R10G (p.Arg10Gly) variant of NSD1 (Q96L73)
R10G (p.Arg10Gly) in NSD1 (Q96L73) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
R10G (p.Arg10Gly) variant details
- p.Arg10Gly
- rs1353809467
- gnomAD 5-177136873-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.11
- CADD 4.27
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available
- Literature evidence available