Name: rs1491521540
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.

rs1491521540

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:196751664 (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: insGTGT(AT)₃ / insGTGT(AT)₄ / insG…
insGTGT(AT)₃ / insGTGT(AT)₄ / insGTGT(AT)₅ / insGTGT(AT)₆ / insGTGT(AT)₇ / insTTAT / insTTATAT / insTT(AT)₃ / insTT(AT)₄ / insTT(AT)₅ / insTT(AT)₆ / insTT(AT)₇ / insTT(AT)₈ / insTT(AT)₉ / insTT(AT)₁₀ / insTT(AT)₁₁ / insTT(AT)₁₂ / insTT(AT)₁₃ / insTT(AT)₁₄ / insTT(AT)₁₅ / insTT(AT)₈GT
Variation Type: Indel Insertion and Deletion
Frequency: insGTGT(AT)₃=0.00000 (0/11854, ALFA)
insGTGT(AT)₄=0.00000 (0/11854, ALFA)
insGTGT(AT)₅=0.00000 (0/11854, ALFA) (+ 12 more)
insGTGT(AT)₇=0.00000 (0/11854, ALFA)
insTTAT=0.00000 (0/11854, ALFA)
insTTATAT=0.00000 (0/11854, ALFA)
insTT(AT)₃=0.00000 (0/11854, ALFA)
insTT(AT)₄=0.00000 (0/11854, ALFA)
insTT(AT)₅=0.00000 (0/11854, ALFA)
insTT(AT)₆=0.00000 (0/11854, ALFA)
insTT(AT)₇=0.00000 (0/11854, ALFA)
insTT(AT)₈=0.00000 (0/11854, ALFA)
insTT(AT)₉=0.00000 (0/11854, ALFA)
insTT(AT)₁₀=0.00000 (0/11854, ALFA)
insTT(AT)₁₁=0.00000 (0/11854, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PAK2 : 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	11854	T=1.00000	TGTGTATATAT=0.00000, TGTGTATATATAT=0.00000, TGTGTATATATATAT=0.00000, TGTGTATATATATATATAT=0.00000, TTTAT=0.00000, TTTATAT=0.00000, TTTATATAT=0.00000, TTTATATATAT=0.00000, TTTATATATATAT=0.00000, TTTATATATATATAT=0.00000, TTTATATATATATATAT=0.00000, TTTATATATATATATATAT=0.00000, TTTATATATATATATATATAT=0.00000, TTTATATATATATATATATATAT=0.00000, TTTATATATATATATATATATATAT=0.00000	1.0	N/A
European	Sub	7618	T=1.0000	TGTGTATATAT=0.0000, TGTGTATATATAT=0.0000, TGTGTATATATATAT=0.0000, TGTGTATATATATATATAT=0.0000, TTTAT=0.0000, TTTATAT=0.0000, TTTATATAT=0.0000, TTTATATATAT=0.0000, TTTATATATATAT=0.0000, TTTATATATATATAT=0.0000, TTTATATATATATATAT=0.0000, TTTATATATATATATATAT=0.0000, TTTATATATATATATATATAT=0.0000, TTTATATATATATATATATATAT=0.0000, TTTATATATATATATATATATATAT=0.0000	1.0	N/A
African	Sub	2810	T=1.0000	TGTGTATATAT=0.0000, TGTGTATATATAT=0.0000, TGTGTATATATATAT=0.0000, TGTGTATATATATATATAT=0.0000, TTTAT=0.0000, TTTATAT=0.0000, TTTATATAT=0.0000, TTTATATATAT=0.0000, TTTATATATATAT=0.0000, TTTATATATATATAT=0.0000, TTTATATATATATATAT=0.0000, TTTATATATATATATATAT=0.0000, TTTATATATATATATATATAT=0.0000, TTTATATATATATATATATATAT=0.0000, TTTATATATATATATATATATATAT=0.0000	1.0	N/A
African Others	Sub	108	T=1.000	TGTGTATATAT=0.000, TGTGTATATATAT=0.000, TGTGTATATATATAT=0.000, TGTGTATATATATATATAT=0.000, TTTAT=0.000, TTTATAT=0.000, TTTATATAT=0.000, TTTATATATAT=0.000, TTTATATATATAT=0.000, TTTATATATATATAT=0.000, TTTATATATATATATAT=0.000, TTTATATATATATATATAT=0.000, TTTATATATATATATATATAT=0.000, TTTATATATATATATATATATAT=0.000, TTTATATATATATATATATATATAT=0.000	1.0	N/A
African American	Sub	2702	T=1.0000	TGTGTATATAT=0.0000, TGTGTATATATAT=0.0000, TGTGTATATATATAT=0.0000, TGTGTATATATATATATAT=0.0000, TTTAT=0.0000, TTTATAT=0.0000, TTTATATAT=0.0000, TTTATATATAT=0.0000, TTTATATATATAT=0.0000, TTTATATATATATAT=0.0000, TTTATATATATATATAT=0.0000, TTTATATATATATATATAT=0.0000, TTTATATATATATATATATAT=0.0000, TTTATATATATATATATATATAT=0.0000, TTTATATATATATATATATATATAT=0.0000	1.0	N/A
Asian	Sub	108	T=1.000	TGTGTATATAT=0.000, TGTGTATATATAT=0.000, TGTGTATATATATAT=0.000, TGTGTATATATATATATAT=0.000, TTTAT=0.000, TTTATAT=0.000, TTTATATAT=0.000, TTTATATATAT=0.000, TTTATATATATAT=0.000, TTTATATATATATAT=0.000, TTTATATATATATATAT=0.000, TTTATATATATATATATAT=0.000, TTTATATATATATATATATAT=0.000, TTTATATATATATATATATATAT=0.000, TTTATATATATATATATATATATAT=0.000	1.0	N/A
East Asian	Sub	84	T=1.00	TGTGTATATAT=0.00, TGTGTATATATAT=0.00, TGTGTATATATATAT=0.00, TGTGTATATATATATATAT=0.00, TTTAT=0.00, TTTATAT=0.00, TTTATATAT=0.00, TTTATATATAT=0.00, TTTATATATATAT=0.00, TTTATATATATATAT=0.00, TTTATATATATATATAT=0.00, TTTATATATATATATATAT=0.00, TTTATATATATATATATATAT=0.00, TTTATATATATATATATATATAT=0.00, TTTATATATATATATATATATATAT=0.00	1.0	N/A
Other Asian	Sub	24	T=1.00	TGTGTATATAT=0.00, TGTGTATATATAT=0.00, TGTGTATATATATAT=0.00, TGTGTATATATATATATAT=0.00, TTTAT=0.00, TTTATAT=0.00, TTTATATAT=0.00, TTTATATATAT=0.00, TTTATATATATAT=0.00, TTTATATATATATAT=0.00, TTTATATATATATATAT=0.00, TTTATATATATATATATAT=0.00, TTTATATATATATATATATAT=0.00, TTTATATATATATATATATATAT=0.00, TTTATATATATATATATATATATAT=0.00	1.0	N/A
Latin American 1	Sub	146	T=1.000	TGTGTATATAT=0.000, TGTGTATATATAT=0.000, TGTGTATATATATAT=0.000, TGTGTATATATATATATAT=0.000, TTTAT=0.000, TTTATAT=0.000, TTTATATAT=0.000, TTTATATATAT=0.000, TTTATATATATAT=0.000, TTTATATATATATAT=0.000, TTTATATATATATATAT=0.000, TTTATATATATATATATAT=0.000, TTTATATATATATATATATAT=0.000, TTTATATATATATATATATATAT=0.000, TTTATATATATATATATATATATAT=0.000	1.0	N/A
Latin American 2	Sub	608	T=1.000	TGTGTATATAT=0.000, TGTGTATATATAT=0.000, TGTGTATATATATAT=0.000, TGTGTATATATATATATAT=0.000, TTTAT=0.000, TTTATAT=0.000, TTTATATAT=0.000, TTTATATATAT=0.000, TTTATATATATAT=0.000, TTTATATATATATAT=0.000, TTTATATATATATATAT=0.000, TTTATATATATATATATAT=0.000, TTTATATATATATATATATAT=0.000, TTTATATATATATATATATATAT=0.000, TTTATATATATATATATATATATAT=0.000	1.0	N/A
South Asian	Sub	94	T=1.00	TGTGTATATAT=0.00, TGTGTATATATAT=0.00, TGTGTATATATATAT=0.00, TGTGTATATATATATATAT=0.00, TTTAT=0.00, TTTATAT=0.00, TTTATATAT=0.00, TTTATATATAT=0.00, TTTATATATATAT=0.00, TTTATATATATATAT=0.00, TTTATATATATATATAT=0.00, TTTATATATATATATATAT=0.00, TTTATATATATATATATATAT=0.00, TTTATATATATATATATATATAT=0.00, TTTATATATATATATATATATATAT=0.00	1.0	N/A
Other	Sub	470	T=1.000	TGTGTATATAT=0.000, TGTGTATATATAT=0.000, TGTGTATATATATAT=0.000, TGTGTATATATATATATAT=0.000, TTTAT=0.000, TTTATAT=0.000, TTTATATAT=0.000, TTTATATATAT=0.000, TTTATATATATAT=0.000, TTTATATATATATAT=0.000, TTTATATATATATATAT=0.000, TTTATATATATATATATAT=0.000, TTTATATATATATATATATAT=0.000, TTTATATATATATATATATATAT=0.000, TTTATATATATATATATATATATAT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11854	T=1.00000	insGTGT(AT)₃=0.00000, insGTGT(AT)₄=0.00000, insGTGT(AT)₅=0.00000, insGTGT(AT)₇=0.00000, insTTAT=0.00000, insTTATAT=0.00000, insTT(AT)₃=0.00000, insTT(AT)₄=0.00000, insTT(AT)₅=0.00000, insTT(AT)₆=0.00000, insTT(AT)₇=0.00000, insTT(AT)₈=0.00000, insTT(AT)₉=0.00000, insTT(AT)₁₀=0.00000, insTT(AT)₁₁=0.00000
Allele Frequency Aggregator	European	Sub	7618	T=1.0000	insGTGT(AT)₃=0.0000, insGTGT(AT)₄=0.0000, insGTGT(AT)₅=0.0000, insGTGT(AT)₇=0.0000, insTTAT=0.0000, insTTATAT=0.0000, insTT(AT)₃=0.0000, insTT(AT)₄=0.0000, insTT(AT)₅=0.0000, insTT(AT)₆=0.0000, insTT(AT)₇=0.0000, insTT(AT)₈=0.0000, insTT(AT)₉=0.0000, insTT(AT)₁₀=0.0000, insTT(AT)₁₁=0.0000
Allele Frequency Aggregator	African	Sub	2810	T=1.0000	insGTGT(AT)₃=0.0000, insGTGT(AT)₄=0.0000, insGTGT(AT)₅=0.0000, insGTGT(AT)₇=0.0000, insTTAT=0.0000, insTTATAT=0.0000, insTT(AT)₃=0.0000, insTT(AT)₄=0.0000, insTT(AT)₅=0.0000, insTT(AT)₆=0.0000, insTT(AT)₇=0.0000, insTT(AT)₈=0.0000, insTT(AT)₉=0.0000, insTT(AT)₁₀=0.0000, insTT(AT)₁₁=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	608	T=1.000	insGTGT(AT)₃=0.000, insGTGT(AT)₄=0.000, insGTGT(AT)₅=0.000, insGTGT(AT)₇=0.000, insTTAT=0.000, insTTATAT=0.000, insTT(AT)₃=0.000, insTT(AT)₄=0.000, insTT(AT)₅=0.000, insTT(AT)₆=0.000, insTT(AT)₇=0.000, insTT(AT)₈=0.000, insTT(AT)₉=0.000, insTT(AT)₁₀=0.000, insTT(AT)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	470	T=1.000	insGTGT(AT)₃=0.000, insGTGT(AT)₄=0.000, insGTGT(AT)₅=0.000, insGTGT(AT)₇=0.000, insTTAT=0.000, insTTATAT=0.000, insTT(AT)₃=0.000, insTT(AT)₄=0.000, insTT(AT)₅=0.000, insTT(AT)₆=0.000, insTT(AT)₇=0.000, insTT(AT)₈=0.000, insTT(AT)₉=0.000, insTT(AT)₁₀=0.000, insTT(AT)₁₁=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	T=1.000	insGTGT(AT)₃=0.000, insGTGT(AT)₄=0.000, insGTGT(AT)₅=0.000, insGTGT(AT)₇=0.000, insTTAT=0.000, insTTATAT=0.000, insTT(AT)₃=0.000, insTT(AT)₄=0.000, insTT(AT)₅=0.000, insTT(AT)₆=0.000, insTT(AT)₇=0.000, insTT(AT)₈=0.000, insTT(AT)₉=0.000, insTT(AT)₁₀=0.000, insTT(AT)₁₁=0.000
Allele Frequency Aggregator	Asian	Sub	108	T=1.000	insGTGT(AT)₃=0.000, insGTGT(AT)₄=0.000, insGTGT(AT)₅=0.000, insGTGT(AT)₇=0.000, insTTAT=0.000, insTTATAT=0.000, insTT(AT)₃=0.000, insTT(AT)₄=0.000, insTT(AT)₅=0.000, insTT(AT)₆=0.000, insTT(AT)₇=0.000, insTT(AT)₈=0.000, insTT(AT)₉=0.000, insTT(AT)₁₀=0.000, insTT(AT)₁₁=0.000
Allele Frequency Aggregator	South Asian	Sub	94	T=1.00	insGTGT(AT)₃=0.00, insGTGT(AT)₄=0.00, insGTGT(AT)₅=0.00, insGTGT(AT)₇=0.00, insTTAT=0.00, insTTATAT=0.00, insTT(AT)₃=0.00, insTT(AT)₄=0.00, insTT(AT)₅=0.00, insTT(AT)₆=0.00, insTT(AT)₇=0.00, insTT(AT)₈=0.00, insTT(AT)₉=0.00, insTT(AT)₁₀=0.00, insTT(AT)₁₁=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 3	NC_000003.12:g.196751664TG[2]TA[3]T[1]
GRCh38.p14 chr 3	NC_000003.12:g.196751664TG[2]TA[4]T[1]
GRCh38.p14 chr 3	NC_000003.12:g.196751664TG[2]TA[5]T[1]
GRCh38.p14 chr 3	NC_000003.12:g.196751664TG[2]TA[6]T[1]
GRCh38.p14 chr 3	NC_000003.12:g.196751664TG[2]TA[7]T[1]
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATATATATAT
GRCh38.p14 chr 3	NC_000003.12:g.196751664_196751665insTTATATATATATATATATGT
GRCh37.p13 chr 3	NC_000003.11:g.196478535TG[2]TA[3]T[1]
GRCh37.p13 chr 3	NC_000003.11:g.196478535TG[2]TA[4]T[1]
GRCh37.p13 chr 3	NC_000003.11:g.196478535TG[2]TA[5]T[1]
GRCh37.p13 chr 3	NC_000003.11:g.196478535TG[2]TA[6]T[1]
GRCh37.p13 chr 3	NC_000003.11:g.196478535TG[2]TA[7]T[1]
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATATATATAT
GRCh37.p13 chr 3	NC_000003.11:g.196478535_196478536insTTATATATATATATATATGT
PAK2 RefSeqGene	NG_009227.1:g.16808TG[2]TA[3]T[1]
PAK2 RefSeqGene	NG_009227.1:g.16808TG[2]TA[4]T[1]
PAK2 RefSeqGene	NG_009227.1:g.16808TG[2]TA[5]T[1]
PAK2 RefSeqGene	NG_009227.1:g.16808TG[2]TA[6]T[1]
PAK2 RefSeqGene	NG_009227.1:g.16808TG[2]TA[7]T[1]
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATATATATAT
PAK2 RefSeqGene	NG_009227.1:g.16808_16809insTTATATATATATATATATGT

Gene: PAK2, p21 (RAC1) activated kinase 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PAK2 transcript	NM_002577.4:c.-22+11507_-… NM_002577.4:c.-22+11507_-22+11508insGTGTATATAT	N/A	Intron Variant
PAK2 transcript variant X1	XM_011512870.3:c.	N/A	Genic Upstream Transcript Variant
PAK2 transcript variant X2	XM_047448218.1:c.	N/A	Genic Upstream Transcript Variant
PAK2 transcript variant X3	XM_047448219.1:c.	N/A	Genic Upstream Transcript 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=	insGTGT(AT)₃	insGTGT(AT)₄	insGTGT(AT)₅	insGTGT(AT)₆	insGTGT(AT)₇	insTTAT	insTTATAT	insTT(AT)₃	insTT(AT)₄	insTT(AT)₅	insTT(AT)₆	insTT(AT)₇	insTT(AT)₈	insTT(AT)₉	insTT(AT)₁₀	insTT(AT)₁₁	insTT(AT)₁₂	insTT(AT)₁₃	insTT(AT)₁₄	insTT(AT)₁₅	insTT(AT)₈GT
GRCh38.p14 chr 3	NC_000003.12:g.196751664=	NC_000003.12:g.196751664TG[2]TA[3]T[1]	NC_000003.12:g.196751664TG[2]TA[4]T[1]	NC_000003.12:g.196751664TG[2]TA[5]T[1]	NC_000003.12:g.196751664TG[2]TA[6]T[1]	NC_000003.12:g.196751664TG[2]TA[7]T[1]	NC_000003.12:g.196751664_196751665insTTAT	NC_000003.12:g.196751664_196751665insTTATAT	NC_000003.12:g.196751664_196751665insTTATATAT	NC_000003.12:g.196751664_196751665insTTATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATATATATATATATAT	NC_000003.12:g.196751664_196751665insTTATATATATATATATATGT
GRCh37.p13 chr 3	NC_000003.11:g.196478535=	NC_000003.11:g.196478535TG[2]TA[3]T[1]	NC_000003.11:g.196478535TG[2]TA[4]T[1]	NC_000003.11:g.196478535TG[2]TA[5]T[1]	NC_000003.11:g.196478535TG[2]TA[6]T[1]	NC_000003.11:g.196478535TG[2]TA[7]T[1]	NC_000003.11:g.196478535_196478536insTTAT	NC_000003.11:g.196478535_196478536insTTATAT	NC_000003.11:g.196478535_196478536insTTATATAT	NC_000003.11:g.196478535_196478536insTTATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATATATATATATATAT	NC_000003.11:g.196478535_196478536insTTATATATATATATATATGT
PAK2 RefSeqGene	NG_009227.1:g.16808=	NG_009227.1:g.16808TG[2]TA[3]T[1]	NG_009227.1:g.16808TG[2]TA[4]T[1]	NG_009227.1:g.16808TG[2]TA[5]T[1]	NG_009227.1:g.16808TG[2]TA[6]T[1]	NG_009227.1:g.16808TG[2]TA[7]T[1]	NG_009227.1:g.16808_16809insTTAT	NG_009227.1:g.16808_16809insTTATAT	NG_009227.1:g.16808_16809insTTATATAT	NG_009227.1:g.16808_16809insTTATATATAT	NG_009227.1:g.16808_16809insTTATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATATATATATATATAT	NG_009227.1:g.16808_16809insTTATATATATATATATATGT
PAK2 transcript	NM_002577.4:c.-22+11507=	NM_002577.4:c.-22+11507_-22+11508insGTGTATATAT	NM_002577.4:c.-22+11507_-22+11508insGTGTATATATAT	NM_002577.4:c.-22+11507_-22+11508insGTGTATATATATAT	NM_002577.4:c.-22+11507_-22+11508insGTGTATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insGTGTATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTAT	NM_002577.4:c.-22+11507_-22+11508insTTATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATATATATATATATAT	NM_002577.4:c.-22+11507_-22+11508insTTATATATATATATATATGT
PAK2 transcript variant X1	XM_005269341.1:c.-22+11507=	XM_005269341.1:c.-22+11507_-22+11508insGTGTATATAT	XM_005269341.1:c.-22+11507_-22+11508insGTGTATATATAT	XM_005269341.1:c.-22+11507_-22+11508insGTGTATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insGTGTATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insGTGTATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTAT	XM_005269341.1:c.-22+11507_-22+11508insTTATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATATATATATATATAT	XM_005269341.1:c.-22+11507_-22+11508insTTATATATATATATATATGT

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#.

18 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4088798681	Apr 26, 2021 (155)
2	GNOMAD	ss4088798682	Apr 26, 2021 (155)
3	GNOMAD	ss4088798683	Apr 26, 2021 (155)
4	GNOMAD	ss4088798684	Apr 26, 2021 (155)
5	GNOMAD	ss4088798685	Apr 26, 2021 (155)
6	GNOMAD	ss4088798686	Apr 26, 2021 (155)
7	GNOMAD	ss4088798687	Apr 26, 2021 (155)
8	GNOMAD	ss4088798688	Apr 26, 2021 (155)
9	GNOMAD	ss4088798689	Apr 26, 2021 (155)
10	GNOMAD	ss4088798690	Apr 26, 2021 (155)
11	GNOMAD	ss4088798691	Apr 26, 2021 (155)
12	GNOMAD	ss4088798692	Apr 26, 2021 (155)
13	GNOMAD	ss4088798693	Apr 26, 2021 (155)
14	GNOMAD	ss4088798694	Apr 26, 2021 (155)
15	GNOMAD	ss4088798695	Apr 26, 2021 (155)
16	GNOMAD	ss4088798696	Apr 26, 2021 (155)
17	GNOMAD	ss4088798697	Apr 26, 2021 (155)
18	GNOMAD	ss4088798698	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137185698 (NC_000003.12:196751663::TGTGTATATA 2/40862) Row 137185699 (NC_000003.12:196751663::TGTGTATATATATATA 1/40862) Row 137185700 (NC_000003.12:196751663::TTTA 18/40858)...	-	Apr 26, 2021 (155)
37	ALFA	NC_000003.12 - 196751664	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
ss4088798681	NC_000003.12:196751663::TGTGTATATA	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATAT	(self)
12575382031	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATAT	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATAT	(self)
12575382031	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATAT	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATATAT	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATATAT	(self)
ss4088798682	NC_000003.12:196751663::TGTGTATATA… NC_000003.12:196751663::TGTGTATATATATATA	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATATATATAT	NC_000003.12:196751663:T:TGTGTATAT… NC_000003.12:196751663:T:TGTGTATATATATATATAT	(self)
ss4088798683	NC_000003.12:196751663::TTTA	NC_000003.12:196751663:T:TTTAT	(self)
12575382031	NC_000003.12:196751663:T:TTTAT	NC_000003.12:196751663:T:TTTAT	(self)
ss4088798684	NC_000003.12:196751663::TTTATA	NC_000003.12:196751663:T:TTTATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATAT	NC_000003.12:196751663:T:TTTATAT	(self)
ss4088798685	NC_000003.12:196751663::TTTATATA	NC_000003.12:196751663:T:TTTATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT	NC_000003.12:196751663:T:TTTATATAT	(self)
ss4088798686	NC_000003.12:196751663::TTTATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATAT	(self)
ss4088798687	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATAT	(self)
ss4088798688	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATAT	(self)
ss4088798689	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATAT	(self)
ss4088798690	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATAT	(self)
ss4088798691	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATAT	(self)
ss4088798692	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATAT	(self)
ss4088798693	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATAT	(self)
12575382031	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATAT	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATAT	(self)
ss4088798694	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATATAT	(self)
ss4088798695	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATATATAT	(self)
ss4088798696	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATATATATAT	(self)
ss4088798697	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATATATATATATATA	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATATATATATATATAT	(self)
ss4088798698	NC_000003.12:196751663::TTTATATATA… NC_000003.12:196751663::TTTATATATATATATATATG	NC_000003.12:196751663:T:TTTATATAT… NC_000003.12:196751663:T:TTTATATATATATATATATGT	(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 rs1491521540

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

rs1491521540