Variant #0000000822 (NC_000012.12:g.25245350C>T, NM_004985.4:c.35G>A (KRAS))

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.25245350C>T
Published as Codon 12 : GGT to GAT
Reference O Zulhabri et al. (2012), dbSNP, (OMIM 0005), ClinVar
DB-ID KRAS_000006 See all 10 reported entries
dbSNP ID rs121913529
Frequency 3/5
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 10:06:06 +08:00 (CST)
Date last edited 2021-08-23 11:38:28 +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>A Codon 12 : GGT to GAT r.(?) p.(Gly12Asp) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

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