Variant #0000417707 (NC_000002.11:g.48026308C>G, NM_000179.2:c.1186C>G (MSH6))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.48026308C>G
DNA change (hg38) g.47799169C>G
Published as L396V
ISCN -
DB-ID MSH6_000118 See all 34 reported entries
Variant remarks mutation rate in MSH6 deficient strain shows functional protein (no details presented)
Reference PubMed: Kolodner 1999
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00551 View details
Owner Rolf Sijmons
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2009-04-24 17:16:00 +02:00 (CEST)
Date last edited 2020-07-14 21:54:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 ?/. 4 c.1186C>G r.1186c>g p.Leu396Val


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