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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs201023701

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:82134-82154 (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
del(A)15 / del(A)12 / del(A)11 / d…

del(A)15 / del(A)12 / del(A)11 / del(A)10 / del(A)9 / del(A)8 / del(A)7 / del(A)6 / del(A)5 / del(A)4 / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)5 / dup(A)8 / dup(A)10 / dup(A)12 / dup(A)13

Variation Type
Indel Insertion and Deletion
Frequency
(A)21=0.0501 (251/5008, 1000G)
del(A)12=0.000 (0/232, ALFA)
del(A)11=0.000 (0/232, ALFA) (+ 10 more)
del(A)10=0.000 (0/232, ALFA)
del(A)9=0.000 (0/232, ALFA)
del(A)8=0.000 (0/232, ALFA)
del(A)6=0.000 (0/232, ALFA)
del(A)5=0.000 (0/232, ALFA)
del(A)4=0.000 (0/232, ALFA)
delAAA=0.000 (0/232, ALFA)
delAA=0.000 (0/232, ALFA)
delA=0.000 (0/232, ALFA)
dupA=0.000 (0/232, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 232 AAAAAAAAAAAAAAAAAAAAA=1.000 AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000
European Sub 82 AAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00
African Sub 128 AAAAAAAAAAAAAAAAAAAAA=1.000 AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000
African Others Sub 0 AAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0
African American Sub 128 AAAAAAAAAAAAAAAAAAAAA=1.000 AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000
Asian Sub 0 AAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0
East Asian Sub 0 AAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0
Other Asian Sub 0 AAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0
Latin American 1 Sub 6 AAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0
Latin American 2 Sub 2 AAAAAAAAAAAAAAAAAAAAA=1.0 AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0
South Asian Sub 0 AAAAAAAAAAAAAAAAAAAAA=0 AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0
Other Sub 14 AAAAAAAAAAAAAAAAAAAAA=1.00 AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00


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
1000Genomes Global Study-wide 5008 (A)21=0.0501 delAA=0.9499
1000Genomes African Sub 1322 (A)21=0.1581 delAA=0.8419
1000Genomes East Asian Sub 1008 (A)21=0.0179 delAA=0.9821
1000Genomes Europe Sub 1006 (A)21=0.0060 delAA=0.9940
1000Genomes South Asian Sub 978 (A)21=0.003 delAA=0.997
1000Genomes American Sub 694 (A)21=0.022 delAA=0.978
Allele Frequency Aggregator Total Global 232 (A)21=1.000 del(A)12=0.000, del(A)11=0.000, del(A)10=0.000, del(A)9=0.000, del(A)8=0.000, del(A)6=0.000, del(A)5=0.000, del(A)4=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator African Sub 128 (A)21=1.000 del(A)12=0.000, del(A)11=0.000, del(A)10=0.000, del(A)9=0.000, del(A)8=0.000, del(A)6=0.000, del(A)5=0.000, del(A)4=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator European Sub 82 (A)21=1.00 del(A)12=0.00, del(A)11=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator Other Sub 14 (A)21=1.00 del(A)12=0.00, del(A)11=0.00, del(A)10=0.00, del(A)9=0.00, del(A)8=0.00, del(A)6=0.00, del(A)5=0.00, del(A)4=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator Latin American 1 Sub 6 (A)21=1.0 del(A)12=0.0, del(A)11=0.0, del(A)10=0.0, del(A)9=0.0, del(A)8=0.0, del(A)6=0.0, del(A)5=0.0, del(A)4=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator Latin American 2 Sub 2 (A)21=1.0 del(A)12=0.0, del(A)11=0.0, del(A)10=0.0, del(A)9=0.0, del(A)8=0.0, del(A)6=0.0, del(A)5=0.0, del(A)4=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator South Asian Sub 0 (A)21=0 del(A)12=0, del(A)11=0, del(A)10=0, del(A)9=0, del(A)8=0, del(A)6=0, del(A)5=0, del(A)4=0, delAAA=0, delAA=0, delA=0, dupA=0
Allele Frequency Aggregator Asian Sub 0 (A)21=0 del(A)12=0, del(A)11=0, del(A)10=0, del(A)9=0, del(A)8=0, del(A)6=0, del(A)5=0, del(A)4=0, delAAA=0, delAA=0, delA=0, dupA=0
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 1 NC_000001.11:g.82140_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82143_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82144_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82145_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82146_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82147_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82148_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82149_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82150_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82151_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82152_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82153_82154del
GRCh38.p14 chr 1 NC_000001.11:g.82154del
GRCh38.p14 chr 1 NC_000001.11:g.82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82153_82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82152_82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82150_82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82147_82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82145_82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82143_82154dup
GRCh38.p14 chr 1 NC_000001.11:g.82142_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82140_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82143_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82144_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82145_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82146_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82147_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82148_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82149_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82150_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82151_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82152_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82153_82154del
GRCh37.p13 chr 1 NC_000001.10:g.82154del
GRCh37.p13 chr 1 NC_000001.10:g.82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82153_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82152_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82150_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82147_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82145_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82143_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82142_82154dup
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 (A)21= del(A)15 del(A)12 del(A)11 del(A)10 del(A)9 del(A)8 del(A)7 del(A)6 del(A)5 del(A)4 delAAA delAA delA dupA dupAA dupAAA dup(A)5 dup(A)8 dup(A)10 dup(A)12 dup(A)13
GRCh38.p14 chr 1 NC_000001.11:g.82134_82154= NC_000001.11:g.82140_82154del NC_000001.11:g.82143_82154del NC_000001.11:g.82144_82154del NC_000001.11:g.82145_82154del NC_000001.11:g.82146_82154del NC_000001.11:g.82147_82154del NC_000001.11:g.82148_82154del NC_000001.11:g.82149_82154del NC_000001.11:g.82150_82154del NC_000001.11:g.82151_82154del NC_000001.11:g.82152_82154del NC_000001.11:g.82153_82154del NC_000001.11:g.82154del NC_000001.11:g.82154dup NC_000001.11:g.82153_82154dup NC_000001.11:g.82152_82154dup NC_000001.11:g.82150_82154dup NC_000001.11:g.82147_82154dup NC_000001.11:g.82145_82154dup NC_000001.11:g.82143_82154dup NC_000001.11:g.82142_82154dup
GRCh37.p13 chr 1 NC_000001.10:g.82134_82154= NC_000001.10:g.82140_82154del NC_000001.10:g.82143_82154del NC_000001.10:g.82144_82154del NC_000001.10:g.82145_82154del NC_000001.10:g.82146_82154del NC_000001.10:g.82147_82154del NC_000001.10:g.82148_82154del NC_000001.10:g.82149_82154del NC_000001.10:g.82150_82154del NC_000001.10:g.82151_82154del NC_000001.10:g.82152_82154del NC_000001.10:g.82153_82154del NC_000001.10:g.82154del NC_000001.10:g.82154dup NC_000001.10:g.82153_82154dup NC_000001.10:g.82152_82154dup NC_000001.10:g.82150_82154dup NC_000001.10:g.82147_82154dup NC_000001.10:g.82145_82154dup NC_000001.10:g.82143_82154dup NC_000001.10:g.82142_82154dup
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#.

42 SubSNP, 29 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss5379928 Mar 15, 2016 (147)
2 GMI ss287939206 May 04, 2012 (137)
3 1000GENOMES ss1367645227 Aug 21, 2014 (142)
4 SWEGEN ss2986142392 Nov 08, 2017 (151)
5 MCHAISSO ss3063573412 Nov 08, 2017 (151)
6 MCHAISSO ss3065282389 Nov 08, 2017 (151)
7 MCHAISSO ss3065282390 Nov 08, 2017 (151)
8 EVA_DECODE ss3685990550 Jul 12, 2019 (153)
9 EVA_DECODE ss3685990551 Jul 12, 2019 (153)
10 EVA_DECODE ss3685990552 Jul 12, 2019 (153)
11 EVA_DECODE ss3685990553 Jul 12, 2019 (153)
12 KHV_HUMAN_GENOMES ss3798742544 Jul 12, 2019 (153)
13 GNOMAD ss3986893474 Apr 25, 2021 (155)
14 GNOMAD ss3986893475 Apr 25, 2021 (155)
15 GNOMAD ss3986893476 Apr 25, 2021 (155)
16 GNOMAD ss3986893477 Apr 25, 2021 (155)
17 GNOMAD ss3986893478 Apr 25, 2021 (155)
18 GNOMAD ss3986893479 Apr 25, 2021 (155)
19 GNOMAD ss3986893480 Apr 25, 2021 (155)
20 GNOMAD ss3986893481 Apr 25, 2021 (155)
21 GNOMAD ss3986893482 Apr 25, 2021 (155)
22 GNOMAD ss3986893483 Apr 25, 2021 (155)
23 GNOMAD ss3986893484 Apr 25, 2021 (155)
24 GNOMAD ss3986893485 Apr 25, 2021 (155)
25 GNOMAD ss3986893486 Apr 25, 2021 (155)
26 GNOMAD ss3986893487 Apr 25, 2021 (155)
27 GNOMAD ss3986893488 Apr 25, 2021 (155)
28 GNOMAD ss3986893489 Apr 25, 2021 (155)
29 GNOMAD ss3986893490 Apr 25, 2021 (155)
30 TOMMO_GENOMICS ss5142034096 Apr 25, 2021 (155)
31 TOMMO_GENOMICS ss5142034097 Apr 25, 2021 (155)
32 TOMMO_GENOMICS ss5142034098 Apr 25, 2021 (155)
33 TOMMO_GENOMICS ss5142034099 Apr 25, 2021 (155)
34 TOMMO_GENOMICS ss5142034100 Apr 25, 2021 (155)
35 HUGCELL_USP ss5442110974 Oct 12, 2022 (156)
36 HUGCELL_USP ss5442110975 Oct 12, 2022 (156)
37 TOMMO_GENOMICS ss5666166882 Oct 12, 2022 (156)
38 TOMMO_GENOMICS ss5666166883 Oct 12, 2022 (156)
39 TOMMO_GENOMICS ss5666166884 Oct 12, 2022 (156)
40 TOMMO_GENOMICS ss5666166885 Oct 12, 2022 (156)
41 TOMMO_GENOMICS ss5666166886 Oct 12, 2022 (156)
42 EVA ss5848748773 Oct 12, 2022 (156)
43 1000Genomes NC_000001.10 - 82134 Oct 11, 2018 (152)
44 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
45 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
46 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
47 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
48 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
49 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
50 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
51 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
52 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
53 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
54 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
55 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
56 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
57 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
58 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
59 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
60 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 8452 (NC_000001.11:82133::A 191/58458)
Row 8453 (NC_000001.11:82133::AA 4/58514)
Row 8454 (NC_000001.11:82133::AAA 8/58510)...

- Apr 25, 2021 (155)
61 8.3KJPN

Submission ignored due to conflicting rows:
Row 3403 (NC_000001.10:82133:AA: 11965/16462)
Row 3404 (NC_000001.10:82133:AAAA: 1325/16462)
Row 3405 (NC_000001.10:82133:AAA: 410/16462)...

- Apr 25, 2021 (155)
62 8.3KJPN

Submission ignored due to conflicting rows:
Row 3403 (NC_000001.10:82133:AA: 11965/16462)
Row 3404 (NC_000001.10:82133:AAAA: 1325/16462)
Row 3405 (NC_000001.10:82133:AAA: 410/16462)...

- Apr 25, 2021 (155)
63 8.3KJPN

Submission ignored due to conflicting rows:
Row 3403 (NC_000001.10:82133:AA: 11965/16462)
Row 3404 (NC_000001.10:82133:AAAA: 1325/16462)
Row 3405 (NC_000001.10:82133:AAA: 410/16462)...

- Apr 25, 2021 (155)
64 8.3KJPN

Submission ignored due to conflicting rows:
Row 3403 (NC_000001.10:82133:AA: 11965/16462)
Row 3404 (NC_000001.10:82133:AAAA: 1325/16462)
Row 3405 (NC_000001.10:82133:AAA: 410/16462)...

- Apr 25, 2021 (155)
65 8.3KJPN

Submission ignored due to conflicting rows:
Row 3403 (NC_000001.10:82133:AA: 11965/16462)
Row 3404 (NC_000001.10:82133:AAAA: 1325/16462)
Row 3405 (NC_000001.10:82133:AAA: 410/16462)...

- Apr 25, 2021 (155)
66 14KJPN

Submission ignored due to conflicting rows:
Row 3986 (NC_000001.11:82133:AA: 21639/26966)
Row 3987 (NC_000001.11:82133:A: 185/26966)
Row 3988 (NC_000001.11:82133:AAAA: 2282/26966)...

- Oct 12, 2022 (156)
67 14KJPN

Submission ignored due to conflicting rows:
Row 3986 (NC_000001.11:82133:AA: 21639/26966)
Row 3987 (NC_000001.11:82133:A: 185/26966)
Row 3988 (NC_000001.11:82133:AAAA: 2282/26966)...

- Oct 12, 2022 (156)
68 14KJPN

Submission ignored due to conflicting rows:
Row 3986 (NC_000001.11:82133:AA: 21639/26966)
Row 3987 (NC_000001.11:82133:A: 185/26966)
Row 3988 (NC_000001.11:82133:AAAA: 2282/26966)...

- Oct 12, 2022 (156)
69 14KJPN

Submission ignored due to conflicting rows:
Row 3986 (NC_000001.11:82133:AA: 21639/26966)
Row 3987 (NC_000001.11:82133:A: 185/26966)
Row 3988 (NC_000001.11:82133:AAAA: 2282/26966)...

- Oct 12, 2022 (156)
70 14KJPN

Submission ignored due to conflicting rows:
Row 3986 (NC_000001.11:82133:AA: 21639/26966)
Row 3987 (NC_000001.11:82133:A: 185/26966)
Row 3988 (NC_000001.11:82133:AAAA: 2282/26966)...

- Oct 12, 2022 (156)
71 ALFA NC_000001.11 - 82134 Apr 25, 2021 (155)
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
ss5379928 NT_077402.2:72135:AAAAAAAAAAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAA

(self)
ss2986142392 NC_000001.10:82133:AAAAAAAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

(self)
ss3986893490 NC_000001.11:82133:AAAAAAAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

(self)
ss3986893489 NC_000001.11:82133:AAAAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA

(self)
ss3986893488 NC_000001.11:82133:AAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

(self)
ss5142034100 NC_000001.10:82133:AAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

(self)
ss3986893487, ss5666166886 NC_000001.11:82133:AAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA

(self)
ss3986893486 NC_000001.11:82133:AAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA

(self)
ss5142034097 NC_000001.10:82133:AAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

(self)
ss3685990553, ss3986893485, ss5666166884 NC_000001.11:82133:AAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

(self)
ss287939206 NC_000001.9:71996:AAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
ss5142034098 NC_000001.10:82133:AAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
ss3986893484, ss5442110975, ss5666166885, ss5848748773 NC_000001.11:82133:AAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
ss3685990552 NC_000001.11:82134:AAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA

(self)
582, ss1367645227, ss5142034096 NC_000001.10:82133:AA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
ss3063573412, ss3065282389, ss3065282390, ss3798742544, ss3986893483, ss5442110974, ss5666166882 NC_000001.11:82133:AA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
ss3685990551 NC_000001.11:82135:AA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA

(self)
ss5142034099 NC_000001.10:82133:A: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss3986893482, ss5666166883 NC_000001.11:82133:A: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss3685990550 NC_000001.11:82136:A: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA

(self)
ss3986893474 NC_000001.11:82133::A NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

(self)
280398392 NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893475 NC_000001.11:82133::AA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893476 NC_000001.11:82133::AAA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893477 NC_000001.11:82133::AAAAA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893478 NC_000001.11:82133::AAAAAAAA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893479 NC_000001.11:82133::AAAAAAAAAA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893480 NC_000001.11:82133::AAAAAAAAAAAA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
ss3986893481 NC_000001.11:82133::AAAAAAAAAAAAA NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

(self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3066326376 NC_000001.11:82133:AAAAAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

ss3066326377 NC_000001.11:82133:AAAAAAAAAAA: NC_000001.11:82133:AAAAAAAAAAAAAAA…

NC_000001.11:82133:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

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 rs201023701

Help

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

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07