A13T (p.Ala13Thr) variant of RAC1 (P63000)
A13T (p.Ala13Thr) in RAC1 (P63000) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A13T (p.Ala13Thr) variant details
- p.Ala13Thr
- NCI-TCGA Cosmic COSV6182
- cosmic curated COSV61822
- Ensembl rs2115193010
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available