H56N (p.His56Asn) variant of TNFRSF13B (O14836)
H56N (p.His56Asn) in TNFRSF13B (O14836) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes published literature.
H56N (p.His56Asn) variant details
- p.His56Asn
- UniProt VAR 064758
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Cited in: Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma. (PMID 21248752)