Annotation Detail
Information
- Associated Genes
- HJV
- Associated Variants
-
HJV p.Cys80Gly (p.C80G)
(
ENST00000497365.5,
ENST00000634927.1,
ENST00000357836.5,
ENST00000475797.1,
ENST00000336751.11,
ENST00000636675.1 )
HJV p.Cys80Gly (p.C80G) ( ENST00000336751.11, ENST00000357836.5, ENST00000475797.1, ENST00000497365.5, ENST00000634927.1, ENST00000636675.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_213653.4(HJV):c.238T>G (p.Cys80Gly) AND not provided
- Observed Origin Sample
- germline
- ClinVar Allele ID
- 212074
- ClinVar RefSeq Alternation Syntax
- NM_202004.4:c.-22+104T>G
- ClinVar RefSeq Alternation Syntax
- NM_001316767.2:c.-22+104T>G
- ClinVar RefSeq Alternation Syntax
- NM_213653.4:c.238T>G
- ClinVar RefSeq Alternation Syntax
- NM_145277.5:c.-102T>G
- ClinVar RefSeq Alternation Syntax
- NM_213652.4:c.-21-894T>G
- ClinVar RefSeq Alternation Syntax
- NM_001379352.1:c.238T>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2015-01-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001377304
- ClinVar Disease
- not provided
Drugs