V13F (p.Val13Phe) variant of SOCS1 (O15524)
V13F (p.Val13Phe) in SOCS1 (O15524) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
V13F (p.Val13Phe) variant details
- p.Val13Phe
- ExAC rs200748141
- TOPMed rs200748141
- gnomAD rs200748141
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- REVEL 0.04
- CADD 23.00
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the Latino/Admixed American population (allele frequency 0.00011)
- Structural context available