G15V (p.Gly15Val) variant of VSIR (Q9H7M9)
G15V (p.Gly15Val) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
G15V (p.Gly15Val) variant details
- p.Gly15Val
- TOPMed rs1840733432
- gnomAD rs1840733432
- Missense
- Variant Prioritization Score for Impact Estimate 0.175
- REVEL 0.07
- CADD 19.40
- PolyPhen-2 0.10
- SIFT 0.06
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available