P37S (p.Pro37Ser) variant of MMAB (Q96EY8)
P37S (p.Pro37Ser) in MMAB (Q96EY8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
P37S (p.Pro37Ser) variant details
- p.Pro37Ser
- gnomAD rs1884735250
- Missense
- Variant Prioritization Score for Impact Estimate 0.196
- REVEL 0.18
- ESM-1b 0.00
- AlphaMissense 0.08
- CADD 15.50
- PolyPhen-2 0.01
- SIFT 0.28
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available