A17G (p.Ala17Gly) variant of ERBB4 (Q15303)
A17G (p.Ala17Gly) in ERBB4 (Q15303) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes variant effect predictions and structural context.
A17G (p.Ala17Gly) variant details
- p.Ala17Gly
- cosmic curated COSV53545
- ExAC rs201202926
- TOPMed rs201202926
- gnomAD rs201202926
- Likely benign
- Missense
- MetaLR 0.07
- MetaSVM -1.03
- SIFT 0.31
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available