V9G (p.Val9Gly) variant of SPTA1 (P02549)
V9G (p.Val9Gly) in SPTA1 (P02549) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data.
V9G (p.Val9Gly) variant details
- p.Val9Gly
- gnomAD rs1655099008
- Missense
- Variant Prioritization Score for Impact Estimate 0.324
- CADD 21.30
- PolyPhen-2 0.03
- SIFT 0.32
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)