Annotation Detail
Information
- Associated Genes
- TARDBP
- Associated Variants
-
TARDBP p.Asn390Ser (p.N390S)
(
ENST00000240185.8,
ENST00000700088.1,
ENST00000621790.4,
ENST00000315091.7,
ENST00000639083.1,
ENST00000616545.4,
ENST00000649624.1,
ENST00000629725.2 )
TARDBP p.Asn390Ser (p.N390S) ( ENST00000700088.1, ENST00000240185.8, ENST00000315091.7, ENST00000616545.4, ENST00000621790.4, ENST00000629725.2, ENST00000639083.1, ENST00000649624.1 ) - Associated Disease
- amyotrophic lateral sclerosis type 10 TARDBP-related frontotemporal dementia
- Source Database
- ClinVar
- Description
- NM_007375.4(TARDBP):c.1169A>G (p.Asn390Ser) AND multiple conditions
- ClinVar Allele ID
- 34330
- ClinVar RefSeq Alternation Syntax
- NM_007375.4:c.1169A>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-07-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001861034
- ClinVar Disease
- TARDBP-related frontotemporal dementia
- ClinVar Disease
- Amyotrophic lateral sclerosis type 10
- Observed Origin Sample
- germline
Drugs