T39T (p.Thr39Thr) variant of ERBB3 (P21860)
T39T (p.Thr39Thr) in ERBB3 (P21860) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
T39T (p.Thr39Thr) variant details
- p.Thr39Thr
- rs749408634
- gnomAD 12-56083785-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0894
- CADD 1.23
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available
- Literature evidence available