Variant #0000002285 (NC_000012.12:g.25227349C>T, NM_004985.4:c.175G>A (KRAS))

Individual ID 00000500
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25227349C>T
Published as A59T
Reference dbSNP, (OMIM 0004), ClinVar
DB-ID KRAS_000012
dbSNP ID rs121913528
Frequency 1/10
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
Date created 2021-03-09 15:10:57 +08:00 (CST)
Date last edited 2021-08-01 13:19:22 +08:00 (CST)
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 +/. - c.175G>A A59T r.(?) p.(Ala59Thr) missense Pathogenic / Likely pathogenic​



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000546 DNA SEQ KRAS 1 Nuur Athirah Binti Mohd Daud