Variant #0000000073 (NC_000012.12:g.25245347C>G, NM_004985.4:c.38G>C (KRAS))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25245347C>G
Published as -
Reference N.A. Abdul Murad et al. (2012)dbSNP
DB-ID KRAS_000005
dbSNP ID rs112445441
Frequency -
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 07:26:39 +08:00 (CST)
Date last edited 2021-09-09 11:51:08 +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     
KRAS NM_004985.4 +/. 1 c.38G>C - r.(?) p.(Gly13Ala) - ClinVar