G64D (p.Gly64Asp) variant of TNFRSF13C (Q96RJ3)
G64D (p.Gly64Asp) in TNFRSF13C (Q96RJ3) is a missense change. Clinical records from EBI and UniProt describe it as benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data.
G64D (p.Gly64Asp) variant details
- p.Gly64Asp
- 1000Genomes rs547352394
- ExAC rs547352394
- TOPMed rs547352394
- gnomAD rs547352394
- Benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.229
- REVEL 0.04
- CADD 19.80
- PolyPhen-2 0.20
- SIFT 0.01
- EBI: Benign (in dbSNP:rs547352394)
- UniProt: Benign (in dbSNP:rs547352394)
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)