ClinVar Miner

List of variants in gene PTPN11 reported as likely benign by GeneDx

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Total variants: 29
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HGVS dbSNP
NM_002834.4(PTPN11):c.*41_*46del rs886048967
NM_002834.4(PTPN11):c.-13G>A rs760374212
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.1047C>T (p.Asn349=) rs1222504763
NM_002834.4(PTPN11):c.1173C>T (p.Ser391=)
NM_002834.4(PTPN11):c.1224+15G>A rs373271861
NM_002834.4(PTPN11):c.1278C>T (p.His426=) rs886038519
NM_002834.4(PTPN11):c.1281C>T (p.Gly427=) rs753173299
NM_002834.4(PTPN11):c.132C>T (p.Ser44=) rs397507502
NM_002834.4(PTPN11):c.137+49A>T rs761259292
NM_002834.4(PTPN11):c.138-4T>G rs959868124
NM_002834.4(PTPN11):c.1448-8C>T rs1555270633
NM_002834.4(PTPN11):c.1467C>T (p.Asp489=) rs539373294
NM_002834.4(PTPN11):c.1599+229G>A
NM_002834.4(PTPN11):c.1649C>T (p.Ala550Val) rs767712281
NM_002834.4(PTPN11):c.1678C>T (p.Leu560Phe) rs397516797
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.333-4T>C rs1555267812
NM_002834.4(PTPN11):c.372A>G (p.Lys124=) rs1035774225
NM_002834.4(PTPN11):c.392A>G (p.Lys131Arg) rs397516805
NM_002834.4(PTPN11):c.526-11T>C rs1555267925
NM_002834.4(PTPN11):c.537C>T (p.Tyr179=) rs141015445
NM_002834.4(PTPN11):c.643-340T>C
NM_002834.4(PTPN11):c.66A>G (p.Thr22=) rs397516808
NM_002834.4(PTPN11):c.853+17C>T rs746692191
NM_002834.4(PTPN11):c.854-19T>G rs751780145
NM_002834.4(PTPN11):c.854-223C>T

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