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45 records found for search term Ptpn7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401884620CV2786526single nucleotide variantNM_002832.4(PTPN7):c.-7C>Anot specified [RCV004363679]uncertain significance1202159409202159409Humanname
597782864CV3585228single nucleotide variantNM_002832.4(PTPN7):c.-5T>Gnot specified [RCV004854041]uncertain significance1202159407202159407Humanname
598182021CV3904968single nucleotide variantNM_002832.4(PTPN7):c.-2G>Anot specified [RCV005265357]uncertain significance1202159404202159404Humanname
401757342CV2734958single nucleotide variantNM_002832.4(PTPN7):c.-21G>Anot specified [RCV004333665]uncertain significance1202159423202159423Humanname
598182001CV3904963single nucleotide variantNM_002832.4(PTPN7):c.-26C>Tnot specified [RCV005265352]uncertain significance1202159428202159428Humanname
156345851CV2372990single nucleotide variantNM_002832.4(PTPN7):c.-104A>Gnot specified [RCV004224022]uncertain significance1202160596202160596Humanname
405689775CV3318493single nucleotide variantNM_002832.4(PTPN7):c.-107C>Anot specified [RCV004445126]uncertain significance1202160599202160599Humanname
8624856CV79971single nucleotide variantNM_080588.2(PTPN7):c.24C>T (p.Ile8=)Malignant melanoma [RCV000060047]not provided1202159496202159496Humanname
405689779CV3318494single nucleotide variantNM_002832.4(PTPN7):c.19G>T (p.Gly7Trp)not specified [RCV004445127]uncertain significance1202159384202159384Humanname
597782872CV3585226single nucleotide variantNM_002832.4(PTPN7):c.13C>T (p.His5Tyr)not specified [RCV004854039]uncertain significance1202159390202159390Humanname
597782868CV3585227single nucleotide variantNM_002832.4(PTPN7):c.10G>T (p.Ala4Ser)not specified [RCV004854040]uncertain significance1202159393202159393Humanname
598182009CV3904965single nucleotide variantNM_002832.4(PTPN7):c.22C>T (p.Arg8Cys)not specified [RCV005265354]likely benign1202159381202159381Humanname
401720558CV2701962single nucleotide variantNM_002832.4(PTPN7):c.55G>A (p.Gly19Arg)not specified [RCV004320562]uncertain significance1202159348202159348Humanname
405689784CV3318495single nucleotide variantNM_002832.3(PTPN7):c.38G>T (p.Gly13Val)not specified [RCV004445128]uncertain significance1202160770202160770Humanname
407450649CV3468455single nucleotide variantNM_002832.3(PTPN7):c.70C>T (p.Arg24Trp)not specified [RCV004662570]uncertain significance1202160738202160738Humanname
407472747CV3468457single nucleotide variantNM_002832.4(PTPN7):c.38C>T (p.Pro13Leu)not specified [RCV004662572]likely benign1202159365202159365Humanname
598182017CV3904967single nucleotide variantNM_002832.4(PTPN7):c.28A>G (p.Arg10Gly)not specified [RCV005265356]uncertain significance1202159375202159375Humanname
156320076CV2197223single nucleotide variantNM_002832.3(PTPN7):c.115G>A (p.Gly39Ser)not specified [RCV004079007]uncertain significance1202160693202160693Humanname
401740225CV2684300single nucleotide variantNM_002832.4(PTPN7):c.172G>A (p.Val58Ile)not specified [RCV004288955]uncertain significance1202158252202158252Humanname
401856815CV2755650single nucleotide variantNM_002832.3(PTPN7):c.137C>T (p.Ala46Val)not specified [RCV004342035]uncertain significance1202160671202160671Humanname
405689789CV3318496single nucleotide variantNM_002832.4(PTPN7):c.255G>T (p.Trp85Cys)not specified [RCV004445129]uncertain significance1202158169202158169Humanname
407472739CV3468454single nucleotide variantNM_002832.4(PTPN7):c.153C>G (p.Asp51Glu)not specified [RCV004662569]uncertain significance1202158271202158271Humanname
407450934CV3468458single nucleotide variantNM_002832.3(PTPN7):c.196C>T (p.Pro66Ser)not specified [RCV004669206]uncertain significance1202160612202160612Humanname
407450654CV3468459single nucleotide variantNM_002832.3(PTPN7):c.179C>T (p.Ser60Phe)not specified [RCV004662573]uncertain significance1202160629202160629Humanname
598182005CV3904964single nucleotide variantNM_002832.3(PTPN7):c.112G>A (p.Glu38Lys)not specified [RCV005265353]uncertain significance1202160696202160696Humanname
156251583CV2286865single nucleotide variantNM_002832.4(PTPN7):c.449T>A (p.Ile150Asn)not specified [RCV004142664]uncertain significance1202155552202155552Humanname
156072418CV2335021single nucleotide variantNM_002832.4(PTPN7):c.944G>A (p.Gly315Glu)not specified [RCV004182111]uncertain significance1202150356202150356Humanname
155915237CV2339087single nucleotide variantNM_002832.4(PTPN7):c.530C>T (p.Ser177Leu)not specified [RCV004187133]uncertain significance1202154262202154262Humanname
156068179CV2341025single nucleotide variantNM_002832.4(PTPN7):c.701G>A (p.Arg234Gln)not specified [RCV004181514]uncertain significance1202153741202153741Humanname
155988002CV2354998single nucleotide variantNM_002832.4(PTPN7):c.593G>A (p.Arg198Gln)not specified [RCV004198399]uncertain significance1202154199202154199Humanname
155931686CV2362617single nucleotide variantNM_002832.4(PTPN7):c.805C>T (p.Arg269Cys)not specified [RCV004215269]uncertain significance1202152612202152612Humanname
156133711CV2383007single nucleotide variantNM_002832.4(PTPN7):c.662G>A (p.Arg221His)not specified [RCV004217592]uncertain significance1202153780202153780Humanname
155956666CV2387332single nucleotide variantNM_002832.4(PTPN7):c.647G>A (p.Gly216Glu)not specified [RCV004238416]uncertain significance1202153795202153795Humanname
155965898CV2396009single nucleotide variantNM_002832.4(PTPN7):c.861C>G (p.Ile287Met)not specified [RCV004237556]uncertain significance1202152556202152556Humanname
329353893CV2439927single nucleotide variantNM_002832.4(PTPN7):c.806G>A (p.Arg269His)not specified [RCV004257961]uncertain significance1202152611202152611Humanname
401737347CV2679289single nucleotide variantNM_002832.4(PTPN7):c.914G>A (p.Arg305Gln)not specified [RCV004285833]uncertain significance1202150386202150386Humanname
401757732CV2707938single nucleotide variantNM_002832.4(PTPN7):c.404G>A (p.Arg135His)not specified [RCV004309203]uncertain significance1202155597202155597Humanname
405689796CV3318497single nucleotide variantNM_002832.4(PTPN7):c.358G>A (p.Ala120Thr)not specified [RCV004445130]uncertain significance1202157772202157772Humanname
405689806CV3318499single nucleotide variantNM_002832.4(PTPN7):c.614T>G (p.Val205Gly)not specified [RCV004445132]uncertain significance1202153828202153828Humanname
407472751CV3468460single nucleotide variantNM_002832.4(PTPN7):c.710C>A (p.Thr237Asn)not specified [RCV004662574]uncertain significance1202153732202153732Humanname
597782880CV3585224single nucleotide variantNM_002832.4(PTPN7):c.568C>T (p.Leu190Phe)not specified [RCV004854037]uncertain significance1202154224202154224Humanname
597782876CV3585225single nucleotide variantNM_002832.4(PTPN7):c.758C>T (p.Ser253Leu)not specified [RCV004854038]uncertain significance1202152659202152659Humanname
598182013CV3904966single nucleotide variantNM_002832.4(PTPN7):c.929A>G (p.Gln310Arg)not specified [RCV005265355]uncertain significance1202150371202150371Humanname
597782860CV3585229single nucleotide variantNM_002832.4(PTPN7):c.1048T>C (p.Tyr350His)not specified [RCV004854042]uncertain significance1202148641202148641Humanname
8629231CV84376single nucleotide variantNM_001199797.1(PTPN7):c.1020C>T (p.Pro340=)Malignant melanoma [RCV000064458]not provided1202152619202152619Humanname