Annotation Detail
Information
- Associated Genes
- DSP
- Associated Variants
-
DSP p.Tyr494Phe (p.Y494F)
(
ENST00000379802.8,
ENST00000418664.3,
ENST00000710359.2,
ENST00000713904.1,
ENST00000713909.1 )
DSP p.Tyr494Phe (p.Y494F) ( ENST00000379802.8, ENST00000418664.3, ENST00000710359.2, ENST00000713904.1, ENST00000713909.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe) AND not specified
- ClinVar Allele ID
- 54027
- ClinVar RefSeq Alternation Syntax
- NM_001319034.2:c.1481A>T
- ClinVar RefSeq Alternation Syntax
- NM_004415.4:c.1481A>T
- ClinVar RefSeq Alternation Syntax
- NM_001008844.3:c.1481A>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2017-04-26
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000037993
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs