M136V (p.Met136Val) variant of GNA13 (Q14344)
M136V (p.Met136Val) in GNA13 (Q14344) 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.
M136V (p.Met136Val) variant details
- p.Met136Val
- Ensembl rs1907933322
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- REVEL 0.25
- MetaLR 0.45
- MetaSVM -0.57
- CADD 16.30
- PolyPhen-2 0.11
- SIFT 0.59
- Most common in the Non-Finnish European population (allele frequency 1.3e-05)