M17T (p.Met17Thr) variant of SLC37A4 (O43826)
M17T (p.Met17Thr) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
M17T (p.Met17Thr) variant details
- p.Met17Thr
- gnomAD rs1197611962
- Missense
- Variant Prioritization Score for Impact Estimate 0.643
- CADD 26.30
- PolyPhen-2 0.96
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available