Variant #0000000826 (NC_000012.12:g.25245350C>A, NM_004985.4:c.35G>T (KRAS))

Individual ID 00000172
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 Codon 12 : GGT to GTT
Reference O Zulhabri et al. (2012), dbSNP, (OMIM 0006), ClinVar
DB-ID KRAS_000007 See all 6 reported entries
dbSNP ID rs121913529
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
Date created 2020-11-22 10:24:24 +08:00 (CST)
Date last edited 2021-08-23 11:39:39 +08:00 (CST)
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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.35G>T Codon 12 : GGT to GTT r.(?) p.(Gly12Val) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000187 DNA PCR;SEQ;SSCA KRAS 2 Nuur Athirah Binti Mohd Daud