Annotation Detail
Information
- Associated Genes
- PRNP
- Associated Variants
-
PRNP p.Ala117Val (p.A117V)
(
ENST00000379440.9,
ENST00000424424.2,
ENST00000430350.2,
ENST00000457586.2 )
PRNP p.Ala117Val (p.A117V) ( ENST00000379440.9, ENST00000424424.2, ENST00000430350.2, ENST00000457586.2 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000311.5(PRNP):c.350C>T (p.Ala117Val) AND Inborn genetic diseases
- ClinVar Allele ID
- 28435
- ClinVar RefSeq Alternation Syntax
- NM_001271561.3:c.*39C>T
- ClinVar RefSeq Alternation Syntax
- NM_000311.5:c.350C>T
- ClinVar RefSeq Alternation Syntax
- NM_001080121.3:c.350C>T
- ClinVar RefSeq Alternation Syntax
- NM_001080122.3:c.350C>T
- ClinVar RefSeq Alternation Syntax
- NM_183079.4:c.350C>T
- ClinVar RefSeq Alternation Syntax
- NM_001080123.3:c.350C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2017-10-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000623716
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs