T13A (p.Thr13Ala) variant of MFN2 (Mitofusin-2)
T13A (p.Thr13Ala) in MFN2 (Mitofusin-2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
T13A (p.Thr13Ala) variant details
- p.Thr13Ala
- Ensembl rs1569802385
- Missense
- Variant Prioritization Score for Impact Estimate 0.218
- REVEL 0.22
- CADD 7.10
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available