M41T (p.Met41Thr) variant of CYP11B1 (P15538)
M41T (p.Met41Thr) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
M41T (p.Met41Thr) variant details
- p.Met41Thr
- rs780845350
- gnomAD 8-142875331-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.105
- CADD 3.43
- Most common in the South Asian population (allele frequency 0.00039)
- Structural context available
- Literature evidence available