S109N (p.Ser109Asn) variant of GRM5 (P41594)
S109N (p.Ser109Asn) in GRM5 (P41594) 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 0.53 / 1. The record also includes population frequency data.
S109N (p.Ser109Asn) variant details
- p.Ser109Asn
- NCI-TCGA Cosmic COSV1005
- NCI-TCGA Cosmic COSV5959
- cosmic curated COSV59599
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.529
- REVEL 0.37
- MetaLR 0.54
- MetaSVM 0.11
- CADD 24.80
- PolyPhen-2 0.97
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)