Name: rs60940244
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.

rs60940244

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:96615242-96615265 (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)₁₅ / del(T)₁₄ / del(T)₁₃ / d…
del(T)₁₅ / del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₁₉ / dup(T)₂₀ / dup(T)₂₁ / dup(T)₂₂ / dup(T)₂₃ / dup(T)₂₄ / ins(T)₂₅ / ins(T)₂₆ / ins(T)₂₇ / ins(T)₂₈ / ins(T)₂₉ / ins(T)₃₀ / ins(T)₃₁ / ins(T)₃₂ / ins(T)₃₃ / ins(T)₃₄ / ins(T)₃₅ / ins(T)₃₈ / ins(T)₄₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₄=0.0000 (0/5306, ALFA)
del(T)₁₃=0.0000 (0/5306, ALFA)
del(T)₁₂=0.0000 (0/5306, ALFA) (+ 19 more)
del(T)₈=0.0000 (0/5306, ALFA)
del(T)₇=0.0000 (0/5306, ALFA)
del(T)₅=0.0000 (0/5306, ALFA)
del(T)₄=0.0000 (0/5306, ALFA)
delTTT=0.0000 (0/5306, ALFA)
delTT=0.0000 (0/5306, ALFA)
delT=0.0000 (0/5306, ALFA)
dupT=0.0000 (0/5306, ALFA)
dupTT=0.0000 (0/5306, ALFA)
dupTTT=0.0000 (0/5306, ALFA)
dup(T)₅=0.0000 (0/5306, ALFA)
dup(T)₆=0.0000 (0/5306, ALFA)
dup(T)₈=0.0000 (0/5306, ALFA)
dup(T)₉=0.0000 (0/5306, ALFA)
dup(T)₁₀=0.0000 (0/5306, ALFA)
dup(T)₁₁=0.0000 (0/5306, ALFA)
dup(T)₁₂=0.0000 (0/5306, ALFA)
dup(T)₁₃=0.0000 (0/5306, ALFA)
(T)₂₄=0.00 (0/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SEM1 : 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	5306	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	3464	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	1104	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	36	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1068	TTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	66	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	50	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	338	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	30	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	236	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	5306	(T)₂₄=1.0000	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₇=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)₅=0.0000, dup(T)₆=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₁=0.0000, dup(T)₁₂=0.0000, dup(T)₁₃=0.0000
Allele Frequency Aggregator	European	Sub	3464	(T)₂₄=1.0000	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₇=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)₅=0.0000, dup(T)₆=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₁=0.0000, dup(T)₁₂=0.0000, dup(T)₁₃=0.0000
Allele Frequency Aggregator	African	Sub	1104	(T)₂₄=1.0000	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₇=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)₅=0.0000, dup(T)₆=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₀=0.0000, dup(T)₁₁=0.0000, dup(T)₁₂=0.0000, dup(T)₁₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	338	(T)₂₄=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₈=0.000, del(T)₇=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)₅=0.000, dup(T)₆=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	Other	Sub	236	(T)₂₄=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₈=0.000, del(T)₇=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)₅=0.000, dup(T)₆=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₀=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₈=0.00, del(T)₇=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)₅=0.00, dup(T)₆=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00
Allele Frequency Aggregator	Asian	Sub	66	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₈=0.00, del(T)₇=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)₅=0.00, dup(T)₆=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(T)₂₄=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₈=0.00, del(T)₇=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)₅=0.00, dup(T)₆=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₄=0.00	del(T)₁₃=1.00

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 7	NC_000007.14:g.96615251_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615252_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615253_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615254_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615256_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615258_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615259_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615261_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615262_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615263_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615264_96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615265del
GRCh38.p14 chr 7	NC_000007.14:g.96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615264_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615263_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615262_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615261_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615260_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615259_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615258_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615257_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615256_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615255_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615254_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615253_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615252_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615251_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615250_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615249_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615248_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615247_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615246_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615245_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615244_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615243_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615242_96615265dup
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244563_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244564_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244565_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244566_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244568_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244570_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244571_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244573_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244574_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244575_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244576_96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244577del
GRCh37.p13 chr 7	NC_000007.13:g.96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244576_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244575_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244574_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244573_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244572_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244571_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244570_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244569_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244568_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244567_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244566_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244565_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244564_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244563_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244562_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244561_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244560_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244559_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244558_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244557_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244556_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244555_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244554_96244577dup
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SEM1 RefSeqGene	NG_009273.2:g.99636_99650del
SEM1 RefSeqGene	NG_009273.2:g.99637_99650del
SEM1 RefSeqGene	NG_009273.2:g.99638_99650del
SEM1 RefSeqGene	NG_009273.2:g.99639_99650del
SEM1 RefSeqGene	NG_009273.2:g.99641_99650del
SEM1 RefSeqGene	NG_009273.2:g.99643_99650del
SEM1 RefSeqGene	NG_009273.2:g.99644_99650del
SEM1 RefSeqGene	NG_009273.2:g.99646_99650del
SEM1 RefSeqGene	NG_009273.2:g.99647_99650del
SEM1 RefSeqGene	NG_009273.2:g.99648_99650del
SEM1 RefSeqGene	NG_009273.2:g.99649_99650del
SEM1 RefSeqGene	NG_009273.2:g.99650del
SEM1 RefSeqGene	NG_009273.2:g.99650dup
SEM1 RefSeqGene	NG_009273.2:g.99649_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99648_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99647_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99646_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99645_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99644_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99643_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99642_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99641_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99640_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99639_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99638_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99637_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99636_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99635_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99634_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99633_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99632_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99631_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99630_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99629_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99628_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99627_99650dup
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
SEM1 RefSeqGene	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: SEM1, SEM1 26S proteasome subunit (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SEM1 transcript variant 9	NM_001393898.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 10	NM_001393899.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 11	NM_001393900.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 12	NM_001393901.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 13	NM_001393902.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 14	NM_001393903.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 15	NM_001393904.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 16	NM_001393905.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 17	NM_001393906.1:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 5	NM_006304.2:c.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant 1	NR_163950.1:n.	N/A	Intron Variant
SEM1 transcript variant 2	NR_163951.1:n.	N/A	Intron Variant
SEM1 transcript variant 3	NR_163952.1:n.	N/A	Intron Variant
SEM1 transcript variant 4	NR_163953.1:n.	N/A	Intron Variant
SEM1 transcript variant 6	NR_163948.1:n.	N/A	Genic Upstream Transcript Variant
SEM1 transcript variant 7	NR_163949.1:n.	N/A	Genic Upstream Transcript Variant
SEM1 transcript variant 8	NR_038948.2:n.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant X1	XR_007060159.1:n.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant X2	XR_007060160.1:n.	N/A	Genic Downstream Transcript Variant
SEM1 transcript variant X3	XR_007060161.1:n.	N/A	Genic 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)₂₄=	del(T)₁₅	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₀	del(T)₈	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	dup(T)₁₉	dup(T)₂₀	dup(T)₂₁	dup(T)₂₂	dup(T)₂₃	dup(T)₂₄	ins(T)₂₅	ins(T)₂₆	ins(T)₂₇	ins(T)₂₈	ins(T)₂₉	ins(T)₃₀	ins(T)₃₁	ins(T)₃₂	ins(T)₃₃	ins(T)₃₄	ins(T)₃₅	ins(T)₃₈	ins(T)₄₈
GRCh38.p14 chr 7	NC_000007.14:g.96615242_96615265=	NC_000007.14:g.96615251_96615265del	NC_000007.14:g.96615252_96615265del	NC_000007.14:g.96615253_96615265del	NC_000007.14:g.96615254_96615265del	NC_000007.14:g.96615256_96615265del	NC_000007.14:g.96615258_96615265del	NC_000007.14:g.96615259_96615265del	NC_000007.14:g.96615261_96615265del	NC_000007.14:g.96615262_96615265del	NC_000007.14:g.96615263_96615265del	NC_000007.14:g.96615264_96615265del	NC_000007.14:g.96615265del	NC_000007.14:g.96615265dup	NC_000007.14:g.96615264_96615265dup	NC_000007.14:g.96615263_96615265dup	NC_000007.14:g.96615262_96615265dup	NC_000007.14:g.96615261_96615265dup	NC_000007.14:g.96615260_96615265dup	NC_000007.14:g.96615259_96615265dup	NC_000007.14:g.96615258_96615265dup	NC_000007.14:g.96615257_96615265dup	NC_000007.14:g.96615256_96615265dup	NC_000007.14:g.96615255_96615265dup	NC_000007.14:g.96615254_96615265dup	NC_000007.14:g.96615253_96615265dup	NC_000007.14:g.96615252_96615265dup	NC_000007.14:g.96615251_96615265dup	NC_000007.14:g.96615250_96615265dup	NC_000007.14:g.96615249_96615265dup	NC_000007.14:g.96615248_96615265dup	NC_000007.14:g.96615247_96615265dup	NC_000007.14:g.96615246_96615265dup	NC_000007.14:g.96615245_96615265dup	NC_000007.14:g.96615244_96615265dup	NC_000007.14:g.96615243_96615265dup	NC_000007.14:g.96615242_96615265dup	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:g.96615265_96615266insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.96244554_96244577=	NC_000007.13:g.96244563_96244577del	NC_000007.13:g.96244564_96244577del	NC_000007.13:g.96244565_96244577del	NC_000007.13:g.96244566_96244577del	NC_000007.13:g.96244568_96244577del	NC_000007.13:g.96244570_96244577del	NC_000007.13:g.96244571_96244577del	NC_000007.13:g.96244573_96244577del	NC_000007.13:g.96244574_96244577del	NC_000007.13:g.96244575_96244577del	NC_000007.13:g.96244576_96244577del	NC_000007.13:g.96244577del	NC_000007.13:g.96244577dup	NC_000007.13:g.96244576_96244577dup	NC_000007.13:g.96244575_96244577dup	NC_000007.13:g.96244574_96244577dup	NC_000007.13:g.96244573_96244577dup	NC_000007.13:g.96244572_96244577dup	NC_000007.13:g.96244571_96244577dup	NC_000007.13:g.96244570_96244577dup	NC_000007.13:g.96244569_96244577dup	NC_000007.13:g.96244568_96244577dup	NC_000007.13:g.96244567_96244577dup	NC_000007.13:g.96244566_96244577dup	NC_000007.13:g.96244565_96244577dup	NC_000007.13:g.96244564_96244577dup	NC_000007.13:g.96244563_96244577dup	NC_000007.13:g.96244562_96244577dup	NC_000007.13:g.96244561_96244577dup	NC_000007.13:g.96244560_96244577dup	NC_000007.13:g.96244559_96244577dup	NC_000007.13:g.96244558_96244577dup	NC_000007.13:g.96244557_96244577dup	NC_000007.13:g.96244556_96244577dup	NC_000007.13:g.96244555_96244577dup	NC_000007.13:g.96244554_96244577dup	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.13:g.96244577_96244578insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SEM1 RefSeqGene	NG_009273.2:g.99627_99650=	NG_009273.2:g.99636_99650del	NG_009273.2:g.99637_99650del	NG_009273.2:g.99638_99650del	NG_009273.2:g.99639_99650del	NG_009273.2:g.99641_99650del	NG_009273.2:g.99643_99650del	NG_009273.2:g.99644_99650del	NG_009273.2:g.99646_99650del	NG_009273.2:g.99647_99650del	NG_009273.2:g.99648_99650del	NG_009273.2:g.99649_99650del	NG_009273.2:g.99650del	NG_009273.2:g.99650dup	NG_009273.2:g.99649_99650dup	NG_009273.2:g.99648_99650dup	NG_009273.2:g.99647_99650dup	NG_009273.2:g.99646_99650dup	NG_009273.2:g.99645_99650dup	NG_009273.2:g.99644_99650dup	NG_009273.2:g.99643_99650dup	NG_009273.2:g.99642_99650dup	NG_009273.2:g.99641_99650dup	NG_009273.2:g.99640_99650dup	NG_009273.2:g.99639_99650dup	NG_009273.2:g.99638_99650dup	NG_009273.2:g.99637_99650dup	NG_009273.2:g.99636_99650dup	NG_009273.2:g.99635_99650dup	NG_009273.2:g.99634_99650dup	NG_009273.2:g.99633_99650dup	NG_009273.2:g.99632_99650dup	NG_009273.2:g.99631_99650dup	NG_009273.2:g.99630_99650dup	NG_009273.2:g.99629_99650dup	NG_009273.2:g.99628_99650dup	NG_009273.2:g.99627_99650dup	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_009273.2:g.99650_99651insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

76 SubSNP, 60 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81154706	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95468898	Feb 05, 2009 (130)
3	GMI	ss288859702	May 04, 2012 (137)
4	BILGI_BIOE	ss666408840	Apr 25, 2013 (138)
5	EVA_GENOME_DK	ss1578683954	Apr 01, 2015 (144)
6	HAMMER_LAB	ss1805123929	Sep 08, 2015 (146)
7	KCHEN_CANCERGENOMICS	ss2632446016	Oct 12, 2018 (152)
8	BEROUKHIMLAB	ss3644244192	Oct 12, 2018 (152)
9	EVA_DECODE	ss3720256829	Jul 13, 2019 (153)
10	EVA_DECODE	ss3720256830	Jul 13, 2019 (153)
11	EVA_DECODE	ss3720256831	Jul 13, 2019 (153)
12	EVA_DECODE	ss3720256832	Jul 13, 2019 (153)
13	ACPOP	ss3734883657	Jul 13, 2019 (153)
14	ACPOP	ss3734883658	Jul 13, 2019 (153)
15	ACPOP	ss3734883659	Jul 13, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3810071770	Jul 13, 2019 (153)
17	KOGIC	ss3962140903	Apr 26, 2020 (154)
18	KOGIC	ss3962140904	Apr 26, 2020 (154)
19	GNOMAD	ss4168987836	Apr 26, 2021 (155)
20	GNOMAD	ss4168987837	Apr 26, 2021 (155)
21	GNOMAD	ss4168987838	Apr 26, 2021 (155)
22	GNOMAD	ss4168987839	Apr 26, 2021 (155)
23	GNOMAD	ss4168987840	Apr 26, 2021 (155)
24	GNOMAD	ss4168987841	Apr 26, 2021 (155)
25	GNOMAD	ss4168987843	Apr 26, 2021 (155)
26	GNOMAD	ss4168987844	Apr 26, 2021 (155)
27	GNOMAD	ss4168987845	Apr 26, 2021 (155)
28	GNOMAD	ss4168987846	Apr 26, 2021 (155)
29	GNOMAD	ss4168987849	Apr 26, 2021 (155)
30	GNOMAD	ss4168987850	Apr 26, 2021 (155)
31	GNOMAD	ss4168987852	Apr 26, 2021 (155)
32	GNOMAD	ss4168987853	Apr 26, 2021 (155)
33	GNOMAD	ss4168987854	Apr 26, 2021 (155)
34	GNOMAD	ss4168987855	Apr 26, 2021 (155)
35	GNOMAD	ss4168987857	Apr 26, 2021 (155)
36	GNOMAD	ss4168987858	Apr 26, 2021 (155)
37	GNOMAD	ss4168987859	Apr 26, 2021 (155)
38	GNOMAD	ss4168987860	Apr 26, 2021 (155)
39	GNOMAD	ss4168987861	Apr 26, 2021 (155)
40	GNOMAD	ss4168987862	Apr 26, 2021 (155)
41	GNOMAD	ss4168987863	Apr 26, 2021 (155)
42	GNOMAD	ss4168987864	Apr 26, 2021 (155)
43	GNOMAD	ss4168987865	Apr 26, 2021 (155)
44	GNOMAD	ss4168987866	Apr 26, 2021 (155)
45	GNOMAD	ss4168987867	Apr 26, 2021 (155)
46	GNOMAD	ss4168987868	Apr 26, 2021 (155)
47	GNOMAD	ss4168987869	Apr 26, 2021 (155)
48	GNOMAD	ss4168987870	Apr 26, 2021 (155)
49	GNOMAD	ss4168987871	Apr 26, 2021 (155)
50	GNOMAD	ss4168987872	Apr 26, 2021 (155)
51	GNOMAD	ss4168987873	Apr 26, 2021 (155)
52	GNOMAD	ss4168987874	Apr 26, 2021 (155)
53	GNOMAD	ss4168987875	Apr 26, 2021 (155)
54	GNOMAD	ss4168987876	Apr 26, 2021 (155)
55	GNOMAD	ss4168987877	Apr 26, 2021 (155)
56	GNOMAD	ss4168987879	Apr 26, 2021 (155)
57	GNOMAD	ss4168987880	Apr 26, 2021 (155)
58	GNOMAD	ss4168987881	Apr 26, 2021 (155)
59	GNOMAD	ss4168987882	Apr 26, 2021 (155)
60	GNOMAD	ss4168987883	Apr 26, 2021 (155)
61	GNOMAD	ss4168987884	Apr 26, 2021 (155)
62	GNOMAD	ss4168987885	Apr 26, 2021 (155)
63	GNOMAD	ss4168987886	Apr 26, 2021 (155)
64	GNOMAD	ss4168987887	Apr 26, 2021 (155)
65	GNOMAD	ss4168987888	Apr 26, 2021 (155)
66	TOMMO_GENOMICS	ss5184558991	Apr 26, 2021 (155)
67	TOMMO_GENOMICS	ss5184558992	Apr 26, 2021 (155)
68	TOMMO_GENOMICS	ss5184558993	Apr 26, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5273953553	Oct 13, 2022 (156)
70	1000G_HIGH_COVERAGE	ss5273953555	Oct 13, 2022 (156)
71	HUGCELL_USP	ss5470933702	Oct 13, 2022 (156)
72	HUGCELL_USP	ss5470933704	Oct 13, 2022 (156)
73	TOMMO_GENOMICS	ss5725235929	Oct 13, 2022 (156)
74	TOMMO_GENOMICS	ss5725235931	Oct 13, 2022 (156)
75	TOMMO_GENOMICS	ss5725235932	Oct 13, 2022 (156)
76	EVA	ss5860001382	Oct 13, 2022 (156)
77	The Danish reference pan genome	NC_000007.13 - 96244554	Apr 26, 2020 (154)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
112	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
113	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
114	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
115	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
116	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
117	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
118	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
119	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
120	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
121	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
122	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
123	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
124	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270002269 (NC_000007.14:96615241::T 134/117076) Row 270002270 (NC_000007.14:96615241::TT 25/117096) Row 270002271 (NC_000007.14:96615241::TTT 17/117102)...	-	Apr 26, 2021 (155)
125	Korean Genome Project Submission ignored due to conflicting rows: Row 18518904 (NC_000007.14:96615242:TTTTTTTTTTTTT: 235/1820) Row 18518905 (NC_000007.14:96615241:TTTTTTTTTTTTTT: 1/1820)	-	Apr 26, 2020 (154)
126	Korean Genome Project Submission ignored due to conflicting rows: Row 18518904 (NC_000007.14:96615242:TTTTTTTTTTTTT: 235/1820) Row 18518905 (NC_000007.14:96615241:TTTTTTTTTTTTTT: 1/1820)	-	Apr 26, 2020 (154)
127	Northern Sweden Submission ignored due to conflicting rows: Row 8168522 (NC_000007.13:96244553::TTTTTTTT 9/578) Row 8168523 (NC_000007.13:96244553:TTTTTTTTTTTTT: 218/578) Row 8168524 (NC_000007.13:96244553::TTTTTTTTT 10/578)	-	Jul 13, 2019 (153)
128	Northern Sweden Submission ignored due to conflicting rows: Row 8168522 (NC_000007.13:96244553::TTTTTTTT 9/578) Row 8168523 (NC_000007.13:96244553:TTTTTTTTTTTTT: 218/578) Row 8168524 (NC_000007.13:96244553::TTTTTTTTT 10/578)	-	Jul 13, 2019 (153)
129	Northern Sweden Submission ignored due to conflicting rows: Row 8168522 (NC_000007.13:96244553::TTTTTTTT 9/578) Row 8168523 (NC_000007.13:96244553:TTTTTTTTTTTTT: 218/578) Row 8168524 (NC_000007.13:96244553::TTTTTTTTT 10/578)	-	Jul 13, 2019 (153)
130	8.3KJPN Submission ignored due to conflicting rows: Row 42528298 (NC_000007.13:96244553:TTTTTTTTTTTTT: 2106/16628) Row 42528299 (NC_000007.13:96244553:TTTTTTTTTTTT: 7/16628) Row 42528300 (NC_000007.13:96244553::TTTTTTTT 5/16628)	-	Apr 26, 2021 (155)
131	8.3KJPN Submission ignored due to conflicting rows: Row 42528298 (NC_000007.13:96244553:TTTTTTTTTTTTT: 2106/16628) Row 42528299 (NC_000007.13:96244553:TTTTTTTTTTTT: 7/16628) Row 42528300 (NC_000007.13:96244553::TTTTTTTT 5/16628)	-	Apr 26, 2021 (155)
132	8.3KJPN Submission ignored due to conflicting rows: Row 42528298 (NC_000007.13:96244553:TTTTTTTTTTTTT: 2106/16628) Row 42528299 (NC_000007.13:96244553:TTTTTTTTTTTT: 7/16628) Row 42528300 (NC_000007.13:96244553::TTTTTTTT 5/16628)	-	Apr 26, 2021 (155)
133	14KJPN Submission ignored due to conflicting rows: Row 59073033 (NC_000007.14:96615241:TTTTTTTTTTTTT: 4192/25402) Row 59073035 (NC_000007.14:96615241:TTTTTTTTTTTT: 12/25402) Row 59073036 (NC_000007.14:96615241::TTTTTTTT 3/25402)	-	Oct 13, 2022 (156)
134	14KJPN Submission ignored due to conflicting rows: Row 59073033 (NC_000007.14:96615241:TTTTTTTTTTTTT: 4192/25402) Row 59073035 (NC_000007.14:96615241:TTTTTTTTTTTT: 12/25402) Row 59073036 (NC_000007.14:96615241::TTTTTTTT 3/25402)	-	Oct 13, 2022 (156)
135	14KJPN Submission ignored due to conflicting rows: Row 59073033 (NC_000007.14:96615241:TTTTTTTTTTTTT: 4192/25402) Row 59073035 (NC_000007.14:96615241:TTTTTTTTTTTT: 12/25402) Row 59073036 (NC_000007.14:96615241::TTTTTTTT 3/25402)	-	Oct 13, 2022 (156)
136	ALFA	NC_000007.14 - 96615242	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
ss4168987888	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3720256829, ss3962140904, ss4168987887	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss288859702	NC_000007.12:96082489:TTTTTTTTTTTT… NC_000007.12:96082489:TTTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
101958, ss666408840, ss1578683954, ss1805123929, ss3644244192, ss3734883658, ss5184558991	NC_000007.13:96244553:TTTTTTTTTTTT… NC_000007.13:96244553:TTTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3810071770, ss4168987886, ss5273953553, ss5470933702, ss5725235929, ss5860001382	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3720256830, ss3962140903	NC_000007.14:96615242:TTTTTTTTTTTT… NC_000007.14:96615242:TTTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5184558992	NC_000007.13:96244553:TTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4168987885, ss5725235931	NC_000007.14:96615241:TTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss2632446016, ss3720256831	NC_000007.14:96615243:TTTTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3720256832	NC_000007.14:96615245:TTTTTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4168987884	NC_000007.14:96615241:TTTTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4168987883	NC_000007.14:96615241:TTTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4168987882, ss5470933704	NC_000007.14:96615241:TTTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4168987881	NC_000007.14:96615241:TTT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987880	NC_000007.14:96615241:TT:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987879	NC_000007.14:96615241:T:	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987836	NC_000007.14:96615241::T	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987837	NC_000007.14:96615241::TT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987838	NC_000007.14:96615241::TTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987839	NC_000007.14:96615241::TTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987840	NC_000007.14:96615241::TTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss81154706, ss95468898	NT_007933.15:34277420::TTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987841	NC_000007.14:96615241::TTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987843	NC_000007.14:96615241::TTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3734883657, ss5184558993	NC_000007.13:96244553::TTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987844, ss5725235932	NC_000007.14:96615241::TTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3734883659	NC_000007.13:96244553::TTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987845	NC_000007.14:96615241::TTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987846	NC_000007.14:96615241::TTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987849, ss5273953555	NC_000007.14:96615241::TTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987850	NC_000007.14:96615241::TTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987852	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5116476111	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987853	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987854	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987855	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987857	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987858	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987859	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987860	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987861	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987862	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987863	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987864	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987865	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987866	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987867	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987868	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987869	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987870	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987871	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987872	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987873	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987874	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987875	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987876	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4168987877	NC_000007.14:96615241::TTTTTTTTTTT… NC_000007.14:96615241::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:96615241:TTTTTTTTTTTT… NC_000007.14:96615241:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs60940244

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

rs60940244