A21G (p.Ala21Gly) variant of ERBB2 (P04626)
A21G (p.Ala21Gly) in ERBB2 (P04626) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes structural context.
A21G (p.Ala21Gly) variant details
- p.Ala21Gly
- rs1004896536
- ClinGen CA399266765
- ClinVar RCV003846921
- TOPMed rs1004896536
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.394
- AlphaMissense 0.17
- MetaLR 0.25
- MetaSVM -0.67
- PolyPhen-2 0.52
- SIFT 0.01
- MutPred 0.35
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available