Name: rs869162947
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.

rs869162947

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:74126348-74126372 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₅ / del(T)₁₄ / del(T)₁₂ / d…
del(T)₁₅ / del(T)₁₄ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₂₂ / dup(T)₂₃ / ins(T)₂₆ / ins(T)₂₇ / ins(T)₃₁ / ins(T)₃₇ / ins(T)₄₃
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00746 (116/15560, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ISLR2 : Intron Variant
LOC283731 : 500B Downstream 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	Alt HMOZ	HTRZ	HWEP
Total	Global	15560	TTTTTTTTTTTTTTTTTTTTTTTTT=0.97770	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00276, TTTTTTTTTTTTTTTTTTTTTTTT=0.00578, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00746, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00084, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00032, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00514, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.986764	0.001456	0.01178	32
European	Sub	12996	TTTTTTTTTTTTTTTTTTTTTTTTT=0.97345	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00331, TTTTTTTTTTTTTTTTTTTTTTTT=0.00693, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00877, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00100, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00038, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00616, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.984377	0.001754	0.013869	32
African	Sub	1476	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	64	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1412	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	90	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	66	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	100	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	470	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	70	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	358	TTTTTTTTTTTTTTTTTTTTTTTTT=0.994	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.988827	0.0	0.011173	0

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	15560	(T)₂₅=0.97770	del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00276, delT=0.00578, dupT=0.00746, dupTT=0.00514, dupTTT=0.00000, dup(T)₄=0.00084, dup(T)₅=0.00000, dup(T)₇=0.00000, ins(T)₂₇=0.00032
Allele Frequency Aggregator	European	Sub	12996	(T)₂₅=0.97345	del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00331, delT=0.00693, dupT=0.00877, dupTT=0.00616, dupTTT=0.00000, dup(T)₄=0.00100, dup(T)₅=0.00000, dup(T)₇=0.00000, ins(T)₂₇=0.00038
Allele Frequency Aggregator	African	Sub	1476	(T)₂₅=1.0000	del(T)₁₅=0.0000, del(T)₁₄=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₇=0.0000, ins(T)₂₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	470	(T)₂₅=1.000	del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000, ins(T)₂₇=0.000
Allele Frequency Aggregator	Other	Sub	358	(T)₂₅=0.994	del(T)₁₅=0.000, del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.006, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000, ins(T)₂₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	100	(T)₂₅=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₇=0.00, ins(T)₂₇=0.00
Allele Frequency Aggregator	Asian	Sub	90	(T)₂₅=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₇=0.00, ins(T)₂₇=0.00
Allele Frequency Aggregator	South Asian	Sub	70	(T)₂₅=1.00	del(T)₁₅=0.00, del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₇=0.00, ins(T)₂₇=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 15	NC_000015.10:g.74126358_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126359_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126361_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126362_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126363_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126364_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126365_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126366_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126367_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126368_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126369_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126370_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126371_74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126372del
GRCh38.p14 chr 15	NC_000015.10:g.74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126371_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126370_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126369_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126368_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126367_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126366_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126365_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126364_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126363_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126351_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126350_74126372dup
GRCh38.p14 chr 15	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.74418699_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418700_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418702_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418703_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418704_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418705_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418706_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418707_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418708_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418709_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418710_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418711_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418712_74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418713del
GRCh37.p13 chr 15	NC_000015.9:g.74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418712_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418711_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418710_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418709_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418708_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418707_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418706_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418705_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418704_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418692_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418691_74418713dup
GRCh37.p13 chr 15	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: ISLR2, immunoglobulin superfamily containing leucine rich repeat 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ISLR2 transcript variant 1	NM_001130136.1:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant 3	NM_001130137.1:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant 4	NM_001130138.2:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant 2	NM_020851.3:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X5	XM_024450003.2:c.-118-484… XM_024450003.2:c.-118-4849_-118-4835del	N/A	Intron Variant
ISLR2 transcript variant X7	XM_024450004.2:c.-118-484… XM_024450004.2:c.-118-4849_-118-4835del	N/A	Intron Variant
ISLR2 transcript variant X1	XM_011521840.4:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X2	XM_011521841.2:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X10	XM_017022446.3:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X4	XM_024450005.2:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X3	XM_024450006.2:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X8	XM_024450007.2:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X9	XM_024450008.2:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X6	XM_047432905.1:c.	N/A	Genic Upstream Transcript Variant
ISLR2 transcript variant X11	XR_931875.4:n.	N/A	Genic Upstream Transcript Variant

Gene: LOC283731, uncharacterized LOC283731 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC283731 transcript variant 1	NR_027073.1:n.	N/A	Downstream Transcript Variant
LOC283731 transcript variant 2	NR_152622.1:n.	N/A	Downstream 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)₂₅=	del(T)₁₅	del(T)₁₄	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₂₂	dup(T)₂₃	ins(T)₂₆	ins(T)₂₇	ins(T)₃₁	ins(T)₃₇	ins(T)₄₃
GRCh38.p14 chr 15	NC_000015.10:g.74126348_74126372=	NC_000015.10:g.74126358_74126372del	NC_000015.10:g.74126359_74126372del	NC_000015.10:g.74126361_74126372del	NC_000015.10:g.74126362_74126372del	NC_000015.10:g.74126363_74126372del	NC_000015.10:g.74126364_74126372del	NC_000015.10:g.74126365_74126372del	NC_000015.10:g.74126366_74126372del	NC_000015.10:g.74126367_74126372del	NC_000015.10:g.74126368_74126372del	NC_000015.10:g.74126369_74126372del	NC_000015.10:g.74126370_74126372del	NC_000015.10:g.74126371_74126372del	NC_000015.10:g.74126372del	NC_000015.10:g.74126372dup	NC_000015.10:g.74126371_74126372dup	NC_000015.10:g.74126370_74126372dup	NC_000015.10:g.74126369_74126372dup	NC_000015.10:g.74126368_74126372dup	NC_000015.10:g.74126367_74126372dup	NC_000015.10:g.74126366_74126372dup	NC_000015.10:g.74126365_74126372dup	NC_000015.10:g.74126364_74126372dup	NC_000015.10:g.74126363_74126372dup	NC_000015.10:g.74126351_74126372dup	NC_000015.10:g.74126350_74126372dup	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:g.74126372_74126373insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.74418689_74418713=	NC_000015.9:g.74418699_74418713del	NC_000015.9:g.74418700_74418713del	NC_000015.9:g.74418702_74418713del	NC_000015.9:g.74418703_74418713del	NC_000015.9:g.74418704_74418713del	NC_000015.9:g.74418705_74418713del	NC_000015.9:g.74418706_74418713del	NC_000015.9:g.74418707_74418713del	NC_000015.9:g.74418708_74418713del	NC_000015.9:g.74418709_74418713del	NC_000015.9:g.74418710_74418713del	NC_000015.9:g.74418711_74418713del	NC_000015.9:g.74418712_74418713del	NC_000015.9:g.74418713del	NC_000015.9:g.74418713dup	NC_000015.9:g.74418712_74418713dup	NC_000015.9:g.74418711_74418713dup	NC_000015.9:g.74418710_74418713dup	NC_000015.9:g.74418709_74418713dup	NC_000015.9:g.74418708_74418713dup	NC_000015.9:g.74418707_74418713dup	NC_000015.9:g.74418706_74418713dup	NC_000015.9:g.74418705_74418713dup	NC_000015.9:g.74418704_74418713dup	NC_000015.9:g.74418692_74418713dup	NC_000015.9:g.74418691_74418713dup	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.9:g.74418713_74418714insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ISLR2 transcript variant X5	XM_024450003.2:c.-118-4859=	XM_024450003.2:c.-118-4849_-118-4835del	XM_024450003.2:c.-118-4848_-118-4835del	XM_024450003.2:c.-118-4846_-118-4835del	XM_024450003.2:c.-118-4845_-118-4835del	XM_024450003.2:c.-118-4844_-118-4835del	XM_024450003.2:c.-118-4843_-118-4835del	XM_024450003.2:c.-118-4842_-118-4835del	XM_024450003.2:c.-118-4841_-118-4835del	XM_024450003.2:c.-118-4840_-118-4835del	XM_024450003.2:c.-118-4839_-118-4835del	XM_024450003.2:c.-118-4838_-118-4835del	XM_024450003.2:c.-118-4837_-118-4835del	XM_024450003.2:c.-118-4836_-118-4835del	XM_024450003.2:c.-118-4835del	XM_024450003.2:c.-118-4835dup	XM_024450003.2:c.-118-4836_-118-4835dup	XM_024450003.2:c.-118-4837_-118-4835dup	XM_024450003.2:c.-118-4838_-118-4835dup	XM_024450003.2:c.-118-4839_-118-4835dup	XM_024450003.2:c.-118-4840_-118-4835dup	XM_024450003.2:c.-118-4841_-118-4835dup	XM_024450003.2:c.-118-4842_-118-4835dup	XM_024450003.2:c.-118-4843_-118-4835dup	XM_024450003.2:c.-118-4844_-118-4835dup	XM_024450003.2:c.-118-4856_-118-4835dup	XM_024450003.2:c.-118-4857_-118-4835dup	XM_024450003.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450003.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450003.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450003.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450003.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ISLR2 transcript variant X7	XM_024450004.2:c.-118-4859=	XM_024450004.2:c.-118-4849_-118-4835del	XM_024450004.2:c.-118-4848_-118-4835del	XM_024450004.2:c.-118-4846_-118-4835del	XM_024450004.2:c.-118-4845_-118-4835del	XM_024450004.2:c.-118-4844_-118-4835del	XM_024450004.2:c.-118-4843_-118-4835del	XM_024450004.2:c.-118-4842_-118-4835del	XM_024450004.2:c.-118-4841_-118-4835del	XM_024450004.2:c.-118-4840_-118-4835del	XM_024450004.2:c.-118-4839_-118-4835del	XM_024450004.2:c.-118-4838_-118-4835del	XM_024450004.2:c.-118-4837_-118-4835del	XM_024450004.2:c.-118-4836_-118-4835del	XM_024450004.2:c.-118-4835del	XM_024450004.2:c.-118-4835dup	XM_024450004.2:c.-118-4836_-118-4835dup	XM_024450004.2:c.-118-4837_-118-4835dup	XM_024450004.2:c.-118-4838_-118-4835dup	XM_024450004.2:c.-118-4839_-118-4835dup	XM_024450004.2:c.-118-4840_-118-4835dup	XM_024450004.2:c.-118-4841_-118-4835dup	XM_024450004.2:c.-118-4842_-118-4835dup	XM_024450004.2:c.-118-4843_-118-4835dup	XM_024450004.2:c.-118-4844_-118-4835dup	XM_024450004.2:c.-118-4856_-118-4835dup	XM_024450004.2:c.-118-4857_-118-4835dup	XM_024450004.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450004.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450004.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450004.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024450004.2:c.-118-4835_-118-4834insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

52 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCMHGSC_JDW	ss103578670	Mar 15, 2016 (147)
2	ACPOP	ss3741063129	Jul 13, 2019 (153)
3	ACPOP	ss3741063130	Jul 13, 2019 (153)
4	ACPOP	ss3741063131	Jul 13, 2019 (153)
5	EVA	ss3834316030	Apr 27, 2020 (154)
6	GNOMAD	ss4291606400	Apr 27, 2021 (155)
7	GNOMAD	ss4291606402	Apr 27, 2021 (155)
8	GNOMAD	ss4291606403	Apr 27, 2021 (155)
9	GNOMAD	ss4291606404	Apr 27, 2021 (155)
10	GNOMAD	ss4291606405	Apr 27, 2021 (155)
11	GNOMAD	ss4291606406	Apr 27, 2021 (155)
12	GNOMAD	ss4291606407	Apr 27, 2021 (155)
13	GNOMAD	ss4291606408	Apr 27, 2021 (155)
14	GNOMAD	ss4291606409	Apr 27, 2021 (155)
15	GNOMAD	ss4291606410	Apr 27, 2021 (155)
16	GNOMAD	ss4291606411	Apr 27, 2021 (155)
17	GNOMAD	ss4291606412	Apr 27, 2021 (155)
18	GNOMAD	ss4291606413	Apr 27, 2021 (155)
19	GNOMAD	ss4291606414	Apr 27, 2021 (155)
20	GNOMAD	ss4291606415	Apr 27, 2021 (155)
21	GNOMAD	ss4291606416	Apr 27, 2021 (155)
22	GNOMAD	ss4291606417	Apr 27, 2021 (155)
23	GNOMAD	ss4291606418	Apr 27, 2021 (155)
24	GNOMAD	ss4291606419	Apr 27, 2021 (155)
25	GNOMAD	ss4291606420	Apr 27, 2021 (155)
26	GNOMAD	ss4291606421	Apr 27, 2021 (155)
27	GNOMAD	ss4291606422	Apr 27, 2021 (155)
28	GNOMAD	ss4291606423	Apr 27, 2021 (155)
29	TOPMED	ss4997076476	Apr 27, 2021 (155)
30	TOPMED	ss4997076477	Apr 27, 2021 (155)
31	TOPMED	ss4997076478	Apr 27, 2021 (155)
32	TOPMED	ss4997076479	Apr 27, 2021 (155)
33	TOPMED	ss4997076480	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5216945857	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5216945858	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5216945859	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5216945860	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5216945861	Apr 27, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5299007829	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5299007830	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5299007832	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5299007833	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5492680262	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5492680263	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5492680264	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5492680265	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5492680266	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5770976333	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5770976334	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5770976336	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5770976337	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5770976338	Oct 16, 2022 (156)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 473805954 (NC_000015.10:74126347::T 3867/86666) Row 473805956 (NC_000015.10:74126347::TT 1722/86638) Row 473805957 (NC_000015.10:74126347::TTT 743/86714)...	-	Apr 27, 2021 (155)
76	Northern Sweden Submission ignored due to conflicting rows: Row 14347994 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 3/584) Row 14347995 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/584) Row 14347996 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTT 3/584)	-	Jul 13, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 14347994 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 3/584) Row 14347995 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/584) Row 14347996 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTT 3/584)	-	Jul 13, 2019 (153)
78	Northern Sweden Submission ignored due to conflicting rows: Row 14347994 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 3/584) Row 14347995 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 2/584) Row 14347996 (NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTT 3/584)	-	Jul 13, 2019 (153)
79	8.3KJPN Submission ignored due to conflicting rows: Row 74915164 (NC_000015.9:74418688:T: 401/16722) Row 74915165 (NC_000015.9:74418688::T 281/16722) Row 74915166 (NC_000015.9:74418688::TTTTT 70/16722)...	-	Apr 27, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 74915164 (NC_000015.9:74418688:T: 401/16722) Row 74915165 (NC_000015.9:74418688::T 281/16722) Row 74915166 (NC_000015.9:74418688::TTTTT 70/16722)...	-	Apr 27, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 74915164 (NC_000015.9:74418688:T: 401/16722) Row 74915165 (NC_000015.9:74418688::T 281/16722) Row 74915166 (NC_000015.9:74418688::TTTTT 70/16722)...	-	Apr 27, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 74915164 (NC_000015.9:74418688:T: 401/16722) Row 74915165 (NC_000015.9:74418688::T 281/16722) Row 74915166 (NC_000015.9:74418688::TTTTT 70/16722)...	-	Apr 27, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 74915164 (NC_000015.9:74418688:T: 401/16722) Row 74915165 (NC_000015.9:74418688::T 281/16722) Row 74915166 (NC_000015.9:74418688::TTTTT 70/16722)...	-	Apr 27, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 104813437 (NC_000015.10:74126347:T: 876/28214) Row 104813438 (NC_000015.10:74126347::T 448/28214) Row 104813440 (NC_000015.10:74126347::TTTT 485/28214)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 104813437 (NC_000015.10:74126347:T: 876/28214) Row 104813438 (NC_000015.10:74126347::T 448/28214) Row 104813440 (NC_000015.10:74126347::TTTT 485/28214)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 104813437 (NC_000015.10:74126347:T: 876/28214) Row 104813438 (NC_000015.10:74126347::T 448/28214) Row 104813440 (NC_000015.10:74126347::TTTT 485/28214)...	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 104813437 (NC_000015.10:74126347:T: 876/28214) Row 104813438 (NC_000015.10:74126347::T 448/28214) Row 104813440 (NC_000015.10:74126347::TTTT 485/28214)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 104813437 (NC_000015.10:74126347:T: 876/28214) Row 104813438 (NC_000015.10:74126347::T 448/28214) Row 104813440 (NC_000015.10:74126347::TTTT 485/28214)...	-	Oct 16, 2022 (156)
89	TopMed Submission ignored due to conflicting rows: Row 212622136 (NC_000015.10:74126347:TTTTTTTTT: 1/264690) Row 212622137 (NC_000015.10:74126347:TTTTTTTTTTT: 1/264690) Row 212622138 (NC_000015.10:74126347:TTTTTTTTTTTT: 7/264690)...	-	Apr 27, 2021 (155)
90	TopMed Submission ignored due to conflicting rows: Row 212622136 (NC_000015.10:74126347:TTTTTTTTT: 1/264690) Row 212622137 (NC_000015.10:74126347:TTTTTTTTTTT: 1/264690) Row 212622138 (NC_000015.10:74126347:TTTTTTTTTTTT: 7/264690)...	-	Apr 27, 2021 (155)
91	TopMed Submission ignored due to conflicting rows: Row 212622136 (NC_000015.10:74126347:TTTTTTTTT: 1/264690) Row 212622137 (NC_000015.10:74126347:TTTTTTTTTTT: 1/264690) Row 212622138 (NC_000015.10:74126347:TTTTTTTTTTTT: 7/264690)...	-	Apr 27, 2021 (155)
92	TopMed Submission ignored due to conflicting rows: Row 212622136 (NC_000015.10:74126347:TTTTTTTTT: 1/264690) Row 212622137 (NC_000015.10:74126347:TTTTTTTTTTT: 1/264690) Row 212622138 (NC_000015.10:74126347:TTTTTTTTTTTT: 7/264690)...	-	Apr 27, 2021 (155)
93	TopMed Submission ignored due to conflicting rows: Row 212622136 (NC_000015.10:74126347:TTTTTTTTT: 1/264690) Row 212622137 (NC_000015.10:74126347:TTTTTTTTTTT: 1/264690) Row 212622138 (NC_000015.10:74126347:TTTTTTTTTTTT: 7/264690)...	-	Apr 27, 2021 (155)
94	ALFA	NC_000015.10 - 74126348	Apr 27, 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
ss4997076480	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4291606423, ss4997076479	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4997076478	NC_000015.10:74126347:TTTTTTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4997076477	NC_000015.10:74126347:TTTTTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5216945861	NC_000015.9:74418688:TTTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4291606422, ss4997076476	NC_000015.10:74126347:TTTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4291606421	NC_000015.10:74126347:TTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4291606420	NC_000015.10:74126347:TTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4291606419	NC_000015.10:74126347:TTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4291606418	NC_000015.10:74126347:TTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606417, ss5299007833	NC_000015.10:74126347:TTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606416, ss5299007832, ss5492680265	NC_000015.10:74126347:TT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5216945857	NC_000015.9:74418688:T:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606415, ss5492680264, ss5770976333	NC_000015.10:74126347:T:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5216945858	NC_000015.9:74418688::T	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606400, ss5299007829, ss5492680262, ss5770976334	NC_000015.10:74126347::T	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss103578670	NT_010194.17:45209270:G:TG	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606402, ss5492680263	NC_000015.10:74126347::TT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606403	NC_000015.10:74126347::TTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3834316030, ss5216945860	NC_000015.9:74418688::TTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606404, ss5299007830, ss5492680266, ss5770976336	NC_000015.10:74126347::TTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5216945859	NC_000015.9:74418688::TTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606405, ss5770976337	NC_000015.10:74126347::TTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606406, ss5770976338	NC_000015.10:74126347::TTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606407	NC_000015.10:74126347::TTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606408	NC_000015.10:74126347::TTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606409	NC_000015.10:74126347::TTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606410	NC_000015.10:74126347::TTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606411	NC_000015.10:74126347::TTTTTTTTTTT… NC_000015.10:74126347::TTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606412	NC_000015.10:74126347::TTTTTTTTTTT… NC_000015.10:74126347::TTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741063131	NC_000015.9:74418688::TTTTTTTTTTTT… NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5765698476	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741063130	NC_000015.9:74418688::TTTTTTTTTTTT… NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606413	NC_000015.10:74126347::TTTTTTTTTTT… NC_000015.10:74126347::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4291606414	NC_000015.10:74126347::TTTTTTTTTTT… NC_000015.10:74126347::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741063129	NC_000015.9:74418688::TTTTTTTTTTTT… NC_000015.9:74418688::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3231892145	NC_000015.10:74126347:TTTTTTTT:	NC_000015.10:74126347:TTTTTTTTTTTT… NC_000015.10:74126347:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

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

No publications for rs869162947

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

rs869162947