List of variants in gene PTPN11 reported as benign 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002834.3(PTPN11):c.-273G>A	rs58805176	0.10884
NM_002834.5(PTPN11):c.14+25G>C	rs7972574	0.05545
NM_002834.5(PTPN11):c.854-21C>T	rs41279090	0.05308
NM_002834.5(PTPN11):c.14+54C>A	rs7973432	0.04259
NM_002834.5(PTPN11):c.1093-9C>A	rs12301915	0.04151
NM_002834.5(PTPN11):c.255C>T (p.His85=)	rs61736914	0.02271
NM_002834.5(PTPN11):c.525+12G>C	rs41304351	0.01035
NM_002834.5(PTPN11):c.1379+20C>T	rs184743462	0.00047
NM_002834.5(PTPN11):c.558G>T (p.Arg186=)	rs200920312	0.00011
NM_002834.5(PTPN11):c.486C>T (p.Asp162=)	rs397507522	0.00009
NM_002834.5(PTPN11):c.990A>C (p.Thr330=)	rs369739920	0.00005
NM_002834.5(PTPN11):c.996C>T (p.Gly332=)	rs397507533	0.00001
NM_002834.5(PTPN11):c.1052G>A (p.Arg351Gln)	rs397507534
NM_002834.5(PTPN11):c.1221A>G (p.Gly407=)	rs532529560

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