Variant #0000002422 (NC_000012.12:g.25227341T>G, KRAS(NM_004985.4):c.183A>C)

Individual ID 00000422
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25227341T>G
Published as -
Reference Wai Kien Yip et al.(2013)
DB-ID KRAS_000010 See all 2 reported entries
dbSNP ID rs17851045
Frequency 1/44
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
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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.183A>C Q61H r.(?) p.(Gln61His) - Pathogenic/Likely pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000443 DNA PCR KRAS 6 Nur Aisyah Athirah