Annotation Detail
Information
- Associated Genes
- DRD2
- Associated Variants
-
DRD2 p.Pro319= (p.P319=)
(
ENST00000346454.7,
ENST00000362072.8,
ENST00000538967.5,
ENST00000542968.5,
ENST00000544518.5 )
DRD2 p.Pro319= (p.P319=) ( ENST00000346454.7, ENST00000362072.8, ENST00000538967.5, ENST00000542968.5, ENST00000544518.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000795.4(DRD2):c.957C>T (p.Pro319=) AND not specified
- ClinVar Allele ID
- 195597
- ClinVar RefSeq Alternation Syntax
- NM_016574.4:c.870C>T
- ClinVar RefSeq Alternation Syntax
- NM_000795.4:c.957C>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2018-03-09
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000179786
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs