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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1491345215

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr13:110253633-110253641 (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
ins(TACA)2CGTATAATTATATGTGTATGTAT …

ins(TACA)2CGTATAATTATATGTGTATGTAT / insTACATATACGTATAATTATATGTGTATGTAT / insTACATATACGTATAATTATATGTGT(ATGT)2ATTACATATACGTATAATTATATGTGTATGTAT / insTACATATACGTATAATTATGTGTATGTAT / insTACATATACTTATAATTATATGTGTATGTAT / insTACATATACTTATAATTATATGTGT(ATGT)2ATTACATATACGTATAATTATATGTGTATGTAT / insTACATATACTTATAATTATGTGTATGTAT

Variation Type
Indel Insertion and Deletion
Frequency
insTACATATACGTATAATTATATGTGTATGTAT=0.00468 (77/16466, 8.3KJPN)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
COL4A1 : Intron Variant
LOC124903212 : Intron 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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
8.3KJPN JAPANESE Study-wide 16466 -

No frequency provided

 insTACATATACGTATAATTATATGTGTATGTAT=0.00468
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 13 NC_000013.11:g.110253633_110253641TGTA[2]TTACATACACGTATAATTATATGTGTATGTAT[1]
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACGTATAATTATATGTGTATGTAT[1]
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641TGTATGTATTACATATACGTATAATTATATGTGTA[2]TGTAT[1]
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACGTATAATTATGTGTATGTAT[1]
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACTTATAATTATATGTGTATGTAT[1]
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACTTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATGTGTATGTAT[1]
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACTTATAATTATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTA[2]TTACATACACGTATAATTATATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACGTATAATTATATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTATGTATTACATATACGTATAATTATATGTGTA[2]TGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACGTATAATTATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACTTATAATTATATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACTTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACTTATAATTATGTGTATGTAT[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATACGTGTATGTAATACATACA[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATACGTATATGTAATACATACA[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATACATACACATATAATTATACGTATATGTAATAC[2]ATACA[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATAC[2]ACATAATTATACGTATATGTAATACATACA[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATAAGTATATGTAATACATACA[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATACGTATATGTAATACATACATACACATATAATTATAAGTATATGTAATACATACA[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517ATAC[2]ACATAATTATAAGTATATGTAATACATACA[1]
Gene: COL4A1, collagen type IV alpha 1 chain (minus strand)
Molecule type Change Amino acid[Codon] SO Term
COL4A1 transcript variant 2 NM_001303110.2:c.85-10899…

NM_001303110.2:c.85-10899_85-10898insATACATACACATATAATTATACGTGTATGTA

 		N/A Intron Variant
COL4A1 transcript variant 1 NM_001845.6:c.85-10899_85…

NM_001845.6:c.85-10899_85-10898insATACATACACATATAATTATACGTGTATGTA

 		N/A Intron Variant
Gene: LOC124903212, uncharacterized LOC124903212 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC124903212 transcript XR_007063872.1:n. N/A Intron 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 (TGTA)2T= ins(TACA)2CGTATAATTATATGTGTATGTAT insTACATATACGTATAATTATATGTGTATGTAT insTACATATACGTATAATTATATGTGT(ATGT)2ATTACATATACGTATAATTATATGTGTATGTAT insTACATATACGTATAATTATGTGTATGTAT insTACATATACTTATAATTATATGTGTATGTAT insTACATATACTTATAATTATATGTGT(ATGT)2ATTACATATACGTATAATTATATGTGTATGTAT insTACATATACTTATAATTATGTGTATGTAT
GRCh38.p14 chr 13 NC_000013.11:g.110253633_110253641= NC_000013.11:g.110253633_110253641TGTA[2]TTACATACACGTATAATTATATGTGTATGTAT[1] NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACGTATAATTATATGTGTATGTAT[1] NC_000013.11:g.110253633_110253641TGTATGTATTACATATACGTATAATTATATGTGTA[2]TGTAT[1] NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACGTATAATTATGTGTATGTAT[1] NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACTTATAATTATATGTGTATGTAT[1] NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACTTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATGTGTATGTAT[1] NC_000013.11:g.110253633_110253641TGTA[2]TTACATATACTTATAATTATGTGTATGTAT[1]
GRCh37.p13 chr 13 NC_000013.10:g.110905980_110905988= NC_000013.10:g.110905980_110905988TGTA[2]TTACATACACGTATAATTATATGTGTATGTAT[1] NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACGTATAATTATATGTGTATGTAT[1] NC_000013.10:g.110905980_110905988TGTATGTATTACATATACGTATAATTATATGTGTA[2]TGTAT[1] NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACGTATAATTATGTGTATGTAT[1] NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACTTATAATTATATGTGTATGTAT[1] NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACTTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATGTGTATGTAT[1] NC_000013.10:g.110905980_110905988TGTA[2]TTACATATACTTATAATTATGTGTATGTAT[1]
COL4A1 RefSeqGene (LRG_1116) NG_011544.2:g.58509_58517= NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATACGTGTATGTAATACATACA[1] NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATACGTATATGTAATACATACA[1] NG_011544.2:g.58509_58517ATACATACACATATAATTATACGTATATGTAATAC[2]ATACA[1] NG_011544.2:g.58509_58517ATAC[2]ACATAATTATACGTATATGTAATACATACA[1] NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATAAGTATATGTAATACATACA[1] NG_011544.2:g.58509_58517ATAC[2]ACATATAATTATACGTATATGTAATACATACATACACATATAATTATAAGTATATGTAATACATACA[1] NG_011544.2:g.58509_58517ATAC[2]ACATAATTATAAGTATATGTAATACATACA[1]
COL4A1 transcript variant 2 NM_001303110.2:c.85-10899= NM_001303110.2:c.85-10899_85-10898insATACATACACATATAATTATACGTGTATGTA NM_001303110.2:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTA NM_001303110.2:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTAATACATACATACACATATAATTATACGTATATGTA NM_001303110.2:c.85-10899_85-10898insATACATACACATAATTATACGTATATGTA NM_001303110.2:c.85-10899_85-10898insATACATACACATATAATTATAAGTATATGTA NM_001303110.2:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTAATACATACATACACATATAATTATAAGTATATGTA NM_001303110.2:c.85-10899_85-10898insATACATACACATAATTATAAGTATATGTA
COL4A1 transcript NM_001845.4:c.85-10899= NM_001845.4:c.85-10899_85-10898insATACATACACATATAATTATACGTGTATGTA NM_001845.4:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTA NM_001845.4:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTAATACATACATACACATATAATTATACGTATATGTA NM_001845.4:c.85-10899_85-10898insATACATACACATAATTATACGTATATGTA NM_001845.4:c.85-10899_85-10898insATACATACACATATAATTATAAGTATATGTA NM_001845.4:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTAATACATACATACACATATAATTATAAGTATATGTA NM_001845.4:c.85-10899_85-10898insATACATACACATAATTATAAGTATATGTA
COL4A1 transcript variant 1 NM_001845.6:c.85-10899= NM_001845.6:c.85-10899_85-10898insATACATACACATATAATTATACGTGTATGTA NM_001845.6:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTA NM_001845.6:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTAATACATACATACACATATAATTATACGTATATGTA NM_001845.6:c.85-10899_85-10898insATACATACACATAATTATACGTATATGTA NM_001845.6:c.85-10899_85-10898insATACATACACATATAATTATAAGTATATGTA NM_001845.6:c.85-10899_85-10898insATACATACACATATAATTATACGTATATGTAATACATACATACACATATAATTATAAGTATATGTA NM_001845.6:c.85-10899_85-10898insATACATACACATAATTATAAGTATATGTA
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#.

14 SubSNP, 12 Frequency submissions
No Submitter Submission ID Date (Build)
1 SWEGEN ss3011720158 Jan 10, 2018 (151)
2 SWEGEN ss3011720159 Jan 10, 2018 (151)
3 ACPOP ss3740137196 Jul 13, 2019 (153)
4 ACPOP ss3740137197 Jul 13, 2019 (153)
5 PACBIO ss3787584735 Jul 13, 2019 (153)
6 GNOMAD ss4273350008 Apr 26, 2021 (155)
7 GNOMAD ss4273350009 Apr 26, 2021 (155)
8 GNOMAD ss4273350010 Apr 26, 2021 (155)
9 GNOMAD ss4273350011 Apr 26, 2021 (155)
10 GNOMAD ss4273350012 Apr 26, 2021 (155)
11 TOMMO_GENOMICS ss5211916163 Apr 26, 2021 (155)
12 HUGCELL_USP ss5489441476 Oct 16, 2022 (156)
13 TOMMO_GENOMICS ss5764318136 Oct 16, 2022 (156)
14 TOMMO_GENOMICS ss5764318137 Oct 16, 2022 (156)
15 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
16 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
17 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
18 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
19 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
20 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
21 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 443221472 (NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG 1/122138)
Row 443221473 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 6524/121920)
Row 443221474 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG 1/122138)...

- Apr 26, 2021 (155)
22 Northern Sweden

Submission ignored due to conflicting rows:
Row 13422061 (NC_000013.10:110905979::TGTATGTATTACATATACGTATAATTATATG 50/590)
Row 13422062 (NC_000013.10:110905979::TGTATGTATTACATATACTTATAATTATATG 7/590)

- Jul 13, 2019 (153)
23 Northern Sweden

Submission ignored due to conflicting rows:
Row 13422061 (NC_000013.10:110905979::TGTATGTATTACATATACGTATAATTATATG 50/590)
Row 13422062 (NC_000013.10:110905979::TGTATGTATTACATATACTTATAATTATATG 7/590)

- Jul 13, 2019 (153)
24 8.3KJPN NC_000013.10 - 110905980 Apr 26, 2021 (155)
25 14KJPN

Submission ignored due to conflicting rows:
Row 98155240 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 122/27736)
Row 98155241 (NC_000013.11:110253632::TGTATGTATTACATATACTTATAATTATATG 1/27736)

- Oct 16, 2022 (156)
26 14KJPN

Submission ignored due to conflicting rows:
Row 98155240 (NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG 122/27736)
Row 98155241 (NC_000013.11:110253632::TGTATGTATTACATATACTTATAATTATATG 1/27736)

- 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
ss4273350008 NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATACACGTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATACACGTATAATTATATGTGTATGTAT

 (self)
69885470, ss3011720158, ss3740137196, ss3787584735, ss5211916163 NC_000013.10:110905979::TGTATGTATT…

NC_000013.10:110905979::TGTATGTATTACATATACGTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACGTATAATTATATGTGTATGTAT

 (self)
ss4273350009, ss5489441476, ss5764318136 NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACGTATAATTATATGTGTATGTAT

 (self)
NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACGTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATGTGTATGTAT

 (self)
ss4273350010 NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATATACGTATAATTATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACGTATAATTATGTGTATGTAT

 (self)
ss3011720159, ss3740137197 NC_000013.10:110905979::TGTATGTATT…

NC_000013.10:110905979::TGTATGTATTACATATACTTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACTTATAATTATATGTGTATGTAT

 (self)
ss4273350011, ss5764318137 NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATATACTTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACTTATAATTATATGTGTATGTAT

 (self)
NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATATACTTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACTTATAATTATATGTGTATGTATGTATTACATATACGTATAATTATATGTGTATGTAT

 (self)
ss4273350012 NC_000013.11:110253632::TGTATGTATT…

NC_000013.11:110253632::TGTATGTATTACATATACTTATAATTATG

 NC_000013.11:110253632:TGTATGTAT:T…

NC_000013.11:110253632:TGTATGTAT:TGTATGTATTACATATACTTATAATTATGTGTATGTAT

 (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 rs1491345215

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.post820+afb47a3d