P101S (p.Pro101Ser) variant of SLC6A3 (Q01959)
P101S (p.Pro101Ser) in SLC6A3 (Q01959) 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 0.85 / 1. The record also includes population frequency data and structural context.
P101S (p.Pro101Ser) variant details
- p.Pro101Ser
- NCI-TCGA Cosmic COSV5436
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.849
- REVEL 0.91
- MetaLR 0.85
- MetaSVM 0.95
- CADD 27.50
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 7.2e-06)
- Structural context available