Annotation Detail
Information
- Associated Genes
- FUS
- Associated Variants
-
FUS p.Arg495Ter (p.R495*)
(
ENST00000254108.12,
ENST00000715542.1,
ENST00000568685.1,
ENST00000380244.8 )
FUS p.Arg495Ter (p.R495*) ( ENST00000254108.12, ENST00000380244.8, ENST00000568685.1, ENST00000715542.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004960.4(FUS):c.1483C>T (p.Arg495Ter) AND not provided
- ClinVar Allele ID
- 38662
- ClinVar RefSeq Alternation Syntax
- NM_001170937.1:c.1471C>T
- ClinVar RefSeq Alternation Syntax
- NR_028388.2:n.1553C>T
- ClinVar RefSeq Alternation Syntax
- NM_001170634.1:c.1480C>T
- ClinVar RefSeq Alternation Syntax
- NM_004960.4:c.1483C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-04-05
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002247377
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs