Annotation Detail
Information
- Associated Genes
- NTRK1
- Associated Variants
-
NTRK1 p.Gly613Val (p.G613V)
(
ENST00000392302.7,
ENST00000368196.7,
ENST00000358660.3,
ENST00000524377.7,
ENST00000674537.2 )
NTRK1 p.Gly613Val (p.G613V) ( ENST00000358660.3, ENST00000368196.7, ENST00000392302.7, ENST00000524377.7, ENST00000674537.2 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_002529.4(NTRK1):c.1838G>T (p.Gly613Val) AND not specified
- ClinVar Allele ID
- 27347
- ClinVar RefSeq Alternation Syntax
- NM_001007792.1:c.1730G>T
- ClinVar RefSeq Alternation Syntax
- NM_001012331.2:c.1820G>T
- ClinVar RefSeq Alternation Syntax
- NM_002529.4:c.1838G>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2021-12-10
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000127263
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs