T16N (p.Thr16Asn) variant of ABCA3 (Q99758)
T16N (p.Thr16Asn) in ABCA3 (Q99758) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T16N (p.Thr16Asn) variant details
- p.Thr16Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available