D19A (p.Asp19Ala) variant of TERF2 (Q15554)
D19A (p.Asp19Ala) in TERF2 (Q15554) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes experimental measurements and structural context.
D19A (p.Asp19Ala) variant details
- p.Asp19Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available
- TERF2 SANT/Myb domain domainome 1.0: score -0.557