Variant #0000417695 (NC_000002.11:g.48018236G>T, NM_000179.2:c.431G>T (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.48018236G>T
DNA change (hg38) g.47791097G>T
Published as p.Ser144Ile
ISCN -
DB-ID MSH6_000923 See all 37 reported entries
Variant remarks in vitro experiments indicate variant has defective ATP hydrolysis and the N-terminal fragment binds to DNA normally.
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) 0.00097 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 2008-12-10 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 ?/. 2 c.431G>T r.(?) p.(Ser144Ile)


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