P690: IDENTIFICATION OF CLINICALLY RELEVANT VARIANT-LEVEL SEX-BIAS IN SF3B1 K700/K666 AND IDH2 R140/R172

Eitemau Tebyg

• P690: IDENTIFICATION OF CLINICALLY RELEVANT VARIANT-LEVEL SEX-BIAS IN SF3B1 K700/K666 AND IDH2 R140/R172
  gan: Maki Sakuma, et al.
  Cyhoeddwyd: (2023-08-01)
• Dual somatic UBA1 Met41 variants with distinct allele frequencies in VEXAS syndrome
  gan: Guiset Carvajal Bedoya, et al.
  Cyhoeddwyd: (2026-09-01)
• Detection of <I>ABL1</I> kinase domain mutations in therapy-naïve <I>BCR-ABL1</I>-positive acute lymphoblastic leukemia
  gan: Constance Baer, et al.
  Cyhoeddwyd: (2021-11-01)
• P554: A case series of 17 patients with VEXAS syndrome due to UBA1 Met41 variants
  gan: Alicia Scocchia, et al.
  Cyhoeddwyd: (2023-01-01)
• “Somatic” and “pathogenic” - is the classification strategy applicable in times of large-scale sequencing?
  gan: Constance Baer, et al.
  Cyhoeddwyd: (2019-08-01)