Annotation Detail
Information
- Associated Genes
- GBA1 LOC106627981
- Associated Variants
-
GBA1 p.Asp482Asn (p.D482N)
(
ENST00000427500.7,
ENST00000368373.8,
ENST00000428024.3,
ENST00000327247.9 )
GBA1 p.Asp482Asn (p.D482N) ( ENST00000327247.9, ENST00000368373.8, ENST00000427500.7, ENST00000428024.3 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000157.4(GBA1):c.1444G>A (p.Asp482Asn) AND not provided
- ClinVar Allele ID
- 19374
- ClinVar RefSeq Alternation Syntax
- NM_001171811.2:c.1183G>A
- ClinVar RefSeq Alternation Syntax
- NM_001005741.3:c.1444G>A
- ClinVar RefSeq Alternation Syntax
- NM_001171812.2:c.1297G>A
- ClinVar RefSeq Alternation Syntax
- NM_001005742.3:c.1444G>A
- ClinVar RefSeq Alternation Syntax
- NM_000157.4:c.1444G>A
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2023-04-01
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001582465
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs