S21W (p.Ser21Trp) variant of TAFAZZIN (Q16635)
S21W (p.Ser21Trp) in TAFAZZIN (Q16635) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
S21W (p.Ser21Trp) variant details
- p.Ser21Trp
- gnomAD X-154413273-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.115
- CADD 4.91
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available