Annotation Detail
Information
- Associated Genes
- AIP
- Associated Variants
-
AIP p.Gln14Ter (p.Q14*)
(
ENST00000528641.7,
ENST00000682659.1,
ENST00000684657.1,
ENST00000684006.1,
ENST00000279146.8,
ENST00000683237.1 )
AIP p.Gln14Ter (p.Q14*) ( ENST00000279146.8, ENST00000528641.7, ENST00000682659.1, ENST00000683237.1, ENST00000684006.1, ENST00000684657.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_003977.4(AIP):c.40C>T (p.Gln14Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 19925
- ClinVar RefSeq Alternation Syntax
- NM_001302960.2:c.40C>T
- ClinVar RefSeq Alternation Syntax
- NM_003977.4:c.40C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-09-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001021869
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs