Annotation Detail
Information
- Associated Genes
- TNFRSF1A
- Associated Variants
-
TNFRSF1A p.Cys59Arg (p.C59R)
(
ENST00000540022.5,
ENST00000162749.7,
ENST00000440083.7 )
TNFRSF1A p.Cys59Arg (p.C59R) ( ENST00000162749.7, ENST00000440083.7, ENST00000540022.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001065.4(TNFRSF1A):c.175T>C (p.Cys59Arg) AND not provided
- ClinVar Allele ID
- 27376
- ClinVar RefSeq Alternation Syntax
- NM_001346092.2:c.-403T>C
- ClinVar RefSeq Alternation Syntax
- NM_001065.4:c.175T>C
- ClinVar RefSeq Alternation Syntax
- NM_001346091.2:c.-131-244T>C
- ClinVar RefSeq Alternation Syntax
- NR_144351.2:n.437T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-02-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000413303
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs