T13T (p.Thr13Thr) variant of MFN2 (Mitofusin-2)
T13T (p.Thr13Thr) in MFN2 (Mitofusin-2) is a synonymous 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.
T13T (p.Thr13Thr) variant details
- p.Thr13Thr
- rs755024220
- gnomAD 1-11989207-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.122
- CADD 5.88
- Most common in the Ashkenazi Jewish population (allele frequency 7.7e-05)
- Structural context available
- Literature evidence available