Annotation Detail
Information
- Associated Genes
- TARDBP
- Associated Variants
-
TARDBP p.Gly294Ala (p.G294A)
(
ENST00000629725.2,
ENST00000649624.1,
ENST00000616545.4,
ENST00000639083.1,
ENST00000315091.7,
ENST00000700088.1,
ENST00000621790.4,
ENST00000240185.8 )
TARDBP p.Gly294Ala (p.G294A) ( ENST00000700088.1, ENST00000240185.8, ENST00000315091.7, ENST00000616545.4, ENST00000621790.4, ENST00000629725.2, ENST00000639083.1, ENST00000649624.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_007375.4(TARDBP):c.881G>C (p.Gly294Ala) AND Inborn genetic diseases
- ClinVar Allele ID
- 20269
- ClinVar RefSeq Alternation Syntax
- NM_007375.4:c.881G>C
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-02-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002371764
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs