Name: rs60642403
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.

rs60642403

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:113072697-113072721 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / 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)₁₁ / dup(T)₁₂ / dup(T)₁₄ / dup(T)₁₆ / dup(T)₁₈ / ins(T)₂₉ / ins(T)₃₂ / ins(T)₃₃ / ins(T)₃₅ / ins(T)₃₇ / ins(T)₃₈ / ins(T)₄₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.02780 (374/13451, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DTX1 : 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	13451	TTTTTTTTTTTTTTTTTTTTTTTTT=0.94952	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00781, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.02780, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01301, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00052, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00134, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.957738	0.011187	0.031075	32
European	Sub	10693	TTTTTTTTTTTTTTTTTTTTTTTTT=0.93669	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00973, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.03498, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01627, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00065, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00168, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.946234	0.014232	0.039534	32
African	Sub	1806	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	70	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1736	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	106	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	80	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	78	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	392	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	66	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	310	TTTTTTTTTTTTTTTTTTTTTTTTT=0.994	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13451	(T)₂₅=0.94952	del(T)₁₄=0.00000, del(T)₁₃=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)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00781, dupT=0.02780, dupTT=0.01301, dupTTT=0.00134, dup(T)₄=0.00052, dup(T)₅=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	European	Sub	10693	(T)₂₅=0.93669	del(T)₁₄=0.00000, del(T)₁₃=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)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00973, dupT=0.03498, dupTT=0.01627, dupTTT=0.00168, dup(T)₄=0.00065, dup(T)₅=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	African	Sub	1806	(T)₂₅=1.0000	del(T)₁₄=0.0000, del(T)₁₃=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)₅=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
Allele Frequency Aggregator	Latin American 2	Sub	392	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=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)₅=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
Allele Frequency Aggregator	Other	Sub	310	(T)₂₅=0.994	del(T)₁₄=0.000, del(T)₁₃=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)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.003, dupT=0.000, dupTT=0.003, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Asian	Sub	106	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₃=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)₅=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
Allele Frequency Aggregator	Latin American 1	Sub	78	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=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)₅=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
Allele Frequency Aggregator	South Asian	Sub	66	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₃=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)₅=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

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 12	NC_000012.12:g.113072708_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072709_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072710_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072711_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072712_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072713_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072714_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072715_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072716_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072717_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072718_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072719_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072720_113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072721del
GRCh38.p14 chr 12	NC_000012.12:g.113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072720_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072719_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072718_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072717_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072716_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072715_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072714_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072713_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072712_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072711_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072710_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072708_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072706_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072704_113072721dup
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 12	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510513_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510514_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510515_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510516_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510517_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510518_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510519_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510520_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510521_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510522_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510523_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510524_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510525_113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510526del
GRCh37.p13 chr 12	NC_000012.11:g.113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510525_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510524_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510523_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510522_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510521_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510520_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510519_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510518_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510517_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510516_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510515_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510513_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510511_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510509_113510526dup
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: DTX1, deltex E3 ubiquitin ligase 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DTX1 transcript	NM_004416.3:c.260-4716_26… NM_004416.3:c.260-4716_260-4703del	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)₂₅=	del(T)₁₄	del(T)₁₃	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)₁₁	dup(T)₁₂	dup(T)₁₄	dup(T)₁₆	dup(T)₁₈	ins(T)₂₉	ins(T)₃₂	ins(T)₃₃	ins(T)₃₅	ins(T)₃₇	ins(T)₃₈	ins(T)₄₆
GRCh38.p14 chr 12	NC_000012.12:g.113072697_113072721=	NC_000012.12:g.113072708_113072721del	NC_000012.12:g.113072709_113072721del	NC_000012.12:g.113072710_113072721del	NC_000012.12:g.113072711_113072721del	NC_000012.12:g.113072712_113072721del	NC_000012.12:g.113072713_113072721del	NC_000012.12:g.113072714_113072721del	NC_000012.12:g.113072715_113072721del	NC_000012.12:g.113072716_113072721del	NC_000012.12:g.113072717_113072721del	NC_000012.12:g.113072718_113072721del	NC_000012.12:g.113072719_113072721del	NC_000012.12:g.113072720_113072721del	NC_000012.12:g.113072721del	NC_000012.12:g.113072721dup	NC_000012.12:g.113072720_113072721dup	NC_000012.12:g.113072719_113072721dup	NC_000012.12:g.113072718_113072721dup	NC_000012.12:g.113072717_113072721dup	NC_000012.12:g.113072716_113072721dup	NC_000012.12:g.113072715_113072721dup	NC_000012.12:g.113072714_113072721dup	NC_000012.12:g.113072713_113072721dup	NC_000012.12:g.113072712_113072721dup	NC_000012.12:g.113072711_113072721dup	NC_000012.12:g.113072710_113072721dup	NC_000012.12:g.113072708_113072721dup	NC_000012.12:g.113072706_113072721dup	NC_000012.12:g.113072704_113072721dup	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:g.113072721_113072722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 12	NC_000012.11:g.113510502_113510526=	NC_000012.11:g.113510513_113510526del	NC_000012.11:g.113510514_113510526del	NC_000012.11:g.113510515_113510526del	NC_000012.11:g.113510516_113510526del	NC_000012.11:g.113510517_113510526del	NC_000012.11:g.113510518_113510526del	NC_000012.11:g.113510519_113510526del	NC_000012.11:g.113510520_113510526del	NC_000012.11:g.113510521_113510526del	NC_000012.11:g.113510522_113510526del	NC_000012.11:g.113510523_113510526del	NC_000012.11:g.113510524_113510526del	NC_000012.11:g.113510525_113510526del	NC_000012.11:g.113510526del	NC_000012.11:g.113510526dup	NC_000012.11:g.113510525_113510526dup	NC_000012.11:g.113510524_113510526dup	NC_000012.11:g.113510523_113510526dup	NC_000012.11:g.113510522_113510526dup	NC_000012.11:g.113510521_113510526dup	NC_000012.11:g.113510520_113510526dup	NC_000012.11:g.113510519_113510526dup	NC_000012.11:g.113510518_113510526dup	NC_000012.11:g.113510517_113510526dup	NC_000012.11:g.113510516_113510526dup	NC_000012.11:g.113510515_113510526dup	NC_000012.11:g.113510513_113510526dup	NC_000012.11:g.113510511_113510526dup	NC_000012.11:g.113510509_113510526dup	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.11:g.113510526_113510527insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DTX1 transcript	NM_004416.2:c.260-4727=	NM_004416.2:c.260-4716_260-4703del	NM_004416.2:c.260-4715_260-4703del	NM_004416.2:c.260-4714_260-4703del	NM_004416.2:c.260-4713_260-4703del	NM_004416.2:c.260-4712_260-4703del	NM_004416.2:c.260-4711_260-4703del	NM_004416.2:c.260-4710_260-4703del	NM_004416.2:c.260-4709_260-4703del	NM_004416.2:c.260-4708_260-4703del	NM_004416.2:c.260-4707_260-4703del	NM_004416.2:c.260-4706_260-4703del	NM_004416.2:c.260-4705_260-4703del	NM_004416.2:c.260-4704_260-4703del	NM_004416.2:c.260-4703del	NM_004416.2:c.260-4703dup	NM_004416.2:c.260-4704_260-4703dup	NM_004416.2:c.260-4705_260-4703dup	NM_004416.2:c.260-4706_260-4703dup	NM_004416.2:c.260-4707_260-4703dup	NM_004416.2:c.260-4708_260-4703dup	NM_004416.2:c.260-4709_260-4703dup	NM_004416.2:c.260-4710_260-4703dup	NM_004416.2:c.260-4711_260-4703dup	NM_004416.2:c.260-4712_260-4703dup	NM_004416.2:c.260-4713_260-4703dup	NM_004416.2:c.260-4714_260-4703dup	NM_004416.2:c.260-4716_260-4703dup	NM_004416.2:c.260-4718_260-4703dup	NM_004416.2:c.260-4720_260-4703dup	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.2:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DTX1 transcript	NM_004416.3:c.260-4727=	NM_004416.3:c.260-4716_260-4703del	NM_004416.3:c.260-4715_260-4703del	NM_004416.3:c.260-4714_260-4703del	NM_004416.3:c.260-4713_260-4703del	NM_004416.3:c.260-4712_260-4703del	NM_004416.3:c.260-4711_260-4703del	NM_004416.3:c.260-4710_260-4703del	NM_004416.3:c.260-4709_260-4703del	NM_004416.3:c.260-4708_260-4703del	NM_004416.3:c.260-4707_260-4703del	NM_004416.3:c.260-4706_260-4703del	NM_004416.3:c.260-4705_260-4703del	NM_004416.3:c.260-4704_260-4703del	NM_004416.3:c.260-4703del	NM_004416.3:c.260-4703dup	NM_004416.3:c.260-4704_260-4703dup	NM_004416.3:c.260-4705_260-4703dup	NM_004416.3:c.260-4706_260-4703dup	NM_004416.3:c.260-4707_260-4703dup	NM_004416.3:c.260-4708_260-4703dup	NM_004416.3:c.260-4709_260-4703dup	NM_004416.3:c.260-4710_260-4703dup	NM_004416.3:c.260-4711_260-4703dup	NM_004416.3:c.260-4712_260-4703dup	NM_004416.3:c.260-4713_260-4703dup	NM_004416.3:c.260-4714_260-4703dup	NM_004416.3:c.260-4716_260-4703dup	NM_004416.3:c.260-4718_260-4703dup	NM_004416.3:c.260-4720_260-4703dup	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_004416.3:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
DTX1 transcript variant X1	XM_005253855.1:c.260-4727=	XM_005253855.1:c.260-4716_260-4703del	XM_005253855.1:c.260-4715_260-4703del	XM_005253855.1:c.260-4714_260-4703del	XM_005253855.1:c.260-4713_260-4703del	XM_005253855.1:c.260-4712_260-4703del	XM_005253855.1:c.260-4711_260-4703del	XM_005253855.1:c.260-4710_260-4703del	XM_005253855.1:c.260-4709_260-4703del	XM_005253855.1:c.260-4708_260-4703del	XM_005253855.1:c.260-4707_260-4703del	XM_005253855.1:c.260-4706_260-4703del	XM_005253855.1:c.260-4705_260-4703del	XM_005253855.1:c.260-4704_260-4703del	XM_005253855.1:c.260-4703del	XM_005253855.1:c.260-4703dup	XM_005253855.1:c.260-4704_260-4703dup	XM_005253855.1:c.260-4705_260-4703dup	XM_005253855.1:c.260-4706_260-4703dup	XM_005253855.1:c.260-4707_260-4703dup	XM_005253855.1:c.260-4708_260-4703dup	XM_005253855.1:c.260-4709_260-4703dup	XM_005253855.1:c.260-4710_260-4703dup	XM_005253855.1:c.260-4711_260-4703dup	XM_005253855.1:c.260-4712_260-4703dup	XM_005253855.1:c.260-4713_260-4703dup	XM_005253855.1:c.260-4714_260-4703dup	XM_005253855.1:c.260-4716_260-4703dup	XM_005253855.1:c.260-4718_260-4703dup	XM_005253855.1:c.260-4720_260-4703dup	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_005253855.1:c.260-4703_260-4702insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

58 SubSNP, 47 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81028605	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95607680	Feb 04, 2009 (130)
3	HUMANGENOME_JCVI	ss97276263	Feb 13, 2009 (130)
4	SWEGEN	ss3010370353	Nov 08, 2017 (151)
5	EVA	ss3833331694	Apr 27, 2020 (154)
6	GNOMAD	ss4259271273	Apr 26, 2021 (155)
7	GNOMAD	ss4259271274	Apr 26, 2021 (155)
8	GNOMAD	ss4259271275	Apr 26, 2021 (155)
9	GNOMAD	ss4259271276	Apr 26, 2021 (155)
10	GNOMAD	ss4259271277	Apr 26, 2021 (155)
11	GNOMAD	ss4259271278	Apr 26, 2021 (155)
12	GNOMAD	ss4259271279	Apr 26, 2021 (155)
13	GNOMAD	ss4259271280	Apr 26, 2021 (155)
14	GNOMAD	ss4259271281	Apr 26, 2021 (155)
15	GNOMAD	ss4259271282	Apr 26, 2021 (155)
16	GNOMAD	ss4259271283	Apr 26, 2021 (155)
17	GNOMAD	ss4259271284	Apr 26, 2021 (155)
18	GNOMAD	ss4259271285	Apr 26, 2021 (155)
19	GNOMAD	ss4259271286	Apr 26, 2021 (155)
20	GNOMAD	ss4259271287	Apr 26, 2021 (155)
21	GNOMAD	ss4259271288	Apr 26, 2021 (155)
22	GNOMAD	ss4259271289	Apr 26, 2021 (155)
23	GNOMAD	ss4259271290	Apr 26, 2021 (155)
24	GNOMAD	ss4259271291	Apr 26, 2021 (155)
25	GNOMAD	ss4259271292	Apr 26, 2021 (155)
26	GNOMAD	ss4259271293	Apr 26, 2021 (155)
27	GNOMAD	ss4259271295	Apr 26, 2021 (155)
28	GNOMAD	ss4259271296	Apr 26, 2021 (155)
29	GNOMAD	ss4259271297	Apr 26, 2021 (155)
30	GNOMAD	ss4259271298	Apr 26, 2021 (155)
31	GNOMAD	ss4259271299	Apr 26, 2021 (155)
32	GNOMAD	ss4259271300	Apr 26, 2021 (155)
33	GNOMAD	ss4259271301	Apr 26, 2021 (155)
34	GNOMAD	ss4259271302	Apr 26, 2021 (155)
35	GNOMAD	ss4259271303	Apr 26, 2021 (155)
36	GNOMAD	ss4259271304	Apr 26, 2021 (155)
37	GNOMAD	ss4259271305	Apr 26, 2021 (155)
38	GNOMAD	ss4259271306	Apr 26, 2021 (155)
39	GNOMAD	ss4259271307	Apr 26, 2021 (155)
40	TOPMED	ss4933267662	Apr 26, 2021 (155)
41	TOPMED	ss4933267663	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5208229307	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5208229308	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5208229309	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5208229310	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5208229311	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5292280311	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5292280312	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5292280313	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5486878579	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5486878580	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5486878581	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5486878582	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5758574370	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5758574371	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5758574373	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5758574374	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5758574375	Oct 16, 2022 (156)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419754717 (NC_000012.12:113072696::TT 2659/66268) Row 419754718 (NC_000012.12:113072696::TTT 388/66314) Row 419754719 (NC_000012.12:113072696::TTTT 494/66314)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 66198614 (NC_000012.11:113510501:TTTTTTTTTTTTTT: 42/16512) Row 66198615 (NC_000012.11:113510501:T: 282/16512) Row 66198616 (NC_000012.11:113510501::T 319/16512)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 66198614 (NC_000012.11:113510501:TTTTTTTTTTTTTT: 42/16512) Row 66198615 (NC_000012.11:113510501:T: 282/16512) Row 66198616 (NC_000012.11:113510501::T 319/16512)...	-	Apr 26, 2021 (155)
95	8.3KJPN Submission ignored due to conflicting rows: Row 66198614 (NC_000012.11:113510501:TTTTTTTTTTTTTT: 42/16512) Row 66198615 (NC_000012.11:113510501:T: 282/16512) Row 66198616 (NC_000012.11:113510501::T 319/16512)...	-	Apr 26, 2021 (155)
96	8.3KJPN Submission ignored due to conflicting rows: Row 66198614 (NC_000012.11:113510501:TTTTTTTTTTTTTT: 42/16512) Row 66198615 (NC_000012.11:113510501:T: 282/16512) Row 66198616 (NC_000012.11:113510501::T 319/16512)...	-	Apr 26, 2021 (155)
97	8.3KJPN Submission ignored due to conflicting rows: Row 66198614 (NC_000012.11:113510501:TTTTTTTTTTTTTT: 42/16512) Row 66198615 (NC_000012.11:113510501:T: 282/16512) Row 66198616 (NC_000012.11:113510501::T 319/16512)...	-	Apr 26, 2021 (155)
98	14KJPN Submission ignored due to conflicting rows: Row 92411474 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 89/26232) Row 92411475 (NC_000012.12:113072696:T: 474/26232) Row 92411477 (NC_000012.12:113072696::T 443/26232)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 92411474 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 89/26232) Row 92411475 (NC_000012.12:113072696:T: 474/26232) Row 92411477 (NC_000012.12:113072696::T 443/26232)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 92411474 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 89/26232) Row 92411475 (NC_000012.12:113072696:T: 474/26232) Row 92411477 (NC_000012.12:113072696::T 443/26232)...	-	Oct 16, 2022 (156)
101	14KJPN Submission ignored due to conflicting rows: Row 92411474 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 89/26232) Row 92411475 (NC_000012.12:113072696:T: 474/26232) Row 92411477 (NC_000012.12:113072696::T 443/26232)...	-	Oct 16, 2022 (156)
102	14KJPN Submission ignored due to conflicting rows: Row 92411474 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 89/26232) Row 92411475 (NC_000012.12:113072696:T: 474/26232) Row 92411477 (NC_000012.12:113072696::T 443/26232)...	-	Oct 16, 2022 (156)
103	TopMed Submission ignored due to conflicting rows: Row 148813319 (NC_000012.12:113072696:TTTTTTTTTT: 4/264690) Row 148813320 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 48/264690)	-	Apr 26, 2021 (155)
104	TopMed Submission ignored due to conflicting rows: Row 148813319 (NC_000012.12:113072696:TTTTTTTTTT: 4/264690) Row 148813320 (NC_000012.12:113072696:TTTTTTTTTTTTTT: 48/264690)	-	Apr 26, 2021 (155)
105	ALFA	NC_000012.12 - 113072697	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
ss5208229307	NC_000012.11:113510501:TTTTTTTTTTT… NC_000012.11:113510501:TTTTTTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4259271307, ss4933267663, ss5758574370	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5208229311	NC_000012.11:113510501:TTTTTTTTTTT… NC_000012.11:113510501:TTTTTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4259271306, ss5758574375	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4259271305	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4259271304, ss4933267662	NC_000012.12:113072696:TTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4259271303	NC_000012.12:113072696:TTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4259271302	NC_000012.12:113072696:TTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4259271301	NC_000012.12:113072696:TTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4259271300, ss5486878582	NC_000012.12:113072696:TTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4259271299	NC_000012.12:113072696:TTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3010370353	NC_000012.11:113510501:TTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271298	NC_000012.12:113072696:TTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271297	NC_000012.12:113072696:TTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271296	NC_000012.12:113072696:TT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5208229308	NC_000012.11:113510501:T:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271295, ss5292280312, ss5486878580, ss5758574371	NC_000012.12:113072696:T:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3833331694, ss5208229309	NC_000012.11:113510501::T	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5292280311, ss5486878581, ss5758574373	NC_000012.12:113072696::T	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss97276263	NT_009775.17:4087031::T	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95607680	NT_009775.17:4087056::T	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5208229310	NC_000012.11:113510501::TT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271273, ss5486878579, ss5758574374	NC_000012.12:113072696::TT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss81028605	NT_009775.17:4087056::TT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271274	NC_000012.12:113072696::TTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271275, ss5292280313	NC_000012.12:113072696::TTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271276	NC_000012.12:113072696::TTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271277	NC_000012.12:113072696::TTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271278	NC_000012.12:113072696::TTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
2456448700	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271279	NC_000012.12:113072696::TTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271280	NC_000012.12:113072696::TTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271281	NC_000012.12:113072696::TTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271282	NC_000012.12:113072696::TTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271283	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271284	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271285	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271286	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271287	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271288	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271289	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271290	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271291	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271292	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4259271293	NC_000012.12:113072696::TTTTTTTTTT… NC_000012.12:113072696::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3182036777	NC_000012.12:113072696:TTTTTTTTTTT:	NC_000012.12:113072696:TTTTTTTTTTT… NC_000012.12:113072696:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs60642403

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

rs60642403