P4S (p.Pro4Ser) variant of GABRG2 (P18507)
P4S (p.Pro4Ser) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
P4S (p.Pro4Ser) variant details
- p.Pro4Ser
- rs1293602718
- gnomAD 5-162036854-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.24
- CADD 17.10
- SIFT 0.14
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available