Name: rs1165643561
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.

rs1165643561

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:48932262-48932290 (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)₂₀ / del(T)₁₉ / del(T)₁₈ / d…
del(T)₂₀ / 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
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₂₀=0.0000 (0/6564, ALFA)
del(T)₁₉=0.0000 (0/6564, ALFA)
del(T)₁₈=0.0000 (0/6564, ALFA) (+ 20 more)
del(T)₁₇=0.0000 (0/6564, ALFA)
del(T)₁₆=0.0000 (0/6564, ALFA)
del(T)₁₅=0.0000 (0/6564, ALFA)
del(T)₁₄=0.0000 (0/6564, ALFA)
del(T)₁₃=0.0000 (0/6564, ALFA)
del(T)₁₂=0.0000 (0/6564, ALFA)
del(T)₁₁=0.0000 (0/6564, ALFA)
del(T)₁₀=0.0000 (0/6564, ALFA)
del(T)₉=0.0000 (0/6564, ALFA)
del(T)₈=0.0000 (0/6564, ALFA)
del(T)₇=0.0000 (0/6564, ALFA)
del(T)₆=0.0000 (0/6564, ALFA)
del(T)₅=0.0000 (0/6564, ALFA)
del(T)₄=0.0000 (0/6564, ALFA)
delTTT=0.0000 (0/6564, ALFA)
delTT=0.0000 (0/6564, ALFA)
delT=0.0000 (0/6564, ALFA)
dupT=0.0000 (0/6564, ALFA)
dupTTT=0.0000 (0/6564, ALFA)
del(T)₁₈=0.026 (9/344, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FKBP11 : 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	6564	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	3806	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2052	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	74	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1978	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	38	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	78	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	292	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	42	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	256	TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	6564	(T)₂₉=1.0000	del(T)₂₀=0.0000, 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
Allele Frequency Aggregator	European	Sub	3806	(T)₂₉=1.0000	del(T)₂₀=0.0000, 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
Allele Frequency Aggregator	African	Sub	2052	(T)₂₉=1.0000	del(T)₂₀=0.0000, 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
Allele Frequency Aggregator	Latin American 2	Sub	292	(T)₂₉=1.000	del(T)₂₀=0.000, 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
Allele Frequency Aggregator	Other	Sub	256	(T)₂₉=1.000	del(T)₂₀=0.000, 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
Allele Frequency Aggregator	Latin American 1	Sub	78	(T)₂₉=1.00	del(T)₂₀=0.00, 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
Allele Frequency Aggregator	South Asian	Sub	42	(T)₂₉=1.00	del(T)₂₀=0.00, 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
Allele Frequency Aggregator	Asian	Sub	38	(T)₂₉=1.00	del(T)₂₀=0.00, 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
Northern Sweden	ACPOP	Study-wide	344	(T)₂₉=0.974	del(T)₁₈=0.026

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 12	NC_000012.12:g.48932271_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932272_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932273_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932274_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932275_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932276_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932277_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932278_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932279_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932280_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932281_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932282_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932283_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932284_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932285_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932286_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932287_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932288_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932289_48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932290del
GRCh38.p14 chr 12	NC_000012.12:g.48932290dup
GRCh38.p14 chr 12	NC_000012.12:g.48932289_48932290dup
GRCh38.p14 chr 12	NC_000012.12:g.48932288_48932290dup
GRCh38.p14 chr 12	NC_000012.12:g.48932287_48932290dup
GRCh38.p14 chr 12	NC_000012.12:g.48932286_48932290dup
GRCh37.p13 chr 12	NC_000012.11:g.49326054_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326055_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326056_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326057_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326058_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326059_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326060_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326061_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326062_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326063_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326064_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326065_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326066_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326067_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326068_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326069_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326070_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326071_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326072_49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326073del
GRCh37.p13 chr 12	NC_000012.11:g.49326073dup
GRCh37.p13 chr 12	NC_000012.11:g.49326072_49326073dup
GRCh37.p13 chr 12	NC_000012.11:g.49326071_49326073dup
GRCh37.p13 chr 12	NC_000012.11:g.49326070_49326073dup
GRCh37.p13 chr 12	NC_000012.11:g.49326069_49326073dup

Gene: FKBP11, FKBP prolyl isomerase 11 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FKBP11 transcript variant 2	NM_001143781.2:c.	N/A	Genic Upstream Transcript Variant
FKBP11 transcript variant 3	NM_001143782.2:c.	N/A	Genic Upstream Transcript Variant
FKBP11 transcript variant 1	NM_016594.3:c.	N/A	Genic Upstream Transcript Variant
FKBP11 transcript variant X1	XM_047428939.1:c.86-1679_… XM_047428939.1:c.86-1679_86-1660del	N/A	Intron Variant
FKBP11 transcript variant X2	XM_047428940.1:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₉=	del(T)₂₀	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
GRCh38.p14 chr 12	NC_000012.12:g.48932262_48932290=	NC_000012.12:g.48932271_48932290del	NC_000012.12:g.48932272_48932290del	NC_000012.12:g.48932273_48932290del	NC_000012.12:g.48932274_48932290del	NC_000012.12:g.48932275_48932290del	NC_000012.12:g.48932276_48932290del	NC_000012.12:g.48932277_48932290del	NC_000012.12:g.48932278_48932290del	NC_000012.12:g.48932279_48932290del	NC_000012.12:g.48932280_48932290del	NC_000012.12:g.48932281_48932290del	NC_000012.12:g.48932282_48932290del	NC_000012.12:g.48932283_48932290del	NC_000012.12:g.48932284_48932290del	NC_000012.12:g.48932285_48932290del	NC_000012.12:g.48932286_48932290del	NC_000012.12:g.48932287_48932290del	NC_000012.12:g.48932288_48932290del	NC_000012.12:g.48932289_48932290del	NC_000012.12:g.48932290del	NC_000012.12:g.48932290dup	NC_000012.12:g.48932289_48932290dup	NC_000012.12:g.48932288_48932290dup	NC_000012.12:g.48932287_48932290dup	NC_000012.12:g.48932286_48932290dup
GRCh37.p13 chr 12	NC_000012.11:g.49326045_49326073=	NC_000012.11:g.49326054_49326073del	NC_000012.11:g.49326055_49326073del	NC_000012.11:g.49326056_49326073del	NC_000012.11:g.49326057_49326073del	NC_000012.11:g.49326058_49326073del	NC_000012.11:g.49326059_49326073del	NC_000012.11:g.49326060_49326073del	NC_000012.11:g.49326061_49326073del	NC_000012.11:g.49326062_49326073del	NC_000012.11:g.49326063_49326073del	NC_000012.11:g.49326064_49326073del	NC_000012.11:g.49326065_49326073del	NC_000012.11:g.49326066_49326073del	NC_000012.11:g.49326067_49326073del	NC_000012.11:g.49326068_49326073del	NC_000012.11:g.49326069_49326073del	NC_000012.11:g.49326070_49326073del	NC_000012.11:g.49326071_49326073del	NC_000012.11:g.49326072_49326073del	NC_000012.11:g.49326073del	NC_000012.11:g.49326073dup	NC_000012.11:g.49326072_49326073dup	NC_000012.11:g.49326071_49326073dup	NC_000012.11:g.49326070_49326073dup	NC_000012.11:g.49326069_49326073dup
FKBP11 transcript variant X1	XM_047428939.1:c.86-1660=	XM_047428939.1:c.86-1679_86-1660del	XM_047428939.1:c.86-1678_86-1660del	XM_047428939.1:c.86-1677_86-1660del	XM_047428939.1:c.86-1676_86-1660del	XM_047428939.1:c.86-1675_86-1660del	XM_047428939.1:c.86-1674_86-1660del	XM_047428939.1:c.86-1673_86-1660del	XM_047428939.1:c.86-1672_86-1660del	XM_047428939.1:c.86-1671_86-1660del	XM_047428939.1:c.86-1670_86-1660del	XM_047428939.1:c.86-1669_86-1660del	XM_047428939.1:c.86-1668_86-1660del	XM_047428939.1:c.86-1667_86-1660del	XM_047428939.1:c.86-1666_86-1660del	XM_047428939.1:c.86-1665_86-1660del	XM_047428939.1:c.86-1664_86-1660del	XM_047428939.1:c.86-1663_86-1660del	XM_047428939.1:c.86-1662_86-1660del	XM_047428939.1:c.86-1661_86-1660del	XM_047428939.1:c.86-1660del	XM_047428939.1:c.86-1660dup	XM_047428939.1:c.86-1661_86-1660dup	XM_047428939.1:c.86-1662_86-1660dup	XM_047428939.1:c.86-1663_86-1660dup	XM_047428939.1:c.86-1664_86-1660dup

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#.

39 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3009657232	Nov 08, 2017 (151)
2	EVA_DECODE	ss3693634619	Jul 13, 2019 (153)
3	EVA_DECODE	ss3693634620	Jul 13, 2019 (153)
4	EVA_DECODE	ss3693634621	Jul 13, 2019 (153)
5	EVA_DECODE	ss3693634622	Jul 13, 2019 (153)
6	EVA_DECODE	ss3693634623	Jul 13, 2019 (153)
7	EVA_DECODE	ss3693634624	Jul 13, 2019 (153)
8	ACPOP	ss3739006827	Jul 13, 2019 (153)
9	KOGIC	ss3971890917	Apr 27, 2020 (154)
10	KOGIC	ss3971890918	Apr 27, 2020 (154)
11	KOGIC	ss3971890919	Apr 27, 2020 (154)
12	KOGIC	ss3971890920	Apr 27, 2020 (154)
13	KOGIC	ss3971890921	Apr 27, 2020 (154)
14	GNOMAD	ss4251471486	Apr 26, 2021 (155)
15	GNOMAD	ss4251471489	Apr 26, 2021 (155)
16	GNOMAD	ss4251471490	Apr 26, 2021 (155)
17	GNOMAD	ss4251471491	Apr 26, 2021 (155)
18	GNOMAD	ss4251471492	Apr 26, 2021 (155)
19	GNOMAD	ss4251471493	Apr 26, 2021 (155)
20	GNOMAD	ss4251471494	Apr 26, 2021 (155)
21	GNOMAD	ss4251471495	Apr 26, 2021 (155)
22	GNOMAD	ss4251471496	Apr 26, 2021 (155)
23	GNOMAD	ss4251471497	Apr 26, 2021 (155)
24	GNOMAD	ss4251471498	Apr 26, 2021 (155)
25	GNOMAD	ss4251471499	Apr 26, 2021 (155)
26	GNOMAD	ss4251471500	Apr 26, 2021 (155)
27	GNOMAD	ss4251471501	Apr 26, 2021 (155)
28	GNOMAD	ss4251471502	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5206231252	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5206231253	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5206231254	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5206231255	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5206231256	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5206231257	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5755991778	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5755991779	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5755991780	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5755991781	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5755991782	Oct 16, 2022 (156)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 406790303 (NC_000012.12:48932261::T 1/29068) Row 406790306 (NC_000012.12:48932261::TT 2/29070) Row 406790307 (NC_000012.12:48932261::TTTT 1/29070)...	-	Apr 26, 2021 (155)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 28268918 (NC_000012.12:48932268:TTTTTTTTTTT: 43/1054) Row 28268919 (NC_000012.12:48932266:TTTTTTTTTTTTT: 30/1054) Row 28268920 (NC_000012.12:48932265:TTTTTTTTTTTTTT: 33/1054)...	-	Apr 27, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 28268918 (NC_000012.12:48932268:TTTTTTTTTTT: 43/1054) Row 28268919 (NC_000012.12:48932266:TTTTTTTTTTTTT: 30/1054) Row 28268920 (NC_000012.12:48932265:TTTTTTTTTTTTTT: 33/1054)...	-	Apr 27, 2020 (154)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 28268918 (NC_000012.12:48932268:TTTTTTTTTTT: 43/1054) Row 28268919 (NC_000012.12:48932266:TTTTTTTTTTTTT: 30/1054) Row 28268920 (NC_000012.12:48932265:TTTTTTTTTTTTTT: 33/1054)...	-	Apr 27, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 28268918 (NC_000012.12:48932268:TTTTTTTTTTT: 43/1054) Row 28268919 (NC_000012.12:48932266:TTTTTTTTTTTTT: 30/1054) Row 28268920 (NC_000012.12:48932265:TTTTTTTTTTTTTT: 33/1054)...	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 28268918 (NC_000012.12:48932268:TTTTTTTTTTT: 43/1054) Row 28268919 (NC_000012.12:48932266:TTTTTTTTTTTTT: 30/1054) Row 28268920 (NC_000012.12:48932265:TTTTTTTTTTTTTT: 33/1054)...	-	Apr 27, 2020 (154)
60	Northern Sweden	NC_000012.11 - 49326045	Jul 13, 2019 (153)
61	8.3KJPN Submission ignored due to conflicting rows: Row 64200559 (NC_000012.11:49326044:TTTTTTTTTTTTT: 452/14594) Row 64200560 (NC_000012.11:49326044:TTTTTTTTTTTTTT: 314/14594) Row 64200561 (NC_000012.11:49326044:TTTTTT: 219/14594)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 64200559 (NC_000012.11:49326044:TTTTTTTTTTTTT: 452/14594) Row 64200560 (NC_000012.11:49326044:TTTTTTTTTTTTTT: 314/14594) Row 64200561 (NC_000012.11:49326044:TTTTTT: 219/14594)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 64200559 (NC_000012.11:49326044:TTTTTTTTTTTTT: 452/14594) Row 64200560 (NC_000012.11:49326044:TTTTTTTTTTTTTT: 314/14594) Row 64200561 (NC_000012.11:49326044:TTTTTT: 219/14594)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 64200559 (NC_000012.11:49326044:TTTTTTTTTTTTT: 452/14594) Row 64200560 (NC_000012.11:49326044:TTTTTTTTTTTTTT: 314/14594) Row 64200561 (NC_000012.11:49326044:TTTTTT: 219/14594)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 64200559 (NC_000012.11:49326044:TTTTTTTTTTTTT: 452/14594) Row 64200560 (NC_000012.11:49326044:TTTTTTTTTTTTTT: 314/14594) Row 64200561 (NC_000012.11:49326044:TTTTTT: 219/14594)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 64200559 (NC_000012.11:49326044:TTTTTTTTTTTTT: 452/14594) Row 64200560 (NC_000012.11:49326044:TTTTTTTTTTTTTT: 314/14594) Row 64200561 (NC_000012.11:49326044:TTTTTT: 219/14594)...	-	Apr 26, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 89828882 (NC_000012.12:48932261:TTTTTTTTTTTTT: 991/26764) Row 89828883 (NC_000012.12:48932261:TTTTTTTTTTTTTTTT: 1553/26764) Row 89828884 (NC_000012.12:48932261:TTTT: 1951/26764)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 89828882 (NC_000012.12:48932261:TTTTTTTTTTTTT: 991/26764) Row 89828883 (NC_000012.12:48932261:TTTTTTTTTTTTTTTT: 1553/26764) Row 89828884 (NC_000012.12:48932261:TTTT: 1951/26764)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 89828882 (NC_000012.12:48932261:TTTTTTTTTTTTT: 991/26764) Row 89828883 (NC_000012.12:48932261:TTTTTTTTTTTTTTTT: 1553/26764) Row 89828884 (NC_000012.12:48932261:TTTT: 1951/26764)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 89828882 (NC_000012.12:48932261:TTTTTTTTTTTTT: 991/26764) Row 89828883 (NC_000012.12:48932261:TTTTTTTTTTTTTTTT: 1553/26764) Row 89828884 (NC_000012.12:48932261:TTTT: 1951/26764)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 89828882 (NC_000012.12:48932261:TTTTTTTTTTTTT: 991/26764) Row 89828883 (NC_000012.12:48932261:TTTTTTTTTTTTTTTT: 1553/26764) Row 89828884 (NC_000012.12:48932261:TTTT: 1951/26764)...	-	Oct 16, 2022 (156)
72	ALFA	NC_000012.12 - 48932262	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
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
12291692, ss3009657232, ss3739006827	NC_000012.11:49326044:TTTTTTTTTTTT… NC_000012.11:49326044:TTTTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4251471502	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4251471501	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5206231256	NC_000012.11:49326044:TTTTTTTTTTTT… NC_000012.11:49326044:TTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3693634619, ss4251471500, ss5755991779	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3971890920	NC_000012.12:48932263:TTTTTTTTTTTT… NC_000012.12:48932263:TTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4251471499	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5206231253	NC_000012.11:49326044:TTTTTTTTTTTT… NC_000012.11:49326044:TTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4251471498	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3693634620	NC_000012.12:48932263:TTTTTTTTTTTT… NC_000012.12:48932263:TTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3971890919	NC_000012.12:48932265:TTTTTTTTTTTT… NC_000012.12:48932265:TTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5206231252	NC_000012.11:49326044:TTTTTTTTTTTT… NC_000012.11:49326044:TTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4251471497, ss5755991778	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3693634621	NC_000012.12:48932264:TTTTTTTTTTTT… NC_000012.12:48932264:TTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3971890918	NC_000012.12:48932266:TTTTTTTTTTTT… NC_000012.12:48932266:TTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4251471496, ss5755991781	NC_000012.12:48932261:TTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3693634622	NC_000012.12:48932265:TTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3971890921	NC_000012.12:48932267:TTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5206231255	NC_000012.11:49326044:TTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4251471495, ss5755991782	NC_000012.12:48932261:TTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3693634623	NC_000012.12:48932266:TTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3971890917	NC_000012.12:48932268:TTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4251471494	NC_000012.12:48932261:TTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3693634624	NC_000012.12:48932267:TTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4251471493	NC_000012.12:48932261:TTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5206231254	NC_000012.11:49326044:TTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4251471492	NC_000012.12:48932261:TTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5206231257	NC_000012.11:49326044:TTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5755991780	NC_000012.12:48932261:TTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4251471486	NC_000012.12:48932261::T	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4251471489	NC_000012.12:48932261::TT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9295542179	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4251471490	NC_000012.12:48932261::TTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4251471491	NC_000012.12:48932261::TTTTT	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3170400272	NC_000012.12:48932261:T:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3170400273	NC_000012.12:48932261:TT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3170400274	NC_000012.12:48932261:TTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
ss3170400276	NC_000012.12:48932261:TTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
ss3170400278	NC_000012.12:48932261:TTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
ss3170400279	NC_000012.12:48932261:TTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
ss3170400290	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTT:	NC_000012.12:48932261:TTTTTTTTTTTT… NC_000012.12:48932261:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT

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

No publications for rs1165643561

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1165643561