Variant #0000000823 (NC_000012.12:g.25245347C>T, KRAS(NM_004985.4):c.38G>A)

Individual ID 00000171
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25245347C>T
Published as Codon 13 : GGC to GAC
Reference O Zulhabri et al. (2012), dbSNP, (OMIM 0003), ClinVar
DB-ID KRAS_000004 See all 7 reported entries
dbSNP ID rs112445441
Frequency 1/5
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
Options




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 Codon 13 : GGC to GAC r.(?) p.(Gly13Asp) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000186 DNA PCR;SEQ;SSCA KRAS 3 Nuur Athirah Binti Mohd Daud