Q61H (p.Gln61His) variant of SHMT2 (P34897)
Q61H (p.Gln61His) 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.
Q61H (p.Gln61His) variant details
- p.Gln61His
- ExAC rs757010542
- TOPMed rs757010542
- gnomAD rs757010542
- Missense
- Variant Prioritization Score for Impact Estimate 0.255
- REVEL 0.06
- CADD 24.30
- PolyPhen-2 0.54
- SIFT 0.07
- Most common in the REMAINING population (allele frequency 0.00013)
- Structural context available