Variant #0000426268 (NC_000002.11:g.47656969C>T, NM_000251.2:c.1165C>T (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47656969C>T
DNA change (hg38) g.47429830C>T
Published as -
ISCN -
DB-ID MSH2_000311 See all 56 reported entries
Variant remarks ICCON data, Prince of Wales Hospital, NSW
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2016-07-07 12:00:00 +02:00 (CEST)
Date last edited 2019-02-22 10:39:02 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 +/. 7 c.1165C>T r.(?) p.(Arg389*)


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