Variant #0000000023 (NC_000002.11:g.47630397T>C, NM_000251.2:c.67T>C (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.47630397T>C
Reference -
DB-ID MSH2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00065 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 10:31:28 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 +?/+? 1 c.67T>C r.(?) p.(Phe23Leu)