Variant #0000000064 (NC_000002.12:g.47476361T>C, NC_000002.12(NM_000251.2):c.2006-6T>C (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.47476361T>C
Published as -
Reference MN Zahary et al.(2012)dbSNP
DB-ID MSH2_000002
dbSNP ID rs2303428
Frequency 34
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 05:06:57 +08:00 (CST)
Date last edited 2021-09-08 11:32:20 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
MSH2 NM_000251.2 -/. 12i c.2006-6T>C - r.(=) p.(=) - ClinVar