Variant #0000011756 (NC_000002.12:g.47643496G>C, MSH2(NM_000251.2):c.1004C>G)

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.47643496G>C
Reference -
DB-ID MSH2_000092 See all 4 reported entries
dbSNP ID rs63750602
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Guillermo Alberto-Instituto Fleming
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
MSH2 NM_000251.2 ?/? 6 c.1004C>G r.(?) p.(Thr335Ser) Hetero no -