H56T (p.His56Thr) variant of SPI1 (Transcription factor PU.1)
H56T (p.His56Thr) in SPI1 (Transcription factor PU.1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
H56T (p.His56Thr) variant details
- p.His56Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available