Variant #0000061742 (NC_000012.11:g.25398284C>A, KRAS(NM_004985.3):c.35G>T)

Individual ID 00034554
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25398284C>A
DNA change (hg38) g.25245350C>A
Published as -
ISCN -
DB-ID KRAS_000002 See all 3 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 Phil Chambers
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRAS NM_004985.3 +/. 2 c.35G>T r.(?) p.(Gly12Val)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000034625 DNA SEQ-NG-I - - KRAS 1 Phil Chambers