Variant #0000426536 (NC_000002.11:g.47703590G>T, NM_000251.2:c.2090G>T (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47703590G>T
DNA change (hg38) g.47476451G>T
Published as C697F
ISCN -
DB-ID MSH2_001569 See all 42 reported entries
Variant remarks {GR:13}
Reference PubMed: Ollila 2006
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rolf Sijmons
Database submission license No license selected
Created by Rolf Sijmons
Date created 2009-02-06 12:00:00 +01:00 (CET)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 +/. 13 c.2090G>T r.2090g>u p.Cys697Phe


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