Annotation Detail
Information
- Associated Genes
- HTR2A
- Associated Variants
-
HTR2A p.Ser34= (p.S34=)
(
ENST00000542664.4,
ENST00000543956.5 )
HTR2A p.Ser34= (p.S34=) ( ENST00000542664.4, ENST00000543956.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000621.5(HTR2A):c.102C>T (p.Ser34=) AND not specified
- ClinVar Allele ID
- 504274
- ClinVar RefSeq Alternation Syntax
- NM_001378924.1:c.102C>T
- ClinVar RefSeq Alternation Syntax
- NM_000621.5:c.102C>T
- ClinVar RefSeq Alternation Syntax
- NM_001165947.5:c.-78+869C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2018-03-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000615560
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs