R26M (p.Arg26Met) variant of SLC34A3 (Q8N130)
R26M (p.Arg26Met) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
R26M (p.Arg26Met) variant details
- p.Arg26Met
- cosmic curated COSV63187
- Missense
- Variant Prioritization Score for Impact Estimate 0.223
- MetaLR 0.04
- MetaSVM -1.05
- CADD 12.30
- PolyPhen-2 0.14
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available