Primary myelofibrosis with concurrent CALR and MPL mutations: A case report

Table 1 Gene mutation list in the primary myelofibrosis patient

Gene	VAF	HGVS	Exonic function
CALR	30.04%	NM_004343: c.1092_1143del (p.364fs)	Frameshift deletion
MPL	50.11%	NM_005373: c.1908A>G (p.X636W)	Nonsynonymous SNV
PIK3R1	3.18%	NM_00181523: c.683delG (p.R228fs)	Frameshift deletion

VAF: Variant allele frequency; HGVS: Human Genome Variation Society; SNV: Single nucleotide variant.