S6F (p.Ser6Phe) variant of SMARCE1 (Q969G3)
S6F (p.Ser6Phe) in SMARCE1 (Q969G3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
S6F (p.Ser6Phe) variant details
- p.Ser6Phe
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10079
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- SMARCE1 High mobility group box domain domainome 1.0: score -0.953