Annotation Detail
Information
- Associated Genes
- GAA
- Associated Variants
-
GAA p.Ser601Trp (p.S601W)
(
ENST00000714057.1,
ENST00000714054.1,
ENST00000577106.6,
ENST00000390015.7,
ENST00000570803.6,
ENST00000714062.1,
ENST00000714058.1,
ENST00000714055.1,
ENST00000302262.8 )
GAA p.Ser601Trp (p.S601W) ( ENST00000302262.8, ENST00000390015.7, ENST00000570803.6, ENST00000577106.6, ENST00000714054.1, ENST00000714055.1, ENST00000714057.1, ENST00000714058.1, ENST00000714062.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000152.5(GAA):c.1802C>G (p.Ser601Trp) AND not provided
- ClinVar Allele ID
- 493217
- ClinVar RefSeq Alternation Syntax
- NM_000152.5:c.1802C>G
- ClinVar RefSeq Alternation Syntax
- NM_001079804.3:c.1802C>G
- ClinVar RefSeq Alternation Syntax
- NM_001079803.3:c.1802C>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2017-05-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000597451
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs