S13N (p.Ser13Asn) variant of RNF207 (RING finger protein 207)
S13N (p.Ser13Asn) in RNF207 (RING finger protein 207) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- 1000Genomes rs201053260
- ESP rs201053260
- ExAC rs201053260
- TOPMed rs201053260
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- REVEL 0.02
- CADD 9.03
- PolyPhen-2 0.01
- SIFT 0.31
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available