P7R (p.Pro7Arg) variant of TNFAIP3 (P21580)
P7R (p.Pro7Arg) in TNFAIP3 (P21580) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
P7R (p.Pro7Arg) variant details
- p.Pro7Arg
- Ensembl rs2114457518
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available