ClinVar Miner

List of variants in gene PTPN11 reported as uncertain significance for not provided

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Total variants: 54
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HGVS dbSNP
NM_002834.4(PTPN11):c.1004A>C (p.Gln335Pro) rs886041622
NM_002834.4(PTPN11):c.103A>C (p.Lys35Gln)
NM_002834.4(PTPN11):c.1048T>G (p.Ser350Ala) rs146571700
NM_002834.4(PTPN11):c.1052G>A (p.Arg351Gln) rs397507534
NM_002834.4(PTPN11):c.1144G>A (p.Val382Ile)
NM_002834.4(PTPN11):c.115G>A (p.Gly39Arg) rs886041585
NM_002834.4(PTPN11):c.1181A>G (p.His394Arg) rs1415532476
NM_002834.4(PTPN11):c.1190C>T (p.Thr397Met) rs767503386
NM_002834.4(PTPN11):c.1261C>T (p.Arg421Trp) rs1355732645
NM_002834.4(PTPN11):c.1262G>A (p.Arg421Gln) rs1420362815
NM_002834.4(PTPN11):c.1282G>A (p.Val428Met) rs397507536
NM_002834.4(PTPN11):c.1327C>T (p.His443Tyr) rs779236638
NM_002834.4(PTPN11):c.132C>T (p.Ser44=) rs397507502
NM_002834.4(PTPN11):c.1361C>T (p.Pro454Leu)
NM_002834.4(PTPN11):c.1379+6A>G rs746958309
NM_002834.4(PTPN11):c.1436T>C (p.Ile479Thr) rs1555270590
NM_002834.4(PTPN11):c.1449T>G (p.Gly483=) rs143238917
NM_002834.4(PTPN11):c.1468G>A (p.Val490Ile)
NM_002834.4(PTPN11):c.1569A>C (p.Glu523Asp)
NM_002834.4(PTPN11):c.1628C>T (p.Thr543Ile) rs1057520397
NM_002834.4(PTPN11):c.1661G>A (p.Ser554Asn) rs1555271397
NM_002834.4(PTPN11):c.166A>G (p.Ile56Val) rs397507504
NM_002834.4(PTPN11):c.1678C>T (p.Leu560Phe) rs397516797
NM_002834.4(PTPN11):c.1696A>T (p.Thr566Ser)
NM_002834.4(PTPN11):c.1697C>T (p.Thr566Met) rs150730493
NM_002834.4(PTPN11):c.173A>G (p.Asn58Ser) rs751437780
NM_002834.4(PTPN11):c.1740T>C (p.Tyr580=) rs139188627
NM_002834.4(PTPN11):c.175A>G (p.Thr59Ala) rs886043790
NM_002834.4(PTPN11):c.215C>T (p.Ala72Val) rs121918454
NM_002834.4(PTPN11):c.244A>G (p.Met82Val) rs397507515
NM_002834.4(PTPN11):c.289G>C (p.Glu97Gln) rs397507516
NM_002834.4(PTPN11):c.327T>G (p.Ser109=) rs1039250039
NM_002834.4(PTPN11):c.330A>C (p.Glu110Asp)
NM_002834.4(PTPN11):c.346C>A (p.His116Asn)
NM_002834.4(PTPN11):c.369G>T (p.Glu123Asp) rs755619262
NM_002834.4(PTPN11):c.440T>G (p.Phe147Cys)
NM_002834.4(PTPN11):c.455G>A (p.Arg152His) rs397507521
NM_002834.4(PTPN11):c.461G>C (p.Gly154Ala) rs376027245
NM_002834.4(PTPN11):c.48A>G (p.Ala16=) rs372736227
NM_002834.4(PTPN11):c.562G>C (p.Asp188His) rs1555267939
NM_002834.4(PTPN11):c.642G>A (p.Gln214=) rs876661383
NM_002834.4(PTPN11):c.652A>T (p.Thr218Ser) rs768555552
NM_002834.4(PTPN11):c.683G>T (p.Ser228Ile) rs748085966
NM_002834.4(PTPN11):c.701G>A (p.Ser234Asn) rs730881220
NM_002834.4(PTPN11):c.788A>G (p.Tyr263Cys)
NM_002834.4(PTPN11):c.794G>A (p.Arg265Gln) rs376607329
NM_002834.4(PTPN11):c.806A>G (p.Gln269Arg) rs794727858
NM_002834.4(PTPN11):c.868G>A (p.Val290Ile) rs1555269782
NM_002834.4(PTPN11):c.879C>G (p.His293Gln) rs117730996
NM_002834.4(PTPN11):c.893A>G (p.Asn298Ser) rs572274623
NM_002834.4(PTPN11):c.913A>G (p.Ile305Val) rs730880995
NM_002834.4(PTPN11):c.933+4A>T
NM_002834.4(PTPN11):c.990A>C (p.Thr330=) rs369739920
NM_002834.4(PTPN11):c.997T>A (p.Cys333Ser) rs730880993

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