Name: rs1491186082
Published: September 21, 2022
License: Open Access

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.

rs1491186082

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:92473113 (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: insAT / insATAT / ins(AT)₃ / ins(A…
insAT / insATAT / ins(AT)₃ / ins(AT)₄ / ins(AT)₅ / ins(AT)₆ / ins(AT)₇ / ins(AT)₇AAATAT / ins(AT)₈ / ins(AT)₉ / ins(AT)₁₀ / ins(AT)₁₁ / ins(AT)₁₂ / ins(AT)₁₃ / ins(AT)₁₄ / ins(AT)₁₅ / ins(AT)₁₆ / ins(AT)₁₇ / ins(AT)₇C(TA)₄T
Variation Type: Indel Insertion and Deletion
Frequency: insAT=0.00000 (0/11388, ALFA)
insATAT=0.00000 (0/11388, ALFA)
ins(AT)₃=0.00000 (0/11388, ALFA) (+ 9 more)
ins(AT)₄=0.00000 (0/11388, ALFA)
ins(AT)₅=0.00000 (0/11388, ALFA)
ins(AT)₆=0.00000 (0/11388, ALFA)
ins(AT)₇=0.00000 (0/11388, ALFA)
ins(AT)₈=0.00000 (0/11388, ALFA)
ins(AT)₉=0.00000 (0/11388, ALFA)
ins(AT)₁₀=0.00000 (0/11388, ALFA)
ins(AT)₁₁=0.00000 (0/11388, ALFA)
ins(AT)₁₂=0.00000 (0/11388, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02397 : Intron 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	11388	T=1.00000	TAT=0.00000, TATAT=0.00000, TATATAT=0.00000, TATATATAT=0.00000, TATATATATAT=0.00000, TATATATATATAT=0.00000, TATATATATATATAT=0.00000, TATATATATATATATAT=0.00000, TATATATATATATATATAT=0.00000, TATATATATATATATATATAT=0.00000, TATATATATATATATATATATAT=0.00000, TATATATATATATATATATATATAT=0.00000	1.0	N/A
European	Sub	7488	T=1.0000	TAT=0.0000, TATAT=0.0000, TATATAT=0.0000, TATATATAT=0.0000, TATATATATAT=0.0000, TATATATATATAT=0.0000, TATATATATATATAT=0.0000, TATATATATATATATAT=0.0000, TATATATATATATATATAT=0.0000, TATATATATATATATATATAT=0.0000, TATATATATATATATATATATAT=0.0000, TATATATATATATATATATATATAT=0.0000	1.0	N/A
African	Sub	2516	T=1.0000	TAT=0.0000, TATAT=0.0000, TATATAT=0.0000, TATATATAT=0.0000, TATATATATAT=0.0000, TATATATATATAT=0.0000, TATATATATATATAT=0.0000, TATATATATATATATAT=0.0000, TATATATATATATATATAT=0.0000, TATATATATATATATATATAT=0.0000, TATATATATATATATATATATAT=0.0000, TATATATATATATATATATATATAT=0.0000	1.0	N/A
African Others	Sub	94	T=1.00	TAT=0.00, TATAT=0.00, TATATAT=0.00, TATATATAT=0.00, TATATATATAT=0.00, TATATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00, TATATATATATATATATATAT=0.00, TATATATATATATATATATATAT=0.00, TATATATATATATATATATATATAT=0.00	1.0	N/A
African American	Sub	2422	T=1.0000	TAT=0.0000, TATAT=0.0000, TATATAT=0.0000, TATATATAT=0.0000, TATATATATAT=0.0000, TATATATATATAT=0.0000, TATATATATATATAT=0.0000, TATATATATATATATAT=0.0000, TATATATATATATATATAT=0.0000, TATATATATATATATATATAT=0.0000, TATATATATATATATATATATAT=0.0000, TATATATATATATATATATATATAT=0.0000	1.0	N/A
Asian	Sub	108	T=1.000	TAT=0.000, TATAT=0.000, TATATAT=0.000, TATATATAT=0.000, TATATATATAT=0.000, TATATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000, TATATATATATATATATATAT=0.000, TATATATATATATATATATATAT=0.000, TATATATATATATATATATATATAT=0.000	1.0	N/A
East Asian	Sub	84	T=1.00	TAT=0.00, TATAT=0.00, TATATAT=0.00, TATATATAT=0.00, TATATATATAT=0.00, TATATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00, TATATATATATATATATATAT=0.00, TATATATATATATATATATATAT=0.00, TATATATATATATATATATATATAT=0.00	1.0	N/A
Other Asian	Sub	24	T=1.00	TAT=0.00, TATAT=0.00, TATATAT=0.00, TATATATAT=0.00, TATATATATAT=0.00, TATATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00, TATATATATATATATATATAT=0.00, TATATATATATATATATATATAT=0.00, TATATATATATATATATATATATAT=0.00	1.0	N/A
Latin American 1	Sub	136	T=1.000	TAT=0.000, TATAT=0.000, TATATAT=0.000, TATATATAT=0.000, TATATATATAT=0.000, TATATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000, TATATATATATATATATATAT=0.000, TATATATATATATATATATATAT=0.000, TATATATATATATATATATATATAT=0.000	1.0	N/A
Latin American 2	Sub	600	T=1.000	TAT=0.000, TATAT=0.000, TATATAT=0.000, TATATATAT=0.000, TATATATATAT=0.000, TATATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000, TATATATATATATATATATAT=0.000, TATATATATATATATATATATAT=0.000, TATATATATATATATATATATATAT=0.000	1.0	N/A
South Asian	Sub	94	T=1.00	TAT=0.00, TATAT=0.00, TATATAT=0.00, TATATATAT=0.00, TATATATATAT=0.00, TATATATATATAT=0.00, TATATATATATATAT=0.00, TATATATATATATATAT=0.00, TATATATATATATATATAT=0.00, TATATATATATATATATATAT=0.00, TATATATATATATATATATATAT=0.00, TATATATATATATATATATATATAT=0.00	1.0	N/A
Other	Sub	446	T=1.000	TAT=0.000, TATAT=0.000, TATATAT=0.000, TATATATAT=0.000, TATATATATAT=0.000, TATATATATATAT=0.000, TATATATATATATAT=0.000, TATATATATATATATAT=0.000, TATATATATATATATATAT=0.000, TATATATATATATATATATAT=0.000, TATATATATATATATATATATAT=0.000, TATATATATATATATATATATATAT=0.000	1.0	N/A

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	11388	T=1.00000	insAT=0.00000, insATAT=0.00000, ins(AT)₃=0.00000, ins(AT)₄=0.00000, ins(AT)₅=0.00000, ins(AT)₆=0.00000, ins(AT)₇=0.00000, ins(AT)₈=0.00000, ins(AT)₉=0.00000, ins(AT)₁₀=0.00000, ins(AT)₁₁=0.00000, ins(AT)₁₂=0.00000
Allele Frequency Aggregator	European	Sub	7488	T=1.0000	insAT=0.0000, insATAT=0.0000, ins(AT)₃=0.0000, ins(AT)₄=0.0000, ins(AT)₅=0.0000, ins(AT)₆=0.0000, ins(AT)₇=0.0000, ins(AT)₈=0.0000, ins(AT)₉=0.0000, ins(AT)₁₀=0.0000, ins(AT)₁₁=0.0000, ins(AT)₁₂=0.0000
Allele Frequency Aggregator	African	Sub	2516	T=1.0000	insAT=0.0000, insATAT=0.0000, ins(AT)₃=0.0000, ins(AT)₄=0.0000, ins(AT)₅=0.0000, ins(AT)₆=0.0000, ins(AT)₇=0.0000, ins(AT)₈=0.0000, ins(AT)₉=0.0000, ins(AT)₁₀=0.0000, ins(AT)₁₁=0.0000, ins(AT)₁₂=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	600	T=1.000	insAT=0.000, insATAT=0.000, ins(AT)₃=0.000, ins(AT)₄=0.000, ins(AT)₅=0.000, ins(AT)₆=0.000, ins(AT)₇=0.000, ins(AT)₈=0.000, ins(AT)₉=0.000, ins(AT)₁₀=0.000, ins(AT)₁₁=0.000, ins(AT)₁₂=0.000
Allele Frequency Aggregator	Other	Sub	446	T=1.000	insAT=0.000, insATAT=0.000, ins(AT)₃=0.000, ins(AT)₄=0.000, ins(AT)₅=0.000, ins(AT)₆=0.000, ins(AT)₇=0.000, ins(AT)₈=0.000, ins(AT)₉=0.000, ins(AT)₁₀=0.000, ins(AT)₁₁=0.000, ins(AT)₁₂=0.000
Allele Frequency Aggregator	Latin American 1	Sub	136	T=1.000	insAT=0.000, insATAT=0.000, ins(AT)₃=0.000, ins(AT)₄=0.000, ins(AT)₅=0.000, ins(AT)₆=0.000, ins(AT)₇=0.000, ins(AT)₈=0.000, ins(AT)₉=0.000, ins(AT)₁₀=0.000, ins(AT)₁₁=0.000, ins(AT)₁₂=0.000
Allele Frequency Aggregator	Asian	Sub	108	T=1.000	insAT=0.000, insATAT=0.000, ins(AT)₃=0.000, ins(AT)₄=0.000, ins(AT)₅=0.000, ins(AT)₆=0.000, ins(AT)₇=0.000, ins(AT)₈=0.000, ins(AT)₉=0.000, ins(AT)₁₀=0.000, ins(AT)₁₁=0.000, ins(AT)₁₂=0.000
Allele Frequency Aggregator	South Asian	Sub	94	T=1.00	insAT=0.00, insATAT=0.00, ins(AT)₃=0.00, ins(AT)₄=0.00, ins(AT)₅=0.00, ins(AT)₆=0.00, ins(AT)₇=0.00, ins(AT)₈=0.00, ins(AT)₉=0.00, ins(AT)₁₀=0.00, ins(AT)₁₁=0.00, ins(AT)₁₂=0.00

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.92473113_92473114insAT
GRCh38.p14 chr 12	NC_000012.12:g.92473113_92473114insATAT
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[3]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[4]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[5]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[6]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[7]
GRCh38.p14 chr 12	NC_000012.12:g.92473113TA[8]AATAT[1]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[8]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[9]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[10]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[11]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[12]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[13]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[14]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[15]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[16]
GRCh38.p14 chr 12	NC_000012.12:g.92473114AT[17]
GRCh38.p14 chr 12	NC_000012.12:g.92473113TA[7]TCTATATATAT[1]
GRCh37.p13 chr 12	NC_000012.11:g.92866889_92866890insAT
GRCh37.p13 chr 12	NC_000012.11:g.92866889_92866890insATAT
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[3]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[4]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[5]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[6]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[7]
GRCh37.p13 chr 12	NC_000012.11:g.92866889TA[8]AATAT[1]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[8]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[9]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[10]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[11]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[12]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[13]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[14]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[15]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[16]
GRCh37.p13 chr 12	NC_000012.11:g.92866890AT[17]
GRCh37.p13 chr 12	NC_000012.11:g.92866889TA[7]TCTATATATAT[1]

Gene: LINC02397, long intergenic non-protein coding RNA 2397 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02397 transcript	NR_144532.1:n.	N/A	Intron Variant

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

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	T=	insAT	insATAT	ins(AT)₃	ins(AT)₄	ins(AT)₅	ins(AT)₆	ins(AT)₇	ins(AT)₇AAATAT	ins(AT)₈	ins(AT)₉	ins(AT)₁₀	ins(AT)₁₁	ins(AT)₁₂	ins(AT)₁₃	ins(AT)₁₄	ins(AT)₁₅	ins(AT)₁₆	ins(AT)₁₇	ins(AT)₇C(TA)₄T
GRCh38.p14 chr 12	NC_000012.12:g.92473113=	NC_000012.12:g.92473113_92473114insAT	NC_000012.12:g.92473113_92473114insATAT	NC_000012.12:g.92473114AT[3]	NC_000012.12:g.92473114AT[4]	NC_000012.12:g.92473114AT[5]	NC_000012.12:g.92473114AT[6]	NC_000012.12:g.92473114AT[7]	NC_000012.12:g.92473113TA[8]AATAT[1]	NC_000012.12:g.92473114AT[8]	NC_000012.12:g.92473114AT[9]	NC_000012.12:g.92473114AT[10]	NC_000012.12:g.92473114AT[11]	NC_000012.12:g.92473114AT[12]	NC_000012.12:g.92473114AT[13]	NC_000012.12:g.92473114AT[14]	NC_000012.12:g.92473114AT[15]	NC_000012.12:g.92473114AT[16]	NC_000012.12:g.92473114AT[17]	NC_000012.12:g.92473113TA[7]TCTATATATAT[1]
GRCh37.p13 chr 12	NC_000012.11:g.92866889=	NC_000012.11:g.92866889_92866890insAT	NC_000012.11:g.92866889_92866890insATAT	NC_000012.11:g.92866890AT[3]	NC_000012.11:g.92866890AT[4]	NC_000012.11:g.92866890AT[5]	NC_000012.11:g.92866890AT[6]	NC_000012.11:g.92866890AT[7]	NC_000012.11:g.92866889TA[8]AATAT[1]	NC_000012.11:g.92866890AT[8]	NC_000012.11:g.92866890AT[9]	NC_000012.11:g.92866890AT[10]	NC_000012.11:g.92866890AT[11]	NC_000012.11:g.92866890AT[12]	NC_000012.11:g.92866890AT[13]	NC_000012.11:g.92866890AT[14]	NC_000012.11:g.92866890AT[15]	NC_000012.11:g.92866890AT[16]	NC_000012.11:g.92866890AT[17]	NC_000012.11:g.92866889TA[7]TCTATATATAT[1]

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#.

32 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3694209087	Jul 13, 2019 (153)
2	EVA_DECODE	ss3694209088	Jul 13, 2019 (153)
3	EVA_DECODE	ss3694209089	Jul 13, 2019 (153)
4	ACPOP	ss3739267778	Jul 13, 2019 (153)
5	ACPOP	ss3739267779	Jul 13, 2019 (153)
6	ACPOP	ss3739267780	Jul 13, 2019 (153)
7	ACPOP	ss3739267781	Jul 13, 2019 (153)
8	GNOMAD	ss4256806834	Apr 26, 2021 (155)
9	GNOMAD	ss4256806835	Apr 26, 2021 (155)
10	GNOMAD	ss4256806836	Apr 26, 2021 (155)
11	GNOMAD	ss4256806837	Apr 26, 2021 (155)
12	GNOMAD	ss4256806838	Apr 26, 2021 (155)
13	GNOMAD	ss4256806839	Apr 26, 2021 (155)
14	GNOMAD	ss4256806840	Apr 26, 2021 (155)
15	GNOMAD	ss4256806841	Apr 26, 2021 (155)
16	GNOMAD	ss4256806842	Apr 26, 2021 (155)
17	GNOMAD	ss4256806843	Apr 26, 2021 (155)
18	GNOMAD	ss4256806844	Apr 26, 2021 (155)
19	GNOMAD	ss4256806845	Apr 26, 2021 (155)
20	GNOMAD	ss4256806846	Apr 26, 2021 (155)
21	GNOMAD	ss4256806847	Apr 26, 2021 (155)
22	GNOMAD	ss4256806848	Apr 26, 2021 (155)
23	GNOMAD	ss4256806849	Apr 26, 2021 (155)
24	GNOMAD	ss4256806850	Apr 26, 2021 (155)
25	GNOMAD	ss4256806851	Apr 26, 2021 (155)
26	GNOMAD	ss4256806852	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5207587365	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5207587366	Apr 26, 2021 (155)
29	HUGCELL_USP	ss5486433562	Oct 13, 2022 (156)
30	HUGCELL_USP	ss5486433564	Oct 13, 2022 (156)
31	TOMMO_GENOMICS	ss5757741931	Oct 13, 2022 (156)
32	TOMMO_GENOMICS	ss5757741933	Oct 13, 2022 (156)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 415658694 (NC_000012.12:92473112::TA 1512/73598) Row 415658695 (NC_000012.12:92473112::TATA 822/73586) Row 415658696 (NC_000012.12:92473112::TATATA 254/73618)...	-	Apr 26, 2021 (155)
52	Northern Sweden Submission ignored due to conflicting rows: Row 12552643 (NC_000012.11:92866888::TATATATATATATATATA 12/548) Row 12552644 (NC_000012.11:92866888::TATATATATATATA 3/548) Row 12552645 (NC_000012.11:92866888::TATA 5/548)...	-	Jul 13, 2019 (153)
53	Northern Sweden Submission ignored due to conflicting rows: Row 12552643 (NC_000012.11:92866888::TATATATATATATATATA 12/548) Row 12552644 (NC_000012.11:92866888::TATATATATATATA 3/548) Row 12552645 (NC_000012.11:92866888::TATA 5/548)...	-	Jul 13, 2019 (153)
54	Northern Sweden Submission ignored due to conflicting rows: Row 12552643 (NC_000012.11:92866888::TATATATATATATATATA 12/548) Row 12552644 (NC_000012.11:92866888::TATATATATATATA 3/548) Row 12552645 (NC_000012.11:92866888::TATA 5/548)...	-	Jul 13, 2019 (153)
55	Northern Sweden Submission ignored due to conflicting rows: Row 12552643 (NC_000012.11:92866888::TATATATATATATATATA 12/548) Row 12552644 (NC_000012.11:92866888::TATATATATATATA 3/548) Row 12552645 (NC_000012.11:92866888::TATA 5/548)...	-	Jul 13, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 65556672 (NC_000012.11:92866888::TATATATATATATATATA 233/16566) Row 65556673 (NC_000012.11:92866888::TATATATATATATATA 232/16566)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 65556672 (NC_000012.11:92866888::TATATATATATATATATA 233/16566) Row 65556673 (NC_000012.11:92866888::TATATATATATATATA 232/16566)	-	Apr 26, 2021 (155)
58	14KJPN Submission ignored due to conflicting rows: Row 91579035 (NC_000012.12:92473112::TATATATATATATATATA 464/27996) Row 91579037 (NC_000012.12:92473112::TATATATATATATATA 419/27996)	-	Oct 13, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 91579035 (NC_000012.12:92473112::TATATATATATATATATA 464/27996) Row 91579037 (NC_000012.12:92473112::TATATATATATATATA 419/27996)	-	Oct 13, 2022 (156)
60	ALFA	NC_000012.12 - 92473113	Apr 26, 2021 (155)

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
ss4256806834, ss5486433564	NC_000012.12:92473112::TA	NC_000012.12:92473112:T:TAT	(self)
4530091660	NC_000012.12:92473112:T:TAT	NC_000012.12:92473112:T:TAT	(self)
ss3739267780	NC_000012.11:92866888::TATA	NC_000012.12:92473112:T:TATAT	(self)
ss4256806835, ss5486433562	NC_000012.12:92473112::TATA	NC_000012.12:92473112:T:TATAT	(self)
4530091660	NC_000012.12:92473112:T:TATAT	NC_000012.12:92473112:T:TATAT	(self)
ss4256806836	NC_000012.12:92473112::TATATA	NC_000012.12:92473112:T:TATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATAT	NC_000012.12:92473112:T:TATATAT	(self)
ss4256806837	NC_000012.12:92473112::TATATATA	NC_000012.12:92473112:T:TATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATAT	NC_000012.12:92473112:T:TATATATAT	(self)
ss4256806838	NC_000012.12:92473112::TATATATATA	NC_000012.12:92473112:T:TATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATAT	NC_000012.12:92473112:T:TATATATATAT	(self)
ss4256806839	NC_000012.12:92473112::TATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATAT	(self)
ss3739267779	NC_000012.11:92866888::TATATATATAT… NC_000012.11:92866888::TATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATAT	(self)
ss4256806840	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATAT	(self)
ss4256806842	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATAAATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATAAATAT	(self)
ss3739267781, ss5207587366	NC_000012.11:92866888::TATATATATAT… NC_000012.11:92866888::TATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATAT	(self)
ss4256806841, ss5757741933	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATAT	(self)
ss3694209089	NC_000012.12:92473113::ATATATATATA… NC_000012.12:92473113::ATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATAT	(self)
ss3739267778, ss5207587365	NC_000012.11:92866888::TATATATATAT… NC_000012.11:92866888::TATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATAT	(self)
ss4256806843, ss5757741931	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATAT	(self)
ss4256806844	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATAT	(self)
ss3694209088	NC_000012.12:92473113::ATATATATATA… NC_000012.12:92473113::ATATATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATAT	(self)
ss4256806845	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATAT	(self)
ss4256806846	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATAT	(self)
4530091660	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATAT	(self)
ss4256806847	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATATAT	(self)
ss3694209087	NC_000012.12:92473113::ATATATATATA… NC_000012.12:92473113::ATATATATATATATATATATATATAT	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATATAT	(self)
ss4256806848	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATATATAT	(self)
ss4256806849	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATATATATAT	(self)
ss4256806850	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATATATATATAT	(self)
ss4256806851	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATATATATATATATATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATATATATATATATATATATAT	(self)
ss4256806852	NC_000012.12:92473112::TATATATATAT… NC_000012.12:92473112::TATATATATATATATCTATATATA	NC_000012.12:92473112:T:TATATATATA… NC_000012.12:92473112:T:TATATATATATATATCTATATATAT	(self)

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

No publications for rs1491186082

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491186082