Genomic variant #0000061744

Individual ID 00034556
Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.25380276T>A
DNA change (hg38) g.25227342T>A
Published as -
ISCN -
DB-ID KRAS_000004
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 1268 View details
Owner Phil Chambers
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
KRAS NM_004985.3 +?/. 3 c.182A>T - r.(?) p.(Gln61Leu)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000034627 DNA SEQ-NG-I - - KRAS 1 Phil Chambers