S150N (p.Ser150Asn) variant of CHM (P24386)
S150N (p.Ser150Asn) in CHM (P24386) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes structural context.
S150N (p.Ser150Asn) variant details
- p.Ser150Asn
- rs1386869495
- NCI-TCGA Cosmic COSV1007
- Ensembl rs1386869495
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.471
- AlphaMissense 0.10
- MetaLR 0.51
- MetaSVM -0.46
- PolyPhen-2 0.82
- SIFT 0.04
- MutPred 0.37
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available