Variant #0000426343 (NC_000002.11:g.47693857G>C, NM_000251.2:c.1571G>C (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47693857G>C
DNA change (hg38) g.47466718G>C
Published as -
ISCN -
DB-ID MSH2_000563 See all 27 reported entries
Variant remarks -
Reference PubMed: Clark 1999
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Michael Woods
Database submission license No license selected
Created by Michael Woods
Date created 2005-11-17 12:00:00 +01:00 (CET)
Date last edited 2020-07-14 21:56:45 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 +?/. 10 c.1571G>C r.1571g>c p.Arg524Pro


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