N49T (p.Asn49Thr) variant of MEF2C (Q06413)
N49T (p.Asn49Thr) in MEF2C (Q06413) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
N49T (p.Asn49Thr) variant details
- p.Asn49Thr
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10042
- NCI-TCGA Cosmic COSV6093
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available