G146R (p.Gly146Arg) variant of SLC6A4 (P31645)
G146R (p.Gly146Arg) in SLC6A4 (P31645) 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 0.99 / 1. The record also includes structural context.
G146R (p.Gly146Arg) variant details
- p.Gly146Arg
- NCI-TCGA Cosmic COSV5556
- cosmic curated COSV55568
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.994
- ESM-1b 1.00
- AlphaMissense 0.99
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available