Annotation Detail

Information
Associated Genes
KRAS
Associated Variants
KRAS p.Gly12Ser (p.G12S) ( ENST00000685328.1, ENST00000256078.10, ENST00000311936.8, ENST00000556131.2, ENST00000557334.6, ENST00000686969.1, ENST00000688940.1, ENST00000692768.1, ENST00000693229.1 )
KRAS p.Gly12Ser (p.G12S) ( ENST00000256078.10, ENST00000311936.8, ENST00000685328.1, ENST00000686969.1, ENST00000556131.2, ENST00000557334.6, ENST00000688940.1, ENST00000692768.1, ENST00000693229.1 )
Associated Disease
Gastric cancer
Source Database
ClinVar
Description
NM_004985.5(KRAS):c.34G>A (p.Gly12Ser) AND Gastric cancer
ClinVar Allele ID
27623
ClinVar RefSeq Alternation Syntax
NM_033360.4:c.34G>A
ClinVar RefSeq Alternation Syntax
NM_001369787.1:c.34G>A
ClinVar RefSeq Alternation Syntax
NM_004985.5:c.34G>A
ClinVar RefSeq Alternation Syntax
NM_001369786.1:c.34G>A
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2007-06-15
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000013414
ClinVar Disease
Gastric cancer
Observed Origin Sample
somatic
Pubmed
7773929
Pubmed
17332249
Drugs