A9G (p.Ala9Gly) variant of RET (P07949)
A9G (p.Ala9Gly) in RET (P07949) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
A9G (p.Ala9Gly) variant details
- p.Ala9Gly
- cosmic curated COSV10968
- Ensembl rs2132497909
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- REVEL 0.19
- MetaLR 0.87
- MetaSVM 0.49
- CADD 13.60
- PolyPhen-2 0.00
- SIFT 0.42
- Most common in the East Asian population (allele frequency 2.8e-05)
- Structural context available