R29G (p.Arg29Gly) variant of ANKRD1 (Q15327)
R29G (p.Arg29Gly) in ANKRD1 (Q15327) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
R29G (p.Arg29Gly) variant details
- p.Arg29Gly
- ExAC rs766683591
- gnomAD rs766683591
- Missense
- Variant Prioritization Score for Impact Estimate 0.219
- REVEL 0.14
- CADD 22.90
- PolyPhen-2 0.01
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available