A12D (p.Ala12Asp) variant of CSRP3 (P50461)
A12D (p.Ala12Asp) in CSRP3 (P50461) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
A12D (p.Ala12Asp) variant details
- p.Ala12Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.86
- MetaSVM 0.81
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available