M69T (p.Met69Thr) variant of CDKN1C (P49918)
M69T (p.Met69Thr) in CDKN1C (P49918) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
M69T (p.Met69Thr) variant details
- p.Met69Thr
- gnomAD 11-2884085-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.111
- CADD 4.29
- Population evidence available
- Structural context available
- Literature evidence available