K77N (p.Lys77Asn) variant of TNFRSF13B (O14836)
K77N (p.Lys77Asn) in TNFRSF13B (O14836) is a missense change. Clinical records from EBI and UniProt describe it as likely benign.
K77N (p.Lys77Asn) variant details
- p.Lys77Asn
- 1000Genomes rs371317735
- ESP rs371317735
- ExAC rs371317735
- TOPMed rs371317735
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign