Name: rs869212842
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.

rs869212842

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:24552354-24552384 (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)₁₉ / del(T)₁₈ / del(T)₁₇ / d…
del(T)₁₉ / del(T)₁₈ / del(T)₁₇ / del(T)₁₆ / del(T)₁₅ / 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
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₉=0.0000 (0/9860, ALFA)
del(T)₁₈=0.0000 (0/9860, ALFA)
del(T)₁₇=0.0000 (0/9860, ALFA) (+ 19 more)
del(T)₁₆=0.0000 (0/9860, ALFA)
del(T)₁₅=0.0000 (0/9860, ALFA)
del(T)₁₄=0.0000 (0/9860, ALFA)
del(T)₁₃=0.0000 (0/9860, ALFA)
del(T)₁₂=0.0000 (0/9860, ALFA)
del(T)₁₁=0.0000 (0/9860, ALFA)
del(T)₁₀=0.0000 (0/9860, ALFA)
del(T)₉=0.0000 (0/9860, ALFA)
del(T)₈=0.0000 (0/9860, ALFA)
del(T)₇=0.0000 (0/9860, ALFA)
del(T)₆=0.0000 (0/9860, ALFA)
del(T)₅=0.0000 (0/9860, ALFA)
del(T)₄=0.0000 (0/9860, ALFA)
delTTT=0.0000 (0/9860, ALFA)
delTT=0.0000 (0/9860, ALFA)
delT=0.0000 (0/9860, ALFA)
dupT=0.0000 (0/9860, ALFA)
dupTTT=0.0000 (0/9860, ALFA)
dup(T)₅=0.0000 (0/9860, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NCOA1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	9860	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	6468	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2192	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2106	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	82	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	64	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	124	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	528	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	78	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	388	TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9860	(T)₃₁=1.0000	del(T)₁₉=0.0000, del(T)₁₈=0.0000, del(T)₁₇=0.0000, del(T)₁₆=0.0000, del(T)₁₅=0.0000, 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, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	6468	(T)₃₁=1.0000	del(T)₁₉=0.0000, del(T)₁₈=0.0000, del(T)₁₇=0.0000, del(T)₁₆=0.0000, del(T)₁₅=0.0000, 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, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	2192	(T)₃₁=1.0000	del(T)₁₉=0.0000, del(T)₁₈=0.0000, del(T)₁₇=0.0000, del(T)₁₆=0.0000, del(T)₁₅=0.0000, 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, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	528	(T)₃₁=1.000	del(T)₁₉=0.000, del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, 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, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	388	(T)₃₁=1.000	del(T)₁₉=0.000, del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, 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, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	124	(T)₃₁=1.000	del(T)₁₉=0.000, del(T)₁₈=0.000, del(T)₁₇=0.000, del(T)₁₆=0.000, del(T)₁₅=0.000, 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, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Asian	Sub	82	(T)₃₁=1.00	del(T)₁₉=0.00, del(T)₁₈=0.00, del(T)₁₇=0.00, del(T)₁₆=0.00, del(T)₁₅=0.00, 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, dupTTT=0.00, dup(T)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	78	(T)₃₁=1.00	del(T)₁₉=0.00, del(T)₁₈=0.00, del(T)₁₇=0.00, del(T)₁₆=0.00, del(T)₁₅=0.00, 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, dupTTT=0.00, dup(T)₅=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 2	NC_000002.12:g.24552366_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552367_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552368_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552369_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552370_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552371_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552372_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552373_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552374_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552375_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552376_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552377_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552378_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552379_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552380_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552381_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552382_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552383_24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552384del
GRCh38.p14 chr 2	NC_000002.12:g.24552384dup
GRCh38.p14 chr 2	NC_000002.12:g.24552383_24552384dup
GRCh38.p14 chr 2	NC_000002.12:g.24552382_24552384dup
GRCh38.p14 chr 2	NC_000002.12:g.24552381_24552384dup
GRCh38.p14 chr 2	NC_000002.12:g.24552380_24552384dup
GRCh38.p14 chr 2	NC_000002.12:g.24552379_24552384dup
GRCh37.p13 chr 2	NC_000002.11:g.24775235_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775236_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775237_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775238_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775239_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775240_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775241_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775242_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775243_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775244_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775245_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775246_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775247_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775248_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775249_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775250_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775251_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775252_24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775253del
GRCh37.p13 chr 2	NC_000002.11:g.24775253dup
GRCh37.p13 chr 2	NC_000002.11:g.24775252_24775253dup
GRCh37.p13 chr 2	NC_000002.11:g.24775251_24775253dup
GRCh37.p13 chr 2	NC_000002.11:g.24775250_24775253dup
GRCh37.p13 chr 2	NC_000002.11:g.24775249_24775253dup
GRCh37.p13 chr 2	NC_000002.11:g.24775248_24775253dup
NCOA1 RefSeqGene	NG_029014.2:g.65317_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65318_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65319_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65320_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65321_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65322_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65323_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65324_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65325_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65326_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65327_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65328_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65329_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65330_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65331_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65332_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65333_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65334_65335del
NCOA1 RefSeqGene	NG_029014.2:g.65335del
NCOA1 RefSeqGene	NG_029014.2:g.65335dup
NCOA1 RefSeqGene	NG_029014.2:g.65334_65335dup
NCOA1 RefSeqGene	NG_029014.2:g.65333_65335dup
NCOA1 RefSeqGene	NG_029014.2:g.65332_65335dup
NCOA1 RefSeqGene	NG_029014.2:g.65331_65335dup
NCOA1 RefSeqGene	NG_029014.2:g.65330_65335dup

Gene: NCOA1, nuclear receptor coactivator 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NCOA1 transcript variant 4	NM_001362950.1:c.-395-119… NM_001362950.1:c.-395-11929_-395-11911del	N/A	Intron Variant
NCOA1 transcript variant 5	NM_001362952.1:c.-395-119… NM_001362952.1:c.-395-11929_-395-11911del	N/A	Intron Variant
NCOA1 transcript variant 6	NM_001362954.1:c.-395-119… NM_001362954.1:c.-395-11929_-395-11911del	N/A	Intron Variant
NCOA1 transcript variant 7	NM_001362955.1:c.-420-115… NM_001362955.1:c.-420-11538_-420-11520del	N/A	Intron Variant
NCOA1 transcript variant 1	NM_003743.5:c.-395-11929_… NM_003743.5:c.-395-11929_-395-11911del	N/A	Intron Variant
NCOA1 transcript variant 2	NM_147223.3:c.-259-32110_… NM_147223.3:c.-259-32110_-259-32092del	N/A	Intron Variant
NCOA1 transcript variant 3	NM_147233.2:c.	N/A	Genic Upstream Transcript Variant
NCOA1 transcript variant X1	XM_047446151.1:c.-259-321… XM_047446151.1:c.-259-32110_-259-32092del	N/A	Intron Variant
NCOA1 transcript variant X2	XM_047446152.1:c.-536-202… XM_047446152.1:c.-536-2023_-536-2005del	N/A	Intron Variant
NCOA1 transcript variant X3	XM_047446153.1:c.-536-202… XM_047446153.1:c.-536-2023_-536-2005del	N/A	Intron Variant
NCOA1 transcript variant X4	XM_047446154.1:c.-536-202… XM_047446154.1:c.-536-2023_-536-2005del	N/A	Intron Variant
NCOA1 transcript variant X5	XM_047446155.1:c.-536-202… XM_047446155.1:c.-536-2023_-536-2005del	N/A	Intron Variant
NCOA1 transcript variant X6	XM_047446156.1:c.-311-321… XM_047446156.1:c.-311-32110_-311-32092del	N/A	Intron Variant
NCOA1 transcript variant X7	XM_047446157.1:c.-259-321… XM_047446157.1:c.-259-32110_-259-32092del	N/A	Intron Variant
NCOA1 transcript variant X8	XM_047446158.1:c.-259-321… XM_047446158.1:c.-259-32110_-259-32092del	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)₃₁=	del(T)₁₉	del(T)₁₈	del(T)₁₇	del(T)₁₆	del(T)₁₅	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
GRCh38.p14 chr 2	NC_000002.12:g.24552354_24552384=	NC_000002.12:g.24552366_24552384del	NC_000002.12:g.24552367_24552384del	NC_000002.12:g.24552368_24552384del	NC_000002.12:g.24552369_24552384del	NC_000002.12:g.24552370_24552384del	NC_000002.12:g.24552371_24552384del	NC_000002.12:g.24552372_24552384del	NC_000002.12:g.24552373_24552384del	NC_000002.12:g.24552374_24552384del	NC_000002.12:g.24552375_24552384del	NC_000002.12:g.24552376_24552384del	NC_000002.12:g.24552377_24552384del	NC_000002.12:g.24552378_24552384del	NC_000002.12:g.24552379_24552384del	NC_000002.12:g.24552380_24552384del	NC_000002.12:g.24552381_24552384del	NC_000002.12:g.24552382_24552384del	NC_000002.12:g.24552383_24552384del	NC_000002.12:g.24552384del	NC_000002.12:g.24552384dup	NC_000002.12:g.24552383_24552384dup	NC_000002.12:g.24552382_24552384dup	NC_000002.12:g.24552381_24552384dup	NC_000002.12:g.24552380_24552384dup	NC_000002.12:g.24552379_24552384dup
GRCh37.p13 chr 2	NC_000002.11:g.24775223_24775253=	NC_000002.11:g.24775235_24775253del	NC_000002.11:g.24775236_24775253del	NC_000002.11:g.24775237_24775253del	NC_000002.11:g.24775238_24775253del	NC_000002.11:g.24775239_24775253del	NC_000002.11:g.24775240_24775253del	NC_000002.11:g.24775241_24775253del	NC_000002.11:g.24775242_24775253del	NC_000002.11:g.24775243_24775253del	NC_000002.11:g.24775244_24775253del	NC_000002.11:g.24775245_24775253del	NC_000002.11:g.24775246_24775253del	NC_000002.11:g.24775247_24775253del	NC_000002.11:g.24775248_24775253del	NC_000002.11:g.24775249_24775253del	NC_000002.11:g.24775250_24775253del	NC_000002.11:g.24775251_24775253del	NC_000002.11:g.24775252_24775253del	NC_000002.11:g.24775253del	NC_000002.11:g.24775253dup	NC_000002.11:g.24775252_24775253dup	NC_000002.11:g.24775251_24775253dup	NC_000002.11:g.24775250_24775253dup	NC_000002.11:g.24775249_24775253dup	NC_000002.11:g.24775248_24775253dup
NCOA1 RefSeqGene	NG_029014.2:g.65305_65335=	NG_029014.2:g.65317_65335del	NG_029014.2:g.65318_65335del	NG_029014.2:g.65319_65335del	NG_029014.2:g.65320_65335del	NG_029014.2:g.65321_65335del	NG_029014.2:g.65322_65335del	NG_029014.2:g.65323_65335del	NG_029014.2:g.65324_65335del	NG_029014.2:g.65325_65335del	NG_029014.2:g.65326_65335del	NG_029014.2:g.65327_65335del	NG_029014.2:g.65328_65335del	NG_029014.2:g.65329_65335del	NG_029014.2:g.65330_65335del	NG_029014.2:g.65331_65335del	NG_029014.2:g.65332_65335del	NG_029014.2:g.65333_65335del	NG_029014.2:g.65334_65335del	NG_029014.2:g.65335del	NG_029014.2:g.65335dup	NG_029014.2:g.65334_65335dup	NG_029014.2:g.65333_65335dup	NG_029014.2:g.65332_65335dup	NG_029014.2:g.65331_65335dup	NG_029014.2:g.65330_65335dup
NCOA1 transcript variant 4	NM_001362950.1:c.-395-11941=	NM_001362950.1:c.-395-11929_-395-11911del	NM_001362950.1:c.-395-11928_-395-11911del	NM_001362950.1:c.-395-11927_-395-11911del	NM_001362950.1:c.-395-11926_-395-11911del	NM_001362950.1:c.-395-11925_-395-11911del	NM_001362950.1:c.-395-11924_-395-11911del	NM_001362950.1:c.-395-11923_-395-11911del	NM_001362950.1:c.-395-11922_-395-11911del	NM_001362950.1:c.-395-11921_-395-11911del	NM_001362950.1:c.-395-11920_-395-11911del	NM_001362950.1:c.-395-11919_-395-11911del	NM_001362950.1:c.-395-11918_-395-11911del	NM_001362950.1:c.-395-11917_-395-11911del	NM_001362950.1:c.-395-11916_-395-11911del	NM_001362950.1:c.-395-11915_-395-11911del	NM_001362950.1:c.-395-11914_-395-11911del	NM_001362950.1:c.-395-11913_-395-11911del	NM_001362950.1:c.-395-11912_-395-11911del	NM_001362950.1:c.-395-11911del	NM_001362950.1:c.-395-11911dup	NM_001362950.1:c.-395-11912_-395-11911dup	NM_001362950.1:c.-395-11913_-395-11911dup	NM_001362950.1:c.-395-11914_-395-11911dup	NM_001362950.1:c.-395-11915_-395-11911dup	NM_001362950.1:c.-395-11916_-395-11911dup
NCOA1 transcript variant 5	NM_001362952.1:c.-395-11941=	NM_001362952.1:c.-395-11929_-395-11911del	NM_001362952.1:c.-395-11928_-395-11911del	NM_001362952.1:c.-395-11927_-395-11911del	NM_001362952.1:c.-395-11926_-395-11911del	NM_001362952.1:c.-395-11925_-395-11911del	NM_001362952.1:c.-395-11924_-395-11911del	NM_001362952.1:c.-395-11923_-395-11911del	NM_001362952.1:c.-395-11922_-395-11911del	NM_001362952.1:c.-395-11921_-395-11911del	NM_001362952.1:c.-395-11920_-395-11911del	NM_001362952.1:c.-395-11919_-395-11911del	NM_001362952.1:c.-395-11918_-395-11911del	NM_001362952.1:c.-395-11917_-395-11911del	NM_001362952.1:c.-395-11916_-395-11911del	NM_001362952.1:c.-395-11915_-395-11911del	NM_001362952.1:c.-395-11914_-395-11911del	NM_001362952.1:c.-395-11913_-395-11911del	NM_001362952.1:c.-395-11912_-395-11911del	NM_001362952.1:c.-395-11911del	NM_001362952.1:c.-395-11911dup	NM_001362952.1:c.-395-11912_-395-11911dup	NM_001362952.1:c.-395-11913_-395-11911dup	NM_001362952.1:c.-395-11914_-395-11911dup	NM_001362952.1:c.-395-11915_-395-11911dup	NM_001362952.1:c.-395-11916_-395-11911dup
NCOA1 transcript variant 6	NM_001362954.1:c.-395-11941=	NM_001362954.1:c.-395-11929_-395-11911del	NM_001362954.1:c.-395-11928_-395-11911del	NM_001362954.1:c.-395-11927_-395-11911del	NM_001362954.1:c.-395-11926_-395-11911del	NM_001362954.1:c.-395-11925_-395-11911del	NM_001362954.1:c.-395-11924_-395-11911del	NM_001362954.1:c.-395-11923_-395-11911del	NM_001362954.1:c.-395-11922_-395-11911del	NM_001362954.1:c.-395-11921_-395-11911del	NM_001362954.1:c.-395-11920_-395-11911del	NM_001362954.1:c.-395-11919_-395-11911del	NM_001362954.1:c.-395-11918_-395-11911del	NM_001362954.1:c.-395-11917_-395-11911del	NM_001362954.1:c.-395-11916_-395-11911del	NM_001362954.1:c.-395-11915_-395-11911del	NM_001362954.1:c.-395-11914_-395-11911del	NM_001362954.1:c.-395-11913_-395-11911del	NM_001362954.1:c.-395-11912_-395-11911del	NM_001362954.1:c.-395-11911del	NM_001362954.1:c.-395-11911dup	NM_001362954.1:c.-395-11912_-395-11911dup	NM_001362954.1:c.-395-11913_-395-11911dup	NM_001362954.1:c.-395-11914_-395-11911dup	NM_001362954.1:c.-395-11915_-395-11911dup	NM_001362954.1:c.-395-11916_-395-11911dup
NCOA1 transcript variant 7	NM_001362955.1:c.-420-11550=	NM_001362955.1:c.-420-11538_-420-11520del	NM_001362955.1:c.-420-11537_-420-11520del	NM_001362955.1:c.-420-11536_-420-11520del	NM_001362955.1:c.-420-11535_-420-11520del	NM_001362955.1:c.-420-11534_-420-11520del	NM_001362955.1:c.-420-11533_-420-11520del	NM_001362955.1:c.-420-11532_-420-11520del	NM_001362955.1:c.-420-11531_-420-11520del	NM_001362955.1:c.-420-11530_-420-11520del	NM_001362955.1:c.-420-11529_-420-11520del	NM_001362955.1:c.-420-11528_-420-11520del	NM_001362955.1:c.-420-11527_-420-11520del	NM_001362955.1:c.-420-11526_-420-11520del	NM_001362955.1:c.-420-11525_-420-11520del	NM_001362955.1:c.-420-11524_-420-11520del	NM_001362955.1:c.-420-11523_-420-11520del	NM_001362955.1:c.-420-11522_-420-11520del	NM_001362955.1:c.-420-11521_-420-11520del	NM_001362955.1:c.-420-11520del	NM_001362955.1:c.-420-11520dup	NM_001362955.1:c.-420-11521_-420-11520dup	NM_001362955.1:c.-420-11522_-420-11520dup	NM_001362955.1:c.-420-11523_-420-11520dup	NM_001362955.1:c.-420-11524_-420-11520dup	NM_001362955.1:c.-420-11525_-420-11520dup
NCOA1 transcript variant 1	NM_003743.5:c.-395-11941=	NM_003743.5:c.-395-11929_-395-11911del	NM_003743.5:c.-395-11928_-395-11911del	NM_003743.5:c.-395-11927_-395-11911del	NM_003743.5:c.-395-11926_-395-11911del	NM_003743.5:c.-395-11925_-395-11911del	NM_003743.5:c.-395-11924_-395-11911del	NM_003743.5:c.-395-11923_-395-11911del	NM_003743.5:c.-395-11922_-395-11911del	NM_003743.5:c.-395-11921_-395-11911del	NM_003743.5:c.-395-11920_-395-11911del	NM_003743.5:c.-395-11919_-395-11911del	NM_003743.5:c.-395-11918_-395-11911del	NM_003743.5:c.-395-11917_-395-11911del	NM_003743.5:c.-395-11916_-395-11911del	NM_003743.5:c.-395-11915_-395-11911del	NM_003743.5:c.-395-11914_-395-11911del	NM_003743.5:c.-395-11913_-395-11911del	NM_003743.5:c.-395-11912_-395-11911del	NM_003743.5:c.-395-11911del	NM_003743.5:c.-395-11911dup	NM_003743.5:c.-395-11912_-395-11911dup	NM_003743.5:c.-395-11913_-395-11911dup	NM_003743.5:c.-395-11914_-395-11911dup	NM_003743.5:c.-395-11915_-395-11911dup	NM_003743.5:c.-395-11916_-395-11911dup
NCOA1 transcript variant 2	NM_147223.3:c.-259-32122=	NM_147223.3:c.-259-32110_-259-32092del	NM_147223.3:c.-259-32109_-259-32092del	NM_147223.3:c.-259-32108_-259-32092del	NM_147223.3:c.-259-32107_-259-32092del	NM_147223.3:c.-259-32106_-259-32092del	NM_147223.3:c.-259-32105_-259-32092del	NM_147223.3:c.-259-32104_-259-32092del	NM_147223.3:c.-259-32103_-259-32092del	NM_147223.3:c.-259-32102_-259-32092del	NM_147223.3:c.-259-32101_-259-32092del	NM_147223.3:c.-259-32100_-259-32092del	NM_147223.3:c.-259-32099_-259-32092del	NM_147223.3:c.-259-32098_-259-32092del	NM_147223.3:c.-259-32097_-259-32092del	NM_147223.3:c.-259-32096_-259-32092del	NM_147223.3:c.-259-32095_-259-32092del	NM_147223.3:c.-259-32094_-259-32092del	NM_147223.3:c.-259-32093_-259-32092del	NM_147223.3:c.-259-32092del	NM_147223.3:c.-259-32092dup	NM_147223.3:c.-259-32093_-259-32092dup	NM_147223.3:c.-259-32094_-259-32092dup	NM_147223.3:c.-259-32095_-259-32092dup	NM_147223.3:c.-259-32096_-259-32092dup	NM_147223.3:c.-259-32097_-259-32092dup
NCOA1 transcript variant X1	XM_005264625.1:c.-395-11941=	XM_005264625.1:c.-395-11929_-395-11911del	XM_005264625.1:c.-395-11928_-395-11911del	XM_005264625.1:c.-395-11927_-395-11911del	XM_005264625.1:c.-395-11926_-395-11911del	XM_005264625.1:c.-395-11925_-395-11911del	XM_005264625.1:c.-395-11924_-395-11911del	XM_005264625.1:c.-395-11923_-395-11911del	XM_005264625.1:c.-395-11922_-395-11911del	XM_005264625.1:c.-395-11921_-395-11911del	XM_005264625.1:c.-395-11920_-395-11911del	XM_005264625.1:c.-395-11919_-395-11911del	XM_005264625.1:c.-395-11918_-395-11911del	XM_005264625.1:c.-395-11917_-395-11911del	XM_005264625.1:c.-395-11916_-395-11911del	XM_005264625.1:c.-395-11915_-395-11911del	XM_005264625.1:c.-395-11914_-395-11911del	XM_005264625.1:c.-395-11913_-395-11911del	XM_005264625.1:c.-395-11912_-395-11911del	XM_005264625.1:c.-395-11911del	XM_005264625.1:c.-395-11911dup	XM_005264625.1:c.-395-11912_-395-11911dup	XM_005264625.1:c.-395-11913_-395-11911dup	XM_005264625.1:c.-395-11914_-395-11911dup	XM_005264625.1:c.-395-11915_-395-11911dup	XM_005264625.1:c.-395-11916_-395-11911dup
NCOA1 transcript variant X1	XM_047446151.1:c.-259-32122=	XM_047446151.1:c.-259-32110_-259-32092del	XM_047446151.1:c.-259-32109_-259-32092del	XM_047446151.1:c.-259-32108_-259-32092del	XM_047446151.1:c.-259-32107_-259-32092del	XM_047446151.1:c.-259-32106_-259-32092del	XM_047446151.1:c.-259-32105_-259-32092del	XM_047446151.1:c.-259-32104_-259-32092del	XM_047446151.1:c.-259-32103_-259-32092del	XM_047446151.1:c.-259-32102_-259-32092del	XM_047446151.1:c.-259-32101_-259-32092del	XM_047446151.1:c.-259-32100_-259-32092del	XM_047446151.1:c.-259-32099_-259-32092del	XM_047446151.1:c.-259-32098_-259-32092del	XM_047446151.1:c.-259-32097_-259-32092del	XM_047446151.1:c.-259-32096_-259-32092del	XM_047446151.1:c.-259-32095_-259-32092del	XM_047446151.1:c.-259-32094_-259-32092del	XM_047446151.1:c.-259-32093_-259-32092del	XM_047446151.1:c.-259-32092del	XM_047446151.1:c.-259-32092dup	XM_047446151.1:c.-259-32093_-259-32092dup	XM_047446151.1:c.-259-32094_-259-32092dup	XM_047446151.1:c.-259-32095_-259-32092dup	XM_047446151.1:c.-259-32096_-259-32092dup	XM_047446151.1:c.-259-32097_-259-32092dup
NCOA1 transcript variant X2	XM_047446152.1:c.-536-2035=	XM_047446152.1:c.-536-2023_-536-2005del	XM_047446152.1:c.-536-2022_-536-2005del	XM_047446152.1:c.-536-2021_-536-2005del	XM_047446152.1:c.-536-2020_-536-2005del	XM_047446152.1:c.-536-2019_-536-2005del	XM_047446152.1:c.-536-2018_-536-2005del	XM_047446152.1:c.-536-2017_-536-2005del	XM_047446152.1:c.-536-2016_-536-2005del	XM_047446152.1:c.-536-2015_-536-2005del	XM_047446152.1:c.-536-2014_-536-2005del	XM_047446152.1:c.-536-2013_-536-2005del	XM_047446152.1:c.-536-2012_-536-2005del	XM_047446152.1:c.-536-2011_-536-2005del	XM_047446152.1:c.-536-2010_-536-2005del	XM_047446152.1:c.-536-2009_-536-2005del	XM_047446152.1:c.-536-2008_-536-2005del	XM_047446152.1:c.-536-2007_-536-2005del	XM_047446152.1:c.-536-2006_-536-2005del	XM_047446152.1:c.-536-2005del	XM_047446152.1:c.-536-2005dup	XM_047446152.1:c.-536-2006_-536-2005dup	XM_047446152.1:c.-536-2007_-536-2005dup	XM_047446152.1:c.-536-2008_-536-2005dup	XM_047446152.1:c.-536-2009_-536-2005dup	XM_047446152.1:c.-536-2010_-536-2005dup
NCOA1 transcript variant X3	XM_047446153.1:c.-536-2035=	XM_047446153.1:c.-536-2023_-536-2005del	XM_047446153.1:c.-536-2022_-536-2005del	XM_047446153.1:c.-536-2021_-536-2005del	XM_047446153.1:c.-536-2020_-536-2005del	XM_047446153.1:c.-536-2019_-536-2005del	XM_047446153.1:c.-536-2018_-536-2005del	XM_047446153.1:c.-536-2017_-536-2005del	XM_047446153.1:c.-536-2016_-536-2005del	XM_047446153.1:c.-536-2015_-536-2005del	XM_047446153.1:c.-536-2014_-536-2005del	XM_047446153.1:c.-536-2013_-536-2005del	XM_047446153.1:c.-536-2012_-536-2005del	XM_047446153.1:c.-536-2011_-536-2005del	XM_047446153.1:c.-536-2010_-536-2005del	XM_047446153.1:c.-536-2009_-536-2005del	XM_047446153.1:c.-536-2008_-536-2005del	XM_047446153.1:c.-536-2007_-536-2005del	XM_047446153.1:c.-536-2006_-536-2005del	XM_047446153.1:c.-536-2005del	XM_047446153.1:c.-536-2005dup	XM_047446153.1:c.-536-2006_-536-2005dup	XM_047446153.1:c.-536-2007_-536-2005dup	XM_047446153.1:c.-536-2008_-536-2005dup	XM_047446153.1:c.-536-2009_-536-2005dup	XM_047446153.1:c.-536-2010_-536-2005dup
NCOA1 transcript variant X4	XM_047446154.1:c.-536-2035=	XM_047446154.1:c.-536-2023_-536-2005del	XM_047446154.1:c.-536-2022_-536-2005del	XM_047446154.1:c.-536-2021_-536-2005del	XM_047446154.1:c.-536-2020_-536-2005del	XM_047446154.1:c.-536-2019_-536-2005del	XM_047446154.1:c.-536-2018_-536-2005del	XM_047446154.1:c.-536-2017_-536-2005del	XM_047446154.1:c.-536-2016_-536-2005del	XM_047446154.1:c.-536-2015_-536-2005del	XM_047446154.1:c.-536-2014_-536-2005del	XM_047446154.1:c.-536-2013_-536-2005del	XM_047446154.1:c.-536-2012_-536-2005del	XM_047446154.1:c.-536-2011_-536-2005del	XM_047446154.1:c.-536-2010_-536-2005del	XM_047446154.1:c.-536-2009_-536-2005del	XM_047446154.1:c.-536-2008_-536-2005del	XM_047446154.1:c.-536-2007_-536-2005del	XM_047446154.1:c.-536-2006_-536-2005del	XM_047446154.1:c.-536-2005del	XM_047446154.1:c.-536-2005dup	XM_047446154.1:c.-536-2006_-536-2005dup	XM_047446154.1:c.-536-2007_-536-2005dup	XM_047446154.1:c.-536-2008_-536-2005dup	XM_047446154.1:c.-536-2009_-536-2005dup	XM_047446154.1:c.-536-2010_-536-2005dup
NCOA1 transcript variant X5	XM_047446155.1:c.-536-2035=	XM_047446155.1:c.-536-2023_-536-2005del	XM_047446155.1:c.-536-2022_-536-2005del	XM_047446155.1:c.-536-2021_-536-2005del	XM_047446155.1:c.-536-2020_-536-2005del	XM_047446155.1:c.-536-2019_-536-2005del	XM_047446155.1:c.-536-2018_-536-2005del	XM_047446155.1:c.-536-2017_-536-2005del	XM_047446155.1:c.-536-2016_-536-2005del	XM_047446155.1:c.-536-2015_-536-2005del	XM_047446155.1:c.-536-2014_-536-2005del	XM_047446155.1:c.-536-2013_-536-2005del	XM_047446155.1:c.-536-2012_-536-2005del	XM_047446155.1:c.-536-2011_-536-2005del	XM_047446155.1:c.-536-2010_-536-2005del	XM_047446155.1:c.-536-2009_-536-2005del	XM_047446155.1:c.-536-2008_-536-2005del	XM_047446155.1:c.-536-2007_-536-2005del	XM_047446155.1:c.-536-2006_-536-2005del	XM_047446155.1:c.-536-2005del	XM_047446155.1:c.-536-2005dup	XM_047446155.1:c.-536-2006_-536-2005dup	XM_047446155.1:c.-536-2007_-536-2005dup	XM_047446155.1:c.-536-2008_-536-2005dup	XM_047446155.1:c.-536-2009_-536-2005dup	XM_047446155.1:c.-536-2010_-536-2005dup
NCOA1 transcript variant X6	XM_047446156.1:c.-311-32122=	XM_047446156.1:c.-311-32110_-311-32092del	XM_047446156.1:c.-311-32109_-311-32092del	XM_047446156.1:c.-311-32108_-311-32092del	XM_047446156.1:c.-311-32107_-311-32092del	XM_047446156.1:c.-311-32106_-311-32092del	XM_047446156.1:c.-311-32105_-311-32092del	XM_047446156.1:c.-311-32104_-311-32092del	XM_047446156.1:c.-311-32103_-311-32092del	XM_047446156.1:c.-311-32102_-311-32092del	XM_047446156.1:c.-311-32101_-311-32092del	XM_047446156.1:c.-311-32100_-311-32092del	XM_047446156.1:c.-311-32099_-311-32092del	XM_047446156.1:c.-311-32098_-311-32092del	XM_047446156.1:c.-311-32097_-311-32092del	XM_047446156.1:c.-311-32096_-311-32092del	XM_047446156.1:c.-311-32095_-311-32092del	XM_047446156.1:c.-311-32094_-311-32092del	XM_047446156.1:c.-311-32093_-311-32092del	XM_047446156.1:c.-311-32092del	XM_047446156.1:c.-311-32092dup	XM_047446156.1:c.-311-32093_-311-32092dup	XM_047446156.1:c.-311-32094_-311-32092dup	XM_047446156.1:c.-311-32095_-311-32092dup	XM_047446156.1:c.-311-32096_-311-32092dup	XM_047446156.1:c.-311-32097_-311-32092dup
NCOA1 transcript variant X7	XM_047446157.1:c.-259-32122=	XM_047446157.1:c.-259-32110_-259-32092del	XM_047446157.1:c.-259-32109_-259-32092del	XM_047446157.1:c.-259-32108_-259-32092del	XM_047446157.1:c.-259-32107_-259-32092del	XM_047446157.1:c.-259-32106_-259-32092del	XM_047446157.1:c.-259-32105_-259-32092del	XM_047446157.1:c.-259-32104_-259-32092del	XM_047446157.1:c.-259-32103_-259-32092del	XM_047446157.1:c.-259-32102_-259-32092del	XM_047446157.1:c.-259-32101_-259-32092del	XM_047446157.1:c.-259-32100_-259-32092del	XM_047446157.1:c.-259-32099_-259-32092del	XM_047446157.1:c.-259-32098_-259-32092del	XM_047446157.1:c.-259-32097_-259-32092del	XM_047446157.1:c.-259-32096_-259-32092del	XM_047446157.1:c.-259-32095_-259-32092del	XM_047446157.1:c.-259-32094_-259-32092del	XM_047446157.1:c.-259-32093_-259-32092del	XM_047446157.1:c.-259-32092del	XM_047446157.1:c.-259-32092dup	XM_047446157.1:c.-259-32093_-259-32092dup	XM_047446157.1:c.-259-32094_-259-32092dup	XM_047446157.1:c.-259-32095_-259-32092dup	XM_047446157.1:c.-259-32096_-259-32092dup	XM_047446157.1:c.-259-32097_-259-32092dup
NCOA1 transcript variant X8	XM_047446158.1:c.-259-32122=	XM_047446158.1:c.-259-32110_-259-32092del	XM_047446158.1:c.-259-32109_-259-32092del	XM_047446158.1:c.-259-32108_-259-32092del	XM_047446158.1:c.-259-32107_-259-32092del	XM_047446158.1:c.-259-32106_-259-32092del	XM_047446158.1:c.-259-32105_-259-32092del	XM_047446158.1:c.-259-32104_-259-32092del	XM_047446158.1:c.-259-32103_-259-32092del	XM_047446158.1:c.-259-32102_-259-32092del	XM_047446158.1:c.-259-32101_-259-32092del	XM_047446158.1:c.-259-32100_-259-32092del	XM_047446158.1:c.-259-32099_-259-32092del	XM_047446158.1:c.-259-32098_-259-32092del	XM_047446158.1:c.-259-32097_-259-32092del	XM_047446158.1:c.-259-32096_-259-32092del	XM_047446158.1:c.-259-32095_-259-32092del	XM_047446158.1:c.-259-32094_-259-32092del	XM_047446158.1:c.-259-32093_-259-32092del	XM_047446158.1:c.-259-32092del	XM_047446158.1:c.-259-32092dup	XM_047446158.1:c.-259-32093_-259-32092dup	XM_047446158.1:c.-259-32094_-259-32092dup	XM_047446158.1:c.-259-32095_-259-32092dup	XM_047446158.1:c.-259-32096_-259-32092dup	XM_047446158.1:c.-259-32097_-259-32092dup

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#.

19 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95266865	Mar 15, 2016 (147)
2	PACBIO	ss3783806256	Jul 12, 2019 (153)
3	KOGIC	ss3947310681	Apr 25, 2020 (154)
4	KOGIC	ss3947310682	Apr 25, 2020 (154)
5	KOGIC	ss3947310683	Apr 25, 2020 (154)
6	KOGIC	ss3947310684	Apr 25, 2020 (154)
7	GNOMAD	ss4037281432	Apr 26, 2021 (155)
8	GNOMAD	ss4037281438	Apr 26, 2021 (155)
9	GNOMAD	ss4037281439	Apr 26, 2021 (155)
10	GNOMAD	ss4037281440	Apr 26, 2021 (155)
11	GNOMAD	ss4037281441	Apr 26, 2021 (155)
12	GNOMAD	ss4037281442	Apr 26, 2021 (155)
13	GNOMAD	ss4037281444	Apr 26, 2021 (155)
14	GNOMAD	ss4037281445	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5678647270	Oct 17, 2022 (156)
16	TOMMO_GENOMICS	ss5678647271	Oct 17, 2022 (156)
17	TOMMO_GENOMICS	ss5678647272	Oct 17, 2022 (156)
18	TOMMO_GENOMICS	ss5678647273	Oct 17, 2022 (156)
19	TOMMO_GENOMICS	ss5678647274	Oct 17, 2022 (156)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51385584 (NC_000002.12:24552353::T 4/36156) Row 51385590 (NC_000002.12:24552353::TT 8/36154) Row 51385591 (NC_000002.12:24552353::TTT 2/36156)...	-	Apr 26, 2021 (155)
28	Korean Genome Project Submission ignored due to conflicting rows: Row 3688682 (NC_000002.12:24552357:TTTTTTTTTTTTT: 49/1116) Row 3688683 (NC_000002.12:24552355:TTTTTTTTTTTTTTT: 63/1116) Row 3688684 (NC_000002.12:24552356:TTTTTTTTTTTTTT: 6/1116)...	-	Apr 25, 2020 (154)
29	Korean Genome Project Submission ignored due to conflicting rows: Row 3688682 (NC_000002.12:24552357:TTTTTTTTTTTTT: 49/1116) Row 3688683 (NC_000002.12:24552355:TTTTTTTTTTTTTTT: 63/1116) Row 3688684 (NC_000002.12:24552356:TTTTTTTTTTTTTT: 6/1116)...	-	Apr 25, 2020 (154)
30	Korean Genome Project Submission ignored due to conflicting rows: Row 3688682 (NC_000002.12:24552357:TTTTTTTTTTTTT: 49/1116) Row 3688683 (NC_000002.12:24552355:TTTTTTTTTTTTTTT: 63/1116) Row 3688684 (NC_000002.12:24552356:TTTTTTTTTTTTTT: 6/1116)...	-	Apr 25, 2020 (154)
31	Korean Genome Project Submission ignored due to conflicting rows: Row 3688682 (NC_000002.12:24552357:TTTTTTTTTTTTT: 49/1116) Row 3688683 (NC_000002.12:24552355:TTTTTTTTTTTTTTT: 63/1116) Row 3688684 (NC_000002.12:24552356:TTTTTTTTTTTTTT: 6/1116)...	-	Apr 25, 2020 (154)
32	14KJPN Submission ignored due to conflicting rows: Row 12484374 (NC_000002.12:24552353:TTTTTTTTTT: 116/20984) Row 12484375 (NC_000002.12:24552353:TTTTTTTTTTTTT: 1521/20984) Row 12484376 (NC_000002.12:24552353:TTTTTTTTTTTTTTT: 2855/20984)...	-	Oct 17, 2022 (156)
33	14KJPN Submission ignored due to conflicting rows: Row 12484374 (NC_000002.12:24552353:TTTTTTTTTT: 116/20984) Row 12484375 (NC_000002.12:24552353:TTTTTTTTTTTTT: 1521/20984) Row 12484376 (NC_000002.12:24552353:TTTTTTTTTTTTTTT: 2855/20984)...	-	Oct 17, 2022 (156)
34	14KJPN Submission ignored due to conflicting rows: Row 12484374 (NC_000002.12:24552353:TTTTTTTTTT: 116/20984) Row 12484375 (NC_000002.12:24552353:TTTTTTTTTTTTT: 1521/20984) Row 12484376 (NC_000002.12:24552353:TTTTTTTTTTTTTTT: 2855/20984)...	-	Oct 17, 2022 (156)
35	14KJPN Submission ignored due to conflicting rows: Row 12484374 (NC_000002.12:24552353:TTTTTTTTTT: 116/20984) Row 12484375 (NC_000002.12:24552353:TTTTTTTTTTTTT: 1521/20984) Row 12484376 (NC_000002.12:24552353:TTTTTTTTTTTTTTT: 2855/20984)...	-	Oct 17, 2022 (156)
36	14KJPN Submission ignored due to conflicting rows: Row 12484374 (NC_000002.12:24552353:TTTTTTTTTT: 116/20984) Row 12484375 (NC_000002.12:24552353:TTTTTTTTTTTTT: 1521/20984) Row 12484376 (NC_000002.12:24552353:TTTTTTTTTTTTTTT: 2855/20984)...	-	Oct 17, 2022 (156)
37	ALFA	NC_000002.12 - 24552354	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:

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3301918855	NC_000002.12:24552353:T:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3301918856	NC_000002.12:24552353:TT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3301918857	NC_000002.12:24552353:TTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3301918858	NC_000002.12:24552353:TTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3301918859	NC_000002.12:24552353:TTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
ss3301918860	NC_000002.12:24552353:TTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
ss3301918861	NC_000002.12:24552353:TTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
ss3301918862	NC_000002.12:24552353:TTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
ss3301918863	NC_000002.12:24552353:TTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
ss3301918868	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

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

No publications for rs869212842

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4037281445	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4037281444	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5678647272	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3947310682	NC_000002.12:24552355:TTTTTTTTTTTT… NC_000002.12:24552355:TTTTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3947310683	NC_000002.12:24552356:TTTTTTTTTTTT… NC_000002.12:24552356:TTTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3783806256	NC_000002.11:24775222:TTTTTTTTTTTT… NC_000002.11:24775222:TTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5678647271	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3947310681	NC_000002.12:24552357:TTTTTTTTTTTT… NC_000002.12:24552357:TTTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5678647273	NC_000002.12:24552353:TTTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5678647274	NC_000002.12:24552353:TTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3947310684	NC_000002.12:24552359:TTTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5678647270	NC_000002.12:24552353:TTTTTTTTTT:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95266865	NT_022184.15:3597113:T:	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4037281432	NC_000002.12:24552353::T	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4037281438	NC_000002.12:24552353::TT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4037281439	NC_000002.12:24552353::TTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4037281440	NC_000002.12:24552353::TTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4037281441	NC_000002.12:24552353::TTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12558096092	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4037281442	NC_000002.12:24552353::TTTTTT	NC_000002.12:24552353:TTTTTTTTTTTT… NC_000002.12:24552353:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs869212842