Annotation Detail
Information
- Associated Genes
- MSH4
- Associated Variants
-
MSH4 p.Ala97Thr (p.A97T)
(
ENST00000263187.4 )
MSH4 p.Ala97Thr (p.A97T) ( ENST00000263187.4 ) - Associated Disease
- spermatogenic failure 2
- Source Database
- ClinVar
- Description
- NM_002440.4(MSH4):c.289G>A (p.Ala97Thr) AND Spermatogenic failure 2
- ClinVar Allele ID
- 2753227
- ClinVar RefSeq Alternation Syntax
- NM_002440.4:c.289G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-04-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003341585
- ClinVar Disease
- Spermatogenic failure 2
- Observed Origin Sample
- germline
Drugs