TINF2 and pulmonary fibrosis: In addition, we analyzed genomic DNA from two paired bone marrow (TB32-M) and peripheral blood (TB32-B) samples from one patient at Stanford Hospital with a history of chronic myelomonocytic leukemia (CMML), pulmonary fibrosis, and a newly discovered and previously unreported frameshift mutation in TIN2 (p.Gln298fs) (Supplementary Data 1).