2:c.4948= | XM_011538764.2:c.4948C>T | XM_011538764.2:c.4948C>A |
| CEP290 transcript variant X9 | XM_011538764.1:c.4948= | XM_011538764.1:c.4948C>T | XM_011538764.1:c.4948C>A |
| CEP290 transcript variant X20 | XM_011538765.4:c.4948= | XM_011538765.4:c.4948C>T | XM_011538765.4:c.4948C>A |
| CEP290 transcript variant X16 | XM_011538765.3:c.4948= | XM_011538765.3:c.4948C>T | XM_011538765.3:c.4948C>A |
| CEP290 transcript variant X16 | XM_011538765.2:c.4948= | XM_011538765.2:c.4948C>T | XM_011538765.2:c.4948C>A |
| CEP290 transcript variant X10 | XM_011538765.1:c.4948= | XM_011538765.1:c.4948C>T | XM_011538765.1:c.4948C>A |
| CEP290 transcript variant X21 | XM_011538766.4:c.3409= | XM_011538766.4:c.3409C>T | XM_011538766.4:c.3409C>A |
| CEP290 transcript variant X17 | XM_011538766.3:c.3409= | XM_011538766.3:c.3409C>T | XM_011538766.3:c.3409C>A |
| CEP290 transcript variant X17 | XM_011538766.2:c.3409= | XM_011538766.2:c.3409C>T | XM_011538766.2:c.3409C>A |
| CEP290 transcript variant X11 | XM_011538766.1:c.3409= | XM_011538766.1:c.3409C>T | XM_011538766.1:c.3409C>A |
| CEP290 transcript variant X4 | XM_011538759.3:c.4948= | XM_011538759.3:c.4948C>T | XM_011538759.3:c.4948C>A |
| CEP290 transcript variant X4 | XM_011538759.2:c.4948= | XM_011538759.2:c.4948C>T | XM_011538759.2:c.4948C>A |
| CEP290 transcript variant X4 | XM_011538759.1:c.4948= | XM_011538759.1:c.4948C>T | XM_011538759.1:c.4948C>A |
| CEP290 transcript variant X5 | XM_011538760.3:c.4948= | XM_011538760.3:c.4948C>T | XM_011538760.3:c.4948C>A |
| CEP290 transcript variant X5 | XM_011538760.2:c.4948= | XM_011538760.2:c.4948C>T | XM_011538760.2:c.4948C>A |
| CEP290 transcript variant X5 | XM_011538760.1:c.4948= | XM_011538760.1:c.4948C>T | XM_011538760.1:c.4948C>A |
| CEP290 transcript variant X6 | XM_017019980.3:c.4948= | XM_017019980.3:c.4948C>T | XM_017019980.3:c.4948C>A |
| CEP290 transcript variant X6 | XM_017019980.2:c.4948= | XM_017019980.2:c.4948C>T | XM_017019980.2:c.4948C>A |
| CEP290 transcript variant X6 | XM_017019980.1:c.4948= | XM_017019980.1:c.4948C>T | XM_017019980.1:c.4948C>A |
| CEP290 transcript variant X7 | XM_011538761.3:c.4948= | XM_011538761.3:c.4948C>T | XM_011538761.3:c.4948C>A |
| CEP290 transcript variant X7 | XM_011538761.2:c.4948= | XM_011538761.2:c.4948C>T | XM_011538761.2:c.4948C>A |
| CEP290 transcript variant X7 | XM_011538761.1:c.4948= | XM_011538761.1:c.4948C>T | XM_011538761.1:c.4948C>A |
| CEP290 transcript variant X8 | XM_017019981.3:c.4948= | XM_017019981.3:c.4948C>T | XM_017019981.3:c.4948C>A |
| CEP290 transcript variant X8 | XM_017019981.2:c.4948= | XM_017019981.2:c.4948C>T | XM_017019981.2:c.4948C>A |
| CEP290 transcript variant X8 | XM_017019981.1:c.4948= | XM_017019981.1:c.4948C>T | XM_017019981.1:c.4948C>A |
| CEP290 transcript variant X17 | XM_017019983.3:c.4066= | XM_017019983.3:c.4066C>T | XM_017019983.3:c.4066C>A |
| CEP290 transcript variant X14 | XM_017019983.2:c.4066= | XM_017019983.2:c.4066C>T | XM_017019983.2:c.4066C>A |
| CEP290 transcript variant X14 | XM_017019983.1:c.4066= | XM_017019983.1:c.4066C>T | XM_017019983.1:c.4066C>A |
| CEP290 transcript variant X9 | XM_017019982.2:c.4948= | XM_017019982.2:c.4948C>T | XM_017019982.2:c.4948C>A |
| CEP290 transcript variant X9 | XM_017019982.1:c.4948= | XM_017019982.1:c.4948C>T | XM_017019982.1:c.4948C>A |
| CEP290 transcript variant X10 | XM_047429558.1:c.4948= | XM_047429558.1:c.4948C>T | XM_047429558.1:c.4948C>A |
| CEP290 transcript variant X14 | XM_047429561.1:c.4180= | XM_047429561.1:c.4180C>T | XM_047429561.1:c.4180C>A |
| CEP290 transcript variant X11 | XM_047429559.1:c.4948= | XM_047429559.1:c.4948C>T | XM_047429559.1:c.4948C>A |
| CEP290 transcript variant X13 | XM_047429560.1:c.4180= | XM_047429560.1:c.4180C>T | XM_047429560.1:c.4180C>A |
| CEP290 transcript variant X16 | XM_047429562.1:c.4087= | XM_047429562.1:c.4087C>T | XM_047429562.1:c.4087C>A |
| CEP290 transcript variant X18 | XM_047429563.1:c.4087= | XM_047429563.1:c.4087C>T | XM_047429563.1:c.4087C>A |
| KIAA0373 transcript | NM_014684.1:c.1267= | NM_014684.1:c.1267C>T | NM_014684.1:c.1267C>A |
| centrosomal protein of 290 kDa | NP_079390.3:p.Arg1363= | NP_079390.3:p.Arg1363Trp | NP_079390.3:p.Arg1363= |
| centrosomal protein of 290 kDa isoform X1 | XP_011537058.1:p.Arg1650= | XP_011537058.1:p.Arg1650Trp | XP_011537058.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X2 | XP_011537060.1:p.Arg1650= | XP_011537060.1:p.Arg1650Trp | XP_011537060.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X1 | XP_011537059.1:p.Arg1650= | XP_011537059.1:p.Arg1650Trp | XP_011537059.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X11 | XP_011537064.1:p.Arg1394= | XP_011537064.1:p.Arg1394Trp | XP_011537064.1:p.Arg1394= |
| centrosomal protein of 290 kDa isoform X13 | XP_011537065.1:p.Arg1363= | XP_011537065.1:p.Arg1363Trp | XP_011537065.1:p.Arg1363= |
| centrosomal protein of 290 kDa isoform X16 | XP_011537066.1:p.Arg1650= | XP_011537066.1:p.Arg1650Trp | XP_011537066.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X17 | XP_011537067.1:p.Arg1650= | XP_011537067.1:p.Arg1650Trp | XP_011537067.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X18 | XP_011537068.1:p.Arg1137= | XP_011537068.1:p.Arg1137Trp | XP_011537068.1:p.Arg1137= |
| centrosomal protein of 290 kDa isoform X3 | XP_011537061.1:p.Arg1650= | XP_011537061.1:p.Arg1650Trp | XP_011537061.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X4 | XP_011537062.1:p.Arg1650= | XP_011537062.1:p.Arg1650Trp | XP_011537062.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X5 | XP_016875469.1:p.Arg1650= | XP_016875469.1:p.Arg1650Trp | XP_016875469.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X6 | XP_011537063.1:p.Arg1650= | XP_011537063.1:p.Arg1650Trp | XP_011537063.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X7 | XP_016875470.1:p.Arg1650= | XP_016875470.1:p.Arg1650Trp | XP_016875470.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X14 | XP_016875472.1:p.Arg1356= | XP_016875472.1:p.Arg1356Trp | XP_016875472.1:p.Arg1356= |
| centrosomal protein of 290 kDa isoform X8 | XP_016875471.1:p.Arg1650= | XP_016875471.1:p.Arg1650Trp | XP_016875471.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X9 | XP_047285514.1:p.Arg1650= | XP_047285514.1:p.Arg1650Trp | XP_047285514.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X12 | XP_047285517.1:p.Arg1394= | XP_047285517.1:p.Arg1394Trp | XP_047285517.1:p.Arg1394= |
| centrosomal protein of 290 kDa isoform X10 | XP_047285515.1:p.Arg1650= | XP_047285515.1:p.Arg1650Trp | XP_047285515.1:p.Arg1650= |
| centrosomal protein of 290 kDa isoform X11 | XP_047285516.1:p.Arg1394= | XP_047285516.1:p.Arg1394Trp | XP_047285516.1:p.Arg1394= |
| centrosomal protein of 290 kDa isoform X13 | XP_047285518.1:p.Arg1363= | XP_047285518.1:p.Arg1363Trp | XP_047285518.1:p.Arg1363= |
| centrosomal protein of 290 kDa isoform X15 | XP_047285519.1:p.Arg1363= | XP_047285519.1:p.Arg1363Trp | XP_047285519.1:p.Arg1363= |
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#.
49 SubSNP,
21 Frequency,
9 ClinVar
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | 1000GENOMES | ss463026090 | Sep 17, 2011 (135) |
| 2 | EXOME_CHIP | ss491471686 | May 04, 2012 (137) |
| 3 | NHLBI-ESP | ss713109383 | Apr 25, 2013 (138) |
| 4 | ILLUMINA | ss780691094 | Sep 08, 2015 (146) |
| 5 | ILLUMINA | ss783364844 | Sep 08, 2015 (146) |
| 6 | 1000GENOMES | ss1346018528 | Aug 21, 2014 (142) |
| 7 | EVA_UK10K_ALSPAC | ss1629107912 | Apr 01, 2015 (144) |
| 8 | EVA_DECODE | ss1641894223 | Apr 01, 2015 (144) |
| 9 | EVA_UK10K_TWINSUK | ss1672101945 | Apr 01, 2015 (144) |
| 10 | EVA_EXAC | ss1691038648 | Apr 01, 2015 (144) |
| 11 | EVA_EXAC | ss1691038649 | Apr 01, 2015 (144) |
| 12 | ILLUMINA | ss1752084730 | Sep 08, 2015 (146) |
| 13 | ILLUMINA | ss1917877027 | Feb 12, 2016 (147) |
| 14 | ILLUMINA | ss1946345501 | Feb 12, 2016 (147) |
| 15 | ILLUMINA | ss1959453691 | Feb 12, 2016 (147) |
| 16 | USC_VALOUEV | ss2155673434 | Dec 20, 2016 (150) |
| 17 | HUMAN_LONGEVITY | ss2191883971 | Dec 20, 2016 (150) |
| 18 | GNOMAD | ss2740022492 | Nov 08, 2017 (151) |
| 19 | GNOMAD | ss2748927666 | Nov 08, 2017 (151) |
| 20 | GNOMAD | ss2913407381 | Nov 08, 2017 (151) |
| 21 | SWEGEN | ss3010097536 | Nov 08, 2017 (151) |
| 22 | ILLUMINA | ss3021451606 | Nov 08, 2017 (151) |
| 23 | ILLUMINA | ss3626931687 | Oct 12, 2018 (152) |
| 24 | ILLUMINA | ss3634515985 | Oct 12, 2018 (152) |
| 25 | ILLUMINA | ss3640223318 | Oct 12, 2018 (152) |
| 26 | ILLUMINA | ss3644598500 | Oct 12, 2018 (152) |
| 27 | ILLUMINA | ss3651832694 | Oct 12, 2018 (152) |
| 28 | EGCUT_WGS | ss3677382456 | Jul 13, 2019 (153) |
| 29 | EVA_DECODE | ss3694156291 | Jul 13, 2019 (153) |
| 30 | ILLUMINA | ss3725343940 | Jul 13, 2019 (153) |
| 31 | ACPOP | ss3739243712 | Jul 13, 2019 (153) |
| 32 | ILLUMINA | ss3744399126 | Jul 13, 2019 (153) |
| 33 | ILLUMINA | ss3744816784 | Jul 13, 2019 (153) |
| 34 | PAGE_CC | ss3771706540 | Jul 13, 2019 (153) |
| 35 | ILLUMINA | ss3772316042 | Jul 13, 2019 (153) |
| 36 | EVA | ss3824755966 | Apr 27, 2020 (154) |
| 37 | SGDP_PRJ | ss3878794295 | Apr 27, 2020 (154) |
| 38 | KRGDB | ss3927490738 | Apr 27, 2020 (154) |
| 39 | TOPMED | ss4927298144 | Apr 26, 2021 (155) |
| 40 | TOMMO_GENOMICS | ss5207459445 | Apr 26, 2021 (155) |
| 41 | 1000G_HIGH_COVERAGE | ss5291690603 | Oct 16, 2022 (156) |
| 42 | EVA | ss5407235581 | Oct 16, 2022 (156) |
| 43 | 1000G_HIGH_COVERAGE | ss5589649524 | Oct 16, 2022 (156) |
| 44 | SANFORD_IMAGENETICS | ss5653654602 | Oct 16, 2022 (156) |
| 45 | TOMMO_GENOMICS | ss5757578124 | Oct 16, 2022 (156) |
| 46 | EVA | ss5847678062 | Oct 16, 2022 (156) |
| 47 | EVA | ss5905391665 | Oct 16, 2022 (156) |
| 48 | EVA | ss5945037159 | Oct 16, 2022 (156) |
| 49 | EVA | ss5979398670 | Oct 16, 2022 (156) |
| 50 | 1000Genomes | NC_000012.11 - 88481664 | Oct 12, 2018 (152) |
| 51 | 1000Genomes_30x | NC_000012.12 - 88087887 | Oct 16, 2022 (156) |
| 52 | The Avon Longitudinal Study of Parents and Children | NC_000012.11 - 88481664 | Oct 12, 2018 (152) |
| 53 | Genetic variation in the Estonian population | NC_000012.11 - 88481664 | Oct 12, 2018 (152) |
| 54 |
ExAC
Submission ignored due to conflicting rows: |
- | Oct 12, 2018 (152) |
| 55 |
ExAC
Submission ignored due to conflicting rows: |
- | Oct 12, 2018 (152) |
| 56 |
gnomAD - Genomes
Submission ignored due to conflicting rows: |
- | Apr 26, 2021 (155) |
| 57 |
gnomAD - Genomes
Submission ignored due to conflicting rows: |
- | Apr 26, 2021 (155) |
| 58 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 59 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 60 | GO Exome Sequencing Project | NC_000012.11 - 88481664 | Oct 12, 2018 (152) |
| 61 | KOREAN population from KRGDB | NC_000012.11 - 88481664 | Apr 27, 2020 (154) |
| 62 | Northern Sweden | NC_000012.11 - 88481664 | Jul 13, 2019 (153) |
| 63 | The PAGE Study | NC_000012.12 - 88087887 | Jul 13, 2019 (153) |
| 64 | SGDP_PRJ | NC_000012.11 - 88481664 | Apr 27, 2020 (154) |
| 65 | Siberian | NC_000012.11 - 88481664 | Apr 27, 2020 (154) |
| 66 | 8.3KJPN | NC_000012.11 - 88481664 | Apr 26, 2021 (155) |
| 67 | 14KJPN | NC_000012.12 - 88087887 | Oct 16, 2022 (156) |
| 68 | TopMed | NC_000012.12 - 88087887 | Apr 26, 2021 (155) |
| 69 | UK 10K study - Twins | NC_000012.11 - 88481664 | Oct 12, 2018 (152) |
| 70 | ALFA | NC_000012.12 - 88087887 | Apr 26, 2021 (155) |
| 71 | ClinVar | RCV000288370.3 | Oct 16, 2022 (156) |
| 72 | ClinVar | RCV000291084.3 | Oct 16, 2022 (156) |
| 73 | ClinVar | RCV000345714.3 | Oct 16, 2022 (156) |
| 74 | ClinVar | RCV000389733.3 | Oct 16, 2022 (156) |
| 75 | ClinVar | RCV000400374.3 | Oct 16, 2022 (156) |
| 76 | ClinVar | RCV000548918.12 | Oct 16, 2022 (156) |
| 77 | ClinVar | RCV001085312.5 | Oct 16, 2022 (156) |
| 78 | ClinVar | RCV001273074.1 | Apr 26, 2021 (155) |
| 79 | ClinVar | RCV001414879.4 | Oct 16, 2022 (156) |
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 |
|---|---|---|---|
| ss1641894223 | NC_000012.10:87005794:G:A | NC_000012.12:88087886:G:A | (self) |
| 58805817, 32644224, 23120704, 1213419, 34668132, 12528577, 30811275, 8189788, 65428752, 32644224, ss463026090, ss491471686, ss713109383, ss780691094, ss783364844, ss1346018528, ss1629107912, ss1672101945, ss1691038648, ss1752084730, ss1917877027, ss1946345501, ss1959453691, ss2155673434, ss2740022492, ss2748927666, ss2913407381, ss3010097536, ss3021451606, ss3626931687, ss3634515985, ss3640223318, ss3644598500, ss3651832694, ss3677382456, ss3739243712, ss3744399126, ss3744816784, ss3772316042, ss3824755966, ss3878794295, ss3927490738, ss5207459445, ss5407235581, ss5653654602, ss5847678062, ss5945037159, ss5979398670 | NC_000012.11:88481663:G:A | NC_000012.12:88087886:G:A | (self) |
| RCV000288370.3, RCV000291084.3, RCV000345714.3, RCV000389733.3, RCV000400374.3, RCV000548918.12, RCV001085312.5, RCV001273074.1, 77175459, 928009, 91415228, 142843801, 2869811023, ss2191883971, ss3694156291, ss3725343940, ss3771706540, ss4927298144, ss5291690603, ss5589649524, ss5757578124, ss5905391665 | NC_000012.12:88087886:G:A | NC_000012.12:88087886:G:A | (self) |
| ss1691038649, ss2740022492, ss2748927666, ss2913407381 | NC_000012.11:88481663:G:T | NC_000012.12:88087886:G:T | (self) |
| RCV001414879.4, 2869811023 | NC_000012.12:88087886:G:T | NC_000012.12:88087886:G:T | (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 rs181121175
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.
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.