S49N (p.Ser49Asn) variant of TNFRSF13C (Q96RJ3)
S49N (p.Ser49Asn) in TNFRSF13C (Q96RJ3) 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.
S49N (p.Ser49Asn) variant details
- p.Ser49Asn
- gnomAD rs1167478636
- Missense
- Variant Prioritization Score for Impact Estimate 0.268
- REVEL 0.06
- CADD 21.80
- PolyPhen-2 0.04
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)