Name: rs1491363494
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.

rs1491363494

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:6816587-6816588 (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: insT / insTTT / insTTTCTTT / ins(T…
insT / insTTT / insTTTCTTT / ins(T)₄ / ins(T)₅ / ins(T)₆ / ins(T)₇ / ins(T)₈ / ins(T)₉ / ins(T)₁₀ / ins(T)₁₁ / ins(T)₁₂ / ins(T)₁₃ / ins(T)₁₄ / ins(T)₁₅ / ins(T)₁₆ / ins(T)₁₇ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂ / ins(T)₂₃ / ins(T)₂₄ / ins(T)₂₅ / ins(T)₂₆ / ins(T)₂₇ / ins(T)₂₈ / ins(T)₂₉ / ins(T)₃₀ / ins(T)₃₁ / ins(T)₃₂ / ins(T)₃₃ / ins(T)₃₄ / ins(T)₃₅ / ins(T)₃₆ / ins(T)₃₇ / ins(T)₃₈ / ins(T)₃₉ / ins(T)₄₀ / ins(T)₄₁ / ins(T)₄₂ / ins(T)₄₇ / ins(T)₄₈ / ins(T)₅₁ / ins(T)₅₃ / ins(T)₅₉
Variation Type: Insertion
Frequency: insTTT=0.00393 (59/15024, 14KJPN)
insTTT=0.00314 (40/12732, 8.3KJPN)
insTTT=0.00000 (0/11862, ALFA) (+ 2 more)
insTTTCTTT=0.00000 (0/11862, ALFA)
insTTT=0.0012 (2/1606, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC00707 : 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	11862	=1.00000	TTT=0.00000, TTTCTTT=0.00000	1.0	N/A
European	Sub	7618	=1.0000	TTT=0.0000, TTTCTTT=0.0000	1.0	N/A
African	Sub	2816	=1.0000	TTT=0.0000, TTTCTTT=0.0000	1.0	N/A
African Others	Sub	108	=1.000	TTT=0.000, TTTCTTT=0.000	1.0	N/A
African American	Sub	2708	=1.0000	TTT=0.0000, TTTCTTT=0.0000	1.0	N/A
Asian	Sub	108	=1.000	TTT=0.000, TTTCTTT=0.000	1.0	N/A
East Asian	Sub	84	=1.00	TTT=0.00, TTTCTTT=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	TTT=0.00, TTTCTTT=0.00	1.0	N/A
Latin American 1	Sub	146	=1.000	TTT=0.000, TTTCTTT=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	TTT=0.000, TTTCTTT=0.000	1.0	N/A
South Asian	Sub	94	=1.00	TTT=0.00, TTTCTTT=0.00	1.0	N/A
Other	Sub	470	=1.000	TTT=0.000, TTTCTTT=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
14KJPN	JAPANESE	Study-wide	15024	- No frequency provided	insTTT=0.00393
8.3KJPN	JAPANESE	Study-wide	12732	- No frequency provided	insTTT=0.00314
Allele Frequency Aggregator	Total	Global	11862	- No frequency provided	insTTT=0.00000, insTTTCTTT=0.00000
Allele Frequency Aggregator	European	Sub	7618	- No frequency provided	insTTT=0.0000, insTTTCTTT=0.0000
Allele Frequency Aggregator	African	Sub	2816	- No frequency provided	insTTT=0.0000, insTTTCTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insTTT=0.000, insTTTCTTT=0.000
Allele Frequency Aggregator	Other	Sub	470	- No frequency provided	insTTT=0.000, insTTTCTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	- No frequency provided	insTTT=0.000, insTTTCTTT=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insTTT=0.000, insTTTCTTT=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insTTT=0.00, insTTTCTTT=0.00
Korean Genome Project	KOREAN	Study-wide	1606	- No frequency provided	insTTT=0.0012

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 10	NC_000010.11:g.6816587_6816588insT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTCTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTCTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LINC00707, long intergenic non-protein coding RNA 707 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC00707 transcript	NR_038291.1: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	=	insT	insTTT	insTTTCTTT	ins(T)₄	ins(T)₅	ins(T)₆	ins(T)₇	ins(T)₈	ins(T)₉	ins(T)₁₀	ins(T)₁₁	ins(T)₁₂	ins(T)₁₃	ins(T)₁₄	ins(T)₁₅	ins(T)₁₆	ins(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂	ins(T)₂₃	ins(T)₂₄	ins(T)₂₅	ins(T)₂₆	ins(T)₂₇	ins(T)₂₈	ins(T)₂₉	ins(T)₃₀	ins(T)₃₁	ins(T)₃₂	ins(T)₃₃	ins(T)₃₄	ins(T)₃₅	ins(T)₃₆	ins(T)₃₇	ins(T)₃₈	ins(T)₃₉	ins(T)₄₀	ins(T)₄₁	ins(T)₄₂	ins(T)₄₇	ins(T)₄₈	ins(T)₅₁	ins(T)₅₃	ins(T)₅₉
GRCh38.p14 chr 10	NC_000010.11:g.6816587_6816588=	NC_000010.11:g.6816587_6816588insT	NC_000010.11:g.6816587_6816588insTTT	NC_000010.11:g.6816587_6816588insTTTCTTT	NC_000010.11:g.6816587_6816588insTTTT	NC_000010.11:g.6816587_6816588insTTTTT	NC_000010.11:g.6816587_6816588insTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:g.6816587_6816588insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 10	NC_000010.10:g.6858549_6858550=	NC_000010.10:g.6858549_6858550insT	NC_000010.10:g.6858549_6858550insTTT	NC_000010.10:g.6858549_6858550insTTTCTTT	NC_000010.10:g.6858549_6858550insTTTT	NC_000010.10:g.6858549_6858550insTTTTT	NC_000010.10:g.6858549_6858550insTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.10:g.6858549_6858550insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

51 SubSNP, 51 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PADH-LAB_SPU	ss1751290996	Jan 10, 2018 (151)
2	KOGIC	ss3967140085	Apr 26, 2020 (154)
3	GNOMAD	ss4212387386	Apr 26, 2021 (155)
4	GNOMAD	ss4212387387	Apr 26, 2021 (155)
5	GNOMAD	ss4212387388	Apr 26, 2021 (155)
6	GNOMAD	ss4212387389	Apr 26, 2021 (155)
7	GNOMAD	ss4212387390	Apr 26, 2021 (155)
8	GNOMAD	ss4212387391	Apr 26, 2021 (155)
9	GNOMAD	ss4212387392	Apr 26, 2021 (155)
10	GNOMAD	ss4212387393	Apr 26, 2021 (155)
11	GNOMAD	ss4212387394	Apr 26, 2021 (155)
12	GNOMAD	ss4212387395	Apr 26, 2021 (155)
13	GNOMAD	ss4212387396	Apr 26, 2021 (155)
14	GNOMAD	ss4212387397	Apr 26, 2021 (155)
15	GNOMAD	ss4212387398	Apr 26, 2021 (155)
16	GNOMAD	ss4212387399	Apr 26, 2021 (155)
17	GNOMAD	ss4212387400	Apr 26, 2021 (155)
18	GNOMAD	ss4212387401	Apr 26, 2021 (155)
19	GNOMAD	ss4212387402	Apr 26, 2021 (155)
20	GNOMAD	ss4212387403	Apr 26, 2021 (155)
21	GNOMAD	ss4212387404	Apr 26, 2021 (155)
22	GNOMAD	ss4212387405	Apr 26, 2021 (155)
23	GNOMAD	ss4212387406	Apr 26, 2021 (155)
24	GNOMAD	ss4212387407	Apr 26, 2021 (155)
25	GNOMAD	ss4212387408	Apr 26, 2021 (155)
26	GNOMAD	ss4212387409	Apr 26, 2021 (155)
27	GNOMAD	ss4212387410	Apr 26, 2021 (155)
28	GNOMAD	ss4212387411	Apr 26, 2021 (155)
29	GNOMAD	ss4212387412	Apr 26, 2021 (155)
30	GNOMAD	ss4212387413	Apr 26, 2021 (155)
31	GNOMAD	ss4212387414	Apr 26, 2021 (155)
32	GNOMAD	ss4212387415	Apr 26, 2021 (155)
33	GNOMAD	ss4212387416	Apr 26, 2021 (155)
34	GNOMAD	ss4212387417	Apr 26, 2021 (155)
35	GNOMAD	ss4212387418	Apr 26, 2021 (155)
36	GNOMAD	ss4212387419	Apr 26, 2021 (155)
37	GNOMAD	ss4212387420	Apr 26, 2021 (155)
38	GNOMAD	ss4212387421	Apr 26, 2021 (155)
39	GNOMAD	ss4212387422	Apr 26, 2021 (155)
40	GNOMAD	ss4212387423	Apr 26, 2021 (155)
41	GNOMAD	ss4212387424	Apr 26, 2021 (155)
42	GNOMAD	ss4212387425	Apr 26, 2021 (155)
43	GNOMAD	ss4212387426	Apr 26, 2021 (155)
44	GNOMAD	ss4212387427	Apr 26, 2021 (155)
45	GNOMAD	ss4212387428	Apr 26, 2021 (155)
46	GNOMAD	ss4212387429	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5196116826	Apr 26, 2021 (155)
48	HUGCELL_USP	ss5478593819	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5478593821	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5478593822	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5740921791	Oct 16, 2022 (156)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 342532308 (NC_000010.11:6816587::T 1/3362) Row 342532309 (NC_000010.11:6816587::TTT 582/3344) Row 342532310 (NC_000010.11:6816587::TTTCTTT 5/3362)...	-	Apr 26, 2021 (155)
99	Korean Genome Project	NC_000010.11 - 6816588	Apr 26, 2020 (154)
100	8.3KJPN	NC_000010.10 - 6858550	Apr 26, 2021 (155)
101	14KJPN	NC_000010.11 - 6816588	Oct 16, 2022 (156)
102	ALFA	NC_000010.11 - 6816588	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:

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

No publications for rs1491363494

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

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4212387386	NC_000010.11:6816587::T	NC_000010.11:6816587::T	(self)
54086133, ss1751290996, ss5196116826	NC_000010.10:6858549::TTT	NC_000010.11:6816587::TTT	(self)
23518086, 74758895, 7911142713, ss3967140085, ss4212387387, ss5478593819, ss5740921791	NC_000010.11:6816587::TTT	NC_000010.11:6816587::TTT	(self)
7911142713, ss4212387388	NC_000010.11:6816587::TTTCTTT	NC_000010.11:6816587::TTTCTTT	(self)
ss4212387389	NC_000010.11:6816587::TTTT	NC_000010.11:6816587::TTTT	(self)
ss4212387390	NC_000010.11:6816587::TTTTT	NC_000010.11:6816587::TTTTT	(self)
ss4212387391	NC_000010.11:6816587::TTTTTT	NC_000010.11:6816587::TTTTTT	(self)
ss4212387392	NC_000010.11:6816587::TTTTTTT	NC_000010.11:6816587::TTTTTTT	(self)
ss4212387393, ss5478593822	NC_000010.11:6816587::TTTTTTTT	NC_000010.11:6816587::TTTTTTTT	(self)
ss4212387394	NC_000010.11:6816587::TTTTTTTTT	NC_000010.11:6816587::TTTTTTTTT	(self)
ss4212387395	NC_000010.11:6816587::TTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTT	(self)
ss4212387396	NC_000010.11:6816587::TTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTT	(self)
ss4212387397	NC_000010.11:6816587::TTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT	(self)
ss4212387398	NC_000010.11:6816587::TTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTTT	(self)
ss4212387399	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTT	(self)
ss4212387400	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTT	(self)
ss4212387401	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTT	(self)
ss4212387402	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTT	(self)
ss4212387403	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTT	(self)
ss4212387404	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTT	(self)
ss4212387405	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTT	(self)
ss4212387406	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387407	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387408	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387409	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387410	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387411, ss5478593821	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387412	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387413	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387414	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387415	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387416	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387417	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387418	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387419	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387420	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387421	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387422	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387423	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387424	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387425	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387426	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387427	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387428	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4212387429	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:6816587::TTTTTTTTTTTT… NC_000010.11:6816587::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491363494