P35S (p.Pro35Ser) variant of GABRG2 (P18507)
P35S (p.Pro35Ser) in GABRG2 (P18507) 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 0.58 / 1. The record also includes population frequency data and structural context.
P35S (p.Pro35Ser) variant details
- p.Pro35Ser
- rs747649928
- NCI-TCGA Cosmic COSV6271
- cosmic curated COSV62717
- NCI-TCGA Cosmic COSV9905
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.585
- CADD 18.10
- PolyPhen-2 0.00
- SIFT 0.25
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available