G86V (p.Gly86Val) variant of MTHFR (P42898)
G86V (p.Gly86Val) in MTHFR (P42898) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.76 / 1. The record also includes population frequency data and structural context.
G86V (p.Gly86Val) variant details
- p.Gly86Val
- gnomAD rs1446205816
- Missense
- Variant Prioritization Score for Impact Estimate 0.756
- REVEL 0.76
- CADD 23.30
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available