S37G (p.Ser37Gly) variant of MECOM (Q03112)
S37G (p.Ser37Gly) in MECOM (Q03112) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data.
S37G (p.Ser37Gly) variant details
- p.Ser37Gly
- gnomAD rs1732372740
- Missense
- Variant Prioritization Score for Impact Estimate 0.363
- CADD 1.46
- PolyPhen-2 0.00
- SIFT 0.51
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)