P18T (p.Pro18Thr) variant of RAD51C (O43502)
P18T (p.Pro18Thr) in RAD51C (O43502) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P18T (p.Pro18Thr) variant details
- p.Pro18Thr
- 1000Genomes rs547142453
- ExAC rs547142453
- gnomAD rs547142453
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available