M79T (p.Met79Thr) variant of MMUT (P22033)
M79T (p.Met79Thr) in MMUT (P22033) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
M79T (p.Met79Thr) variant details
- p.Met79Thr
- gnomAD rs1478816235
- Missense
- Variant Prioritization Score for Impact Estimate 0.272
- REVEL 0.31
- CADD 0.33
- PolyPhen-2 0.00
- SIFT 0.49
- Most common in the South Asian population (allele frequency 7e-05)
- Structural context available