P16S (p.Pro16Ser) variant of SPI1 (Transcription factor PU.1)
P16S (p.Pro16Ser) 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.
P16S (p.Pro16Ser) variant details
- p.Pro16Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available