N41D (p.Asn41Asp) variant of SOS1 (Son of sevenless homolog 1)
N41D (p.Asn41Asp) in SOS1 (Son of sevenless homolog 1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
N41D (p.Asn41Asp) variant details
- p.Asn41Asp
- cosmic curated COSV67673
- Missense
- Variant Prioritization Score for Impact Estimate 0.358
- REVEL 0.20
- CADD 20.40
- PolyPhen-2 0.00
- SIFT 0.53
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available