T7N (p.Thr7Asn) variant of KRT6B (Keratin, type II cytoskeletal 6B)
T7N (p.Thr7Asn) in KRT6B (Keratin, type II cytoskeletal 6B) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
T7N (p.Thr7Asn) variant details
- p.Thr7Asn
- ExAC rs759200378
- TOPMed rs759200378
- gnomAD rs759200378
- Missense
- Variant Prioritization Score for Impact Estimate 0.142
- REVEL 0.08
- CADD 14.00
- PolyPhen-2 0.00
- SIFT 0.01
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available