Y46D (p.Tyr46Asp) variant of ERBB3 (P21860)
Y46D (p.Tyr46Asp) in ERBB3 (P21860) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
Y46D (p.Tyr46Asp) variant details
- p.Tyr46Asp
- NCI-TCGA Cosmic COSV9991
- cosmic curated COSV99916
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.45
- MetaSVM -0.09
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available