S42N (p.Ser42Asn) variant of TNFRSF1A (P19438)
S42N (p.Ser42Asn) in TNFRSF1A (P19438) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
S42N (p.Ser42Asn) variant details
- p.Ser42Asn
- TOPMed rs200140274
- gnomAD rs200140274
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available