G26W (p.Gly26Trp) variant of TAFAZZIN (Q16635)
G26W (p.Gly26Trp) in TAFAZZIN (Q16635) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
G26W (p.Gly26Trp) variant details
- p.Gly26Trp
- rs376540475
- gnomAD X-154413284-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0822
- CADD 0.22
- Most common in the Middle Eastern population (allele frequency 0.00099)
- Structural context available
- Literature evidence available