Annotation Detail
Information
- Associated Genes
- AIP LOC130006206
- Associated Variants
-
AIP p.Gly47_Arg54del (p.G47_R54del)
(
ENST00000279146.8,
ENST00000684006.1,
ENST00000683237.1,
ENST00000528641.7,
ENST00000683856.1,
ENST00000684657.1,
ENST00000682659.1 )
AIP p.Gly47_Arg54del (p.G47_R54del) ( ENST00000279146.8, ENST00000528641.7, ENST00000682659.1, ENST00000683237.1, ENST00000683856.1, ENST00000684006.1, ENST00000684657.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_003977.4(AIP):c.140_163del (p.Gly47_Arg54del) AND not provided
- ClinVar Allele ID
- 49585
- ClinVar RefSeq Alternation Syntax
- NM_001302960.2:c.140_163del
- ClinVar RefSeq Alternation Syntax
- NM_003977.4:c.140_163del
- ClinVar RefSeq Alternation Syntax
- NM_001302959.2:c.-38_-15del
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-04-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001852688
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs