C37W (p.Cys37Trp) variant of GNA13 (Q14344)
C37W (p.Cys37Trp) in GNA13 (Q14344) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
C37W (p.Cys37Trp) variant details
- p.Cys37Trp
- NCI-TCGA Cosmic COSV7147
- gnomAD rs1431023781
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.