Variant #0000417720 (NC_000002.11:g.48027755T>C, NM_000179.2:c.2633T>C (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.48027755T>C
DNA change (hg38) g.47800616T>C
Published as p.Val878Ala
ISCN -
DB-ID MSH6_000772 See all 68 reported entries
Variant remarks in vitro experiments indicate that this variant has reduced function
Reference PubMed: Cyr and Heinen 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00512 View details
Owner Michael Woods
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2008-12-11 12:00:00 +01:00 (CET)
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.2633T>C r.(?) p.(Val878Ala)


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