Name: rs1156363999
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.

rs1156363999

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:35455406-35455433 (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)₂₁ / del(T)₁₉ / del(T)₁₈ / d…
del(T)₂₁ / 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 / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₂₁=0.00000 (0/10584, ALFA)
del(T)₁₉=0.00000 (0/10584, ALFA)
del(T)₁₈=0.00000 (0/10584, ALFA) (+ 28 more)
del(T)₁₇=0.00000 (0/10584, ALFA)
del(T)₁₆=0.00000 (0/10584, ALFA)
del(T)₁₅=0.00000 (0/10584, ALFA)
del(T)₁₄=0.00000 (0/10584, ALFA)
del(T)₁₃=0.00000 (0/10584, ALFA)
del(T)₁₂=0.00000 (0/10584, ALFA)
del(T)₁₁=0.00000 (0/10584, ALFA)
del(T)₁₀=0.00000 (0/10584, ALFA)
del(T)₉=0.00000 (0/10584, ALFA)
del(T)₈=0.00000 (0/10584, ALFA)
del(T)₇=0.00000 (0/10584, ALFA)
del(T)₆=0.00000 (0/10584, ALFA)
del(T)₅=0.00000 (0/10584, ALFA)
del(T)₄=0.00000 (0/10584, ALFA)
delTTT=0.00000 (0/10584, ALFA)
delTT=0.00000 (0/10584, ALFA)
delT=0.00000 (0/10584, ALFA)
dupT=0.00000 (0/10584, ALFA)
dupTT=0.00000 (0/10584, ALFA)
dupTTT=0.00000 (0/10584, ALFA)
dup(T)₄=0.00000 (0/10584, ALFA)
dup(T)₅=0.00000 (0/10584, ALFA)
dup(T)₆=0.00000 (0/10584, ALFA)
dup(T)₇=0.00000 (0/10584, ALFA)
dup(T)₈=0.00000 (0/10584, ALFA)
dup(T)₉=0.00000 (0/10584, ALFA)
dup(T)₁₀=0.00000 (0/10584, ALFA)
dup(T)₇=0.006 (6/938, Korea1K)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MCM5 : 500B Downstream 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	10584	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00000	TTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7302	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	1998	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	78	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1920	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTT=0.0000, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	98	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	76	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	120	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	556	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	90	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTT=0.00, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	420	TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTT=0.000, 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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	10584	(T)₂₈=1.00000	del(T)₂₁=0.00000, del(T)₁₉=0.00000, del(T)₁₈=0.00000, del(T)₁₇=0.00000, del(T)₁₆=0.00000, del(T)₁₅=0.00000, del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000, dup(T)₈=0.00000, dup(T)₉=0.00000, dup(T)₁₀=0.00000
Allele Frequency Aggregator	European	Sub	7302	(T)₂₈=1.0000	del(T)₂₁=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, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000
Allele Frequency Aggregator	African	Sub	1998	(T)₂₈=1.0000	del(T)₂₁=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, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	556	(T)₂₈=1.000	del(T)₂₁=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, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Other	Sub	420	(T)₂₈=1.000	del(T)₂₁=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, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Latin American 1	Sub	120	(T)₂₈=1.000	del(T)₂₁=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, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000
Allele Frequency Aggregator	Asian	Sub	98	(T)₂₈=1.00	del(T)₂₁=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, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Allele Frequency Aggregator	South Asian	Sub	90	(T)₂₈=1.00	del(T)₂₁=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, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00
Korean Genome Project	KOREAN	Study-wide	938	- No frequency provided	dup(T)₇=0.006

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 22	NC_000022.11:g.35455413_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455415_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455416_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455417_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455418_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455419_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455420_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455421_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455422_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455423_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455424_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455425_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455426_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455427_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455428_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455429_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455430_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455431_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455432_35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455433del
GRCh38.p14 chr 22	NC_000022.11:g.35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455432_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455431_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455430_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455429_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455428_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455427_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455426_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455425_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455424_35455433dup
GRCh38.p14 chr 22	NC_000022.11:g.35455423_35455433dup
GRCh37.p13 chr 22	NC_000022.10:g.35851406_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851408_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851409_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851410_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851411_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851412_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851413_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851414_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851415_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851416_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851417_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851418_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851419_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851420_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851421_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851422_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851423_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851424_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851425_35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851426del
GRCh37.p13 chr 22	NC_000022.10:g.35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851425_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851424_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851423_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851422_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851421_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851420_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851419_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851418_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851417_35851426dup
GRCh37.p13 chr 22	NC_000022.10:g.35851416_35851426dup

Gene: MCM5, minichromosome maintenance complex component 5 (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
MCM5 transcript	NM_006739.4:c.	N/A	N/A
MCM5 transcript variant X1	XM_006724242.5:c.	N/A	Downstream Transcript Variant
MCM5 transcript variant X2	XM_047441366.1:c.	N/A	Downstream 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)₂₈=	del(T)₂₁	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	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁
GRCh38.p14 chr 22	NC_000022.11:g.35455406_35455433=	NC_000022.11:g.35455413_35455433del	NC_000022.11:g.35455415_35455433del	NC_000022.11:g.35455416_35455433del	NC_000022.11:g.35455417_35455433del	NC_000022.11:g.35455418_35455433del	NC_000022.11:g.35455419_35455433del	NC_000022.11:g.35455420_35455433del	NC_000022.11:g.35455421_35455433del	NC_000022.11:g.35455422_35455433del	NC_000022.11:g.35455423_35455433del	NC_000022.11:g.35455424_35455433del	NC_000022.11:g.35455425_35455433del	NC_000022.11:g.35455426_35455433del	NC_000022.11:g.35455427_35455433del	NC_000022.11:g.35455428_35455433del	NC_000022.11:g.35455429_35455433del	NC_000022.11:g.35455430_35455433del	NC_000022.11:g.35455431_35455433del	NC_000022.11:g.35455432_35455433del	NC_000022.11:g.35455433del	NC_000022.11:g.35455433dup	NC_000022.11:g.35455432_35455433dup	NC_000022.11:g.35455431_35455433dup	NC_000022.11:g.35455430_35455433dup	NC_000022.11:g.35455429_35455433dup	NC_000022.11:g.35455428_35455433dup	NC_000022.11:g.35455427_35455433dup	NC_000022.11:g.35455426_35455433dup	NC_000022.11:g.35455425_35455433dup	NC_000022.11:g.35455424_35455433dup	NC_000022.11:g.35455423_35455433dup
GRCh37.p13 chr 22	NC_000022.10:g.35851399_35851426=	NC_000022.10:g.35851406_35851426del	NC_000022.10:g.35851408_35851426del	NC_000022.10:g.35851409_35851426del	NC_000022.10:g.35851410_35851426del	NC_000022.10:g.35851411_35851426del	NC_000022.10:g.35851412_35851426del	NC_000022.10:g.35851413_35851426del	NC_000022.10:g.35851414_35851426del	NC_000022.10:g.35851415_35851426del	NC_000022.10:g.35851416_35851426del	NC_000022.10:g.35851417_35851426del	NC_000022.10:g.35851418_35851426del	NC_000022.10:g.35851419_35851426del	NC_000022.10:g.35851420_35851426del	NC_000022.10:g.35851421_35851426del	NC_000022.10:g.35851422_35851426del	NC_000022.10:g.35851423_35851426del	NC_000022.10:g.35851424_35851426del	NC_000022.10:g.35851425_35851426del	NC_000022.10:g.35851426del	NC_000022.10:g.35851426dup	NC_000022.10:g.35851425_35851426dup	NC_000022.10:g.35851424_35851426dup	NC_000022.10:g.35851423_35851426dup	NC_000022.10:g.35851422_35851426dup	NC_000022.10:g.35851421_35851426dup	NC_000022.10:g.35851420_35851426dup	NC_000022.10:g.35851419_35851426dup	NC_000022.10:g.35851418_35851426dup	NC_000022.10:g.35851417_35851426dup	NC_000022.10:g.35851416_35851426dup

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#.

31 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3708190272	Jul 13, 2019 (153)
2	EVA_DECODE	ss3708190273	Jul 13, 2019 (153)
3	EVA_DECODE	ss3708190274	Jul 13, 2019 (153)
4	KOGIC	ss3983632650	Apr 27, 2020 (154)
5	GNOMAD	ss4364514145	Apr 26, 2021 (155)
6	GNOMAD	ss4364514166	Apr 26, 2021 (155)
7	GNOMAD	ss4364514167	Apr 26, 2021 (155)
8	GNOMAD	ss4364514168	Apr 26, 2021 (155)
9	GNOMAD	ss4364514169	Apr 26, 2021 (155)
10	GNOMAD	ss4364514170	Apr 26, 2021 (155)
11	GNOMAD	ss4364514171	Apr 26, 2021 (155)
12	GNOMAD	ss4364514172	Apr 26, 2021 (155)
13	GNOMAD	ss4364514173	Apr 26, 2021 (155)
14	GNOMAD	ss4364514174	Apr 26, 2021 (155)
15	GNOMAD	ss4364514175	Apr 26, 2021 (155)
16	GNOMAD	ss4364514176	Apr 26, 2021 (155)
17	GNOMAD	ss4364514177	Apr 26, 2021 (155)
18	GNOMAD	ss4364514178	Apr 26, 2021 (155)
19	GNOMAD	ss4364514179	Apr 26, 2021 (155)
20	GNOMAD	ss4364514180	Apr 26, 2021 (155)
21	GNOMAD	ss4364514181	Apr 26, 2021 (155)
22	GNOMAD	ss4364514182	Apr 26, 2021 (155)
23	GNOMAD	ss4364514183	Apr 26, 2021 (155)
24	GNOMAD	ss4364514184	Apr 26, 2021 (155)
25	GNOMAD	ss4364514185	Apr 26, 2021 (155)
26	GNOMAD	ss4364514186	Apr 26, 2021 (155)
27	GNOMAD	ss4364514187	Apr 26, 2021 (155)
28	GNOMAD	ss4364514188	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5793714893	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5793714894	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5793714895	Oct 16, 2022 (156)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569825860 (NC_000022.11:35455405::T 17/12166) Row 569825881 (NC_000022.11:35455405::TT 39/12158) Row 569825882 (NC_000022.11:35455405::TTT 92/12160)...	-	Apr 26, 2021 (155)
56	Korean Genome Project	NC_000022.11 - 35455418	Apr 27, 2020 (154)
57	14KJPN Submission ignored due to conflicting rows: Row 127551997 (NC_000022.11:35455405::TTTT 199/16484) Row 127551998 (NC_000022.11:35455405::TTTTTT 62/16484) Row 127551999 (NC_000022.11:35455405::TT 121/16484)	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 127551997 (NC_000022.11:35455405::TTTT 199/16484) Row 127551998 (NC_000022.11:35455405::TTTTTT 62/16484) Row 127551999 (NC_000022.11:35455405::TT 121/16484)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 127551997 (NC_000022.11:35455405::TTTT 199/16484) Row 127551998 (NC_000022.11:35455405::TTTTTT 62/16484) Row 127551999 (NC_000022.11:35455405::TT 121/16484)	-	Oct 16, 2022 (156)
60	ALFA	NC_000022.11 - 35455406	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
ss3377040311	NC_000022.11:35455405:TTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
ss3377040315	NC_000022.11:35455405:TTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
ss3377040323	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT
ss3377040325	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT
ss3377040326	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

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

No publications for rs1156363999

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
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4364514188	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4364514187	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4364514186	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4364514185	NC_000022.11:35455405:TTTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4364514184	NC_000022.11:35455405:TTTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4364514183	NC_000022.11:35455405:TTTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4364514182	NC_000022.11:35455405:TTTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4364514181	NC_000022.11:35455405:TTTTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514180	NC_000022.11:35455405:TTTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514179	NC_000022.11:35455405:TTTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514178	NC_000022.11:35455405:TTTT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514177	NC_000022.11:35455405:TT:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514176	NC_000022.11:35455405:T:	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514145	NC_000022.11:35455405::T	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514166, ss5793714895	NC_000022.11:35455405::TT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3708190272, ss4364514167	NC_000022.11:35455405::TTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514168, ss5793714893	NC_000022.11:35455405::TTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3708190273, ss4364514169	NC_000022.11:35455405::TTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514170, ss5793714894	NC_000022.11:35455405::TTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3708190274, ss4364514171	NC_000022.11:35455405::TTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
40010651, ss3983632650	NC_000022.11:35455417::TTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514172	NC_000022.11:35455405::TTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514173	NC_000022.11:35455405::TTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514174	NC_000022.11:35455405::TTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
845201746	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4364514175	NC_000022.11:35455405::TTTTTTTTTTT	NC_000022.11:35455405:TTTTTTTTTTTT… NC_000022.11:35455405:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1156363999