ClinVar Miner

List of variants in gene PTPN11 reported as likely benign for not provided

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Total variants: 16
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HGVS dbSNP
NM_002834.4(PTPN11):c.1011G>A (p.Thr337=) rs371951288
NM_002834.4(PTPN11):c.1023T>C (p.Phe341=) rs762516252
NM_002834.4(PTPN11):c.1173C>T (p.Ser391=)
NM_002834.4(PTPN11):c.1278C>T (p.His426=) rs886038519
NM_002834.4(PTPN11):c.132C>T (p.Ser44=) rs397507502
NM_002834.4(PTPN11):c.1599+229G>A
NM_002834.4(PTPN11):c.1649C>T (p.Ala550Val) rs767712281
NM_002834.4(PTPN11):c.1658C>T (p.Thr553Met) rs148176616
NM_002834.4(PTPN11):c.1682C>T (p.Pro561Leu) rs141140214
NM_002834.4(PTPN11):c.1740T>C (p.Tyr580=) rs139188627
NM_002834.4(PTPN11):c.392A>G (p.Lys131Arg) rs397516805
NM_002834.4(PTPN11):c.526-8C>A rs184804143
NM_002834.4(PTPN11):c.537C>T (p.Tyr179=) rs141015445
NM_002834.4(PTPN11):c.643-340T>C
NM_002834.4(PTPN11):c.854-223C>T
NM_002834.4(PTPN11):c.925A>G (p.Ile309Val) rs201787206

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