Variant #0000001263 (NC_000012.12:g.25245345C>T, KRAS(NM_004985.4):c.40G>A)

Individual ID 00000250
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25245345C>T
Published as V14I
Reference dbSNP, (OMIM 0012), ClinVar
DB-ID KRAS_000011
dbSNP ID rs104894365
Frequency 1/3
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.40G>A V14I r.(?) p.(Val14Ile) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000265 DNA IHC;SEQ-NG KRAS 3 Nuur Athirah Binti Mohd Daud