Annotation Detail
Information
- Associated Genes
- SLC22A4 MIR3936HG
- Associated Variants
-
SLC22A4 p.Ile306Thr (p.I306T)
(
ENST00000200652.4 )
SLC22A4 p.Ile306Thr (p.I306T) ( ENST00000200652.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_003059.3(SLC22A4):c.917T>C (p.Ile306Thr) AND not provided
- ClinVar Allele ID
- 1258632
- ClinVar RefSeq Alternation Syntax
- NM_003059.3:c.917T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001684177
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs