Name: rs1491495436
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.

rs1491495436

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:110293871-110293872 (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: insA / insATA / insATATA / ins(AT)…
insA / insATA / insATATA / ins(AT)₃A / ins(AT)₄A / ins(AT)₅A / ins(AT)₆A / ins(AT)₇A / ins(AT)₈A / ins(AT)₉A / ins(AT)₁₀A / ins(AT)₁₁A / insG
Variation Type: Insertion
Frequency: insA=0.00000 (0/11520, ALFA)
insATA=0.00000 (0/11520, ALFA)
insATATA=0.00000 (0/11520, ALFA) (+ 3 more)
ins(AT)₃A=0.00000 (0/11520, ALFA)
ins(AT)₄A=0.00000 (0/11520, ALFA)
ins(AT)₅A=0.00000 (0/11520, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ATP2A2 : 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	11520	=1.00000	A=0.00000, ATA=0.00000, ATATA=0.00000, ATATATA=0.00000, ATATATATA=0.00000, ATATATATATA=0.00000	1.0	N/A
European	Sub	7488	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000	1.0	N/A
African	Sub	2634	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000	1.0	N/A
African Others	Sub	102	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000	1.0	N/A
African American	Sub	2532	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATA=0.0000	1.0	N/A
Asian	Sub	108	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000	1.0	N/A
East Asian	Sub	84	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00	1.0	N/A
Latin American 1	Sub	142	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000	1.0	N/A
Latin American 2	Sub	600	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=0.000	1.0	N/A
South Asian	Sub	94	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATA=0.00	1.0	N/A
Other	Sub	454	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATA=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	11520	- No frequency provided	insA=0.00000, insATA=0.00000, insATATA=0.00000, ins(AT)₃A=0.00000, ins(AT)₄A=0.00000, ins(AT)₅A=0.00000
Allele Frequency Aggregator	European	Sub	7488	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₅A=0.0000
Allele Frequency Aggregator	African	Sub	2634	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₅A=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	600	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000
Allele Frequency Aggregator	Other	Sub	454	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	142	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₅A=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insA=0.00, insATA=0.00, insATATA=0.00, ins(AT)₃A=0.00, ins(AT)₄A=0.00, ins(AT)₅A=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.110293871_110293872insA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insATATATATATATATATATATATA
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872insG
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insATATATATATATATATATATATA
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677insG
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insATATATATATATATATATATATA
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246insG

Gene: ATP2A2, ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ATP2A2 transcript variant a	NM_001681.4:c.324+1747_32… NM_001681.4:c.324+1747_324+1748insA	N/A	Intron Variant
ATP2A2 transcript variant b	NM_170665.4:c.324+1747_32… NM_170665.4:c.324+1747_324+1748insA	N/A	Intron Variant
ATP2A2 transcript variant X2	XM_005253888.4:c.324+1747… XM_005253888.4:c.324+1747_324+1748insA	N/A	Intron Variant
ATP2A2 transcript variant X1	XM_011538402.4:c.324+1747… XM_011538402.4:c.324+1747_324+1748insA	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	=	insA	insATA	insATATA	ins(AT)₃A	ins(AT)₄A	ins(AT)₅A	ins(AT)₆A	ins(AT)₇A	ins(AT)₈A	ins(AT)₉A	ins(AT)₁₀A	ins(AT)₁₁A	insG
GRCh38.p14 chr 12	NC_000012.12:g.110293871_110293872=	NC_000012.12:g.110293871_110293872insA	NC_000012.12:g.110293871_110293872insATA	NC_000012.12:g.110293871_110293872insATATA	NC_000012.12:g.110293871_110293872insATATATA	NC_000012.12:g.110293871_110293872insATATATATA	NC_000012.12:g.110293871_110293872insATATATATATA	NC_000012.12:g.110293871_110293872insATATATATATATA	NC_000012.12:g.110293871_110293872insATATATATATATATA	NC_000012.12:g.110293871_110293872insATATATATATATATATA	NC_000012.12:g.110293871_110293872insATATATATATATATATATA	NC_000012.12:g.110293871_110293872insATATATATATATATATATATA	NC_000012.12:g.110293871_110293872insATATATATATATATATATATATA	NC_000012.12:g.110293871_110293872insG
GRCh37.p13 chr 12	NC_000012.11:g.110731676_110731677=	NC_000012.11:g.110731676_110731677insA	NC_000012.11:g.110731676_110731677insATA	NC_000012.11:g.110731676_110731677insATATA	NC_000012.11:g.110731676_110731677insATATATA	NC_000012.11:g.110731676_110731677insATATATATA	NC_000012.11:g.110731676_110731677insATATATATATA	NC_000012.11:g.110731676_110731677insATATATATATATA	NC_000012.11:g.110731676_110731677insATATATATATATATA	NC_000012.11:g.110731676_110731677insATATATATATATATATA	NC_000012.11:g.110731676_110731677insATATATATATATATATATA	NC_000012.11:g.110731676_110731677insATATATATATATATATATATA	NC_000012.11:g.110731676_110731677insATATATATATATATATATATATA	NC_000012.11:g.110731676_110731677insG
ATP2A2 RefSeqGene	NG_007097.2:g.17245_17246=	NG_007097.2:g.17245_17246insA	NG_007097.2:g.17245_17246insATA	NG_007097.2:g.17245_17246insATATA	NG_007097.2:g.17245_17246insATATATA	NG_007097.2:g.17245_17246insATATATATA	NG_007097.2:g.17245_17246insATATATATATA	NG_007097.2:g.17245_17246insATATATATATATA	NG_007097.2:g.17245_17246insATATATATATATATA	NG_007097.2:g.17245_17246insATATATATATATATATA	NG_007097.2:g.17245_17246insATATATATATATATATATA	NG_007097.2:g.17245_17246insATATATATATATATATATATA	NG_007097.2:g.17245_17246insATATATATATATATATATATATA	NG_007097.2:g.17245_17246insG
ATP2A2 transcript variant a	NM_001681.3:c.324+1748=	NM_001681.3:c.324+1747_324+1748insA	NM_001681.3:c.324+1747_324+1748insATA	NM_001681.3:c.324+1747_324+1748insATATA	NM_001681.3:c.324+1747_324+1748insATATATA	NM_001681.3:c.324+1747_324+1748insATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATATATATATATA	NM_001681.3:c.324+1747_324+1748insATATATATATATATATATATATA	NM_001681.3:c.324+1747_324+1748insG
ATP2A2 transcript variant a	NM_001681.4:c.324+1748=	NM_001681.4:c.324+1747_324+1748insA	NM_001681.4:c.324+1747_324+1748insATA	NM_001681.4:c.324+1747_324+1748insATATA	NM_001681.4:c.324+1747_324+1748insATATATA	NM_001681.4:c.324+1747_324+1748insATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATATATATATATA	NM_001681.4:c.324+1747_324+1748insATATATATATATATATATATATA	NM_001681.4:c.324+1747_324+1748insG
ATP2A2 transcript variant b	NM_170665.3:c.324+1748=	NM_170665.3:c.324+1747_324+1748insA	NM_170665.3:c.324+1747_324+1748insATA	NM_170665.3:c.324+1747_324+1748insATATA	NM_170665.3:c.324+1747_324+1748insATATATA	NM_170665.3:c.324+1747_324+1748insATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATATATATATATA	NM_170665.3:c.324+1747_324+1748insATATATATATATATATATATATA	NM_170665.3:c.324+1747_324+1748insG
ATP2A2 transcript variant b	NM_170665.4:c.324+1748=	NM_170665.4:c.324+1747_324+1748insA	NM_170665.4:c.324+1747_324+1748insATA	NM_170665.4:c.324+1747_324+1748insATATA	NM_170665.4:c.324+1747_324+1748insATATATA	NM_170665.4:c.324+1747_324+1748insATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATATATATATATA	NM_170665.4:c.324+1747_324+1748insATATATATATATATATATATATA	NM_170665.4:c.324+1747_324+1748insG
ATP2A2 transcript variant X1	XM_005253887.1:c.324+1748=	XM_005253887.1:c.324+1747_324+1748insA	XM_005253887.1:c.324+1747_324+1748insATA	XM_005253887.1:c.324+1747_324+1748insATATA	XM_005253887.1:c.324+1747_324+1748insATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATATATATATATA	XM_005253887.1:c.324+1747_324+1748insATATATATATATATATATATATA	XM_005253887.1:c.324+1747_324+1748insG
ATP2A2 transcript variant X3	XM_005253888.1:c.324+1748=	XM_005253888.1:c.324+1747_324+1748insA	XM_005253888.1:c.324+1747_324+1748insATA	XM_005253888.1:c.324+1747_324+1748insATATA	XM_005253888.1:c.324+1747_324+1748insATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATATATATATATA	XM_005253888.1:c.324+1747_324+1748insATATATATATATATATATATATA	XM_005253888.1:c.324+1747_324+1748insG
ATP2A2 transcript variant X2	XM_005253888.4:c.324+1748=	XM_005253888.4:c.324+1747_324+1748insA	XM_005253888.4:c.324+1747_324+1748insATA	XM_005253888.4:c.324+1747_324+1748insATATA	XM_005253888.4:c.324+1747_324+1748insATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATATATATATATA	XM_005253888.4:c.324+1747_324+1748insATATATATATATATATATATATA	XM_005253888.4:c.324+1747_324+1748insG
ATP2A2 transcript variant X1	XM_011538402.4:c.324+1748=	XM_011538402.4:c.324+1747_324+1748insA	XM_011538402.4:c.324+1747_324+1748insATA	XM_011538402.4:c.324+1747_324+1748insATATA	XM_011538402.4:c.324+1747_324+1748insATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATATATATATATA	XM_011538402.4:c.324+1747_324+1748insATATATATATATATATATATATA	XM_011538402.4:c.324+1747_324+1748insG

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#.

26 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3694458273	Jul 13, 2019 (153)
2	EVA_DECODE	ss3694458274	Jul 13, 2019 (153)
3	EVA_DECODE	ss3694458275	Jul 13, 2019 (153)
4	ACPOP	ss3739379927	Jul 13, 2019 (153)
5	ACPOP	ss3739379928	Jul 13, 2019 (153)
6	ACPOP	ss3739379929	Jul 13, 2019 (153)
7	GNOMAD	ss4258936969	Apr 26, 2021 (155)
8	GNOMAD	ss4258936970	Apr 26, 2021 (155)
9	GNOMAD	ss4258936971	Apr 26, 2021 (155)
10	GNOMAD	ss4258936972	Apr 26, 2021 (155)
11	GNOMAD	ss4258936973	Apr 26, 2021 (155)
12	GNOMAD	ss4258936974	Apr 26, 2021 (155)
13	GNOMAD	ss4258936975	Apr 26, 2021 (155)
14	GNOMAD	ss4258936976	Apr 26, 2021 (155)
15	GNOMAD	ss4258936977	Apr 26, 2021 (155)
16	GNOMAD	ss4258936978	Apr 26, 2021 (155)
17	GNOMAD	ss4258936979	Apr 26, 2021 (155)
18	GNOMAD	ss4258936980	Apr 26, 2021 (155)
19	GNOMAD	ss4258936981	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5208144605	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5208144606	Apr 26, 2021 (155)
22	1000G_HIGH_COVERAGE	ss5292219217	Oct 16, 2022 (156)
23	HUGCELL_USP	ss5486824373	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5758459409	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5758459410	Oct 16, 2022 (156)
26	YY_MCH	ss5813643748	Oct 16, 2022 (156)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419206718 (NC_000012.12:110293871::A 3378/72276) Row 419206719 (NC_000012.12:110293871::ATA 180/72302) Row 419206720 (NC_000012.12:110293871::ATATA 19/72314)...	-	Apr 26, 2021 (155)
40	Northern Sweden Submission ignored due to conflicting rows: Row 12664792 (NC_000012.11:110731676:: 553/570, NC_000012.11:110731676::A 17/570) Row 12664793 (NC_000012.11:110731676:: 569/570, NC_000012.11:110731676::ATATATATATATATATATA 1/570) Row 12664794 (NC_000012.11:110731676:: 569/570, NC_000012.11:110731676::ATA 1/570)	-	Jul 13, 2019 (153)
41	Northern Sweden Submission ignored due to conflicting rows: Row 12664792 (NC_000012.11:110731676:: 553/570, NC_000012.11:110731676::A 17/570) Row 12664793 (NC_000012.11:110731676:: 569/570, NC_000012.11:110731676::ATATATATATATATATATA 1/570) Row 12664794 (NC_000012.11:110731676:: 569/570, NC_000012.11:110731676::ATA 1/570)	-	Jul 13, 2019 (153)
42	Northern Sweden Submission ignored due to conflicting rows: Row 12664792 (NC_000012.11:110731676:: 553/570, NC_000012.11:110731676::A 17/570) Row 12664793 (NC_000012.11:110731676:: 569/570, NC_000012.11:110731676::ATATATATATATATATATA 1/570) Row 12664794 (NC_000012.11:110731676:: 569/570, NC_000012.11:110731676::ATA 1/570)	-	Jul 13, 2019 (153)
43	8.3KJPN Submission ignored due to conflicting rows: Row 66113912 (NC_000012.11:110731676::ATATATA 1/14184) Row 66113913 (NC_000012.11:110731676::A 9/14184)	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 66113912 (NC_000012.11:110731676::ATATATA 1/14184) Row 66113913 (NC_000012.11:110731676::A 9/14184)	-	Apr 26, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 92296513 (NC_000012.12:110293871::A 15/20198) Row 92296514 (NC_000012.12:110293871::G 1/20198)	-	Oct 16, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 92296513 (NC_000012.12:110293871::A 15/20198) Row 92296514 (NC_000012.12:110293871::G 1/20198)	-	Oct 16, 2022 (156)
47	ALFA	NC_000012.12 - 110293872	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
ss3739379927, ss5208144606	NC_000012.11:110731676::A	NC_000012.12:110293871::A	(self)
10329299386, ss3694458273, ss4258936969, ss5292219217, ss5486824373, ss5758459409, ss5813643748	NC_000012.12:110293871::A	NC_000012.12:110293871::A	(self)
ss3739379929	NC_000012.11:110731676::ATA	NC_000012.12:110293871::ATA	(self)
10329299386, ss3694458274, ss4258936970	NC_000012.12:110293871::ATA	NC_000012.12:110293871::ATA	(self)
10329299386, ss3694458275, ss4258936971	NC_000012.12:110293871::ATATA	NC_000012.12:110293871::ATATA	(self)
ss5208144605	NC_000012.11:110731676::ATATATA	NC_000012.12:110293871::ATATATA	(self)
10329299386, ss4258936972	NC_000012.12:110293871::ATATATA	NC_000012.12:110293871::ATATATA	(self)
10329299386, ss4258936973	NC_000012.12:110293871::ATATATATA	NC_000012.12:110293871::ATATATATA	(self)
10329299386, ss4258936974	NC_000012.12:110293871::ATATATATATA	NC_000012.12:110293871::ATATATATATA	(self)
ss4258936975	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATA	(self)
ss4258936976	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATA	(self)
ss4258936977	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATA	(self)
ss3739379928	NC_000012.11:110731676::ATATATATAT… NC_000012.11:110731676::ATATATATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATA	(self)
ss4258936978	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATA	(self)
ss4258936979	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATATA	(self)
ss4258936980	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATATATA	NC_000012.12:110293871::ATATATATAT… NC_000012.12:110293871::ATATATATATATATATATATATA	(self)
ss4258936981, ss5758459410	NC_000012.12:110293871::G	NC_000012.12:110293871::G	(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 rs1491495436

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

rs1491495436