Variant #0000466828 (NC_000012.11:g.25398279C>T, KRAS(NM_004985.3):c.40G>A)

Individual ID 00226346
Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25398279C>T
DNA change (hg38) g.25245345C>T
Published as -
ISCN -
DB-ID KRAS_000032 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Lisa-Marie Niestroj
Database submission license No license selected
Created by Lisa-Marie Niestroj
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRAS NM_004985.3 +?/. - c.40G>A r.(?) p.(Val14Ile)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000227428 DNA SEQ-NG Brain tissue gene panel KRAS 1 Lisa-Marie Niestroj