N16S (p.Asn16Ser) variant of MYCN (N-myc proto-oncogene protein)
N16S (p.Asn16Ser) in MYCN (N-myc proto-oncogene protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
N16S (p.Asn16Ser) variant details
- p.Asn16Ser
- rs1007593827
- gnomAD 2-15940606-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.344
- CADD 19.60
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available