Q27H (p.Gln27His) variant of SHMT2 (P34897)
Q27H (p.Gln27His) in SHMT2 (P34897) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
Q27H (p.Gln27His) variant details
- p.Gln27His
- TOPMed rs1165343011
- Missense
- Variant Prioritization Score for Impact Estimate 0.246
- REVEL 0.17
- CADD 21.20
- Most common in the African/African-American population (allele frequency 0.00027)
- Structural context available