Annotation Detail
Information
- Associated Genes
- TNFRSF1A
- Associated Variants
-
TNFRSF1A c.625+10A>G
(
ENST00000162749.7,
ENST00000540022.5,
ENST00000440083.7 )
TNFRSF1A c.625+10A>G ( ENST00000162749.7, ENST00000440083.7, ENST00000540022.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001065.4(TNFRSF1A):c.625+10A>G AND not specified
- ClinVar Allele ID
- 45724
- ClinVar RefSeq Alternation Syntax
- NM_001346091.2:c.301+10A>G
- ClinVar RefSeq Alternation Syntax
- NM_001065.4:c.625+10A>G
- ClinVar RefSeq Alternation Syntax
- NM_001346092.2:c.166+10A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-11-12
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000244183
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs