Annotation Detail

Information
Associated Genes
KRAS
Associated Variants
KRAS p.Lys147Glu (p.K147E) ( ENST00000557334.6, ENST00000311936.8, ENST00000693229.1, ENST00000256078.10, ENST00000688940.1, ENST00000692768.1, ENST00000685328.1 )
KRAS p.Lys147Glu (p.K147E) ( ENST00000256078.10, ENST00000311936.8, ENST00000557334.6, ENST00000685328.1, ENST00000688940.1, ENST00000692768.1, ENST00000693229.1 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_033360.4(KRAS):c.439A>G (p.Lys147Glu) AND not provided
ClinVar Allele ID
40606
ClinVar RefSeq Alternation Syntax
NM_001369787.1:c.439A>G
ClinVar RefSeq Alternation Syntax
NM_004985.5:c.439A>G
ClinVar RefSeq Alternation Syntax
NM_033360.4:c.439A>G
ClinVar RefSeq Alternation Syntax
NM_001369786.1:c.439A>G
Clinical Significance Description
Pathogenic/Likely pathogenic
Clinical Significance Last Update
2023-06-14
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000520244
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs