Annotation Detail
Information
- Associated Genes
- SOD1
- Associated Variants
-
SOD1 p.Asp97Asn (p.D97N)
(
ENST00000270142.11,
ENST00000389995.4 )
SOD1 p.Asp97Asn (p.D97N) ( ENST00000270142.11, ENST00000389995.4 ) - Associated Disease
- Amyotrophic lateral sclerosis 1, autosomal recessive
- Source Database
- ClinVar
- Description
- NM_000454.5(SOD1):c.289G>A (p.Asp97Asn) AND Amyotrophic lateral sclerosis 1, autosomal recessive
- ClinVar Allele ID
- 29822
- ClinVar RefSeq Alternation Syntax
- NM_000454.5:c.289G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2001-02-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000015906
- ClinVar Disease
- Amyotrophic lateral sclerosis 1, autosomal recessive
- Observed Origin Sample
- germline
- Pubmed
- 10809943
- Pubmed
- 11220750
Drugs