T56A (p.Thr56Ala) variant of VCP (P55072)
T56A (p.Thr56Ala) in VCP (P55072) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of not provided. The record also includes structural context.
T56A (p.Thr56Ala) variant details
- p.Thr56Ala
- rs2490373952
- ClinGen CA373294389
- ClinVar RCV003425656
- Likely pathogenic
- not provided
- Missense
- ClinVar: Likely pathogenic (not provided)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available