V61M (p.Val61Met) variant of CHRNA4 (P43681)
V61M (p.Val61Met) in CHRNA4 (P43681) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Familial sleep-related hypermotor epilepsy. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and published literature.
V61M (p.Val61Met) variant details
- p.Val61Met
- rs150451372
- ClinGen CA9957953
- ClinVar RCV001928271
- ESP rs150451372
- Uncertain significance
- Familial sleep-related hypermotor epilepsy
- Missense
- Variant Prioritization Score for Impact Estimate 0.318
- REVEL 0.09
- CADD 22.80
- PolyPhen-2 0.38
- SIFT 0.03
- ClinVar: Uncertain significance (Familial sleep-related hypermotor epilepsy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the African/African-American population (allele frequency 3e-05)
- Cited in: Autosomal Dominant Sleep-Related Hypermotor (Hyperkinetic) Epilepsy. (PMID 20301348)