Name: rs869115663
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.

rs869115663

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:127466505-127466530 (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)₁₃ / del(T)₁₂ / del(T)₁₁ / d…
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
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.00000 (0/10634, ALFA)
del(T)₁₂=0.00000 (0/10634, ALFA)
del(T)₁₁=0.00000 (0/10634, ALFA) (+ 18 more)
del(T)₁₀=0.00000 (0/10634, ALFA)
del(T)₉=0.00000 (0/10634, ALFA)
del(T)₈=0.00000 (0/10634, ALFA)
del(T)₇=0.00000 (0/10634, ALFA)
del(T)₆=0.00000 (0/10634, ALFA)
del(T)₅=0.00000 (0/10634, ALFA)
del(T)₄=0.00000 (0/10634, ALFA)
delTTT=0.00000 (0/10634, ALFA)
delTT=0.00000 (0/10634, ALFA)
delT=0.00000 (0/10634, ALFA)
dupT=0.00000 (0/10634, ALFA)
dupTT=0.00000 (0/10634, ALFA)
dupTTT=0.00000 (0/10634, ALFA)
dup(T)₄=0.00000 (0/10634, ALFA)
dup(T)₅=0.00000 (0/10634, ALFA)
dup(T)₆=0.00000 (0/10634, ALFA)
dup(T)₇=0.00000 (0/10634, ALFA)
dup(T)₈=0.00000 (0/10634, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LRSAM1 : 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	10634	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	6798	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2588	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	102	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2486	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	76	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	58	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	130	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	550	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	82	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	410	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	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, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	10634	(T)₂₆=1.00000	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
Allele Frequency Aggregator	European	Sub	6798	(T)₂₆=1.0000	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
Allele Frequency Aggregator	African	Sub	2588	(T)₂₆=1.0000	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
Allele Frequency Aggregator	Latin American 2	Sub	550	(T)₂₆=1.000	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
Allele Frequency Aggregator	Other	Sub	410	(T)₂₆=1.000	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
Allele Frequency Aggregator	Latin American 1	Sub	130	(T)₂₆=1.000	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
Allele Frequency Aggregator	South Asian	Sub	82	(T)₂₆=1.00	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
Allele Frequency Aggregator	Asian	Sub	76	(T)₂₆=1.00	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

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 9	NC_000009.12:g.127466518_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466519_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466520_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466521_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466522_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466523_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466524_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466525_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466526_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466527_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466528_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466529_127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466530del
GRCh38.p14 chr 9	NC_000009.12:g.127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466529_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466528_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466527_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466526_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466525_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466524_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466523_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466522_127466530dup
GRCh38.p14 chr 9	NC_000009.12:g.127466521_127466530dup
GRCh37.p13 chr 9	NC_000009.11:g.130228797_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228798_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228799_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228800_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228801_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228802_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228803_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228804_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228805_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228806_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228807_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228808_130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228809del
GRCh37.p13 chr 9	NC_000009.11:g.130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228808_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228807_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228806_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228805_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228804_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228803_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228802_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228801_130228809dup
GRCh37.p13 chr 9	NC_000009.11:g.130228800_130228809dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20033_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20034_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20035_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20036_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20037_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20038_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20039_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20040_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20041_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20042_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20043_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20044_20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20045del
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20044_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20043_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20042_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20041_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20040_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20039_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20038_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20037_20045dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20036_20045dup

Gene: LRSAM1, leucine rich repeat and sterile alpha motif containing 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LRSAM1 transcript variant 2	NM_001005373.4:c.529-1222… NM_001005373.4:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant 3	NM_001005374.4:c.529-1222… NM_001005374.4:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant 4	NM_001190723.3:c.529-1222… NM_001190723.3:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant 5	NM_001384142.1:c.529-1222… NM_001384142.1:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant 6	NM_001384143.1:c.529-1222… NM_001384143.1:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant 7	NM_001384144.1:c.-256-122… NM_001384144.1:c.-256-1222_-256-1210del	N/A	Intron Variant
LRSAM1 transcript variant 1	NM_138361.5:c.529-1222_52… NM_138361.5:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant 8	NR_168891.1:n.	N/A	Intron Variant
LRSAM1 transcript variant 9	NR_168892.1:n.	N/A	Intron Variant
LRSAM1 transcript variant X1	XM_047424058.1:c.529-1222… XM_047424058.1:c.529-1222_529-1210del	N/A	Intron Variant
LRSAM1 transcript variant X2	XM_047424059.1:c.-171+414… XM_047424059.1:c.-171+4145_-171+4157del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₆=	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
GRCh38.p14 chr 9	NC_000009.12:g.127466505_127466530=	NC_000009.12:g.127466518_127466530del	NC_000009.12:g.127466519_127466530del	NC_000009.12:g.127466520_127466530del	NC_000009.12:g.127466521_127466530del	NC_000009.12:g.127466522_127466530del	NC_000009.12:g.127466523_127466530del	NC_000009.12:g.127466524_127466530del	NC_000009.12:g.127466525_127466530del	NC_000009.12:g.127466526_127466530del	NC_000009.12:g.127466527_127466530del	NC_000009.12:g.127466528_127466530del	NC_000009.12:g.127466529_127466530del	NC_000009.12:g.127466530del	NC_000009.12:g.127466530dup	NC_000009.12:g.127466529_127466530dup	NC_000009.12:g.127466528_127466530dup	NC_000009.12:g.127466527_127466530dup	NC_000009.12:g.127466526_127466530dup	NC_000009.12:g.127466525_127466530dup	NC_000009.12:g.127466524_127466530dup	NC_000009.12:g.127466523_127466530dup	NC_000009.12:g.127466522_127466530dup	NC_000009.12:g.127466521_127466530dup
GRCh37.p13 chr 9	NC_000009.11:g.130228784_130228809=	NC_000009.11:g.130228797_130228809del	NC_000009.11:g.130228798_130228809del	NC_000009.11:g.130228799_130228809del	NC_000009.11:g.130228800_130228809del	NC_000009.11:g.130228801_130228809del	NC_000009.11:g.130228802_130228809del	NC_000009.11:g.130228803_130228809del	NC_000009.11:g.130228804_130228809del	NC_000009.11:g.130228805_130228809del	NC_000009.11:g.130228806_130228809del	NC_000009.11:g.130228807_130228809del	NC_000009.11:g.130228808_130228809del	NC_000009.11:g.130228809del	NC_000009.11:g.130228809dup	NC_000009.11:g.130228808_130228809dup	NC_000009.11:g.130228807_130228809dup	NC_000009.11:g.130228806_130228809dup	NC_000009.11:g.130228805_130228809dup	NC_000009.11:g.130228804_130228809dup	NC_000009.11:g.130228803_130228809dup	NC_000009.11:g.130228802_130228809dup	NC_000009.11:g.130228801_130228809dup	NC_000009.11:g.130228800_130228809dup
LRSAM1 RefSeqGene (LRG_373)	NG_032008.1:g.20020_20045=	NG_032008.1:g.20033_20045del	NG_032008.1:g.20034_20045del	NG_032008.1:g.20035_20045del	NG_032008.1:g.20036_20045del	NG_032008.1:g.20037_20045del	NG_032008.1:g.20038_20045del	NG_032008.1:g.20039_20045del	NG_032008.1:g.20040_20045del	NG_032008.1:g.20041_20045del	NG_032008.1:g.20042_20045del	NG_032008.1:g.20043_20045del	NG_032008.1:g.20044_20045del	NG_032008.1:g.20045del	NG_032008.1:g.20045dup	NG_032008.1:g.20044_20045dup	NG_032008.1:g.20043_20045dup	NG_032008.1:g.20042_20045dup	NG_032008.1:g.20041_20045dup	NG_032008.1:g.20040_20045dup	NG_032008.1:g.20039_20045dup	NG_032008.1:g.20038_20045dup	NG_032008.1:g.20037_20045dup	NG_032008.1:g.20036_20045dup
LRSAM1 transcript variant 2	NM_001005373.3:c.529-1235=	NM_001005373.3:c.529-1222_529-1210del	NM_001005373.3:c.529-1221_529-1210del	NM_001005373.3:c.529-1220_529-1210del	NM_001005373.3:c.529-1219_529-1210del	NM_001005373.3:c.529-1218_529-1210del	NM_001005373.3:c.529-1217_529-1210del	NM_001005373.3:c.529-1216_529-1210del	NM_001005373.3:c.529-1215_529-1210del	NM_001005373.3:c.529-1214_529-1210del	NM_001005373.3:c.529-1213_529-1210del	NM_001005373.3:c.529-1212_529-1210del	NM_001005373.3:c.529-1211_529-1210del	NM_001005373.3:c.529-1210del	NM_001005373.3:c.529-1210dup	NM_001005373.3:c.529-1211_529-1210dup	NM_001005373.3:c.529-1212_529-1210dup	NM_001005373.3:c.529-1213_529-1210dup	NM_001005373.3:c.529-1214_529-1210dup	NM_001005373.3:c.529-1215_529-1210dup	NM_001005373.3:c.529-1216_529-1210dup	NM_001005373.3:c.529-1217_529-1210dup	NM_001005373.3:c.529-1218_529-1210dup	NM_001005373.3:c.529-1219_529-1210dup
LRSAM1 transcript variant 2	NM_001005373.4:c.529-1235=	NM_001005373.4:c.529-1222_529-1210del	NM_001005373.4:c.529-1221_529-1210del	NM_001005373.4:c.529-1220_529-1210del	NM_001005373.4:c.529-1219_529-1210del	NM_001005373.4:c.529-1218_529-1210del	NM_001005373.4:c.529-1217_529-1210del	NM_001005373.4:c.529-1216_529-1210del	NM_001005373.4:c.529-1215_529-1210del	NM_001005373.4:c.529-1214_529-1210del	NM_001005373.4:c.529-1213_529-1210del	NM_001005373.4:c.529-1212_529-1210del	NM_001005373.4:c.529-1211_529-1210del	NM_001005373.4:c.529-1210del	NM_001005373.4:c.529-1210dup	NM_001005373.4:c.529-1211_529-1210dup	NM_001005373.4:c.529-1212_529-1210dup	NM_001005373.4:c.529-1213_529-1210dup	NM_001005373.4:c.529-1214_529-1210dup	NM_001005373.4:c.529-1215_529-1210dup	NM_001005373.4:c.529-1216_529-1210dup	NM_001005373.4:c.529-1217_529-1210dup	NM_001005373.4:c.529-1218_529-1210dup	NM_001005373.4:c.529-1219_529-1210dup
LRSAM1 transcript variant 3	NM_001005374.3:c.529-1235=	NM_001005374.3:c.529-1222_529-1210del	NM_001005374.3:c.529-1221_529-1210del	NM_001005374.3:c.529-1220_529-1210del	NM_001005374.3:c.529-1219_529-1210del	NM_001005374.3:c.529-1218_529-1210del	NM_001005374.3:c.529-1217_529-1210del	NM_001005374.3:c.529-1216_529-1210del	NM_001005374.3:c.529-1215_529-1210del	NM_001005374.3:c.529-1214_529-1210del	NM_001005374.3:c.529-1213_529-1210del	NM_001005374.3:c.529-1212_529-1210del	NM_001005374.3:c.529-1211_529-1210del	NM_001005374.3:c.529-1210del	NM_001005374.3:c.529-1210dup	NM_001005374.3:c.529-1211_529-1210dup	NM_001005374.3:c.529-1212_529-1210dup	NM_001005374.3:c.529-1213_529-1210dup	NM_001005374.3:c.529-1214_529-1210dup	NM_001005374.3:c.529-1215_529-1210dup	NM_001005374.3:c.529-1216_529-1210dup	NM_001005374.3:c.529-1217_529-1210dup	NM_001005374.3:c.529-1218_529-1210dup	NM_001005374.3:c.529-1219_529-1210dup
LRSAM1 transcript variant 3	NM_001005374.4:c.529-1235=	NM_001005374.4:c.529-1222_529-1210del	NM_001005374.4:c.529-1221_529-1210del	NM_001005374.4:c.529-1220_529-1210del	NM_001005374.4:c.529-1219_529-1210del	NM_001005374.4:c.529-1218_529-1210del	NM_001005374.4:c.529-1217_529-1210del	NM_001005374.4:c.529-1216_529-1210del	NM_001005374.4:c.529-1215_529-1210del	NM_001005374.4:c.529-1214_529-1210del	NM_001005374.4:c.529-1213_529-1210del	NM_001005374.4:c.529-1212_529-1210del	NM_001005374.4:c.529-1211_529-1210del	NM_001005374.4:c.529-1210del	NM_001005374.4:c.529-1210dup	NM_001005374.4:c.529-1211_529-1210dup	NM_001005374.4:c.529-1212_529-1210dup	NM_001005374.4:c.529-1213_529-1210dup	NM_001005374.4:c.529-1214_529-1210dup	NM_001005374.4:c.529-1215_529-1210dup	NM_001005374.4:c.529-1216_529-1210dup	NM_001005374.4:c.529-1217_529-1210dup	NM_001005374.4:c.529-1218_529-1210dup	NM_001005374.4:c.529-1219_529-1210dup
LRSAM1 transcript variant 4	NM_001190723.2:c.529-1235=	NM_001190723.2:c.529-1222_529-1210del	NM_001190723.2:c.529-1221_529-1210del	NM_001190723.2:c.529-1220_529-1210del	NM_001190723.2:c.529-1219_529-1210del	NM_001190723.2:c.529-1218_529-1210del	NM_001190723.2:c.529-1217_529-1210del	NM_001190723.2:c.529-1216_529-1210del	NM_001190723.2:c.529-1215_529-1210del	NM_001190723.2:c.529-1214_529-1210del	NM_001190723.2:c.529-1213_529-1210del	NM_001190723.2:c.529-1212_529-1210del	NM_001190723.2:c.529-1211_529-1210del	NM_001190723.2:c.529-1210del	NM_001190723.2:c.529-1210dup	NM_001190723.2:c.529-1211_529-1210dup	NM_001190723.2:c.529-1212_529-1210dup	NM_001190723.2:c.529-1213_529-1210dup	NM_001190723.2:c.529-1214_529-1210dup	NM_001190723.2:c.529-1215_529-1210dup	NM_001190723.2:c.529-1216_529-1210dup	NM_001190723.2:c.529-1217_529-1210dup	NM_001190723.2:c.529-1218_529-1210dup	NM_001190723.2:c.529-1219_529-1210dup
LRSAM1 transcript variant 4	NM_001190723.3:c.529-1235=	NM_001190723.3:c.529-1222_529-1210del	NM_001190723.3:c.529-1221_529-1210del	NM_001190723.3:c.529-1220_529-1210del	NM_001190723.3:c.529-1219_529-1210del	NM_001190723.3:c.529-1218_529-1210del	NM_001190723.3:c.529-1217_529-1210del	NM_001190723.3:c.529-1216_529-1210del	NM_001190723.3:c.529-1215_529-1210del	NM_001190723.3:c.529-1214_529-1210del	NM_001190723.3:c.529-1213_529-1210del	NM_001190723.3:c.529-1212_529-1210del	NM_001190723.3:c.529-1211_529-1210del	NM_001190723.3:c.529-1210del	NM_001190723.3:c.529-1210dup	NM_001190723.3:c.529-1211_529-1210dup	NM_001190723.3:c.529-1212_529-1210dup	NM_001190723.3:c.529-1213_529-1210dup	NM_001190723.3:c.529-1214_529-1210dup	NM_001190723.3:c.529-1215_529-1210dup	NM_001190723.3:c.529-1216_529-1210dup	NM_001190723.3:c.529-1217_529-1210dup	NM_001190723.3:c.529-1218_529-1210dup	NM_001190723.3:c.529-1219_529-1210dup
LRSAM1 transcript variant 5	NM_001384142.1:c.529-1235=	NM_001384142.1:c.529-1222_529-1210del	NM_001384142.1:c.529-1221_529-1210del	NM_001384142.1:c.529-1220_529-1210del	NM_001384142.1:c.529-1219_529-1210del	NM_001384142.1:c.529-1218_529-1210del	NM_001384142.1:c.529-1217_529-1210del	NM_001384142.1:c.529-1216_529-1210del	NM_001384142.1:c.529-1215_529-1210del	NM_001384142.1:c.529-1214_529-1210del	NM_001384142.1:c.529-1213_529-1210del	NM_001384142.1:c.529-1212_529-1210del	NM_001384142.1:c.529-1211_529-1210del	NM_001384142.1:c.529-1210del	NM_001384142.1:c.529-1210dup	NM_001384142.1:c.529-1211_529-1210dup	NM_001384142.1:c.529-1212_529-1210dup	NM_001384142.1:c.529-1213_529-1210dup	NM_001384142.1:c.529-1214_529-1210dup	NM_001384142.1:c.529-1215_529-1210dup	NM_001384142.1:c.529-1216_529-1210dup	NM_001384142.1:c.529-1217_529-1210dup	NM_001384142.1:c.529-1218_529-1210dup	NM_001384142.1:c.529-1219_529-1210dup
LRSAM1 transcript variant 6	NM_001384143.1:c.529-1235=	NM_001384143.1:c.529-1222_529-1210del	NM_001384143.1:c.529-1221_529-1210del	NM_001384143.1:c.529-1220_529-1210del	NM_001384143.1:c.529-1219_529-1210del	NM_001384143.1:c.529-1218_529-1210del	NM_001384143.1:c.529-1217_529-1210del	NM_001384143.1:c.529-1216_529-1210del	NM_001384143.1:c.529-1215_529-1210del	NM_001384143.1:c.529-1214_529-1210del	NM_001384143.1:c.529-1213_529-1210del	NM_001384143.1:c.529-1212_529-1210del	NM_001384143.1:c.529-1211_529-1210del	NM_001384143.1:c.529-1210del	NM_001384143.1:c.529-1210dup	NM_001384143.1:c.529-1211_529-1210dup	NM_001384143.1:c.529-1212_529-1210dup	NM_001384143.1:c.529-1213_529-1210dup	NM_001384143.1:c.529-1214_529-1210dup	NM_001384143.1:c.529-1215_529-1210dup	NM_001384143.1:c.529-1216_529-1210dup	NM_001384143.1:c.529-1217_529-1210dup	NM_001384143.1:c.529-1218_529-1210dup	NM_001384143.1:c.529-1219_529-1210dup
LRSAM1 transcript variant 7	NM_001384144.1:c.-256-1235=	NM_001384144.1:c.-256-1222_-256-1210del	NM_001384144.1:c.-256-1221_-256-1210del	NM_001384144.1:c.-256-1220_-256-1210del	NM_001384144.1:c.-256-1219_-256-1210del	NM_001384144.1:c.-256-1218_-256-1210del	NM_001384144.1:c.-256-1217_-256-1210del	NM_001384144.1:c.-256-1216_-256-1210del	NM_001384144.1:c.-256-1215_-256-1210del	NM_001384144.1:c.-256-1214_-256-1210del	NM_001384144.1:c.-256-1213_-256-1210del	NM_001384144.1:c.-256-1212_-256-1210del	NM_001384144.1:c.-256-1211_-256-1210del	NM_001384144.1:c.-256-1210del	NM_001384144.1:c.-256-1210dup	NM_001384144.1:c.-256-1211_-256-1210dup	NM_001384144.1:c.-256-1212_-256-1210dup	NM_001384144.1:c.-256-1213_-256-1210dup	NM_001384144.1:c.-256-1214_-256-1210dup	NM_001384144.1:c.-256-1215_-256-1210dup	NM_001384144.1:c.-256-1216_-256-1210dup	NM_001384144.1:c.-256-1217_-256-1210dup	NM_001384144.1:c.-256-1218_-256-1210dup	NM_001384144.1:c.-256-1219_-256-1210dup
LRSAM1 transcript variant 1	NM_138361.5:c.529-1235=	NM_138361.5:c.529-1222_529-1210del	NM_138361.5:c.529-1221_529-1210del	NM_138361.5:c.529-1220_529-1210del	NM_138361.5:c.529-1219_529-1210del	NM_138361.5:c.529-1218_529-1210del	NM_138361.5:c.529-1217_529-1210del	NM_138361.5:c.529-1216_529-1210del	NM_138361.5:c.529-1215_529-1210del	NM_138361.5:c.529-1214_529-1210del	NM_138361.5:c.529-1213_529-1210del	NM_138361.5:c.529-1212_529-1210del	NM_138361.5:c.529-1211_529-1210del	NM_138361.5:c.529-1210del	NM_138361.5:c.529-1210dup	NM_138361.5:c.529-1211_529-1210dup	NM_138361.5:c.529-1212_529-1210dup	NM_138361.5:c.529-1213_529-1210dup	NM_138361.5:c.529-1214_529-1210dup	NM_138361.5:c.529-1215_529-1210dup	NM_138361.5:c.529-1216_529-1210dup	NM_138361.5:c.529-1217_529-1210dup	NM_138361.5:c.529-1218_529-1210dup	NM_138361.5:c.529-1219_529-1210dup
LRSAM1 transcript variant X1	XM_047424058.1:c.529-1235=	XM_047424058.1:c.529-1222_529-1210del	XM_047424058.1:c.529-1221_529-1210del	XM_047424058.1:c.529-1220_529-1210del	XM_047424058.1:c.529-1219_529-1210del	XM_047424058.1:c.529-1218_529-1210del	XM_047424058.1:c.529-1217_529-1210del	XM_047424058.1:c.529-1216_529-1210del	XM_047424058.1:c.529-1215_529-1210del	XM_047424058.1:c.529-1214_529-1210del	XM_047424058.1:c.529-1213_529-1210del	XM_047424058.1:c.529-1212_529-1210del	XM_047424058.1:c.529-1211_529-1210del	XM_047424058.1:c.529-1210del	XM_047424058.1:c.529-1210dup	XM_047424058.1:c.529-1211_529-1210dup	XM_047424058.1:c.529-1212_529-1210dup	XM_047424058.1:c.529-1213_529-1210dup	XM_047424058.1:c.529-1214_529-1210dup	XM_047424058.1:c.529-1215_529-1210dup	XM_047424058.1:c.529-1216_529-1210dup	XM_047424058.1:c.529-1217_529-1210dup	XM_047424058.1:c.529-1218_529-1210dup	XM_047424058.1:c.529-1219_529-1210dup
LRSAM1 transcript variant X2	XM_047424059.1:c.-171+4132=	XM_047424059.1:c.-171+4145_-171+4157del	XM_047424059.1:c.-171+4146_-171+4157del	XM_047424059.1:c.-171+4147_-171+4157del	XM_047424059.1:c.-171+4148_-171+4157del	XM_047424059.1:c.-171+4149_-171+4157del	XM_047424059.1:c.-171+4150_-171+4157del	XM_047424059.1:c.-171+4151_-171+4157del	XM_047424059.1:c.-171+4152_-171+4157del	XM_047424059.1:c.-171+4153_-171+4157del	XM_047424059.1:c.-171+4154_-171+4157del	XM_047424059.1:c.-171+4155_-171+4157del	XM_047424059.1:c.-171+4156_-171+4157del	XM_047424059.1:c.-171+4157del	XM_047424059.1:c.-171+4157dup	XM_047424059.1:c.-171+4156_-171+4157dup	XM_047424059.1:c.-171+4155_-171+4157dup	XM_047424059.1:c.-171+4154_-171+4157dup	XM_047424059.1:c.-171+4153_-171+4157dup	XM_047424059.1:c.-171+4152_-171+4157dup	XM_047424059.1:c.-171+4151_-171+4157dup	XM_047424059.1:c.-171+4150_-171+4157dup	XM_047424059.1:c.-171+4149_-171+4157dup	XM_047424059.1:c.-171+4148_-171+4157dup

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#.

27 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95527304	Mar 15, 2016 (147)
2	HUMANGENOME_JCVI	ss95527305	Mar 15, 2016 (147)
3	EVA_DECODE	ss3724803413	Jul 13, 2019 (153)
4	EVA_DECODE	ss3724803414	Jul 13, 2019 (153)
5	GNOMAD	ss4209897071	Apr 26, 2021 (155)
6	GNOMAD	ss4209897109	Apr 26, 2021 (155)
7	GNOMAD	ss4209897110	Apr 26, 2021 (155)
8	GNOMAD	ss4209897111	Apr 26, 2021 (155)
9	GNOMAD	ss4209897112	Apr 26, 2021 (155)
10	GNOMAD	ss4209897113	Apr 26, 2021 (155)
11	GNOMAD	ss4209897114	Apr 26, 2021 (155)
12	GNOMAD	ss4209897115	Apr 26, 2021 (155)
13	GNOMAD	ss4209897116	Apr 26, 2021 (155)
14	GNOMAD	ss4209897117	Apr 26, 2021 (155)
15	GNOMAD	ss4209897118	Apr 26, 2021 (155)
16	GNOMAD	ss4209897119	Apr 26, 2021 (155)
17	GNOMAD	ss4209897120	Apr 26, 2021 (155)
18	GNOMAD	ss4209897121	Apr 26, 2021 (155)
19	GNOMAD	ss4209897122	Apr 26, 2021 (155)
20	GNOMAD	ss4209897123	Apr 26, 2021 (155)
21	GNOMAD	ss4209897124	Apr 26, 2021 (155)
22	GNOMAD	ss4209897125	Apr 26, 2021 (155)
23	GNOMAD	ss4209897126	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5739983953	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5739983954	Oct 16, 2022 (156)
26	TOMMO_GENOMICS	ss5739983956	Oct 16, 2022 (156)
27	TOMMO_GENOMICS	ss5739983957	Oct 16, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 338432957 (NC_000009.12:127466504::T 88/23114) Row 338432995 (NC_000009.12:127466504::TT 80/23116) Row 338432996 (NC_000009.12:127466504::TTTT 10/23126)...	-	Apr 26, 2021 (155)
47	14KJPN Submission ignored due to conflicting rows: Row 73821057 (NC_000009.12:127466504::T 1202/26412) Row 73821058 (NC_000009.12:127466504:TTT: 237/26412) Row 73821060 (NC_000009.12:127466504::TT 602/26412)...	-	Oct 16, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 73821057 (NC_000009.12:127466504::T 1202/26412) Row 73821058 (NC_000009.12:127466504:TTT: 237/26412) Row 73821060 (NC_000009.12:127466504::TT 602/26412)...	-	Oct 16, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 73821057 (NC_000009.12:127466504::T 1202/26412) Row 73821058 (NC_000009.12:127466504:TTT: 237/26412) Row 73821060 (NC_000009.12:127466504::TT 602/26412)...	-	Oct 16, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 73821057 (NC_000009.12:127466504::T 1202/26412) Row 73821058 (NC_000009.12:127466504:TTT: 237/26412) Row 73821060 (NC_000009.12:127466504::TT 602/26412)...	-	Oct 16, 2022 (156)
51	ALFA	NC_000009.12 - 127466505	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
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4209897126	NC_000009.12:127466504:TTTTTTTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4209897125	NC_000009.12:127466504:TTTTTTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4209897124	NC_000009.12:127466504:TTTTTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4209897123	NC_000009.12:127466504:TTTTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4209897122	NC_000009.12:127466504:TTTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4209897121	NC_000009.12:127466504:TTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4209897120	NC_000009.12:127466504:TTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897119	NC_000009.12:127466504:TTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897118, ss5739983954	NC_000009.12:127466504:TTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897117	NC_000009.12:127466504:TT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897116, ss5739983957	NC_000009.12:127466504:T:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95527304	NT_008470.19:59393316:T:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897071, ss5739983953	NC_000009.12:127466504::T	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897109, ss5739983956	NC_000009.12:127466504::TT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724803413	NC_000009.12:127466504::TTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897110	NC_000009.12:127466504::TTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897111	NC_000009.12:127466504::TTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724803414, ss4209897112	NC_000009.12:127466504::TTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897113	NC_000009.12:127466504::TTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13267863189	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897114	NC_000009.12:127466504::TTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4209897115	NC_000009.12:127466504::TTTTTTTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95527305	NT_008470.19:59393341:C:TTTTTTTTTTC	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3601283932	NC_000009.12:127466504::TTTTT	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ss3601283947	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTT:	NC_000009.12:127466504:TTTTTTTTTTT… NC_000009.12:127466504:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs869115663

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

rs869115663