Name: rs371276467
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.

rs371276467

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:60645457-60645493 (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(GT)₁₂ / del(GT)₁₁ / del(GT)₈ /…
del(GT)₁₂ / del(GT)₁₁ / del(GT)₈ / del(GT)₇ / del(GT)₆ / del(GT)₅ / del(GT)₄ / del(GT)₃ / delGTGT / delGT / dupGT / dupGTGT / dup(GT)₃ / dup(GT)₄ / dup(GT)₅ / dup(GT)₆ / dup(GT)₇ / dup(GT)₈ / dup(GT)₉ / dup(GT)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: (TG)₁₈T=0.3028 (1738/5740, ALFA)
dupGT=0.1911 (957/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPM1D : 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	5740	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.3028	TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0014, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0214, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.5075, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1106, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0533, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0030, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.351267	0.50388	0.144853	32
European	Sub	4572	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1262	TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0017, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0269, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.6363, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.1385, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0667, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0037, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	0.073279	0.720207	0.206514	32
African	Sub	1050	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0000	TGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	52	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
African American	Sub	998	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.000	TGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	16	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	8	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.0	TGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	34	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=1.00	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	TGTGTGTGTGTGT=0, TGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0	0	0	0	N/A
Other	Sub	60	TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.88	TGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.07, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.03, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.02, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT=0.00	0.928571	0.035714	0.035714	7

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	5740	(TG)₁₈T=0.3028	del(GT)₁₂=0.0000, del(GT)₁₁=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0014, delGT=0.0214, dupGT=0.5075, dupGTGT=0.1106, dup(GT)₃=0.0533, dup(GT)₄=0.0030, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000
Allele Frequency Aggregator	European	Sub	4572	(TG)₁₈T=0.1262	del(GT)₁₂=0.0000, del(GT)₁₁=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0017, delGT=0.0269, dupGT=0.6363, dupGTGT=0.1385, dup(GT)₃=0.0667, dup(GT)₄=0.0037, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000
Allele Frequency Aggregator	African	Sub	1050	(TG)₁₈T=1.0000	del(GT)₁₂=0.0000, del(GT)₁₁=0.0000, del(GT)₈=0.0000, del(GT)₇=0.0000, del(GT)₆=0.0000, del(GT)₅=0.0000, del(GT)₄=0.0000, del(GT)₃=0.0000, delGTGT=0.0000, delGT=0.0000, dupGT=0.0000, dupGTGT=0.0000, dup(GT)₃=0.0000, dup(GT)₄=0.0000, dup(GT)₅=0.0000, dup(GT)₆=0.0000, dup(GT)₇=0.0000, dup(GT)₈=0.0000, dup(GT)₉=0.0000
Allele Frequency Aggregator	Other	Sub	60	(TG)₁₈T=0.88	del(GT)₁₂=0.00, del(GT)₁₁=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.07, dupGTGT=0.03, dup(GT)₃=0.02, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00
Allele Frequency Aggregator	Latin American 2	Sub	34	(TG)₁₈T=1.00	del(GT)₁₂=0.00, del(GT)₁₁=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00
Allele Frequency Aggregator	Asian	Sub	16	(TG)₁₈T=1.00	del(GT)₁₂=0.00, del(GT)₁₁=0.00, del(GT)₈=0.00, del(GT)₇=0.00, del(GT)₆=0.00, del(GT)₅=0.00, del(GT)₄=0.00, del(GT)₃=0.00, delGTGT=0.00, delGT=0.00, dupGT=0.00, dupGTGT=0.00, dup(GT)₃=0.00, dup(GT)₄=0.00, dup(GT)₅=0.00, dup(GT)₆=0.00, dup(GT)₇=0.00, dup(GT)₈=0.00, dup(GT)₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(TG)₁₈T=1.0	del(GT)₁₂=0.0, del(GT)₁₁=0.0, del(GT)₈=0.0, del(GT)₇=0.0, del(GT)₆=0.0, del(GT)₅=0.0, del(GT)₄=0.0, del(GT)₃=0.0, delGTGT=0.0, delGT=0.0, dupGT=0.0, dupGTGT=0.0, dup(GT)₃=0.0, dup(GT)₄=0.0, dup(GT)₅=0.0, dup(GT)₆=0.0, dup(GT)₇=0.0, dup(GT)₈=0.0, dup(GT)₉=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(TG)₁₈T=0	del(GT)₁₂=0, del(GT)₁₁=0, del(GT)₈=0, del(GT)₇=0, del(GT)₆=0, del(GT)₅=0, del(GT)₄=0, del(GT)₃=0, delGTGT=0, delGT=0, dupGT=0, dupGTGT=0, dup(GT)₃=0, dup(GT)₄=0, dup(GT)₅=0, dup(GT)₆=0, dup(GT)₇=0, dup(GT)₈=0, dup(GT)₉=0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupGT=0.1911
1000Genomes	African	Sub	1322	- No frequency provided	dupGT=0.1362
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupGT=0.1587
1000Genomes	Europe	Sub	1006	- No frequency provided	dupGT=0.2296
1000Genomes	South Asian	Sub	978	- No frequency provided	dupGT=0.252
1000Genomes	American	Sub	694	- No frequency provided	dupGT=0.202

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 17	NC_000017.11:g.60645458GT[6]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[7]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[10]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[11]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[12]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[13]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[14]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[15]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[16]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[17]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[19]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[20]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[21]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[22]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[23]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[24]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[25]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[26]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[27]
GRCh38.p14 chr 17	NC_000017.11:g.60645458GT[28]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[6]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[7]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[10]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[11]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[12]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[13]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[14]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[15]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[16]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[17]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[19]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[20]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[21]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[22]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[23]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[24]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[25]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[26]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[27]
GRCh37.p13 chr 17	NC_000017.10:g.58722819GT[28]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[6]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[7]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[10]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[11]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[12]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[13]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[14]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[15]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[16]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[17]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[19]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[20]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[21]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[22]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[23]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[24]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[25]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[26]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[27]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50266GT[28]

Gene: PPM1D, protein phosphatase, Mg2+/Mn2+ dependent 1D (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPM1D transcript	NM_003620.4:c.827-2435TG[… NM_003620.4:c.827-2435TG[6]	N/A	Intron Variant
PPM1D transcript variant X1	XR_007065507.1:n.	N/A	Intron Variant
PPM1D transcript variant X2	XR_934577.3:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(TG)₁₈T=	del(GT)₁₂	del(GT)₁₁	del(GT)₈	del(GT)₇	del(GT)₆	del(GT)₅	del(GT)₄	del(GT)₃	delGTGT	delGT	dupGT	dupGTGT	dup(GT)₃	dup(GT)₄	dup(GT)₅	dup(GT)₆	dup(GT)₇	dup(GT)₈	dup(GT)₉	dup(GT)₁₀
GRCh38.p14 chr 17	NC_000017.11:g.60645457_60645493=	NC_000017.11:g.60645458GT[6]	NC_000017.11:g.60645458GT[7]	NC_000017.11:g.60645458GT[10]	NC_000017.11:g.60645458GT[11]	NC_000017.11:g.60645458GT[12]	NC_000017.11:g.60645458GT[13]	NC_000017.11:g.60645458GT[14]	NC_000017.11:g.60645458GT[15]	NC_000017.11:g.60645458GT[16]	NC_000017.11:g.60645458GT[17]	NC_000017.11:g.60645458GT[19]	NC_000017.11:g.60645458GT[20]	NC_000017.11:g.60645458GT[21]	NC_000017.11:g.60645458GT[22]	NC_000017.11:g.60645458GT[23]	NC_000017.11:g.60645458GT[24]	NC_000017.11:g.60645458GT[25]	NC_000017.11:g.60645458GT[26]	NC_000017.11:g.60645458GT[27]	NC_000017.11:g.60645458GT[28]
GRCh37.p13 chr 17	NC_000017.10:g.58722818_58722854=	NC_000017.10:g.58722819GT[6]	NC_000017.10:g.58722819GT[7]	NC_000017.10:g.58722819GT[10]	NC_000017.10:g.58722819GT[11]	NC_000017.10:g.58722819GT[12]	NC_000017.10:g.58722819GT[13]	NC_000017.10:g.58722819GT[14]	NC_000017.10:g.58722819GT[15]	NC_000017.10:g.58722819GT[16]	NC_000017.10:g.58722819GT[17]	NC_000017.10:g.58722819GT[19]	NC_000017.10:g.58722819GT[20]	NC_000017.10:g.58722819GT[21]	NC_000017.10:g.58722819GT[22]	NC_000017.10:g.58722819GT[23]	NC_000017.10:g.58722819GT[24]	NC_000017.10:g.58722819GT[25]	NC_000017.10:g.58722819GT[26]	NC_000017.10:g.58722819GT[27]	NC_000017.10:g.58722819GT[28]
PPM1D RefSeqGene (LRG_770)	NG_023265.1:g.50265_50301=	NG_023265.1:g.50266GT[6]	NG_023265.1:g.50266GT[7]	NG_023265.1:g.50266GT[10]	NG_023265.1:g.50266GT[11]	NG_023265.1:g.50266GT[12]	NG_023265.1:g.50266GT[13]	NG_023265.1:g.50266GT[14]	NG_023265.1:g.50266GT[15]	NG_023265.1:g.50266GT[16]	NG_023265.1:g.50266GT[17]	NG_023265.1:g.50266GT[19]	NG_023265.1:g.50266GT[20]	NG_023265.1:g.50266GT[21]	NG_023265.1:g.50266GT[22]	NG_023265.1:g.50266GT[23]	NG_023265.1:g.50266GT[24]	NG_023265.1:g.50266GT[25]	NG_023265.1:g.50266GT[26]	NG_023265.1:g.50266GT[27]	NG_023265.1:g.50266GT[28]
PPM1D transcript	NM_003620.3:c.827-2435=	NM_003620.3:c.827-2435TG[6]	NM_003620.3:c.827-2435TG[7]	NM_003620.3:c.827-2435TG[10]	NM_003620.3:c.827-2435TG[11]	NM_003620.3:c.827-2435TG[12]	NM_003620.3:c.827-2435TG[13]	NM_003620.3:c.827-2435TG[14]	NM_003620.3:c.827-2435TG[15]	NM_003620.3:c.827-2435TG[16]	NM_003620.3:c.827-2435TG[17]	NM_003620.3:c.827-2435TG[19]	NM_003620.3:c.827-2435TG[20]	NM_003620.3:c.827-2435TG[21]	NM_003620.3:c.827-2435TG[22]	NM_003620.3:c.827-2435TG[23]	NM_003620.3:c.827-2435TG[24]	NM_003620.3:c.827-2435TG[25]	NM_003620.3:c.827-2435TG[26]	NM_003620.3:c.827-2435TG[27]	NM_003620.3:c.827-2435TG[28]
PPM1D transcript	NM_003620.4:c.827-2435=	NM_003620.4:c.827-2435TG[6]	NM_003620.4:c.827-2435TG[7]	NM_003620.4:c.827-2435TG[10]	NM_003620.4:c.827-2435TG[11]	NM_003620.4:c.827-2435TG[12]	NM_003620.4:c.827-2435TG[13]	NM_003620.4:c.827-2435TG[14]	NM_003620.4:c.827-2435TG[15]	NM_003620.4:c.827-2435TG[16]	NM_003620.4:c.827-2435TG[17]	NM_003620.4:c.827-2435TG[19]	NM_003620.4:c.827-2435TG[20]	NM_003620.4:c.827-2435TG[21]	NM_003620.4:c.827-2435TG[22]	NM_003620.4:c.827-2435TG[23]	NM_003620.4:c.827-2435TG[24]	NM_003620.4:c.827-2435TG[25]	NM_003620.4:c.827-2435TG[26]	NM_003620.4:c.827-2435TG[27]	NM_003620.4:c.827-2435TG[28]
PPM1D transcript variant X1	XM_005257742.1:c.827-2435=	XM_005257742.1:c.827-2435TG[6]	XM_005257742.1:c.827-2435TG[7]	XM_005257742.1:c.827-2435TG[10]	XM_005257742.1:c.827-2435TG[11]	XM_005257742.1:c.827-2435TG[12]	XM_005257742.1:c.827-2435TG[13]	XM_005257742.1:c.827-2435TG[14]	XM_005257742.1:c.827-2435TG[15]	XM_005257742.1:c.827-2435TG[16]	XM_005257742.1:c.827-2435TG[17]	XM_005257742.1:c.827-2435TG[19]	XM_005257742.1:c.827-2435TG[20]	XM_005257742.1:c.827-2435TG[21]	XM_005257742.1:c.827-2435TG[22]	XM_005257742.1:c.827-2435TG[23]	XM_005257742.1:c.827-2435TG[24]	XM_005257742.1:c.827-2435TG[25]	XM_005257742.1:c.827-2435TG[26]	XM_005257742.1:c.827-2435TG[27]	XM_005257742.1:c.827-2435TG[28]

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#.

49 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81966210	Oct 12, 2018 (152)
2	HUMANGENOME_JCVI	ss95697893	Oct 12, 2018 (152)
3	GMI	ss289332564	Oct 12, 2018 (152)
4	SSMP	ss664367585	Apr 01, 2015 (144)
5	BILGI_BIOE	ss666695905	Apr 25, 2013 (138)
6	1000GENOMES	ss1376801743	Aug 21, 2014 (142)
7	PADH-LAB_SPU	ss1713967793	Sep 08, 2015 (146)
8	URBANLAB	ss3650680477	Oct 12, 2018 (152)
9	PACBIO	ss3788239324	Jul 13, 2019 (153)
10	PACBIO	ss3793190003	Jul 13, 2019 (153)
11	PACBIO	ss3798075800	Jul 13, 2019 (153)
12	KHV_HUMAN_GENOMES	ss3820074494	Jul 13, 2019 (153)
13	GNOMAD	ss4313784583	Apr 26, 2021 (155)
14	GNOMAD	ss4313784584	Apr 26, 2021 (155)
15	GNOMAD	ss4313784585	Apr 26, 2021 (155)
16	GNOMAD	ss4313784586	Apr 26, 2021 (155)
17	GNOMAD	ss4313784587	Apr 26, 2021 (155)
18	GNOMAD	ss4313784588	Apr 26, 2021 (155)
19	GNOMAD	ss4313784589	Apr 26, 2021 (155)
20	GNOMAD	ss4313784590	Apr 26, 2021 (155)
21	GNOMAD	ss4313784591	Apr 26, 2021 (155)
22	GNOMAD	ss4313784592	Apr 26, 2021 (155)
23	GNOMAD	ss4313784594	Apr 26, 2021 (155)
24	GNOMAD	ss4313784595	Apr 26, 2021 (155)
25	GNOMAD	ss4313784596	Apr 26, 2021 (155)
26	GNOMAD	ss4313784597	Apr 26, 2021 (155)
27	GNOMAD	ss4313784598	Apr 26, 2021 (155)
28	GNOMAD	ss4313784599	Apr 26, 2021 (155)
29	GNOMAD	ss4313784600	Apr 26, 2021 (155)
30	GNOMAD	ss4313784601	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5222994326	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5222994327	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5222994328	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5222994329	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5222994330	Apr 26, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5303562553	Oct 16, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5303562554	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5496565017	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5496565018	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5496565019	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5496565020	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5496565021	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5779384031	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5779384032	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5779384033	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5779384034	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5779384036	Oct 16, 2022 (156)
48	EVA	ss5834147329	Oct 16, 2022 (156)
49	EVA	ss5834147330	Oct 16, 2022 (156)
50	1000Genomes	NC_000017.10 - 58722818	Oct 12, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 510856318 (NC_000017.11:60645456::TG 59473/113142) Row 510856319 (NC_000017.11:60645456::TGTG 13005/113346) Row 510856320 (NC_000017.11:60645456::TGTGTG 4374/113440)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 80963633 (NC_000017.10:58722817:TG: 2839/16760) Row 80963634 (NC_000017.10:58722817::TGTGTG 235/16760) Row 80963635 (NC_000017.10:58722817::TG 6925/16760)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 80963633 (NC_000017.10:58722817:TG: 2839/16760) Row 80963634 (NC_000017.10:58722817::TGTGTG 235/16760) Row 80963635 (NC_000017.10:58722817::TG 6925/16760)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 80963633 (NC_000017.10:58722817:TG: 2839/16760) Row 80963634 (NC_000017.10:58722817::TGTGTG 235/16760) Row 80963635 (NC_000017.10:58722817::TG 6925/16760)...	-	Apr 26, 2021 (155)
72	8.3KJPN Submission ignored due to conflicting rows: Row 80963633 (NC_000017.10:58722817:TG: 2839/16760) Row 80963634 (NC_000017.10:58722817::TGTGTG 235/16760) Row 80963635 (NC_000017.10:58722817::TG 6925/16760)...	-	Apr 26, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 80963633 (NC_000017.10:58722817:TG: 2839/16760) Row 80963634 (NC_000017.10:58722817::TGTGTG 235/16760) Row 80963635 (NC_000017.10:58722817::TG 6925/16760)...	-	Apr 26, 2021 (155)
74	14KJPN Submission ignored due to conflicting rows: Row 113221135 (NC_000017.11:60645456:TG: 4289/28062) Row 113221136 (NC_000017.11:60645456::TG 11074/28062) Row 113221137 (NC_000017.11:60645456:TGTG: 290/28062)...	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 113221135 (NC_000017.11:60645456:TG: 4289/28062) Row 113221136 (NC_000017.11:60645456::TG 11074/28062) Row 113221137 (NC_000017.11:60645456:TGTG: 290/28062)...	-	Oct 16, 2022 (156)
76	14KJPN Submission ignored due to conflicting rows: Row 113221135 (NC_000017.11:60645456:TG: 4289/28062) Row 113221136 (NC_000017.11:60645456::TG 11074/28062) Row 113221137 (NC_000017.11:60645456:TGTG: 290/28062)...	-	Oct 16, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 113221135 (NC_000017.11:60645456:TG: 4289/28062) Row 113221136 (NC_000017.11:60645456::TG 11074/28062) Row 113221137 (NC_000017.11:60645456:TGTG: 290/28062)...	-	Oct 16, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 113221135 (NC_000017.11:60645456:TG: 4289/28062) Row 113221136 (NC_000017.11:60645456::TG 11074/28062) Row 113221137 (NC_000017.11:60645456:TGTG: 290/28062)...	-	Oct 16, 2022 (156)
79	ALFA	NC_000017.11 - 60645457	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
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT	(self)
ss4313784601	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784600	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784599	NC_000017.11:60645456:TGTGTGTGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784598	NC_000017.11:60645456:TGTGTGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784597	NC_000017.11:60645456:TGTGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784596	NC_000017.11:60645456:TGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5222994330	NC_000017.10:58722817:TGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784595, ss5496565021, ss5779384033	NC_000017.11:60645456:TGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5222994326	NC_000017.10:58722817:TG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784594, ss5496565019, ss5779384031	NC_000017.11:60645456:TG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss289332564	NC_000017.9:56077636::GT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
72393863, ss666695905, ss1376801743, ss1713967793, ss3788239324, ss3793190003, ss3798075800, ss5222994328, ss5834147329	NC_000017.10:58722817::TG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3820074494, ss4313784583, ss5303562553, ss5496565017, ss5779384032	NC_000017.11:60645456::TG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss3650680477	NC_000017.11:60645469::GT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss81966210, ss95697893	NT_010783.15:23997006::GT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss664367585, ss5222994329, ss5834147330	NC_000017.10:58722817::TGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784584, ss5496565018, ss5779384034	NC_000017.11:60645456::TGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss5222994327	NC_000017.10:58722817::TGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784585, ss5303562554, ss5496565020, ss5779384036	NC_000017.11:60645456::TGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784586	NC_000017.11:60645456::TGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784587	NC_000017.11:60645456::TGTGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784588	NC_000017.11:60645456::TGTGTGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784589	NC_000017.11:60645456::TGTGTGTGTGT… NC_000017.11:60645456::TGTGTGTGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784590	NC_000017.11:60645456::TGTGTGTGTGT… NC_000017.11:60645456::TGTGTGTGTGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784591	NC_000017.11:60645456::TGTGTGTGTGT… NC_000017.11:60645456::TGTGTGTGTGTGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
11581904154	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)
ss4313784592	NC_000017.11:60645456::TGTGTGTGTGT… NC_000017.11:60645456::TGTGTGTGTGTGTGTGTGTG	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3266090039	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTG:	NC_000017.11:60645456:TGTGTGTGTGTG… NC_000017.11:60645456:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT

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

No publications for rs371276467

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs371276467