P17S (p.Pro17Ser) variant of MCCC2 (Q9HCC0)
P17S (p.Pro17Ser) in MCCC2 (Q9HCC0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
P17S (p.Pro17Ser) variant details
- p.Pro17Ser
- ExAC rs780891559
- TOPMed rs780891559
- gnomAD rs780891559
- Missense
- Variant Prioritization Score for Impact Estimate 0.231
- REVEL 0.26
- CADD 6.41
- PolyPhen-2 0.00
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available