Annotation Detail
Information
- Associated Genes
- GALT
- Associated Variants
-
GALT p.Asn314Asp (p.N314D)
(
ENST00000378842.8,
ENST00000450095.6 )
GALT p.Asn314Asp (p.N314D) ( ENST00000378842.8, ENST00000450095.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000155.4(GALT):c.940A>G (p.Asn314Asp) AND not provided
- ClinVar Allele ID
- 18652
- ClinVar RefSeq Alternation Syntax
- NM_000155.4:c.940A>G
- ClinVar RefSeq Alternation Syntax
- NM_001258332.2:c.613A>G
- Clinical Significance Description
- Conflicting interpretations of pathogenicity; other
- Clinical Significance Last Update
- 2024-04-01
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000078243
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs