M56I (p.Met56Ile) variant of SHMT2 (P34897)
M56I (p.Met56Ile) in SHMT2 (P34897) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
M56I (p.Met56Ile) variant details
- p.Met56Ile
- gnomAD rs1162516961
- Missense
- Variant Prioritization Score for Impact Estimate 0.266
- REVEL 0.09
- CADD 21.00
- PolyPhen-2 0.00
- SIFT 0.63
- Most common in the Non-Finnish European population (allele frequency 0.00024)
- Structural context available