ClinVar Miner

List of variants in gene PTPN11 reported as likely benign

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Gene type:
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Total variants: 77
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HGVS dbSNP
NM_002834.3(PTPN11):c.*13A>G rs201957261
NM_002834.4(PTPN11):c.*1006del rs146940557
NM_002834.4(PTPN11):c.*1157_*1159ATG[14] rs80269561
NM_002834.4(PTPN11):c.*1374G>C rs139266170
NM_002834.4(PTPN11):c.*2927T>A rs190612693
NM_002834.4(PTPN11):c.*41_*46del rs886048967
NM_002834.4(PTPN11):c.*670G>A rs112287134
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.1093-9C>A rs12301915
NM_002834.4(PTPN11):c.1161C>T (p.Asn387=) rs727505180
NM_002834.4(PTPN11):c.1173C>T (p.Ser391=)
NM_002834.4(PTPN11):c.1174G>A (p.Ala392Thr) rs774356443
NM_002834.4(PTPN11):c.1191G>T (p.Thr397=) rs775571445
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.1379+20C>T rs184743462
NM_002834.4(PTPN11):c.138-4T>G rs959868124
NM_002834.4(PTPN11):c.1380-4G>T rs750640531
NM_002834.4(PTPN11):c.1404G>A (p.Thr468=) rs587781130
NM_002834.4(PTPN11):c.1404G>C (p.Thr468=) rs587781130
NM_002834.4(PTPN11):c.1448-5C>T rs554790621
NM_002834.4(PTPN11):c.1448-8C>T rs1555270633
NM_002834.4(PTPN11):c.1449T>G (p.Gly483=) rs143238917
NM_002834.4(PTPN11):c.1467C>T (p.Asp489=) rs539373294
NM_002834.4(PTPN11):c.1551G>A (p.Ala517=) rs727504377
NM_002834.4(PTPN11):c.1599+229G>A
NM_002834.4(PTPN11):c.1620C>T (p.His540=) rs587781132
NM_002834.4(PTPN11):c.162C>T (p.Ile54=) rs1207829516
NM_002834.4(PTPN11):c.1649C>T (p.Ala550Val) rs767712281
NM_002834.4(PTPN11):c.1650G>A (p.Ala550=) rs374896287
NM_002834.4(PTPN11):c.1658C>T (p.Thr553Met) rs148176616
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.1683G>A (p.Pro561=) rs397516798
NM_002834.4(PTPN11):c.1740T>C (p.Tyr580=) rs139188627
NM_002834.4(PTPN11):c.1746C>T (p.Asn582=) rs397516800
NM_002834.4(PTPN11):c.255C>T (p.His85=) rs61736914
NM_002834.4(PTPN11):c.315A>T (p.Ala105=) rs397516804
NM_002834.4(PTPN11):c.333-3T>C rs146749153
NM_002834.4(PTPN11):c.333-4T>C rs1555267812
NM_002834.4(PTPN11):c.372A>G (p.Lys124=) rs1035774225
NM_002834.4(PTPN11):c.381T>C (p.Thr127=) rs757004128
NM_002834.4(PTPN11):c.392A>G (p.Lys131Arg) rs397516805
NM_002834.4(PTPN11):c.426C>T (p.Ser142=) rs199498784
NM_002834.4(PTPN11):c.438T>C (p.Asp146=) rs1566168661
NM_002834.4(PTPN11):c.486C>T (p.Asp162=) rs397507522
NM_002834.4(PTPN11):c.48A>G (p.Ala16=) rs372736227
NM_002834.4(PTPN11):c.519C>G (p.Arg173=) rs767425313
NM_002834.4(PTPN11):c.526-11T>C rs1555267925
NM_002834.4(PTPN11):c.526-17T>C rs375184329
NM_002834.4(PTPN11):c.526-33_526-31del rs142777663
NM_002834.4(PTPN11):c.526-8C>A rs184804143
NM_002834.4(PTPN11):c.537C>T (p.Tyr179=) rs141015445
NM_002834.4(PTPN11):c.540C>T (p.Asp180=) rs753269427
NM_002834.4(PTPN11):c.556C>T (p.Arg186Trp) rs143433437
NM_002834.4(PTPN11):c.558G>T (p.Arg186=) rs200920312
NM_002834.4(PTPN11):c.624A>G (p.Thr208=) rs864622409
NM_002834.4(PTPN11):c.643-340T>C
NM_002834.4(PTPN11):c.643-6dup rs758889732
NM_002834.4(PTPN11):c.643-7C>T rs1555268066
NM_002834.4(PTPN11):c.66A>G (p.Thr22=) rs397516808
NM_002834.4(PTPN11):c.831T>C (p.Asn277=) rs876657567
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
NM_002834.4(PTPN11):c.874C>T (p.Leu292=) rs930267460
NM_002834.4(PTPN11):c.925A>G (p.Ile309Val) rs201787206
NM_002834.4(PTPN11):c.933+25T>C rs727505386
NM_002834.4(PTPN11):c.951G>A (p.Lys317=) rs576405446
NM_002834.4(PTPN11):c.990A>C (p.Thr330=) rs369739920
NM_002834.4(PTPN11):c.996C>T (p.Gly332=) rs397507533

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