Annotation Detail
Information
- Associated Genes
- MTOR
- Associated Variants
-
MTOR p.Pro2213Ser (p.P2213S)
(
ENST00000361445.9,
ENST00000703140.1 )
MTOR p.Pro2213Ser (p.P2213S) ( ENST00000361445.9, ENST00000703140.1 ) - Associated Disease
- melanoma
- Source Database
- ClinVar
- Description
- NM_004958.4(MTOR):c.6637C>T (p.Pro2213Ser) AND Melanoma
- ClinVar Allele ID
- 363237
- ClinVar RefSeq Alternation Syntax
- NM_004958.4:c.6637C>T
- Clinical Significance Description
- not provided
- Clinical Significance Last Update
- 2016-03-10
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000428626
- ClinVar Disease
- Melanoma
- Observed Origin Sample
- somatic
Drugs