Annotation Detail

Information
Associated Genes
HRAS LRRC56
Associated Variants
HRAS p.Gly12Val (p.G12V) ( ENST00000397594.7, ENST00000311189.8, ENST00000397596.6, ENST00000417302.7, ENST00000451590.5 )
HRAS p.Gly12Val (p.G12V) ( ENST00000311189.8, ENST00000397594.7, ENST00000397596.6, ENST00000417302.7, ENST00000451590.5 )
Associated Disease
Malignant tumor of urinary bladder
Source Database
ClinVar
Description
NM_005343.4(HRAS):c.35G>T (p.Gly12Val) AND Malignant tumor of urinary bladder
ClinVar Allele ID
27639
ClinVar RefSeq Alternation Syntax
NM_001318054.2:c.-285G>T
ClinVar RefSeq Alternation Syntax
NM_005343.4:c.35G>T
ClinVar RefSeq Alternation Syntax
NM_176795.5:c.35G>T
ClinVar RefSeq Alternation Syntax
NM_001130442.3:c.35G>T
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2012-04-01
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000013431
ClinVar Disease
Malignant tumor of urinary bladder
Observed Origin Sample
somatic
Pubmed
22499344
Pubmed
6092966
Pubmed
16170316
Pubmed
2999610
Pubmed
7177195
Pubmed
6330729
Pubmed
3537694
Pubmed
17412879
Pubmed
8960317
Drugs