P13S (p.Pro13Ser) variant of SLC34A3 (Q8N130)
P13S (p.Pro13Ser) in SLC34A3 (Q8N130) 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 0.37 / 1. The record also includes population frequency data and structural context.
P13S (p.Pro13Ser) variant details
- p.Pro13Ser
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10074
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.367
- MetaLR 0.04
- MetaSVM -0.98
- CADD 5.14
- PolyPhen-2 0.00
- SIFT 0.12
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available