List of variants in gene MPL reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005373.3(MPL):c.391+5G>C	rs752453717	0.00012
NM_005373.3(MPL):c.769C>T (p.Arg257Cys)	rs121913611	0.00011
NM_005373.3(MPL):c.1609C>T (p.Arg537Trp)	rs148784027	0.00003
NM_005373.3(MPL):c.1305G>C (p.Trp435Cys)	rs1006158872	0.00001
NM_005373.3(MPL):c.317C>T (p.Pro106Leu)	rs750046020	0.00001
NM_005373.3(MPL):c.1454C>T (p.Thr485Ile)	rs974626632
NM_005373.3(MPL):c.1545G>A (p.Trp515Ter)
NM_005373.3(MPL):c.1545_1546dup (p.Gln516fs)	rs2545686090
NM_005373.3(MPL):c.1653+1del	rs755257605
NM_005373.3(MPL):c.1781T>G (p.Leu594Trp)	rs1448812001

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