List of variants in gene PTPN11 reported as likely pathogenic for bone cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.1471C>G (p.Pro491Ala)	rs397507539	0.00001
NM_002834.5(PTPN11):c.175A>G (p.Thr59Ala)	rs886043790	0.00001
NM_002834.5(PTPN11):c.1232C>T (p.Thr411Met)	rs121918467
NM_002834.5(PTPN11):c.1282G>T (p.Val428Leu)	rs397507536
NM_002834.5(PTPN11):c.1471C>A (p.Pro491Thr)	rs397507539
NM_002834.5(PTPN11):c.1472C>A (p.Pro491His)	rs397507540
NM_002834.5(PTPN11):c.1502G>A (p.Arg501Lys)	rs397507543
NM_002834.5(PTPN11):c.167T>C (p.Ile56Thr)	rs1052382672
NM_002834.5(PTPN11):c.205G>A (p.Glu69Lys)	rs397507511
NM_002834.5(PTPN11):c.209A>G (p.Lys70Arg)	rs397516801
NM_002834.5(PTPN11):c.214G>A (p.Ala72Thr)	rs121918453
NM_002834.5(PTPN11):c.2T>G (p.Met1Arg)
NM_002834.5(PTPN11):c.691C>T (p.Arg231Ter)	rs2038154558
NM_002834.5(PTPN11):c.787T>A (p.Tyr263Asn)	rs2540445590
NM_002834.5(PTPN11):c.802G>A (p.Gly268Ser)	rs397507527
NM_002834.5(PTPN11):c.853T>G (p.Phe285Val)	rs397507531

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