Annotation Detail
Information
- Associated Genes
- NOD1
- Associated Variants
-
NOD1 p.Asp372Asn (p.D372N)
(
ENST00000222823.9 )
NOD1 p.Asp372Asn (p.D372N) ( ENST00000222823.9 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_006092.4(NOD1):c.1114G>A (p.Asp372Asn) AND not provided
- ClinVar Allele ID
- 710971
- ClinVar RefSeq Alternation Syntax
- NM_006092.4:c.1114G>A
- ClinVar RefSeq Alternation Syntax
- NM_001354849.2:c.1114G>A
- ClinVar RefSeq Alternation Syntax
- NR_149002.2:n.1644G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-01-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000970161
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs