Annotation Detail
Information
- Associated Genes
- CYP1B1
- Associated Variants
-
CYP1B1 p.Ala119Ser (p.A119S)
(
ENST00000490576.2,
ENST00000494864.1,
ENST00000610745.5,
ENST00000614273.1,
ENST00000714520.1 )
CYP1B1 p.Ala119Ser (p.A119S) ( ENST00000490576.2, ENST00000494864.1, ENST00000610745.5, ENST00000614273.1, ENST00000714520.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000104.4(CYP1B1):c.355G>T (p.Ala119Ser) AND not specified
- ClinVar Allele ID
- 98346
- ClinVar RefSeq Alternation Syntax
- NM_000104.4:c.355G>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2021-12-03
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000078127
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs