Variant #0000000072 (NC_000012.12:g.25245347C>T, KRAS(NM_004985.4):c.38G>A)

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>T
Published as -
Reference N.A. Abdul Murad et al. (2012)dbSNP
DB-ID KRAS_000004 See all 7 reported entries
dbSNP ID rs112445441
Frequency 76
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
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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>A - r.(?) p.(Gly13Asp) - ClinVar