A14T (p.Ala14Thr) variant of ERBB2 (P04626)
A14T (p.Ala14Thr) in ERBB2 (P04626) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
A14T (p.Ala14Thr) variant details
- p.Ala14Thr
- gnomAD rs1442246817
- Missense
- Variant Prioritization Score for Impact Estimate 0.358
- REVEL 0.26
- CADD 19.90
- PolyPhen-2 0.07
- SIFT 0.39
- Most common in the Non-Finnish European population (allele frequency 9.7e-07)
- Structural context available