Name: rs1491544464
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.

rs1491544464

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:27525108 (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: insTGCG / insTGCGCG / insT(GC)₃G /…
insTGCG / insTGCGCG / insT(GC)₃G / insT(GC)₄G / insT(GC)₅G / insT(GC)₆G / insTGTGCG / insTGTGCGCG / insTGTG(CG)₃ / insTGTG(CG)₄ / insTGTG(CG)₅ / insTGTG(CG)₆ / insTGTG(CG)₇ / ins(TG)₃CG / ins(TG)₃CGCG / ins(TG)₃(CG)₃ / ins(TG)₃(CG)₄ / ins(TG)₃(CG)₅ / ins(TG)₃(CG)₆ / ins(TG)₄CG / ins(TG)₄CGCG / ins(TG)₄(CG)₃ / ins(TG)₄(CG)₄ / ins(TG)₄(CG)₅ / ins(TG)₅CG / ins(TG)₅CGCG / ins(TG)₅(CG)₃ / ins(TG)₆CG / ins(TG)₆(CG)₄ / ins(TG)₇CG / ins(TG)₇(CG)₃ / ins(TG)₉CG
Variation Type: Indel Insertion and Deletion
Frequency: insTGCG=0.00000 (0/11714, ALFA)
insTGCGCG=0.00000 (0/11714, ALFA)
insT(GC)₃G=0.00000 (0/11714, ALFA) (+ 23 more)
insT(GC)₄G=0.00000 (0/11714, ALFA)
insT(GC)₅G=0.00000 (0/11714, ALFA)
insT(GC)₆G=0.00000 (0/11714, ALFA)
insTGTGCG=0.00000 (0/11714, ALFA)
insTGTGCGCG=0.00000 (0/11714, ALFA)
insTGTG(CG)₃=0.00000 (0/11714, ALFA)
insTGTG(CG)₄=0.00000 (0/11714, ALFA)
insTGTG(CG)₅=0.00000 (0/11714, ALFA)
ins(TG)₃CG=0.00000 (0/11714, ALFA)
ins(TG)₃CGCG=0.00000 (0/11714, ALFA)
ins(TG)₃(CG)₃=0.00000 (0/11714, ALFA)
ins(TG)₃(CG)₄=0.00000 (0/11714, ALFA)
ins(TG)₃(CG)₅=0.00000 (0/11714, ALFA)
ins(TG)₄CG=0.00000 (0/11714, ALFA)
ins(TG)₄CGCG=0.00000 (0/11714, ALFA)
ins(TG)₄(CG)₃=0.00000 (0/11714, ALFA)
ins(TG)₄(CG)₄=0.00000 (0/11714, ALFA)
ins(TG)₅CG=0.00000 (0/11714, ALFA)
ins(TG)₅CGCG=0.00000 (0/11714, ALFA)
ins(TG)₅(CG)₃=0.00000 (0/11714, ALFA)
ins(TG)₆CG=0.00000 (0/11714, ALFA)
ins(TG)₇CG=0.00000 (0/11714, ALFA)
ins(TG)₇(CG)₃=0.00000 (0/11714, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: EPHX2 : 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	11714	G=1.00000	GTGCG=0.00000, GTGCGCG=0.00000, GTGCGCGCG=0.00000, GTGCGCGCGCG=0.00000, GTGCGCGCGCGCG=0.00000, GTGCGCGCGCGCGCG=0.00000, GTGTGCG=0.00000, GTGTGCGCG=0.00000, GTGTGCGCGCG=0.00000, GTGTGCGCGCGCG=0.00000, GTGTGCGCGCGCGCG=0.00000, GTGTGTGCG=0.00000, GTGTGTGCGCG=0.00000, GTGTGTGCGCGCG=0.00000, GTGTGTGCGCGCGCG=0.00000, GTGTGTGCGCGCGCGCG=0.00000, GTGTGTGTGCG=0.00000, GTGTGTGTGCGCG=0.00000, GTGTGTGTGCGCGCG=0.00000, GTGTGTGTGCGCGCGCG=0.00000, GTGTGTGTGTGCG=0.00000, GTGTGTGTGTGCGCG=0.00000, GTGTGTGTGTGCGCGCG=0.00000, GTGTGTGTGTGTGCG=0.00000, GTGTGTGTGTGTGTGCG=0.00000, GTGTGTGTGTGTGTGCGCGCG=0.00000	1.0	N/A
European	Sub	7592	G=1.0000	GTGCG=0.0000, GTGCGCG=0.0000, GTGCGCGCG=0.0000, GTGCGCGCGCG=0.0000, GTGCGCGCGCGCG=0.0000, GTGCGCGCGCGCGCG=0.0000, GTGTGCG=0.0000, GTGTGCGCG=0.0000, GTGTGCGCGCG=0.0000, GTGTGCGCGCGCG=0.0000, GTGTGCGCGCGCGCG=0.0000, GTGTGTGCG=0.0000, GTGTGTGCGCG=0.0000, GTGTGTGCGCGCG=0.0000, GTGTGTGCGCGCGCG=0.0000, GTGTGTGCGCGCGCGCG=0.0000, GTGTGTGTGCG=0.0000, GTGTGTGTGCGCG=0.0000, GTGTGTGTGCGCGCG=0.0000, GTGTGTGTGCGCGCGCG=0.0000, GTGTGTGTGTGCG=0.0000, GTGTGTGTGTGCGCG=0.0000, GTGTGTGTGTGCGCGCG=0.0000, GTGTGTGTGTGTGCG=0.0000, GTGTGTGTGTGTGTGCG=0.0000, GTGTGTGTGTGTGTGCGCGCG=0.0000	1.0	N/A
African	Sub	2710	G=1.0000	GTGCG=0.0000, GTGCGCG=0.0000, GTGCGCGCG=0.0000, GTGCGCGCGCG=0.0000, GTGCGCGCGCGCG=0.0000, GTGCGCGCGCGCGCG=0.0000, GTGTGCG=0.0000, GTGTGCGCG=0.0000, GTGTGCGCGCG=0.0000, GTGTGCGCGCGCG=0.0000, GTGTGCGCGCGCGCG=0.0000, GTGTGTGCG=0.0000, GTGTGTGCGCG=0.0000, GTGTGTGCGCGCG=0.0000, GTGTGTGCGCGCGCG=0.0000, GTGTGTGCGCGCGCGCG=0.0000, GTGTGTGTGCG=0.0000, GTGTGTGTGCGCG=0.0000, GTGTGTGTGCGCGCG=0.0000, GTGTGTGTGCGCGCGCG=0.0000, GTGTGTGTGTGCG=0.0000, GTGTGTGTGTGCGCG=0.0000, GTGTGTGTGTGCGCGCG=0.0000, GTGTGTGTGTGTGCG=0.0000, GTGTGTGTGTGTGTGCG=0.0000, GTGTGTGTGTGTGTGCGCGCG=0.0000	1.0	N/A
African Others	Sub	102	G=1.000	GTGCG=0.000, GTGCGCG=0.000, GTGCGCGCG=0.000, GTGCGCGCGCG=0.000, GTGCGCGCGCGCG=0.000, GTGCGCGCGCGCGCG=0.000, GTGTGCG=0.000, GTGTGCGCG=0.000, GTGTGCGCGCG=0.000, GTGTGCGCGCGCG=0.000, GTGTGCGCGCGCGCG=0.000, GTGTGTGCG=0.000, GTGTGTGCGCG=0.000, GTGTGTGCGCGCG=0.000, GTGTGTGCGCGCGCG=0.000, GTGTGTGCGCGCGCGCG=0.000, GTGTGTGTGCG=0.000, GTGTGTGTGCGCG=0.000, GTGTGTGTGCGCGCG=0.000, GTGTGTGTGCGCGCGCG=0.000, GTGTGTGTGTGCG=0.000, GTGTGTGTGTGCGCG=0.000, GTGTGTGTGTGCGCGCG=0.000, GTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCGCGCG=0.000	1.0	N/A
African American	Sub	2608	G=1.0000	GTGCG=0.0000, GTGCGCG=0.0000, GTGCGCGCG=0.0000, GTGCGCGCGCG=0.0000, GTGCGCGCGCGCG=0.0000, GTGCGCGCGCGCGCG=0.0000, GTGTGCG=0.0000, GTGTGCGCG=0.0000, GTGTGCGCGCG=0.0000, GTGTGCGCGCGCG=0.0000, GTGTGCGCGCGCGCG=0.0000, GTGTGTGCG=0.0000, GTGTGTGCGCG=0.0000, GTGTGTGCGCGCG=0.0000, GTGTGTGCGCGCGCG=0.0000, GTGTGTGCGCGCGCGCG=0.0000, GTGTGTGTGCG=0.0000, GTGTGTGTGCGCG=0.0000, GTGTGTGTGCGCGCG=0.0000, GTGTGTGTGCGCGCGCG=0.0000, GTGTGTGTGTGCG=0.0000, GTGTGTGTGTGCGCG=0.0000, GTGTGTGTGTGCGCGCG=0.0000, GTGTGTGTGTGTGCG=0.0000, GTGTGTGTGTGTGTGCG=0.0000, GTGTGTGTGTGTGTGCGCGCG=0.0000	1.0	N/A
Asian	Sub	108	G=1.000	GTGCG=0.000, GTGCGCG=0.000, GTGCGCGCG=0.000, GTGCGCGCGCG=0.000, GTGCGCGCGCGCG=0.000, GTGCGCGCGCGCGCG=0.000, GTGTGCG=0.000, GTGTGCGCG=0.000, GTGTGCGCGCG=0.000, GTGTGCGCGCGCG=0.000, GTGTGCGCGCGCGCG=0.000, GTGTGTGCG=0.000, GTGTGTGCGCG=0.000, GTGTGTGCGCGCG=0.000, GTGTGTGCGCGCGCG=0.000, GTGTGTGCGCGCGCGCG=0.000, GTGTGTGTGCG=0.000, GTGTGTGTGCGCG=0.000, GTGTGTGTGCGCGCG=0.000, GTGTGTGTGCGCGCGCG=0.000, GTGTGTGTGTGCG=0.000, GTGTGTGTGTGCGCG=0.000, GTGTGTGTGTGCGCGCG=0.000, GTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCGCGCG=0.000	1.0	N/A
East Asian	Sub	84	G=1.00	GTGCG=0.00, GTGCGCG=0.00, GTGCGCGCG=0.00, GTGCGCGCGCG=0.00, GTGCGCGCGCGCG=0.00, GTGCGCGCGCGCGCG=0.00, GTGTGCG=0.00, GTGTGCGCG=0.00, GTGTGCGCGCG=0.00, GTGTGCGCGCGCG=0.00, GTGTGCGCGCGCGCG=0.00, GTGTGTGCG=0.00, GTGTGTGCGCG=0.00, GTGTGTGCGCGCG=0.00, GTGTGTGCGCGCGCG=0.00, GTGTGTGCGCGCGCGCG=0.00, GTGTGTGTGCG=0.00, GTGTGTGTGCGCG=0.00, GTGTGTGTGCGCGCG=0.00, GTGTGTGTGCGCGCGCG=0.00, GTGTGTGTGTGCG=0.00, GTGTGTGTGTGCGCG=0.00, GTGTGTGTGTGCGCGCG=0.00, GTGTGTGTGTGTGCG=0.00, GTGTGTGTGTGTGTGCG=0.00, GTGTGTGTGTGTGTGCGCGCG=0.00	1.0	N/A
Other Asian	Sub	24	G=1.00	GTGCG=0.00, GTGCGCG=0.00, GTGCGCGCG=0.00, GTGCGCGCGCG=0.00, GTGCGCGCGCGCG=0.00, GTGCGCGCGCGCGCG=0.00, GTGTGCG=0.00, GTGTGCGCG=0.00, GTGTGCGCGCG=0.00, GTGTGCGCGCGCG=0.00, GTGTGCGCGCGCGCG=0.00, GTGTGTGCG=0.00, GTGTGTGCGCG=0.00, GTGTGTGCGCGCG=0.00, GTGTGTGCGCGCGCG=0.00, GTGTGTGCGCGCGCGCG=0.00, GTGTGTGTGCG=0.00, GTGTGTGTGCGCG=0.00, GTGTGTGTGCGCGCG=0.00, GTGTGTGTGCGCGCGCG=0.00, GTGTGTGTGTGCG=0.00, GTGTGTGTGTGCGCG=0.00, GTGTGTGTGTGCGCGCG=0.00, GTGTGTGTGTGTGCG=0.00, GTGTGTGTGTGTGTGCG=0.00, GTGTGTGTGTGTGTGCGCGCG=0.00	1.0	N/A
Latin American 1	Sub	144	G=1.000	GTGCG=0.000, GTGCGCG=0.000, GTGCGCGCG=0.000, GTGCGCGCGCG=0.000, GTGCGCGCGCGCG=0.000, GTGCGCGCGCGCGCG=0.000, GTGTGCG=0.000, GTGTGCGCG=0.000, GTGTGCGCGCG=0.000, GTGTGCGCGCGCG=0.000, GTGTGCGCGCGCGCG=0.000, GTGTGTGCG=0.000, GTGTGTGCGCG=0.000, GTGTGTGCGCGCG=0.000, GTGTGTGCGCGCGCG=0.000, GTGTGTGCGCGCGCGCG=0.000, GTGTGTGTGCG=0.000, GTGTGTGTGCGCG=0.000, GTGTGTGTGCGCGCG=0.000, GTGTGTGTGCGCGCGCG=0.000, GTGTGTGTGTGCG=0.000, GTGTGTGTGTGCGCG=0.000, GTGTGTGTGTGCGCGCG=0.000, GTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCGCGCG=0.000	1.0	N/A
Latin American 2	Sub	608	G=1.000	GTGCG=0.000, GTGCGCG=0.000, GTGCGCGCG=0.000, GTGCGCGCGCG=0.000, GTGCGCGCGCGCG=0.000, GTGCGCGCGCGCGCG=0.000, GTGTGCG=0.000, GTGTGCGCG=0.000, GTGTGCGCGCG=0.000, GTGTGCGCGCGCG=0.000, GTGTGCGCGCGCGCG=0.000, GTGTGTGCG=0.000, GTGTGTGCGCG=0.000, GTGTGTGCGCGCG=0.000, GTGTGTGCGCGCGCG=0.000, GTGTGTGCGCGCGCGCG=0.000, GTGTGTGTGCG=0.000, GTGTGTGTGCGCG=0.000, GTGTGTGTGCGCGCG=0.000, GTGTGTGTGCGCGCGCG=0.000, GTGTGTGTGTGCG=0.000, GTGTGTGTGTGCGCG=0.000, GTGTGTGTGTGCGCGCG=0.000, GTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCGCGCG=0.000	1.0	N/A
South Asian	Sub	88	G=1.00	GTGCG=0.00, GTGCGCG=0.00, GTGCGCGCG=0.00, GTGCGCGCGCG=0.00, GTGCGCGCGCGCG=0.00, GTGCGCGCGCGCGCG=0.00, GTGTGCG=0.00, GTGTGCGCG=0.00, GTGTGCGCGCG=0.00, GTGTGCGCGCGCG=0.00, GTGTGCGCGCGCGCG=0.00, GTGTGTGCG=0.00, GTGTGTGCGCG=0.00, GTGTGTGCGCGCG=0.00, GTGTGTGCGCGCGCG=0.00, GTGTGTGCGCGCGCGCG=0.00, GTGTGTGTGCG=0.00, GTGTGTGTGCGCG=0.00, GTGTGTGTGCGCGCG=0.00, GTGTGTGTGCGCGCGCG=0.00, GTGTGTGTGTGCG=0.00, GTGTGTGTGTGCGCG=0.00, GTGTGTGTGTGCGCGCG=0.00, GTGTGTGTGTGTGCG=0.00, GTGTGTGTGTGTGTGCG=0.00, GTGTGTGTGTGTGTGCGCGCG=0.00	1.0	N/A
Other	Sub	464	G=1.000	GTGCG=0.000, GTGCGCG=0.000, GTGCGCGCG=0.000, GTGCGCGCGCG=0.000, GTGCGCGCGCGCG=0.000, GTGCGCGCGCGCGCG=0.000, GTGTGCG=0.000, GTGTGCGCG=0.000, GTGTGCGCGCG=0.000, GTGTGCGCGCGCG=0.000, GTGTGCGCGCGCGCG=0.000, GTGTGTGCG=0.000, GTGTGTGCGCG=0.000, GTGTGTGCGCGCG=0.000, GTGTGTGCGCGCGCG=0.000, GTGTGTGCGCGCGCGCG=0.000, GTGTGTGTGCG=0.000, GTGTGTGTGCGCG=0.000, GTGTGTGTGCGCGCG=0.000, GTGTGTGTGCGCGCGCG=0.000, GTGTGTGTGTGCG=0.000, GTGTGTGTGTGCGCG=0.000, GTGTGTGTGTGCGCGCG=0.000, GTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCG=0.000, GTGTGTGTGTGTGTGCGCGCG=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	11714	G=1.00000	insTGCG=0.00000, insTGCGCG=0.00000, insT(GC)₃G=0.00000, insT(GC)₄G=0.00000, insT(GC)₅G=0.00000, insT(GC)₆G=0.00000, insTGTGCG=0.00000, insTGTGCGCG=0.00000, insTGTG(CG)₃=0.00000, insTGTG(CG)₄=0.00000, insTGTG(CG)₅=0.00000, ins(TG)₃CG=0.00000, ins(TG)₃CGCG=0.00000, ins(TG)₃(CG)₃=0.00000, ins(TG)₃(CG)₄=0.00000, ins(TG)₃(CG)₅=0.00000, ins(TG)₄CG=0.00000, ins(TG)₄CGCG=0.00000, ins(TG)₄(CG)₃=0.00000, ins(TG)₄(CG)₄=0.00000, ins(TG)₅CG=0.00000, ins(TG)₅CGCG=0.00000, ins(TG)₅(CG)₃=0.00000, ins(TG)₆CG=0.00000, ins(TG)₇CG=0.00000, ins(TG)₇(CG)₃=0.00000
Allele Frequency Aggregator	European	Sub	7592	G=1.0000	insTGCG=0.0000, insTGCGCG=0.0000, insT(GC)₃G=0.0000, insT(GC)₄G=0.0000, insT(GC)₅G=0.0000, insT(GC)₆G=0.0000, insTGTGCG=0.0000, insTGTGCGCG=0.0000, insTGTG(CG)₃=0.0000, insTGTG(CG)₄=0.0000, insTGTG(CG)₅=0.0000, ins(TG)₃CG=0.0000, ins(TG)₃CGCG=0.0000, ins(TG)₃(CG)₃=0.0000, ins(TG)₃(CG)₄=0.0000, ins(TG)₃(CG)₅=0.0000, ins(TG)₄CG=0.0000, ins(TG)₄CGCG=0.0000, ins(TG)₄(CG)₃=0.0000, ins(TG)₄(CG)₄=0.0000, ins(TG)₅CG=0.0000, ins(TG)₅CGCG=0.0000, ins(TG)₅(CG)₃=0.0000, ins(TG)₆CG=0.0000, ins(TG)₇CG=0.0000, ins(TG)₇(CG)₃=0.0000
Allele Frequency Aggregator	African	Sub	2710	G=1.0000	insTGCG=0.0000, insTGCGCG=0.0000, insT(GC)₃G=0.0000, insT(GC)₄G=0.0000, insT(GC)₅G=0.0000, insT(GC)₆G=0.0000, insTGTGCG=0.0000, insTGTGCGCG=0.0000, insTGTG(CG)₃=0.0000, insTGTG(CG)₄=0.0000, insTGTG(CG)₅=0.0000, ins(TG)₃CG=0.0000, ins(TG)₃CGCG=0.0000, ins(TG)₃(CG)₃=0.0000, ins(TG)₃(CG)₄=0.0000, ins(TG)₃(CG)₅=0.0000, ins(TG)₄CG=0.0000, ins(TG)₄CGCG=0.0000, ins(TG)₄(CG)₃=0.0000, ins(TG)₄(CG)₄=0.0000, ins(TG)₅CG=0.0000, ins(TG)₅CGCG=0.0000, ins(TG)₅(CG)₃=0.0000, ins(TG)₆CG=0.0000, ins(TG)₇CG=0.0000, ins(TG)₇(CG)₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	608	G=1.000	insTGCG=0.000, insTGCGCG=0.000, insT(GC)₃G=0.000, insT(GC)₄G=0.000, insT(GC)₅G=0.000, insT(GC)₆G=0.000, insTGTGCG=0.000, insTGTGCGCG=0.000, insTGTG(CG)₃=0.000, insTGTG(CG)₄=0.000, insTGTG(CG)₅=0.000, ins(TG)₃CG=0.000, ins(TG)₃CGCG=0.000, ins(TG)₃(CG)₃=0.000, ins(TG)₃(CG)₄=0.000, ins(TG)₃(CG)₅=0.000, ins(TG)₄CG=0.000, ins(TG)₄CGCG=0.000, ins(TG)₄(CG)₃=0.000, ins(TG)₄(CG)₄=0.000, ins(TG)₅CG=0.000, ins(TG)₅CGCG=0.000, ins(TG)₅(CG)₃=0.000, ins(TG)₆CG=0.000, ins(TG)₇CG=0.000, ins(TG)₇(CG)₃=0.000
Allele Frequency Aggregator	Other	Sub	464	G=1.000	insTGCG=0.000, insTGCGCG=0.000, insT(GC)₃G=0.000, insT(GC)₄G=0.000, insT(GC)₅G=0.000, insT(GC)₆G=0.000, insTGTGCG=0.000, insTGTGCGCG=0.000, insTGTG(CG)₃=0.000, insTGTG(CG)₄=0.000, insTGTG(CG)₅=0.000, ins(TG)₃CG=0.000, ins(TG)₃CGCG=0.000, ins(TG)₃(CG)₃=0.000, ins(TG)₃(CG)₄=0.000, ins(TG)₃(CG)₅=0.000, ins(TG)₄CG=0.000, ins(TG)₄CGCG=0.000, ins(TG)₄(CG)₃=0.000, ins(TG)₄(CG)₄=0.000, ins(TG)₅CG=0.000, ins(TG)₅CGCG=0.000, ins(TG)₅(CG)₃=0.000, ins(TG)₆CG=0.000, ins(TG)₇CG=0.000, ins(TG)₇(CG)₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	G=1.000	insTGCG=0.000, insTGCGCG=0.000, insT(GC)₃G=0.000, insT(GC)₄G=0.000, insT(GC)₅G=0.000, insT(GC)₆G=0.000, insTGTGCG=0.000, insTGTGCGCG=0.000, insTGTG(CG)₃=0.000, insTGTG(CG)₄=0.000, insTGTG(CG)₅=0.000, ins(TG)₃CG=0.000, ins(TG)₃CGCG=0.000, ins(TG)₃(CG)₃=0.000, ins(TG)₃(CG)₄=0.000, ins(TG)₃(CG)₅=0.000, ins(TG)₄CG=0.000, ins(TG)₄CGCG=0.000, ins(TG)₄(CG)₃=0.000, ins(TG)₄(CG)₄=0.000, ins(TG)₅CG=0.000, ins(TG)₅CGCG=0.000, ins(TG)₅(CG)₃=0.000, ins(TG)₆CG=0.000, ins(TG)₇CG=0.000, ins(TG)₇(CG)₃=0.000
Allele Frequency Aggregator	Asian	Sub	108	G=1.000	insTGCG=0.000, insTGCGCG=0.000, insT(GC)₃G=0.000, insT(GC)₄G=0.000, insT(GC)₅G=0.000, insT(GC)₆G=0.000, insTGTGCG=0.000, insTGTGCGCG=0.000, insTGTG(CG)₃=0.000, insTGTG(CG)₄=0.000, insTGTG(CG)₅=0.000, ins(TG)₃CG=0.000, ins(TG)₃CGCG=0.000, ins(TG)₃(CG)₃=0.000, ins(TG)₃(CG)₄=0.000, ins(TG)₃(CG)₅=0.000, ins(TG)₄CG=0.000, ins(TG)₄CGCG=0.000, ins(TG)₄(CG)₃=0.000, ins(TG)₄(CG)₄=0.000, ins(TG)₅CG=0.000, ins(TG)₅CGCG=0.000, ins(TG)₅(CG)₃=0.000, ins(TG)₆CG=0.000, ins(TG)₇CG=0.000, ins(TG)₇(CG)₃=0.000
Allele Frequency Aggregator	South Asian	Sub	88	G=1.00	insTGCG=0.00, insTGCGCG=0.00, insT(GC)₃G=0.00, insT(GC)₄G=0.00, insT(GC)₅G=0.00, insT(GC)₆G=0.00, insTGTGCG=0.00, insTGTGCGCG=0.00, insTGTG(CG)₃=0.00, insTGTG(CG)₄=0.00, insTGTG(CG)₅=0.00, ins(TG)₃CG=0.00, ins(TG)₃CGCG=0.00, ins(TG)₃(CG)₃=0.00, ins(TG)₃(CG)₄=0.00, ins(TG)₃(CG)₅=0.00, ins(TG)₄CG=0.00, ins(TG)₄CGCG=0.00, ins(TG)₄(CG)₃=0.00, ins(TG)₄(CG)₄=0.00, ins(TG)₅CG=0.00, ins(TG)₅CGCG=0.00, ins(TG)₅(CG)₃=0.00, ins(TG)₆CG=0.00, ins(TG)₇CG=0.00, ins(TG)₇(CG)₃=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 8	NC_000008.11:g.27525108_27525109insTGCG
GRCh38.p14 chr 8	NC_000008.11:g.27525108_27525109insTGCGCG
GRCh38.p14 chr 8	NC_000008.11:g.27525108_27525109insTGCGCGCG
GRCh38.p14 chr 8	NC_000008.11:g.27525108_27525109insTGCGCGCGCG
GRCh38.p14 chr 8	NC_000008.11:g.27525108_27525109insTGCGCGCGCGCG
GRCh38.p14 chr 8	NC_000008.11:g.27525108_27525109insTGCGCGCGCGCGCG
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GCG[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GC[2]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GC[3]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GC[4]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GC[5]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GC[6]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[2]GC[7]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[3]GCG[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[3]GC[2]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[3]GC[3]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[3]GC[4]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[3]GC[5]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[3]GC[6]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[4]GCG[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[4]GC[2]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[4]GC[3]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[4]GC[4]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[4]GC[5]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[5]GCG[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[5]GC[2]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[5]GC[3]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[6]GCG[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[6]GC[4]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[7]GCG[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[7]GC[3]G[1]
GRCh38.p14 chr 8	NC_000008.11:g.27525108GT[9]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625_27382626insTGCG
GRCh37.p13 chr 8	NC_000008.10:g.27382625_27382626insTGCGCG
GRCh37.p13 chr 8	NC_000008.10:g.27382625_27382626insTGCGCGCG
GRCh37.p13 chr 8	NC_000008.10:g.27382625_27382626insTGCGCGCGCG
GRCh37.p13 chr 8	NC_000008.10:g.27382625_27382626insTGCGCGCGCGCG
GRCh37.p13 chr 8	NC_000008.10:g.27382625_27382626insTGCGCGCGCGCGCG
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GC[2]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GC[3]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GC[4]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GC[5]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GC[6]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[2]GC[7]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[3]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[3]GC[2]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[3]GC[3]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[3]GC[4]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[3]GC[5]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[3]GC[6]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[4]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[4]GC[2]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[4]GC[3]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[4]GC[4]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[4]GC[5]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[5]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[5]GC[2]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[5]GC[3]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[6]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[6]GC[4]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[7]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[7]GC[3]G[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625GT[9]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981_38982insTGCG
EPHX2 RefSeqGene	NG_012064.1:g.38981_38982insTGCGCG
EPHX2 RefSeqGene	NG_012064.1:g.38981_38982insTGCGCGCG
EPHX2 RefSeqGene	NG_012064.1:g.38981_38982insTGCGCGCGCG
EPHX2 RefSeqGene	NG_012064.1:g.38981_38982insTGCGCGCGCGCG
EPHX2 RefSeqGene	NG_012064.1:g.38981_38982insTGCGCGCGCGCGCG
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GC[2]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GC[3]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GC[4]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GC[5]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GC[6]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[2]GC[7]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[3]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[3]GC[2]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[3]GC[3]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[3]GC[4]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[3]GC[5]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[3]GC[6]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[4]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[4]GC[2]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[4]GC[3]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[4]GC[4]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[4]GC[5]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[5]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[5]GC[2]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[5]GC[3]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[6]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[6]GC[4]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[7]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[7]GC[3]G[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981GT[9]GCG[1]

Gene: EPHX2, epoxide hydrolase 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
EPHX2 transcript variant 2	NM_001256482.2:c.900-254_… NM_001256482.2:c.900-254_900-253insTGCG	N/A	Intron Variant
EPHX2 transcript variant 3	NM_001256483.2:c.861-254_… NM_001256483.2:c.861-254_861-253insTGCG	N/A	Intron Variant
EPHX2 transcript variant 4	NM_001256484.2:c.900-254_… NM_001256484.2:c.900-254_900-253insTGCG	N/A	Intron Variant
EPHX2 transcript variant 1	NM_001979.6:c.1059-254_10… NM_001979.6:c.1059-254_1059-253insTGCG	N/A	Intron Variant
EPHX2 transcript variant X1	XM_017013199.2:c.936-254_… XM_017013199.2:c.936-254_936-253insTGCG	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	G=	insTGCG	insTGCGCG	insT(GC)₃G	insT(GC)₄G	insT(GC)₅G	insT(GC)₆G	insTGTGCG	insTGTGCGCG	insTGTG(CG)₃	insTGTG(CG)₄	insTGTG(CG)₅	insTGTG(CG)₆	insTGTG(CG)₇	ins(TG)₃CG	ins(TG)₃CGCG	ins(TG)₃(CG)₃	ins(TG)₃(CG)₄	ins(TG)₃(CG)₅	ins(TG)₃(CG)₆	ins(TG)₄CG	ins(TG)₄CGCG	ins(TG)₄(CG)₃	ins(TG)₄(CG)₄	ins(TG)₄(CG)₅	ins(TG)₅CG	ins(TG)₅CGCG	ins(TG)₅(CG)₃	ins(TG)₆CG	ins(TG)₆(CG)₄	ins(TG)₇CG	ins(TG)₇(CG)₃	ins(TG)₉CG
GRCh38.p14 chr 8	NC_000008.11:g.27525108=	NC_000008.11:g.27525108_27525109insTGCG	NC_000008.11:g.27525108_27525109insTGCGCG	NC_000008.11:g.27525108_27525109insTGCGCGCG	NC_000008.11:g.27525108_27525109insTGCGCGCGCG	NC_000008.11:g.27525108_27525109insTGCGCGCGCGCG	NC_000008.11:g.27525108_27525109insTGCGCGCGCGCGCG	NC_000008.11:g.27525108GT[2]GCG[1]	NC_000008.11:g.27525108GT[2]GC[2]G[1]	NC_000008.11:g.27525108GT[2]GC[3]G[1]	NC_000008.11:g.27525108GT[2]GC[4]G[1]	NC_000008.11:g.27525108GT[2]GC[5]G[1]	NC_000008.11:g.27525108GT[2]GC[6]G[1]	NC_000008.11:g.27525108GT[2]GC[7]G[1]	NC_000008.11:g.27525108GT[3]GCG[1]	NC_000008.11:g.27525108GT[3]GC[2]G[1]	NC_000008.11:g.27525108GT[3]GC[3]G[1]	NC_000008.11:g.27525108GT[3]GC[4]G[1]	NC_000008.11:g.27525108GT[3]GC[5]G[1]	NC_000008.11:g.27525108GT[3]GC[6]G[1]	NC_000008.11:g.27525108GT[4]GCG[1]	NC_000008.11:g.27525108GT[4]GC[2]G[1]	NC_000008.11:g.27525108GT[4]GC[3]G[1]	NC_000008.11:g.27525108GT[4]GC[4]G[1]	NC_000008.11:g.27525108GT[4]GC[5]G[1]	NC_000008.11:g.27525108GT[5]GCG[1]	NC_000008.11:g.27525108GT[5]GC[2]G[1]	NC_000008.11:g.27525108GT[5]GC[3]G[1]	NC_000008.11:g.27525108GT[6]GCG[1]	NC_000008.11:g.27525108GT[6]GC[4]G[1]	NC_000008.11:g.27525108GT[7]GCG[1]	NC_000008.11:g.27525108GT[7]GC[3]G[1]	NC_000008.11:g.27525108GT[9]GCG[1]
GRCh37.p13 chr 8	NC_000008.10:g.27382625=	NC_000008.10:g.27382625_27382626insTGCG	NC_000008.10:g.27382625_27382626insTGCGCG	NC_000008.10:g.27382625_27382626insTGCGCGCG	NC_000008.10:g.27382625_27382626insTGCGCGCGCG	NC_000008.10:g.27382625_27382626insTGCGCGCGCGCG	NC_000008.10:g.27382625_27382626insTGCGCGCGCGCGCG	NC_000008.10:g.27382625GT[2]GCG[1]	NC_000008.10:g.27382625GT[2]GC[2]G[1]	NC_000008.10:g.27382625GT[2]GC[3]G[1]	NC_000008.10:g.27382625GT[2]GC[4]G[1]	NC_000008.10:g.27382625GT[2]GC[5]G[1]	NC_000008.10:g.27382625GT[2]GC[6]G[1]	NC_000008.10:g.27382625GT[2]GC[7]G[1]	NC_000008.10:g.27382625GT[3]GCG[1]	NC_000008.10:g.27382625GT[3]GC[2]G[1]	NC_000008.10:g.27382625GT[3]GC[3]G[1]	NC_000008.10:g.27382625GT[3]GC[4]G[1]	NC_000008.10:g.27382625GT[3]GC[5]G[1]	NC_000008.10:g.27382625GT[3]GC[6]G[1]	NC_000008.10:g.27382625GT[4]GCG[1]	NC_000008.10:g.27382625GT[4]GC[2]G[1]	NC_000008.10:g.27382625GT[4]GC[3]G[1]	NC_000008.10:g.27382625GT[4]GC[4]G[1]	NC_000008.10:g.27382625GT[4]GC[5]G[1]	NC_000008.10:g.27382625GT[5]GCG[1]	NC_000008.10:g.27382625GT[5]GC[2]G[1]	NC_000008.10:g.27382625GT[5]GC[3]G[1]	NC_000008.10:g.27382625GT[6]GCG[1]	NC_000008.10:g.27382625GT[6]GC[4]G[1]	NC_000008.10:g.27382625GT[7]GCG[1]	NC_000008.10:g.27382625GT[7]GC[3]G[1]	NC_000008.10:g.27382625GT[9]GCG[1]
EPHX2 RefSeqGene	NG_012064.1:g.38981=	NG_012064.1:g.38981_38982insTGCG	NG_012064.1:g.38981_38982insTGCGCG	NG_012064.1:g.38981_38982insTGCGCGCG	NG_012064.1:g.38981_38982insTGCGCGCGCG	NG_012064.1:g.38981_38982insTGCGCGCGCGCG	NG_012064.1:g.38981_38982insTGCGCGCGCGCGCG	NG_012064.1:g.38981GT[2]GCG[1]	NG_012064.1:g.38981GT[2]GC[2]G[1]	NG_012064.1:g.38981GT[2]GC[3]G[1]	NG_012064.1:g.38981GT[2]GC[4]G[1]	NG_012064.1:g.38981GT[2]GC[5]G[1]	NG_012064.1:g.38981GT[2]GC[6]G[1]	NG_012064.1:g.38981GT[2]GC[7]G[1]	NG_012064.1:g.38981GT[3]GCG[1]	NG_012064.1:g.38981GT[3]GC[2]G[1]	NG_012064.1:g.38981GT[3]GC[3]G[1]	NG_012064.1:g.38981GT[3]GC[4]G[1]	NG_012064.1:g.38981GT[3]GC[5]G[1]	NG_012064.1:g.38981GT[3]GC[6]G[1]	NG_012064.1:g.38981GT[4]GCG[1]	NG_012064.1:g.38981GT[4]GC[2]G[1]	NG_012064.1:g.38981GT[4]GC[3]G[1]	NG_012064.1:g.38981GT[4]GC[4]G[1]	NG_012064.1:g.38981GT[4]GC[5]G[1]	NG_012064.1:g.38981GT[5]GCG[1]	NG_012064.1:g.38981GT[5]GC[2]G[1]	NG_012064.1:g.38981GT[5]GC[3]G[1]	NG_012064.1:g.38981GT[6]GCG[1]	NG_012064.1:g.38981GT[6]GC[4]G[1]	NG_012064.1:g.38981GT[7]GCG[1]	NG_012064.1:g.38981GT[7]GC[3]G[1]	NG_012064.1:g.38981GT[9]GCG[1]
EPHX2 transcript variant 2	NM_001256482.1:c.900-254=	NM_001256482.1:c.900-254_900-253insTGCG	NM_001256482.1:c.900-254_900-253insTGCGCG	NM_001256482.1:c.900-254_900-253insTGCGCGCG	NM_001256482.1:c.900-254_900-253insTGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGCGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGCG	NM_001256482.1:c.900-254_900-253insTGTGCGCG	NM_001256482.1:c.900-254_900-253insTGTGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGCGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGCGCGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGCG	NM_001256482.1:c.900-254_900-253insTGTGTGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGCGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGCGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGTGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGTGCGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGTGTGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGTGTGCGCGCG	NM_001256482.1:c.900-254_900-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 2	NM_001256482.2:c.900-254=	NM_001256482.2:c.900-254_900-253insTGCG	NM_001256482.2:c.900-254_900-253insTGCGCG	NM_001256482.2:c.900-254_900-253insTGCGCGCG	NM_001256482.2:c.900-254_900-253insTGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGCGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGCG	NM_001256482.2:c.900-254_900-253insTGTGCGCG	NM_001256482.2:c.900-254_900-253insTGTGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGCGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGCGCGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGCG	NM_001256482.2:c.900-254_900-253insTGTGTGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGCGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGCGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGTGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGTGCGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGTGTGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGTGTGCGCGCG	NM_001256482.2:c.900-254_900-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 3	NM_001256483.1:c.861-254=	NM_001256483.1:c.861-254_861-253insTGCG	NM_001256483.1:c.861-254_861-253insTGCGCG	NM_001256483.1:c.861-254_861-253insTGCGCGCG	NM_001256483.1:c.861-254_861-253insTGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGCGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGCG	NM_001256483.1:c.861-254_861-253insTGTGCGCG	NM_001256483.1:c.861-254_861-253insTGTGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGCGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGCGCGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGCG	NM_001256483.1:c.861-254_861-253insTGTGTGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGCGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGCGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGTGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGTGCGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGTGTGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGTGTGCGCGCG	NM_001256483.1:c.861-254_861-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 3	NM_001256483.2:c.861-254=	NM_001256483.2:c.861-254_861-253insTGCG	NM_001256483.2:c.861-254_861-253insTGCGCG	NM_001256483.2:c.861-254_861-253insTGCGCGCG	NM_001256483.2:c.861-254_861-253insTGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGCGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGCG	NM_001256483.2:c.861-254_861-253insTGTGCGCG	NM_001256483.2:c.861-254_861-253insTGTGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGCGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGCGCGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGCG	NM_001256483.2:c.861-254_861-253insTGTGTGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGCGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGCGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGTGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGTGCGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGTGTGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGTGTGCGCGCG	NM_001256483.2:c.861-254_861-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 4	NM_001256484.1:c.900-254=	NM_001256484.1:c.900-254_900-253insTGCG	NM_001256484.1:c.900-254_900-253insTGCGCG	NM_001256484.1:c.900-254_900-253insTGCGCGCG	NM_001256484.1:c.900-254_900-253insTGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGCGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGCG	NM_001256484.1:c.900-254_900-253insTGTGCGCG	NM_001256484.1:c.900-254_900-253insTGTGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGCGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGCGCGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGCG	NM_001256484.1:c.900-254_900-253insTGTGTGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGCGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGCGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGTGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGTGCGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGTGTGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGTGTGCGCGCG	NM_001256484.1:c.900-254_900-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 4	NM_001256484.2:c.900-254=	NM_001256484.2:c.900-254_900-253insTGCG	NM_001256484.2:c.900-254_900-253insTGCGCG	NM_001256484.2:c.900-254_900-253insTGCGCGCG	NM_001256484.2:c.900-254_900-253insTGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGCGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGCG	NM_001256484.2:c.900-254_900-253insTGTGCGCG	NM_001256484.2:c.900-254_900-253insTGTGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGCGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGCGCGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGCG	NM_001256484.2:c.900-254_900-253insTGTGTGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGCGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGCGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGTGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGTGCGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGTGTGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGTGTGCGCGCG	NM_001256484.2:c.900-254_900-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 1	NM_001979.5:c.1059-254=	NM_001979.5:c.1059-254_1059-253insTGCG	NM_001979.5:c.1059-254_1059-253insTGCGCG	NM_001979.5:c.1059-254_1059-253insTGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGCGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGCG	NM_001979.5:c.1059-254_1059-253insTGTGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGCGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGCGCGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGCGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGCGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGTGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGTGCGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGTGTGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGTGTGCGCGCG	NM_001979.5:c.1059-254_1059-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant 1	NM_001979.6:c.1059-254=	NM_001979.6:c.1059-254_1059-253insTGCG	NM_001979.6:c.1059-254_1059-253insTGCGCG	NM_001979.6:c.1059-254_1059-253insTGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGCGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGCG	NM_001979.6:c.1059-254_1059-253insTGTGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGCGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGCGCGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGCGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGCGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGTGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGTGCGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGTGTGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGTGTGCGCGCG	NM_001979.6:c.1059-254_1059-253insTGTGTGTGTGTGTGTGTGCG
EPHX2 transcript variant X1	XM_017013199.2:c.936-254=	XM_017013199.2:c.936-254_936-253insTGCG	XM_017013199.2:c.936-254_936-253insTGCGCG	XM_017013199.2:c.936-254_936-253insTGCGCGCG	XM_017013199.2:c.936-254_936-253insTGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGCGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGCG	XM_017013199.2:c.936-254_936-253insTGTGCGCG	XM_017013199.2:c.936-254_936-253insTGTGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGCGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGCGCGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGCG	XM_017013199.2:c.936-254_936-253insTGTGTGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGCGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGCGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGTGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGTGCGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGTGTGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGTGTGCGCGCG	XM_017013199.2:c.936-254_936-253insTGTGTGTGTGTGTGTGTGCG

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#.

36 SubSNP, 34 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss82355912	Oct 12, 2018 (152)
2	MCHAISSO	ss3066194380	Jan 10, 2018 (151)
3	GNOMAD	ss4181338247	Apr 26, 2021 (155)
4	GNOMAD	ss4181338248	Apr 26, 2021 (155)
5	GNOMAD	ss4181338249	Apr 26, 2021 (155)
6	GNOMAD	ss4181338250	Apr 26, 2021 (155)
7	GNOMAD	ss4181338251	Apr 26, 2021 (155)
8	GNOMAD	ss4181338252	Apr 26, 2021 (155)
9	GNOMAD	ss4181338253	Apr 26, 2021 (155)
10	GNOMAD	ss4181338254	Apr 26, 2021 (155)
11	GNOMAD	ss4181338255	Apr 26, 2021 (155)
12	GNOMAD	ss4181338256	Apr 26, 2021 (155)
13	GNOMAD	ss4181338257	Apr 26, 2021 (155)
14	GNOMAD	ss4181338258	Apr 26, 2021 (155)
15	GNOMAD	ss4181338259	Apr 26, 2021 (155)
16	GNOMAD	ss4181338260	Apr 26, 2021 (155)
17	GNOMAD	ss4181338261	Apr 26, 2021 (155)
18	GNOMAD	ss4181338262	Apr 26, 2021 (155)
19	GNOMAD	ss4181338263	Apr 26, 2021 (155)
20	GNOMAD	ss4181338264	Apr 26, 2021 (155)
21	GNOMAD	ss4181338265	Apr 26, 2021 (155)
22	GNOMAD	ss4181338266	Apr 26, 2021 (155)
23	GNOMAD	ss4181338267	Apr 26, 2021 (155)
24	GNOMAD	ss4181338268	Apr 26, 2021 (155)
25	GNOMAD	ss4181338269	Apr 26, 2021 (155)
26	GNOMAD	ss4181338270	Apr 26, 2021 (155)
27	GNOMAD	ss4181338271	Apr 26, 2021 (155)
28	GNOMAD	ss4181338272	Apr 26, 2021 (155)
29	GNOMAD	ss4181338273	Apr 26, 2021 (155)
30	GNOMAD	ss4181338274	Apr 26, 2021 (155)
31	GNOMAD	ss4181338275	Apr 26, 2021 (155)
32	TOPMED	ss4780104785	Apr 26, 2021 (155)
33	TOPMED	ss4780104786	Apr 26, 2021 (155)
34	HUGCELL_USP	ss5473170706	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5729613202	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5729613203	Oct 16, 2022 (156)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 290898027 (NC_000008.11:27525107::GTGC 523/95354) Row 290898028 (NC_000008.11:27525107::GTGCGC 57/95402) Row 290898029 (NC_000008.11:27525107::GTGCGCGC 69/95412)...	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 63450306 (NC_000008.11:27525107::GTGC 66/28030) Row 63450307 (NC_000008.11:27525107::GTGCGCGCGCGC 50/28030)	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 63450306 (NC_000008.11:27525107::GTGC 66/28030) Row 63450307 (NC_000008.11:27525107::GTGCGCGCGCGC 50/28030)	-	Oct 16, 2022 (156)
68	TopMed Submission ignored due to conflicting rows: Row 617482345 (NC_000008.11:27525107::GTGTGTGTGCGCGCGC 1/264690) Row 617482346 (NC_000008.11:27525107::GTGTGTGTGTGTGTGCGCGC 1/264690)	-	Apr 26, 2021 (155)
69	TopMed Submission ignored due to conflicting rows: Row 617482345 (NC_000008.11:27525107::GTGTGTGTGCGCGCGC 1/264690) Row 617482346 (NC_000008.11:27525107::GTGTGTGTGTGTGTGCGCGC 1/264690)	-	Apr 26, 2021 (155)
70	ALFA	NC_000008.11 - 27525108	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
ss4181338247, ss5473170706, ss5729613202	NC_000008.11:27525107::GTGC	NC_000008.11:27525107:G:GTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGCG	NC_000008.11:27525107:G:GTGCG	(self)
ss82355912	NT_167187.1:15240771::TGCG	NC_000008.11:27525107:G:GTGCG	(self)
ss4181338248	NC_000008.11:27525107::GTGCGC	NC_000008.11:27525107:G:GTGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGCGCG	NC_000008.11:27525107:G:GTGCGCG	(self)
ss4181338249	NC_000008.11:27525107::GTGCGCGC	NC_000008.11:27525107:G:GTGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGCGCGCG	NC_000008.11:27525107:G:GTGCGCGCG	(self)
ss4181338250	NC_000008.11:27525107::GTGCGCGCGC	NC_000008.11:27525107:G:GTGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGCGCGCGCG	NC_000008.11:27525107:G:GTGCGCGCGCG	(self)
ss4181338251, ss5729613203	NC_000008.11:27525107::GTGCGCGCGCGC	NC_000008.11:27525107:G:GTGCGCGCGC… NC_000008.11:27525107:G:GTGCGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGCGCGCGC… NC_000008.11:27525107:G:GTGCGCGCGCGCG	NC_000008.11:27525107:G:GTGCGCGCGC… NC_000008.11:27525107:G:GTGCGCGCGCGCG	(self)
ss4181338252	NC_000008.11:27525107::GTGCGCGCGCG… NC_000008.11:27525107::GTGCGCGCGCGCGC	NC_000008.11:27525107:G:GTGCGCGCGC… NC_000008.11:27525107:G:GTGCGCGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGCGCGCGC… NC_000008.11:27525107:G:GTGCGCGCGCGCGCG	NC_000008.11:27525107:G:GTGCGCGCGC… NC_000008.11:27525107:G:GTGCGCGCGCGCGCG	(self)
ss4181338253	NC_000008.11:27525107::GTGTGC	NC_000008.11:27525107:G:GTGTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGCG	NC_000008.11:27525107:G:GTGTGCG	(self)
ss4181338254	NC_000008.11:27525107::GTGTGCGC	NC_000008.11:27525107:G:GTGTGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGCGCG	NC_000008.11:27525107:G:GTGTGCGCG	(self)
ss4181338255	NC_000008.11:27525107::GTGTGCGCGC	NC_000008.11:27525107:G:GTGTGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGCGCGCG	NC_000008.11:27525107:G:GTGTGCGCGCG	(self)
ss4181338256	NC_000008.11:27525107::GTGTGCGCGCGC	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCG	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCG	(self)
ss4181338257	NC_000008.11:27525107::GTGTGCGCGCG… NC_000008.11:27525107::GTGTGCGCGCGCGC	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCGCG	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCGCG	(self)
ss4181338258	NC_000008.11:27525107::GTGTGCGCGCG… NC_000008.11:27525107::GTGTGCGCGCGCGCGC	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCGCGCG	(self)
ss4181338259	NC_000008.11:27525107::GTGTGCGCGCG… NC_000008.11:27525107::GTGTGCGCGCGCGCGCGC	NC_000008.11:27525107:G:GTGTGCGCGC… NC_000008.11:27525107:G:GTGTGCGCGCGCGCGCGCG	(self)
ss3066194380, ss4181338260	NC_000008.11:27525107::GTGTGTGC	NC_000008.11:27525107:G:GTGTGTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGCG	NC_000008.11:27525107:G:GTGTGTGCG	(self)
ss4181338261	NC_000008.11:27525107::GTGTGTGCGC	NC_000008.11:27525107:G:GTGTGTGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGCGCG	NC_000008.11:27525107:G:GTGTGTGCGCG	(self)
ss4181338262	NC_000008.11:27525107::GTGTGTGCGCGC	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCG	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCG	(self)
ss4181338263	NC_000008.11:27525107::GTGTGTGCGCG… NC_000008.11:27525107::GTGTGTGCGCGCGC	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCG	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCG	(self)
ss4181338264	NC_000008.11:27525107::GTGTGTGCGCG… NC_000008.11:27525107::GTGTGTGCGCGCGCGC	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCGCG	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCGCG	(self)
ss4181338265	NC_000008.11:27525107::GTGTGTGCGCG… NC_000008.11:27525107::GTGTGTGCGCGCGCGCGC	NC_000008.11:27525107:G:GTGTGTGCGC… NC_000008.11:27525107:G:GTGTGTGCGCGCGCGCGCG	(self)
ss4181338266	NC_000008.11:27525107::GTGTGTGTGC	NC_000008.11:27525107:G:GTGTGTGTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGCG	NC_000008.11:27525107:G:GTGTGTGTGCG	(self)
ss4181338267	NC_000008.11:27525107::GTGTGTGTGCGC	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCG	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCG	(self)
ss4181338268	NC_000008.11:27525107::GTGTGTGTGCG… NC_000008.11:27525107::GTGTGTGTGCGCGC	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCG	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCG	(self)
ss4780104785	NC_000008.11:27525107::GTGTGTGTGCG… NC_000008.11:27525107::GTGTGTGTGCGCGCGC	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCGCG	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCGCG	(self)
ss4181338269	NC_000008.11:27525107::GTGTGTGTGCG… NC_000008.11:27525107::GTGTGTGTGCGCGCGCGC	NC_000008.11:27525107:G:GTGTGTGTGC… NC_000008.11:27525107:G:GTGTGTGTGCGCGCGCGCG	(self)
ss4181338270	NC_000008.11:27525107::GTGTGTGTGTGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCG	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCG	(self)
ss4181338271	NC_000008.11:27525107::GTGTGTGTGTG… NC_000008.11:27525107::GTGTGTGTGTGCGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCGCG	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCGCGCG	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGCGCGCG	(self)
ss4181338272	NC_000008.11:27525107::GTGTGTGTGTG… NC_000008.11:27525107::GTGTGTGTGTGTGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGCG	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGCG	(self)
ss4181338273	NC_000008.11:27525107::GTGTGTGTGTG… NC_000008.11:27525107::GTGTGTGTGTGTGCGCGCGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGCGCGCGCG	(self)
ss4181338274	NC_000008.11:27525107::GTGTGTGTGTG… NC_000008.11:27525107::GTGTGTGTGTGTGTGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGCG	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGCG	(self)
ss4780104786	NC_000008.11:27525107::GTGTGTGTGTG… NC_000008.11:27525107::GTGTGTGTGTGTGTGCGCGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGCGCGCG	(self)
2345757059	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGCGCGCG	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGCGCGCG	(self)
ss4181338275	NC_000008.11:27525107::GTGTGTGTGTG… NC_000008.11:27525107::GTGTGTGTGTGTGTGTGTGC	NC_000008.11:27525107:G:GTGTGTGTGT… NC_000008.11:27525107:G:GTGTGTGTGTGTGTGTGTGCG	(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 rs1491544464

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
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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

rs1491544464