M13T (p.Met13Thr) variant of DDC (P20711)
M13T (p.Met13Thr) in DDC (P20711) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
M13T (p.Met13Thr) variant details
- p.Met13Thr
- TOPMed rs2044724209
- gnomAD rs2044724209
- Missense
- Variant Prioritization Score for Impact Estimate 0.534
- REVEL 0.48
- CADD 23.30
- PolyPhen-2 0.41
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available