Variant #0000000913 (NC_000012.12:g.25245350C>A, KRAS(NM_004985.4):c.35G>T)

Individual ID 00000184
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25245350C>A
Published as G12V
Reference Wai Kien Yip et al. (2013), dbSNP, (OMIM 0006), ClinVar
DB-ID KRAS_000007 See all 6 reported entries
dbSNP ID rs121913529
Frequency 1/44
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
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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 +/. - c.35G>T G12V r.(?) p.(Gly12Val) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000199 DNA SEQ KRAS 6 Nuur Athirah Binti Mohd Daud