S76T (p.Ser76Thr) variant of KRT6B (Keratin, type II cytoskeletal 6B)
S76T (p.Ser76Thr) in KRT6B (Keratin, type II cytoskeletal 6B) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
S76T (p.Ser76Thr) variant details
- p.Ser76Thr
- gnomAD rs1305904902
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.05
- CADD 21.00
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available