H162R (p.His162Arg) variant of MED13L (Q71F56)
H162R (p.His162Arg) in MED13L (Q71F56) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes structural context.
H162R (p.His162Arg) variant details
- p.His162Arg
- gnomAD rs1303284486
- Missense
- Variant Prioritization Score for Impact Estimate 0.202
- ESM-1b 0.00
- AlphaMissense 0.75
- Structural context available