Variant #0000071912 (NC_000012.11:g.25398285C>T, KRAS(NM_004985.3):c.34G>A)

Individual ID 00043992
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.25398285C>T
DNA change (hg38) g.25245351C>T
Published as -
ISCN -
DB-ID KRAS_000012 See all 2 reported entries
Variant remarks -
Reference PubMed: Joyce 2016
ClinVar ID -
dbSNP ID rs121913530
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Pia Ostergaard
Database submission license No license selected
Created by Pia Ostergaard
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRAS NM_004985.3 +?/. 1 c.34G>A r.(?) p.(Gly12Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000044098 DNA SEQ blood - KRAS 1 Pia Ostergaard