T38M (p.Thr38Met) variant of MCL1 (Q07820)
T38M (p.Thr38Met) in MCL1 (Q07820) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
T38M (p.Thr38Met) variant details
- p.Thr38Met
- TOPMed rs1168893169
- gnomAD rs1168893169
- Missense
- Variant Prioritization Score for Impact Estimate 0.148
- REVEL 0.06
- CADD 14.20
- PolyPhen-2 0.00
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available