M16R (p.Met16Arg) variant of CDKN1B (P46527)
M16R (p.Met16Arg) in CDKN1B (P46527) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
M16R (p.Met16Arg) variant details
- p.Met16Arg
- TOPMed rs1411029555
- gnomAD rs1411029555
- Missense
- Variant Prioritization Score for Impact Estimate 0.384
- REVEL 0.46
- CADD 23.10
- PolyPhen-2 0.00
- SIFT 0.04
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available