Annotation Detail
Information
- Associated Genes
- TNFRSF1A
- Associated Variants
-
TNFRSF1A p.Thr79Met (p.T79M)
(
ENST00000162749.7,
ENST00000540022.5,
ENST00000440083.7 )
TNFRSF1A p.Thr79Met (p.T79M) ( ENST00000162749.7, ENST00000440083.7, ENST00000540022.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001065.4(TNFRSF1A):c.236C>T (p.Thr79Met) AND not provided
- ClinVar Allele ID
- 27375
- ClinVar RefSeq Alternation Syntax
- NM_001065.4:c.236C>T
- ClinVar RefSeq Alternation Syntax
- NR_144351.2:n.498C>T
- ClinVar RefSeq Alternation Syntax
- NM_001346091.2:c.-89C>T
- ClinVar RefSeq Alternation Syntax
- NM_001346092.2:c.-342C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-01-03
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000414218
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs