Q28P (p.Gln28Pro) variant of SLC6A4 (P31645)
Q28P (p.Gln28Pro) 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 0.13 / 1. The record also includes population frequency data and structural context.
Q28P (p.Gln28Pro) variant details
- p.Gln28Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.125
- REVEL 0.09
- ESM-1b 0.00
- AlphaMissense 0.08
- MetaLR 0.13
- MetaSVM -0.96
- CADD 4.63
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available