N11I (p.Asn11Ile) variant of SLC30A8 (Q8IWU4)
N11I (p.Asn11Ile) in SLC30A8 (Q8IWU4) 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.
N11I (p.Asn11Ile) variant details
- p.Asn11Ile
- TOPMed rs1821312496
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.17
- CADD 19.10
- PolyPhen-2 0.01
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.2e-05)
- Structural context available