W17G (p.Trp17Gly) variant of TAFAZZIN (Q16635)
W17G (p.Trp17Gly) in TAFAZZIN (Q16635) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
W17G (p.Trp17Gly) variant details
- p.Trp17Gly
- gnomAD X-154411892-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.575
- CADD 25.90
- PolyPhen-2 0.99
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available