ClinVar Miner

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

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Total variants: 29
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HGVS dbSNP
NM_002834.4(PTPN11):c.1093A>C (p.Ser365Arg) rs1566183223
NM_002834.4(PTPN11):c.1124A>G (p.Tyr375Cys) rs41299183
NM_002834.4(PTPN11):c.1162G>A (p.Val388Ile) rs749523268
NM_002834.4(PTPN11):c.119A>G (p.Asp40Gly) rs397516795
NM_002834.4(PTPN11):c.1225-7A>G rs727504397
NM_002834.4(PTPN11):c.1226G>C (p.Gly409Ala) rs201247699
NM_002834.4(PTPN11):c.1366G>A (p.Val456Met) rs397516796
NM_002834.4(PTPN11):c.1374C>A (p.His458Gln) rs727504393
NM_002834.4(PTPN11):c.1382C>G (p.Ala461Gly) rs397509344
NM_002834.4(PTPN11):c.1495T>A (p.Ser499Thr) rs1566186813
NM_002834.4(PTPN11):c.1594G>A (p.Glu532Lys) rs587778634
NM_002834.4(PTPN11):c.1642T>C (p.Ser548Pro) rs1057517907
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.1713-5T>A rs876657964
NM_002834.4(PTPN11):c.1724A>G (p.Asp575Gly) rs397516799
NM_002834.4(PTPN11):c.173A>G (p.Asn58Ser) rs751437780
NM_002834.4(PTPN11):c.272A>G (p.Lys91Arg) rs869312744
NM_002834.4(PTPN11):c.333-3T>C rs146749153
NM_002834.4(PTPN11):c.348T>A (p.His116Gln) rs1482410266
NM_002834.4(PTPN11):c.392A>G (p.Lys131Arg) rs397516805
NM_002834.4(PTPN11):c.556C>T (p.Arg186Trp) rs143433437
NM_002834.4(PTPN11):c.562G>A (p.Asp188Asn) rs1555267939
NM_002834.4(PTPN11):c.642G>A (p.Gln214=) rs876661383
NM_002834.4(PTPN11):c.652A>G (p.Thr218Ala) rs768555552
NM_002834.4(PTPN11):c.661A>T (p.Ile221Leu) rs397516806
NM_002834.4(PTPN11):c.827A>G (p.Lys276Arg) rs777603059
NM_002834.4(PTPN11):c.858T>A (p.Asp286Glu) rs397516811
NM_002834.4(PTPN11):c.931A>G (p.Met311Val) rs774939392

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