Name: rs567222914
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.

rs567222914

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:119017777-119017799 (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)₁₃ / del(T)₁₁ / d…
del(T)₁₅ / del(T)₁₃ / 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)₁₀ / dup(T)₁₁ / ins(T)₁₂A(T)₂₃ / dup(T)₁₅ / dup(T)₁₉ / dup(T)₂₁ / ins(T)₂₆ / ins(T)₂₈ / ins(T)₄₀
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.02033 (282/13874, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IGSF11 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	13874	TTTTTTTTTTTTTTTTTTTTTTT=0.94479	TTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.02033, TTTTTTTTTTTTTTTTTTTTTT=0.01535, TTTTTTTTTTTTTTTTTTTTTTTT=0.01615, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00296, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00043	0.963874	0.001691	0.034435	18
European	Sub	11742	TTTTTTTTTTTTTTTTTTTTTTT=0.93502	TTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.02376, TTTTTTTTTTTTTTTTTTTTTT=0.01814, TTTTTTTTTTTTTTTTTTTTTTTT=0.01908, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00349, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00051	0.957161	0.001839	0.041	12
African	Sub	1362	TTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	52	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1310	TTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	70	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	54	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	96	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	254	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	68	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	282	TTTTTTTTTTTTTTTTTTTTTTT=0.989	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.011, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.985816	0.007092	0.007092	33

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	13874	(T)₂₃=0.94479	del(T)₁₅=0.00000, del(T)₁₃=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)₅=0.00000, delTTT=0.00000, delTT=0.02033, delT=0.01535, dupT=0.01615, dupTT=0.00296, ins(T)₂₈=0.00043
Allele Frequency Aggregator	European	Sub	11742	(T)₂₃=0.93502	del(T)₁₅=0.00000, del(T)₁₃=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)₅=0.00000, delTTT=0.00000, delTT=0.02376, delT=0.01814, dupT=0.01908, dupTT=0.00349, ins(T)₂₈=0.00051
Allele Frequency Aggregator	African	Sub	1362	(T)₂₃=1.0000	del(T)₁₅=0.0000, del(T)₁₃=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)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, ins(T)₂₈=0.0000
Allele Frequency Aggregator	Other	Sub	282	(T)₂₃=0.989	del(T)₁₅=0.000, del(T)₁₃=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)₅=0.000, delTTT=0.000, delTT=0.011, delT=0.000, dupT=0.000, dupTT=0.000, ins(T)₂₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	254	(T)₂₃=1.000	del(T)₁₅=0.000, del(T)₁₃=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)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, ins(T)₂₈=0.000
Allele Frequency Aggregator	Latin American 1	Sub	96	(T)₂₃=1.00	del(T)₁₅=0.00, del(T)₁₃=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)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₂₈=0.00
Allele Frequency Aggregator	Asian	Sub	70	(T)₂₃=1.00	del(T)₁₅=0.00, del(T)₁₃=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)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₂₈=0.00
Allele Frequency Aggregator	South Asian	Sub	68	(T)₂₃=1.00	del(T)₁₅=0.00, del(T)₁₃=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)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₂₈=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.119017785_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017787_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017789_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017790_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017791_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017792_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017793_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017794_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017795_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017796_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017797_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017798_119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017799del
GRCh38.p14 chr 3	NC_000003.12:g.119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017798_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017797_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017796_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017795_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017794_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017793_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017792_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017790_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017789_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017777_119017799T[35]ATTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.119017785_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017781_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017779_119017799dup
GRCh38.p14 chr 3	NC_000003.12:g.119017799_119017800insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.119017799_119017800insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.119017799_119017800insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.118736632_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736634_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736636_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736637_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736638_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736639_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736640_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736641_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736642_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736643_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736644_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736645_118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736646del
GRCh37.p13 chr 3	NC_000003.11:g.118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736645_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736644_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736643_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736642_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736641_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736640_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736639_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736637_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736636_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736624_118736646T[35]ATTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.118736632_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736628_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736626_118736646dup
GRCh37.p13 chr 3	NC_000003.11:g.118736646_118736647insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.118736646_118736647insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.118736646_118736647insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: IGSF11, immunoglobulin superfamily member 11 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IGSF11 transcript variant 2	NM_001015887.3:c.52+16740… NM_001015887.3:c.52+16740_52+16754del	N/A	Intron Variant
IGSF11 transcript variant 3	NM_001353318.2:c.52+16740… NM_001353318.2:c.52+16740_52+16754del	N/A	Intron Variant
IGSF11 transcript variant 4	NM_001353319.2:c.52+16740… NM_001353319.2:c.52+16740_52+16754del	N/A	Intron Variant
IGSF11 transcript variant 5	NM_001353320.2:c.49+87353… NM_001353320.2:c.49+87353_49+87367del	N/A	Intron Variant
IGSF11 transcript variant 6	NM_001353321.2:c.52+16740… NM_001353321.2:c.52+16740_52+16754del	N/A	Intron Variant
IGSF11 transcript variant 7	NM_001353322.2:c.49+87353… NM_001353322.2:c.49+87353_49+87367del	N/A	Intron Variant
IGSF11 transcript variant 8	NM_001353323.2:c.52+16740… NM_001353323.2:c.52+16740_52+16754del	N/A	Intron Variant
IGSF11 transcript variant 9	NM_001353324.2:c.52+16740… NM_001353324.2:c.52+16740_52+16754del	N/A	Intron Variant
IGSF11 transcript variant 10	NM_001353325.2:c.-216+167… NM_001353325.2:c.-216+16740_-216+16754del	N/A	Intron Variant
IGSF11 transcript variant 11	NM_001353326.2:c.-216+167… NM_001353326.2:c.-216+16740_-216+16754del	N/A	Intron Variant
IGSF11 transcript variant 1	NM_152538.4:c.49+87353_49… NM_152538.4:c.49+87353_49+87367del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₃=	del(T)₁₅	del(T)₁₃	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)₁₀	dup(T)₁₁	ins(T)₁₂A(T)₂₃	dup(T)₁₅	dup(T)₁₉	dup(T)₂₁	ins(T)₂₆	ins(T)₂₈	ins(T)₄₀
GRCh38.p14 chr 3	NC_000003.12:g.119017777_119017799=	NC_000003.12:g.119017785_119017799del	NC_000003.12:g.119017787_119017799del	NC_000003.12:g.119017789_119017799del	NC_000003.12:g.119017790_119017799del	NC_000003.12:g.119017791_119017799del	NC_000003.12:g.119017792_119017799del	NC_000003.12:g.119017793_119017799del	NC_000003.12:g.119017794_119017799del	NC_000003.12:g.119017795_119017799del	NC_000003.12:g.119017796_119017799del	NC_000003.12:g.119017797_119017799del	NC_000003.12:g.119017798_119017799del	NC_000003.12:g.119017799del	NC_000003.12:g.119017799dup	NC_000003.12:g.119017798_119017799dup	NC_000003.12:g.119017797_119017799dup	NC_000003.12:g.119017796_119017799dup	NC_000003.12:g.119017795_119017799dup	NC_000003.12:g.119017794_119017799dup	NC_000003.12:g.119017793_119017799dup	NC_000003.12:g.119017792_119017799dup	NC_000003.12:g.119017790_119017799dup	NC_000003.12:g.119017789_119017799dup	NC_000003.12:g.119017777_119017799T[35]ATTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.119017785_119017799dup	NC_000003.12:g.119017781_119017799dup	NC_000003.12:g.119017779_119017799dup	NC_000003.12:g.119017799_119017800insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.119017799_119017800insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.119017799_119017800insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.118736624_118736646=	NC_000003.11:g.118736632_118736646del	NC_000003.11:g.118736634_118736646del	NC_000003.11:g.118736636_118736646del	NC_000003.11:g.118736637_118736646del	NC_000003.11:g.118736638_118736646del	NC_000003.11:g.118736639_118736646del	NC_000003.11:g.118736640_118736646del	NC_000003.11:g.118736641_118736646del	NC_000003.11:g.118736642_118736646del	NC_000003.11:g.118736643_118736646del	NC_000003.11:g.118736644_118736646del	NC_000003.11:g.118736645_118736646del	NC_000003.11:g.118736646del	NC_000003.11:g.118736646dup	NC_000003.11:g.118736645_118736646dup	NC_000003.11:g.118736644_118736646dup	NC_000003.11:g.118736643_118736646dup	NC_000003.11:g.118736642_118736646dup	NC_000003.11:g.118736641_118736646dup	NC_000003.11:g.118736640_118736646dup	NC_000003.11:g.118736639_118736646dup	NC_000003.11:g.118736637_118736646dup	NC_000003.11:g.118736636_118736646dup	NC_000003.11:g.118736624_118736646T[35]ATTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.118736632_118736646dup	NC_000003.11:g.118736628_118736646dup	NC_000003.11:g.118736626_118736646dup	NC_000003.11:g.118736646_118736647insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.118736646_118736647insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.118736646_118736647insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGSF11 transcript variant 2	NM_001015887.1:c.52+16754=	NM_001015887.1:c.52+16740_52+16754del	NM_001015887.1:c.52+16742_52+16754del	NM_001015887.1:c.52+16744_52+16754del	NM_001015887.1:c.52+16745_52+16754del	NM_001015887.1:c.52+16746_52+16754del	NM_001015887.1:c.52+16747_52+16754del	NM_001015887.1:c.52+16748_52+16754del	NM_001015887.1:c.52+16749_52+16754del	NM_001015887.1:c.52+16750_52+16754del	NM_001015887.1:c.52+16751_52+16754del	NM_001015887.1:c.52+16752_52+16754del	NM_001015887.1:c.52+16753_52+16754del	NM_001015887.1:c.52+16754del	NM_001015887.1:c.52+16754dup	NM_001015887.1:c.52+16753_52+16754dup	NM_001015887.1:c.52+16752_52+16754dup	NM_001015887.1:c.52+16751_52+16754dup	NM_001015887.1:c.52+16750_52+16754dup	NM_001015887.1:c.52+16749_52+16754dup	NM_001015887.1:c.52+16748_52+16754dup	NM_001015887.1:c.52+16747_52+16754dup	NM_001015887.1:c.52+16745_52+16754dup	NM_001015887.1:c.52+16744_52+16754dup	NM_001015887.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001015887.1:c.52+16740_52+16754dup	NM_001015887.1:c.52+16736_52+16754dup	NM_001015887.1:c.52+16734_52+16754dup	NM_001015887.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001015887.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001015887.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 2	NM_001015887.3:c.52+16754=	NM_001015887.3:c.52+16740_52+16754del	NM_001015887.3:c.52+16742_52+16754del	NM_001015887.3:c.52+16744_52+16754del	NM_001015887.3:c.52+16745_52+16754del	NM_001015887.3:c.52+16746_52+16754del	NM_001015887.3:c.52+16747_52+16754del	NM_001015887.3:c.52+16748_52+16754del	NM_001015887.3:c.52+16749_52+16754del	NM_001015887.3:c.52+16750_52+16754del	NM_001015887.3:c.52+16751_52+16754del	NM_001015887.3:c.52+16752_52+16754del	NM_001015887.3:c.52+16753_52+16754del	NM_001015887.3:c.52+16754del	NM_001015887.3:c.52+16754dup	NM_001015887.3:c.52+16753_52+16754dup	NM_001015887.3:c.52+16752_52+16754dup	NM_001015887.3:c.52+16751_52+16754dup	NM_001015887.3:c.52+16750_52+16754dup	NM_001015887.3:c.52+16749_52+16754dup	NM_001015887.3:c.52+16748_52+16754dup	NM_001015887.3:c.52+16747_52+16754dup	NM_001015887.3:c.52+16745_52+16754dup	NM_001015887.3:c.52+16744_52+16754dup	NM_001015887.3:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001015887.3:c.52+16740_52+16754dup	NM_001015887.3:c.52+16736_52+16754dup	NM_001015887.3:c.52+16734_52+16754dup	NM_001015887.3:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001015887.3:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001015887.3:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 3	NM_001353318.2:c.52+16754=	NM_001353318.2:c.52+16740_52+16754del	NM_001353318.2:c.52+16742_52+16754del	NM_001353318.2:c.52+16744_52+16754del	NM_001353318.2:c.52+16745_52+16754del	NM_001353318.2:c.52+16746_52+16754del	NM_001353318.2:c.52+16747_52+16754del	NM_001353318.2:c.52+16748_52+16754del	NM_001353318.2:c.52+16749_52+16754del	NM_001353318.2:c.52+16750_52+16754del	NM_001353318.2:c.52+16751_52+16754del	NM_001353318.2:c.52+16752_52+16754del	NM_001353318.2:c.52+16753_52+16754del	NM_001353318.2:c.52+16754del	NM_001353318.2:c.52+16754dup	NM_001353318.2:c.52+16753_52+16754dup	NM_001353318.2:c.52+16752_52+16754dup	NM_001353318.2:c.52+16751_52+16754dup	NM_001353318.2:c.52+16750_52+16754dup	NM_001353318.2:c.52+16749_52+16754dup	NM_001353318.2:c.52+16748_52+16754dup	NM_001353318.2:c.52+16747_52+16754dup	NM_001353318.2:c.52+16745_52+16754dup	NM_001353318.2:c.52+16744_52+16754dup	NM_001353318.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353318.2:c.52+16740_52+16754dup	NM_001353318.2:c.52+16736_52+16754dup	NM_001353318.2:c.52+16734_52+16754dup	NM_001353318.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353318.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353318.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 4	NM_001353319.2:c.52+16754=	NM_001353319.2:c.52+16740_52+16754del	NM_001353319.2:c.52+16742_52+16754del	NM_001353319.2:c.52+16744_52+16754del	NM_001353319.2:c.52+16745_52+16754del	NM_001353319.2:c.52+16746_52+16754del	NM_001353319.2:c.52+16747_52+16754del	NM_001353319.2:c.52+16748_52+16754del	NM_001353319.2:c.52+16749_52+16754del	NM_001353319.2:c.52+16750_52+16754del	NM_001353319.2:c.52+16751_52+16754del	NM_001353319.2:c.52+16752_52+16754del	NM_001353319.2:c.52+16753_52+16754del	NM_001353319.2:c.52+16754del	NM_001353319.2:c.52+16754dup	NM_001353319.2:c.52+16753_52+16754dup	NM_001353319.2:c.52+16752_52+16754dup	NM_001353319.2:c.52+16751_52+16754dup	NM_001353319.2:c.52+16750_52+16754dup	NM_001353319.2:c.52+16749_52+16754dup	NM_001353319.2:c.52+16748_52+16754dup	NM_001353319.2:c.52+16747_52+16754dup	NM_001353319.2:c.52+16745_52+16754dup	NM_001353319.2:c.52+16744_52+16754dup	NM_001353319.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353319.2:c.52+16740_52+16754dup	NM_001353319.2:c.52+16736_52+16754dup	NM_001353319.2:c.52+16734_52+16754dup	NM_001353319.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353319.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353319.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 5	NM_001353320.2:c.49+87367=	NM_001353320.2:c.49+87353_49+87367del	NM_001353320.2:c.49+87355_49+87367del	NM_001353320.2:c.49+87357_49+87367del	NM_001353320.2:c.49+87358_49+87367del	NM_001353320.2:c.49+87359_49+87367del	NM_001353320.2:c.49+87360_49+87367del	NM_001353320.2:c.49+87361_49+87367del	NM_001353320.2:c.49+87362_49+87367del	NM_001353320.2:c.49+87363_49+87367del	NM_001353320.2:c.49+87364_49+87367del	NM_001353320.2:c.49+87365_49+87367del	NM_001353320.2:c.49+87366_49+87367del	NM_001353320.2:c.49+87367del	NM_001353320.2:c.49+87367dup	NM_001353320.2:c.49+87366_49+87367dup	NM_001353320.2:c.49+87365_49+87367dup	NM_001353320.2:c.49+87364_49+87367dup	NM_001353320.2:c.49+87363_49+87367dup	NM_001353320.2:c.49+87362_49+87367dup	NM_001353320.2:c.49+87361_49+87367dup	NM_001353320.2:c.49+87360_49+87367dup	NM_001353320.2:c.49+87358_49+87367dup	NM_001353320.2:c.49+87357_49+87367dup	NM_001353320.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353320.2:c.49+87353_49+87367dup	NM_001353320.2:c.49+87349_49+87367dup	NM_001353320.2:c.49+87347_49+87367dup	NM_001353320.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353320.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353320.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 6	NM_001353321.2:c.52+16754=	NM_001353321.2:c.52+16740_52+16754del	NM_001353321.2:c.52+16742_52+16754del	NM_001353321.2:c.52+16744_52+16754del	NM_001353321.2:c.52+16745_52+16754del	NM_001353321.2:c.52+16746_52+16754del	NM_001353321.2:c.52+16747_52+16754del	NM_001353321.2:c.52+16748_52+16754del	NM_001353321.2:c.52+16749_52+16754del	NM_001353321.2:c.52+16750_52+16754del	NM_001353321.2:c.52+16751_52+16754del	NM_001353321.2:c.52+16752_52+16754del	NM_001353321.2:c.52+16753_52+16754del	NM_001353321.2:c.52+16754del	NM_001353321.2:c.52+16754dup	NM_001353321.2:c.52+16753_52+16754dup	NM_001353321.2:c.52+16752_52+16754dup	NM_001353321.2:c.52+16751_52+16754dup	NM_001353321.2:c.52+16750_52+16754dup	NM_001353321.2:c.52+16749_52+16754dup	NM_001353321.2:c.52+16748_52+16754dup	NM_001353321.2:c.52+16747_52+16754dup	NM_001353321.2:c.52+16745_52+16754dup	NM_001353321.2:c.52+16744_52+16754dup	NM_001353321.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353321.2:c.52+16740_52+16754dup	NM_001353321.2:c.52+16736_52+16754dup	NM_001353321.2:c.52+16734_52+16754dup	NM_001353321.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353321.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353321.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 7	NM_001353322.2:c.49+87367=	NM_001353322.2:c.49+87353_49+87367del	NM_001353322.2:c.49+87355_49+87367del	NM_001353322.2:c.49+87357_49+87367del	NM_001353322.2:c.49+87358_49+87367del	NM_001353322.2:c.49+87359_49+87367del	NM_001353322.2:c.49+87360_49+87367del	NM_001353322.2:c.49+87361_49+87367del	NM_001353322.2:c.49+87362_49+87367del	NM_001353322.2:c.49+87363_49+87367del	NM_001353322.2:c.49+87364_49+87367del	NM_001353322.2:c.49+87365_49+87367del	NM_001353322.2:c.49+87366_49+87367del	NM_001353322.2:c.49+87367del	NM_001353322.2:c.49+87367dup	NM_001353322.2:c.49+87366_49+87367dup	NM_001353322.2:c.49+87365_49+87367dup	NM_001353322.2:c.49+87364_49+87367dup	NM_001353322.2:c.49+87363_49+87367dup	NM_001353322.2:c.49+87362_49+87367dup	NM_001353322.2:c.49+87361_49+87367dup	NM_001353322.2:c.49+87360_49+87367dup	NM_001353322.2:c.49+87358_49+87367dup	NM_001353322.2:c.49+87357_49+87367dup	NM_001353322.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353322.2:c.49+87353_49+87367dup	NM_001353322.2:c.49+87349_49+87367dup	NM_001353322.2:c.49+87347_49+87367dup	NM_001353322.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353322.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353322.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 8	NM_001353323.2:c.52+16754=	NM_001353323.2:c.52+16740_52+16754del	NM_001353323.2:c.52+16742_52+16754del	NM_001353323.2:c.52+16744_52+16754del	NM_001353323.2:c.52+16745_52+16754del	NM_001353323.2:c.52+16746_52+16754del	NM_001353323.2:c.52+16747_52+16754del	NM_001353323.2:c.52+16748_52+16754del	NM_001353323.2:c.52+16749_52+16754del	NM_001353323.2:c.52+16750_52+16754del	NM_001353323.2:c.52+16751_52+16754del	NM_001353323.2:c.52+16752_52+16754del	NM_001353323.2:c.52+16753_52+16754del	NM_001353323.2:c.52+16754del	NM_001353323.2:c.52+16754dup	NM_001353323.2:c.52+16753_52+16754dup	NM_001353323.2:c.52+16752_52+16754dup	NM_001353323.2:c.52+16751_52+16754dup	NM_001353323.2:c.52+16750_52+16754dup	NM_001353323.2:c.52+16749_52+16754dup	NM_001353323.2:c.52+16748_52+16754dup	NM_001353323.2:c.52+16747_52+16754dup	NM_001353323.2:c.52+16745_52+16754dup	NM_001353323.2:c.52+16744_52+16754dup	NM_001353323.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353323.2:c.52+16740_52+16754dup	NM_001353323.2:c.52+16736_52+16754dup	NM_001353323.2:c.52+16734_52+16754dup	NM_001353323.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353323.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353323.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 9	NM_001353324.2:c.52+16754=	NM_001353324.2:c.52+16740_52+16754del	NM_001353324.2:c.52+16742_52+16754del	NM_001353324.2:c.52+16744_52+16754del	NM_001353324.2:c.52+16745_52+16754del	NM_001353324.2:c.52+16746_52+16754del	NM_001353324.2:c.52+16747_52+16754del	NM_001353324.2:c.52+16748_52+16754del	NM_001353324.2:c.52+16749_52+16754del	NM_001353324.2:c.52+16750_52+16754del	NM_001353324.2:c.52+16751_52+16754del	NM_001353324.2:c.52+16752_52+16754del	NM_001353324.2:c.52+16753_52+16754del	NM_001353324.2:c.52+16754del	NM_001353324.2:c.52+16754dup	NM_001353324.2:c.52+16753_52+16754dup	NM_001353324.2:c.52+16752_52+16754dup	NM_001353324.2:c.52+16751_52+16754dup	NM_001353324.2:c.52+16750_52+16754dup	NM_001353324.2:c.52+16749_52+16754dup	NM_001353324.2:c.52+16748_52+16754dup	NM_001353324.2:c.52+16747_52+16754dup	NM_001353324.2:c.52+16745_52+16754dup	NM_001353324.2:c.52+16744_52+16754dup	NM_001353324.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353324.2:c.52+16740_52+16754dup	NM_001353324.2:c.52+16736_52+16754dup	NM_001353324.2:c.52+16734_52+16754dup	NM_001353324.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353324.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353324.2:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 10	NM_001353325.2:c.-216+16754=	NM_001353325.2:c.-216+16740_-216+16754del	NM_001353325.2:c.-216+16742_-216+16754del	NM_001353325.2:c.-216+16744_-216+16754del	NM_001353325.2:c.-216+16745_-216+16754del	NM_001353325.2:c.-216+16746_-216+16754del	NM_001353325.2:c.-216+16747_-216+16754del	NM_001353325.2:c.-216+16748_-216+16754del	NM_001353325.2:c.-216+16749_-216+16754del	NM_001353325.2:c.-216+16750_-216+16754del	NM_001353325.2:c.-216+16751_-216+16754del	NM_001353325.2:c.-216+16752_-216+16754del	NM_001353325.2:c.-216+16753_-216+16754del	NM_001353325.2:c.-216+16754del	NM_001353325.2:c.-216+16754dup	NM_001353325.2:c.-216+16753_-216+16754dup	NM_001353325.2:c.-216+16752_-216+16754dup	NM_001353325.2:c.-216+16751_-216+16754dup	NM_001353325.2:c.-216+16750_-216+16754dup	NM_001353325.2:c.-216+16749_-216+16754dup	NM_001353325.2:c.-216+16748_-216+16754dup	NM_001353325.2:c.-216+16747_-216+16754dup	NM_001353325.2:c.-216+16745_-216+16754dup	NM_001353325.2:c.-216+16744_-216+16754dup	NM_001353325.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353325.2:c.-216+16740_-216+16754dup	NM_001353325.2:c.-216+16736_-216+16754dup	NM_001353325.2:c.-216+16734_-216+16754dup	NM_001353325.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353325.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353325.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 11	NM_001353326.2:c.-216+16754=	NM_001353326.2:c.-216+16740_-216+16754del	NM_001353326.2:c.-216+16742_-216+16754del	NM_001353326.2:c.-216+16744_-216+16754del	NM_001353326.2:c.-216+16745_-216+16754del	NM_001353326.2:c.-216+16746_-216+16754del	NM_001353326.2:c.-216+16747_-216+16754del	NM_001353326.2:c.-216+16748_-216+16754del	NM_001353326.2:c.-216+16749_-216+16754del	NM_001353326.2:c.-216+16750_-216+16754del	NM_001353326.2:c.-216+16751_-216+16754del	NM_001353326.2:c.-216+16752_-216+16754del	NM_001353326.2:c.-216+16753_-216+16754del	NM_001353326.2:c.-216+16754del	NM_001353326.2:c.-216+16754dup	NM_001353326.2:c.-216+16753_-216+16754dup	NM_001353326.2:c.-216+16752_-216+16754dup	NM_001353326.2:c.-216+16751_-216+16754dup	NM_001353326.2:c.-216+16750_-216+16754dup	NM_001353326.2:c.-216+16749_-216+16754dup	NM_001353326.2:c.-216+16748_-216+16754dup	NM_001353326.2:c.-216+16747_-216+16754dup	NM_001353326.2:c.-216+16745_-216+16754dup	NM_001353326.2:c.-216+16744_-216+16754dup	NM_001353326.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_001353326.2:c.-216+16740_-216+16754dup	NM_001353326.2:c.-216+16736_-216+16754dup	NM_001353326.2:c.-216+16734_-216+16754dup	NM_001353326.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353326.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001353326.2:c.-216+16754_-216+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 1	NM_152538.2:c.49+87367=	NM_152538.2:c.49+87353_49+87367del	NM_152538.2:c.49+87355_49+87367del	NM_152538.2:c.49+87357_49+87367del	NM_152538.2:c.49+87358_49+87367del	NM_152538.2:c.49+87359_49+87367del	NM_152538.2:c.49+87360_49+87367del	NM_152538.2:c.49+87361_49+87367del	NM_152538.2:c.49+87362_49+87367del	NM_152538.2:c.49+87363_49+87367del	NM_152538.2:c.49+87364_49+87367del	NM_152538.2:c.49+87365_49+87367del	NM_152538.2:c.49+87366_49+87367del	NM_152538.2:c.49+87367del	NM_152538.2:c.49+87367dup	NM_152538.2:c.49+87366_49+87367dup	NM_152538.2:c.49+87365_49+87367dup	NM_152538.2:c.49+87364_49+87367dup	NM_152538.2:c.49+87363_49+87367dup	NM_152538.2:c.49+87362_49+87367dup	NM_152538.2:c.49+87361_49+87367dup	NM_152538.2:c.49+87360_49+87367dup	NM_152538.2:c.49+87358_49+87367dup	NM_152538.2:c.49+87357_49+87367dup	NM_152538.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_152538.2:c.49+87353_49+87367dup	NM_152538.2:c.49+87349_49+87367dup	NM_152538.2:c.49+87347_49+87367dup	NM_152538.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152538.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152538.2:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant 1	NM_152538.4:c.49+87367=	NM_152538.4:c.49+87353_49+87367del	NM_152538.4:c.49+87355_49+87367del	NM_152538.4:c.49+87357_49+87367del	NM_152538.4:c.49+87358_49+87367del	NM_152538.4:c.49+87359_49+87367del	NM_152538.4:c.49+87360_49+87367del	NM_152538.4:c.49+87361_49+87367del	NM_152538.4:c.49+87362_49+87367del	NM_152538.4:c.49+87363_49+87367del	NM_152538.4:c.49+87364_49+87367del	NM_152538.4:c.49+87365_49+87367del	NM_152538.4:c.49+87366_49+87367del	NM_152538.4:c.49+87367del	NM_152538.4:c.49+87367dup	NM_152538.4:c.49+87366_49+87367dup	NM_152538.4:c.49+87365_49+87367dup	NM_152538.4:c.49+87364_49+87367dup	NM_152538.4:c.49+87363_49+87367dup	NM_152538.4:c.49+87362_49+87367dup	NM_152538.4:c.49+87361_49+87367dup	NM_152538.4:c.49+87360_49+87367dup	NM_152538.4:c.49+87358_49+87367dup	NM_152538.4:c.49+87357_49+87367dup	NM_152538.4:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	NM_152538.4:c.49+87353_49+87367dup	NM_152538.4:c.49+87349_49+87367dup	NM_152538.4:c.49+87347_49+87367dup	NM_152538.4:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152538.4:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_152538.4:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant X1	XM_005247144.1:c.49+87367=	XM_005247144.1:c.49+87353_49+87367del	XM_005247144.1:c.49+87355_49+87367del	XM_005247144.1:c.49+87357_49+87367del	XM_005247144.1:c.49+87358_49+87367del	XM_005247144.1:c.49+87359_49+87367del	XM_005247144.1:c.49+87360_49+87367del	XM_005247144.1:c.49+87361_49+87367del	XM_005247144.1:c.49+87362_49+87367del	XM_005247144.1:c.49+87363_49+87367del	XM_005247144.1:c.49+87364_49+87367del	XM_005247144.1:c.49+87365_49+87367del	XM_005247144.1:c.49+87366_49+87367del	XM_005247144.1:c.49+87367del	XM_005247144.1:c.49+87367dup	XM_005247144.1:c.49+87366_49+87367dup	XM_005247144.1:c.49+87365_49+87367dup	XM_005247144.1:c.49+87364_49+87367dup	XM_005247144.1:c.49+87363_49+87367dup	XM_005247144.1:c.49+87362_49+87367dup	XM_005247144.1:c.49+87361_49+87367dup	XM_005247144.1:c.49+87360_49+87367dup	XM_005247144.1:c.49+87358_49+87367dup	XM_005247144.1:c.49+87357_49+87367dup	XM_005247144.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	XM_005247144.1:c.49+87353_49+87367dup	XM_005247144.1:c.49+87349_49+87367dup	XM_005247144.1:c.49+87347_49+87367dup	XM_005247144.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247144.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247144.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant X2	XM_005247145.1:c.49+87367=	XM_005247145.1:c.49+87353_49+87367del	XM_005247145.1:c.49+87355_49+87367del	XM_005247145.1:c.49+87357_49+87367del	XM_005247145.1:c.49+87358_49+87367del	XM_005247145.1:c.49+87359_49+87367del	XM_005247145.1:c.49+87360_49+87367del	XM_005247145.1:c.49+87361_49+87367del	XM_005247145.1:c.49+87362_49+87367del	XM_005247145.1:c.49+87363_49+87367del	XM_005247145.1:c.49+87364_49+87367del	XM_005247145.1:c.49+87365_49+87367del	XM_005247145.1:c.49+87366_49+87367del	XM_005247145.1:c.49+87367del	XM_005247145.1:c.49+87367dup	XM_005247145.1:c.49+87366_49+87367dup	XM_005247145.1:c.49+87365_49+87367dup	XM_005247145.1:c.49+87364_49+87367dup	XM_005247145.1:c.49+87363_49+87367dup	XM_005247145.1:c.49+87362_49+87367dup	XM_005247145.1:c.49+87361_49+87367dup	XM_005247145.1:c.49+87360_49+87367dup	XM_005247145.1:c.49+87358_49+87367dup	XM_005247145.1:c.49+87357_49+87367dup	XM_005247145.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	XM_005247145.1:c.49+87353_49+87367dup	XM_005247145.1:c.49+87349_49+87367dup	XM_005247145.1:c.49+87347_49+87367dup	XM_005247145.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247145.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247145.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant X3	XM_005247146.1:c.52+16754=	XM_005247146.1:c.52+16740_52+16754del	XM_005247146.1:c.52+16742_52+16754del	XM_005247146.1:c.52+16744_52+16754del	XM_005247146.1:c.52+16745_52+16754del	XM_005247146.1:c.52+16746_52+16754del	XM_005247146.1:c.52+16747_52+16754del	XM_005247146.1:c.52+16748_52+16754del	XM_005247146.1:c.52+16749_52+16754del	XM_005247146.1:c.52+16750_52+16754del	XM_005247146.1:c.52+16751_52+16754del	XM_005247146.1:c.52+16752_52+16754del	XM_005247146.1:c.52+16753_52+16754del	XM_005247146.1:c.52+16754del	XM_005247146.1:c.52+16754dup	XM_005247146.1:c.52+16753_52+16754dup	XM_005247146.1:c.52+16752_52+16754dup	XM_005247146.1:c.52+16751_52+16754dup	XM_005247146.1:c.52+16750_52+16754dup	XM_005247146.1:c.52+16749_52+16754dup	XM_005247146.1:c.52+16748_52+16754dup	XM_005247146.1:c.52+16747_52+16754dup	XM_005247146.1:c.52+16745_52+16754dup	XM_005247146.1:c.52+16744_52+16754dup	XM_005247146.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	XM_005247146.1:c.52+16740_52+16754dup	XM_005247146.1:c.52+16736_52+16754dup	XM_005247146.1:c.52+16734_52+16754dup	XM_005247146.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247146.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247146.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant X4	XM_005247147.1:c.49+87367=	XM_005247147.1:c.49+87353_49+87367del	XM_005247147.1:c.49+87355_49+87367del	XM_005247147.1:c.49+87357_49+87367del	XM_005247147.1:c.49+87358_49+87367del	XM_005247147.1:c.49+87359_49+87367del	XM_005247147.1:c.49+87360_49+87367del	XM_005247147.1:c.49+87361_49+87367del	XM_005247147.1:c.49+87362_49+87367del	XM_005247147.1:c.49+87363_49+87367del	XM_005247147.1:c.49+87364_49+87367del	XM_005247147.1:c.49+87365_49+87367del	XM_005247147.1:c.49+87366_49+87367del	XM_005247147.1:c.49+87367del	XM_005247147.1:c.49+87367dup	XM_005247147.1:c.49+87366_49+87367dup	XM_005247147.1:c.49+87365_49+87367dup	XM_005247147.1:c.49+87364_49+87367dup	XM_005247147.1:c.49+87363_49+87367dup	XM_005247147.1:c.49+87362_49+87367dup	XM_005247147.1:c.49+87361_49+87367dup	XM_005247147.1:c.49+87360_49+87367dup	XM_005247147.1:c.49+87358_49+87367dup	XM_005247147.1:c.49+87357_49+87367dup	XM_005247147.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	XM_005247147.1:c.49+87353_49+87367dup	XM_005247147.1:c.49+87349_49+87367dup	XM_005247147.1:c.49+87347_49+87367dup	XM_005247147.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247147.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247147.1:c.49+87367_49+87368insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGSF11 transcript variant X5	XM_005247148.1:c.52+16754=	XM_005247148.1:c.52+16740_52+16754del	XM_005247148.1:c.52+16742_52+16754del	XM_005247148.1:c.52+16744_52+16754del	XM_005247148.1:c.52+16745_52+16754del	XM_005247148.1:c.52+16746_52+16754del	XM_005247148.1:c.52+16747_52+16754del	XM_005247148.1:c.52+16748_52+16754del	XM_005247148.1:c.52+16749_52+16754del	XM_005247148.1:c.52+16750_52+16754del	XM_005247148.1:c.52+16751_52+16754del	XM_005247148.1:c.52+16752_52+16754del	XM_005247148.1:c.52+16753_52+16754del	XM_005247148.1:c.52+16754del	XM_005247148.1:c.52+16754dup	XM_005247148.1:c.52+16753_52+16754dup	XM_005247148.1:c.52+16752_52+16754dup	XM_005247148.1:c.52+16751_52+16754dup	XM_005247148.1:c.52+16750_52+16754dup	XM_005247148.1:c.52+16749_52+16754dup	XM_005247148.1:c.52+16748_52+16754dup	XM_005247148.1:c.52+16747_52+16754dup	XM_005247148.1:c.52+16745_52+16754dup	XM_005247148.1:c.52+16744_52+16754dup	XM_005247148.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA	XM_005247148.1:c.52+16740_52+16754dup	XM_005247148.1:c.52+16736_52+16754dup	XM_005247148.1:c.52+16734_52+16754dup	XM_005247148.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247148.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005247148.1:c.52+16754_52+16755insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

55 SubSNP, 42 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42060782	Mar 15, 2016 (147)
2	HGSV	ss77833549	Aug 21, 2014 (142)
3	SSMP	ss663348676	Apr 01, 2015 (144)
4	SWEGEN	ss2993056303	Jan 10, 2018 (151)
5	EVA	ss3828032277	Apr 25, 2020 (154)
6	GNOMAD	ss4079344643	Apr 26, 2021 (155)
7	GNOMAD	ss4079344644	Apr 26, 2021 (155)
8	GNOMAD	ss4079344645	Apr 26, 2021 (155)
9	GNOMAD	ss4079344646	Apr 26, 2021 (155)
10	GNOMAD	ss4079344647	Apr 26, 2021 (155)
11	GNOMAD	ss4079344648	Apr 26, 2021 (155)
12	GNOMAD	ss4079344649	Apr 26, 2021 (155)
13	GNOMAD	ss4079344650	Apr 26, 2021 (155)
14	GNOMAD	ss4079344651	Apr 26, 2021 (155)
15	GNOMAD	ss4079344652	Apr 26, 2021 (155)
16	GNOMAD	ss4079344653	Apr 26, 2021 (155)
17	GNOMAD	ss4079344654	Apr 26, 2021 (155)
18	GNOMAD	ss4079344655	Apr 26, 2021 (155)
19	GNOMAD	ss4079344656	Apr 26, 2021 (155)
20	GNOMAD	ss4079344657	Apr 26, 2021 (155)
21	GNOMAD	ss4079344658	Apr 26, 2021 (155)
22	GNOMAD	ss4079344659	Apr 26, 2021 (155)
23	GNOMAD	ss4079344660	Apr 26, 2021 (155)
24	GNOMAD	ss4079344661	Apr 26, 2021 (155)
25	GNOMAD	ss4079344662	Apr 26, 2021 (155)
26	GNOMAD	ss4079344663	Apr 26, 2021 (155)
27	GNOMAD	ss4079344664	Apr 26, 2021 (155)
28	GNOMAD	ss4079344665	Apr 26, 2021 (155)
29	GNOMAD	ss4079344666	Apr 26, 2021 (155)
30	GNOMAD	ss4079344667	Apr 26, 2021 (155)
31	GNOMAD	ss4079344668	Apr 26, 2021 (155)
32	GNOMAD	ss4079344669	Apr 26, 2021 (155)
33	GNOMAD	ss4079344670	Apr 26, 2021 (155)
34	TOPMED	ss4580709742	Apr 26, 2021 (155)
35	TOPMED	ss4580709743	Apr 26, 2021 (155)
36	TOPMED	ss4580709744	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5161196771	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5161196772	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5161196773	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5161196774	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5161196775	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5255732036	Oct 12, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5255732037	Oct 12, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5255732038	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5255732039	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5454909977	Oct 12, 2022 (156)
47	HUGCELL_USP	ss5454909978	Oct 12, 2022 (156)
48	HUGCELL_USP	ss5454909979	Oct 12, 2022 (156)
49	HUGCELL_USP	ss5454909980	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5454909981	Oct 12, 2022 (156)
51	TOMMO_GENOMICS	ss5693957331	Oct 12, 2022 (156)
52	TOMMO_GENOMICS	ss5693957332	Oct 12, 2022 (156)
53	TOMMO_GENOMICS	ss5693957333	Oct 12, 2022 (156)
54	TOMMO_GENOMICS	ss5693957334	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5693957335	Oct 12, 2022 (156)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121347504 (NC_000003.12:119017776::T 4866/92220) Row 121347505 (NC_000003.12:119017776::TT 559/92116) Row 121347506 (NC_000003.12:119017776::TTT 59/92224)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 19166078 (NC_000003.11:118736623:TT: 1840/16598) Row 19166079 (NC_000003.11:118736623::T 815/16598) Row 19166080 (NC_000003.11:118736623:T: 56/16598)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 19166078 (NC_000003.11:118736623:TT: 1840/16598) Row 19166079 (NC_000003.11:118736623::T 815/16598) Row 19166080 (NC_000003.11:118736623:T: 56/16598)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 19166078 (NC_000003.11:118736623:TT: 1840/16598) Row 19166079 (NC_000003.11:118736623::T 815/16598) Row 19166080 (NC_000003.11:118736623:T: 56/16598)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 19166078 (NC_000003.11:118736623:TT: 1840/16598) Row 19166079 (NC_000003.11:118736623::T 815/16598) Row 19166080 (NC_000003.11:118736623:T: 56/16598)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 19166078 (NC_000003.11:118736623:TT: 1840/16598) Row 19166079 (NC_000003.11:118736623::T 815/16598) Row 19166080 (NC_000003.11:118736623:T: 56/16598)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 27794435 (NC_000003.12:119017776:TT: 3493/27968) Row 27794436 (NC_000003.12:119017776::T 1260/27968) Row 27794437 (NC_000003.12:119017776:T: 101/27968)...	-	Oct 12, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 27794435 (NC_000003.12:119017776:TT: 3493/27968) Row 27794436 (NC_000003.12:119017776::T 1260/27968) Row 27794437 (NC_000003.12:119017776:T: 101/27968)...	-	Oct 12, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 27794435 (NC_000003.12:119017776:TT: 3493/27968) Row 27794436 (NC_000003.12:119017776::T 1260/27968) Row 27794437 (NC_000003.12:119017776:T: 101/27968)...	-	Oct 12, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 27794435 (NC_000003.12:119017776:TT: 3493/27968) Row 27794436 (NC_000003.12:119017776::T 1260/27968) Row 27794437 (NC_000003.12:119017776:T: 101/27968)...	-	Oct 12, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 27794435 (NC_000003.12:119017776:TT: 3493/27968) Row 27794436 (NC_000003.12:119017776::T 1260/27968) Row 27794437 (NC_000003.12:119017776:T: 101/27968)...	-	Oct 12, 2022 (156)
94	TopMed Submission ignored due to conflicting rows: Row 418087297 (NC_000003.12:119017776:TTTTTTTTT: 1/264690) Row 418087298 (NC_000003.12:119017776:TTTTTTTTTT: 1/264690) Row 418087299 (NC_000003.12:119017776:TTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
95	TopMed Submission ignored due to conflicting rows: Row 418087297 (NC_000003.12:119017776:TTTTTTTTT: 1/264690) Row 418087298 (NC_000003.12:119017776:TTTTTTTTTT: 1/264690) Row 418087299 (NC_000003.12:119017776:TTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
96	TopMed Submission ignored due to conflicting rows: Row 418087297 (NC_000003.12:119017776:TTTTTTTTT: 1/264690) Row 418087298 (NC_000003.12:119017776:TTTTTTTTTT: 1/264690) Row 418087299 (NC_000003.12:119017776:TTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
97	ALFA	NC_000003.12 - 119017777	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4079344670	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4079344669	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4079344668, ss4580709744	NC_000003.12:119017776:TTTTTTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4079344667, ss4580709743	NC_000003.12:119017776:TTTTTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4079344666, ss4580709742	NC_000003.12:119017776:TTTTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5161196775	NC_000003.11:118736623:TTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4079344665	NC_000003.12:119017776:TTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4079344664	NC_000003.12:119017776:TTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4079344663	NC_000003.12:119017776:TTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4079344662	NC_000003.12:119017776:TTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5161196774	NC_000003.11:118736623:TTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4079344661, ss5255732039, ss5454909981, ss5693957335	NC_000003.12:119017776:TTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss77833549	NC_000003.9:120219334:TT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss2993056303, ss5161196771	NC_000003.11:118736623:TT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344660, ss5255732038, ss5454909980, ss5693957331	NC_000003.12:119017776:TT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss42060782	NT_005612.16:25231790:TT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5161196773	NC_000003.11:118736623:T:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344659, ss5255732037, ss5454909978, ss5693957333	NC_000003.12:119017776:T:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss663348676, ss5161196772	NC_000003.11:118736623::T	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344643, ss5255732036, ss5454909977, ss5693957332	NC_000003.12:119017776::T	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3828032277	NC_000003.11:118736623::TT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344644, ss5454909979, ss5693957334	NC_000003.12:119017776::TT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344645	NC_000003.12:119017776::TTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344646	NC_000003.12:119017776::TTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344647	NC_000003.12:119017776::TTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344648	NC_000003.12:119017776::TTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344649	NC_000003.12:119017776::TTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344650	NC_000003.12:119017776::TTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344651	NC_000003.12:119017776::TTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344652	NC_000003.12:119017776::TTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344657	NC_000003.12:119017776::TTTTTTTTTT… NC_000003.12:119017776::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTA	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344653	NC_000003.12:119017776::TTTTTTTTTT… NC_000003.12:119017776::TTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344654	NC_000003.12:119017776::TTTTTTTTTT… NC_000003.12:119017776::TTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344655	NC_000003.12:119017776::TTTTTTTTTT… NC_000003.12:119017776::TTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344656	NC_000003.12:119017776::TTTTTTTTTT… NC_000003.12:119017776::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14041308280	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4079344658	NC_000003.12:119017776::TTTTTTTTTT… NC_000003.12:119017776::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3403311225	NC_000003.12:119017776:TTTTTTTT:	NC_000003.12:119017776:TTTTTTTTTTT… NC_000003.12:119017776:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

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

No publications for rs567222914

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

rs567222914