Annotation Detail
Information
- Associated Genes
- TIRAP
- Associated Variants
-
TIRAP c.-92-11A>G
(
ENST00000392678.7,
ENST00000700489.1,
ENST00000392680.6,
ENST00000392679.6,
ENST00000700488.1,
ENST00000700491.1,
ENST00000700492.1,
ENST00000700495.1,
ENST00000700490.1 )
TIRAP c.-92-11A>G ( ENST00000392678.7, ENST00000392679.6, ENST00000392680.6, ENST00000700488.1, ENST00000700489.1, ENST00000700490.1, ENST00000700491.1, ENST00000700492.1, ENST00000700495.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001318777.2(TIRAP):c.-92-11A>G AND not specified
- ClinVar Allele ID
- 2849536
- ClinVar RefSeq Alternation Syntax
- NM_001318777.2:c.-92-11A>G
- ClinVar RefSeq Alternation Syntax
- NM_148910.3:c.-92-11A>G
- ClinVar RefSeq Alternation Syntax
- NM_001318776.2:c.-92-11A>G
- ClinVar RefSeq Alternation Syntax
- NM_001039661.2:c.-92-11A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003490393
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs