Y37H (p.Tyr37His) variant of ITGA6 (Integrin alpha-6)
Y37H (p.Tyr37His) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
Y37H (p.Tyr37His) variant details
- p.Tyr37His
- ExAC rs746019316
- TOPMed rs746019316
- gnomAD rs746019316
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- CADD 15.90
- PolyPhen-2 0.00
- SIFT 0.17
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available