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75 records found for search term Sgip1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156090733CV2256530single nucleotide variantNM_032291.4(SGIP1):c.4A>G (p.Met2Val)not specified [RCV004118731]uncertain significance16653436266534362Humanname
405706639CV3321600single nucleotide variantNM_032291.4(SGIP1):c.22C>T (p.Arg8Cys)not specified [RCV004447874]uncertain significance16662585866625858Humanname
156331243CV2218134single nucleotide variantNM_032291.4(SGIP1):c.41G>C (p.Gly14Ala)not specified [RCV004086561]uncertain significance16662587766625877Humanname
155983048CV2239945single nucleotide variantNM_032291.4(SGIP1):c.40G>A (p.Gly14Arg)not specified [RCV004110746]uncertain significance16662587666625876Humanname
401740719CV2681508single nucleotide variantNM_032291.4(SGIP1):c.46C>T (p.Arg16Trp)not specified [RCV004292042]uncertain significance16662588266625882Humanname
405706686CV3321607single nucleotide variantNM_032291.4(SGIP1):c.89G>C (p.Arg30Thr)not specified [RCV004447881]uncertain significance16663308466633084Humanname
597673052CV3595721single nucleotide variantNM_032291.4(SGIP1):c.68A>G (p.Asp23Gly)not specified [RCV004856638]uncertain significance16662590466625904Humanname
401868490CV2767252single nucleotide variantNM_032291.4(SGIP1):c.115G>A (p.Glu39Lys)not specified [RCV004349426]uncertain significance16663595966635959Humanname
405706614CV3321596single nucleotide variantNM_032291.4(SGIP1):c.205G>A (p.Ala69Thr)not specified [RCV004447870]uncertain significance16663981066639810Humanname
407490189CV3484079single nucleotide variantNM_032291.4(SGIP1):c.149G>A (p.Arg50His)not specified [RCV004666228]uncertain significance16663599366635993Humanname
597672987CV3595713single nucleotide variantNM_032291.4(SGIP1):c.206C>T (p.Ala69Val)not specified [RCV004856630]uncertain significance16663981166639811Humanname
597673013CV3595716single nucleotide variantNM_032291.4(SGIP1):c.165A>T (p.Lys55Asn)not specified [RCV004856633]uncertain significance16663600966636009Humanname
598166848CV3921220single nucleotide variantNM_032291.4(SGIP1):c.125A>G (p.Tyr42Cys)not specified [RCV005283731]uncertain significance16663596966635969Humanname
15180460CV707498single nucleotide variantNM_032291.4(SGIP1):c.1290G>A (p.Ser430=)not provided [RCV000974159]benign16668234466682344Humanname
156142495CV2208536single nucleotide variantNM_032291.4(SGIP1):c.811C>T (p.Pro271Ser)not specified [RCV004091066]uncertain significance16667974966679749Humanname
156334288CV2230902single nucleotide variantNM_032291.4(SGIP1):c.479G>T (p.Ser160Ile)not specified [RCV004092374]uncertain significance16666753766667537Humanname
155917802CV2275068single nucleotide variantNM_032291.4(SGIP1):c.892G>T (p.Val298Leu)not specified [RCV004136887]uncertain significance16668194666681946Humanname
156107092CV2303885single nucleotide variantNM_032291.4(SGIP1):c.911T>C (p.Val304Ala)not specified [RCV004168169]uncertain significance16668196566681965Humanname
156075742CV2350900single nucleotide variantNM_032291.4(SGIP1):c.724C>T (p.Pro242Ser)not specified [RCV004211737]uncertain significance16667708166677081Humanname
156186199CV2377931single nucleotide variantNM_032291.4(SGIP1):c.476G>A (p.Arg159His)not specified [RCV004230497]uncertain significance16666753466667534Humanname
401893944CV2770141single nucleotide variantNM_032291.4(SGIP1):c.952A>G (p.Thr318Ala)not specified [RCV004356042]uncertain significance16668200666682006Humanname
401887320CV2773366single nucleotide variantNM_032291.4(SGIP1):c.733A>G (p.Thr245Ala)not specified [RCV004354016]uncertain significance16667709066677090Humanname
401898840CV2782747single nucleotide variantNM_032291.4(SGIP1):c.670T>G (p.Trp224Gly)not specified [RCV004359747]uncertain significance16667702766677027Humanname
401895178CV2789752single nucleotide variantNM_032291.4(SGIP1):c.389T>C (p.Leu130Pro)not specified [RCV004361866]uncertain significance16664364966643649Humanname
405706647CV3321601single nucleotide variantNM_032291.4(SGIP1):c.359A>G (p.Lys120Arg)not specified [RCV004447875]uncertain significance16664361966643619Humanname
405706667CV3321604single nucleotide variantNM_032291.4(SGIP1):c.505T>C (p.Ser169Pro)not specified [RCV004447878]uncertain significance16667101666671016Humanname
405706675CV3321605single nucleotide variantNM_032291.4(SGIP1):c.533G>C (p.Arg178Pro)not specified [RCV004447879]uncertain significance16667196866671968Humanname
405706681CV3321606single nucleotide variantNM_032291.4(SGIP1):c.838G>A (p.Val280Ile)not specified [RCV004447880]likely benign16668189266681892Humanname
405706695CV3321608single nucleotide variantNM_032291.4(SGIP1):c.953C>T (p.Thr318Ile)not specified [RCV004447882]uncertain significance16668200766682007Humanname
407492672CV3484080single nucleotide variantNM_032291.4(SGIP1):c.448C>G (p.Pro150Ala)not specified [RCV004667220]uncertain significance16664370866643708Humanname
407490192CV3484081single nucleotide variantNM_032291.4(SGIP1):c.650T>C (p.Leu217Pro)not specified [RCV004666229]uncertain significance16667700766677007Humanname
407490195CV3484084single nucleotide variantNM_032291.4(SGIP1):c.535T>C (p.Ser179Pro)not specified [RCV004666230]uncertain significance16667197066671970Humanname
407492684CV3484087single nucleotide variantNM_032291.4(SGIP1):c.830C>A (p.Ala277Asp)not specified [RCV004667223]uncertain significance16668188466681884Humanname
597672997CV3595714single nucleotide variantNM_032291.4(SGIP1):c.657T>A (p.Asp219Glu)not specified [RCV004856631]uncertain significance16667701466677014Humanname
597673057CV3595722single nucleotide variantNM_032291.4(SGIP1):c.766G>T (p.Val256Leu)not specified [RCV004856639]uncertain significance16667970466679704Humanname
597673065CV3595724single nucleotide variantNM_032291.4(SGIP1):c.871T>G (p.Leu291Val)not specified [RCV004856640]uncertain significance16668192566681925Humanname
598166855CV3921221single nucleotide variantNM_032291.4(SGIP1):c.500A>T (p.Asn167Ile)not specified [RCV005283732]uncertain significance16667101166671011Humanname
156235707CV2245454single nucleotide variantNM_032291.4(SGIP1):c.1115C>G (p.Ser372Trp)not specified [RCV004109234]uncertain significance16668216966682169Humanname
156364314CV2271891single nucleotide variantNM_032291.4(SGIP1):c.1699A>T (p.Thr567Ser)not specified [RCV004130984]uncertain significance16671936266719362Humanname
155917537CV2274915single nucleotide variantNM_032291.4(SGIP1):c.1448G>A (p.Arg483Lys)not specified [RCV004134978]uncertain significance16669019466690194Humanname
156255961CV2277547single nucleotide variantNM_032291.4(SGIP1):c.1003T>C (p.Ser335Pro)not specified [RCV004145235]uncertain significance16668205766682057Humanname
155929351CV2356778single nucleotide variantNM_032291.4(SGIP1):c.2266A>T (p.Ile756Phe)not specified [RCV004202121]uncertain significance16674068966740689Humanname
156385494CV2364480single nucleotide variantNM_032291.4(SGIP1):c.1602C>A (p.Asp534Glu)not specified [RCV004217350]uncertain significance16669546566695465Humanname
156307341CV2369685single nucleotide variantNM_032291.4(SGIP1):c.1199C>A (p.Pro400His)not specified [RCV004215085]uncertain significance16668225366682253Humanname
156214280CV2385907single nucleotide variantNM_032291.4(SGIP1):c.1545G>C (p.Leu515Phe)not specified [RCV004226945]uncertain significance16669029166690291Humanname
329363153CV2467142single nucleotide variantNM_032291.4(SGIP1):c.1088C>T (p.Pro363Leu)not specified [RCV004282866]uncertain significance16668214266682142Humanname
401736033CV2689240single nucleotide variantNM_032291.4(SGIP1):c.1187C>A (p.Thr396Lys)not specified [RCV004306084]uncertain significance16668224166682241Humanname
401737931CV2700826single nucleotide variantNM_032291.4(SGIP1):c.1069C>T (p.Pro357Ser)not specified [RCV004307104]uncertain significance16668212366682123Humanname
401732958CV2702309single nucleotide variantNM_032291.4(SGIP1):c.1919C>G (p.Ala640Gly)not specified [RCV004314636]uncertain significance16673376866733768Humanname
401896505CV2780874single nucleotide variantNM_032291.4(SGIP1):c.2110C>G (p.Arg704Gly)not specified [RCV004354421]uncertain significance16673941366739413Humanname
405706566CV3321590single nucleotide variantNM_032291.4(SGIP1):c.1073C>T (p.Thr358Ile)not specified [RCV004447864]uncertain significance16668212766682127Humanname
405706573CV3321591single nucleotide variantNM_032291.4(SGIP1):c.1125T>G (p.Asn375Lys)not specified [RCV004447865]uncertain significance16668217966682179Humanname
405706581CV3321592single nucleotide variantNM_032291.4(SGIP1):c.1579C>A (p.Gln527Lys)not specified [RCV004447866]uncertain significance16669544266695442Humanname
405706589CV3321593single nucleotide variantNM_032291.4(SGIP1):c.1841G>A (p.Arg614Gln)not specified [RCV004447867]uncertain significance16672936266729362Humanname
405706595CV3321594single nucleotide variantNM_032291.4(SGIP1):c.2000C>T (p.Thr667Ile)not specified [RCV004447868]uncertain significance16673384966733849Humanname
405706601CV3321595single nucleotide variantNM_032291.4(SGIP1):c.2047A>G (p.Ile683Val)not specified [RCV004447869]uncertain significance16673935066739350Humanname
405706620CV3321597single nucleotide variantNM_032291.4(SGIP1):c.2110C>T (p.Arg704Cys)not specified [RCV004447871]uncertain significance16673941366739413Humanname
405706627CV3321598single nucleotide variantNM_032291.4(SGIP1):c.2135A>T (p.Asp712Val)not specified [RCV004447872]uncertain significance16673943866739438Humanname
405707206CV3321599single nucleotide variantNM_032291.4(SGIP1):c.2275A>C (p.Ile759Leu)not specified [RCV004447873]uncertain significance16674069866740698Humanname
407492676CV3484082single nucleotide variantNM_032291.4(SGIP1):c.1456A>G (p.Ser486Gly)not specified [RCV004667221]uncertain significance16669020266690202Humanname
407492680CV3484083single nucleotide variantNM_032291.4(SGIP1):c.2144C>T (p.Thr715Met)not specified [RCV004667222]uncertain significance16673944766739447Humanname
407490199CV3484085single nucleotide variantNM_032291.4(SGIP1):c.2057C>T (p.Thr686Ile)not specified [RCV004666231]uncertain significance16673936066739360Humanname
407490202CV3484086single nucleotide variantNM_032291.4(SGIP1):c.1460C>T (p.Pro487Leu)not specified [RCV004666232]uncertain significance16669020666690206Humanname
597672978CV3595712single nucleotide variantNM_032291.4(SGIP1):c.1228A>G (p.Thr410Ala)not specified [RCV004856629]uncertain significance16668228266682282Humanname
597673006CV3595715single nucleotide variantNM_032291.4(SGIP1):c.1913A>G (p.Asn638Ser)not specified [RCV004856632]uncertain significance16673376266733762Humanname
597673479CV3595717single nucleotide variantNM_032291.4(SGIP1):c.1750G>A (p.Val584Ile)not specified [RCV004856634]uncertain significance16672927166729271Humanname
597673028CV3595718single nucleotide variantNM_032291.4(SGIP1):c.1118C>T (p.Pro373Leu)not specified [RCV004856635]uncertain significance16668217266682172Humanname
597673035CV3595719single nucleotide variantNM_032291.4(SGIP1):c.1927A>G (p.Lys643Glu)not specified [RCV004856636]uncertain significance16673377666733776Humanname
597673042CV3595720single nucleotide variantNM_032291.4(SGIP1):c.2045G>A (p.Gly682Asp)not specified [RCV004856637]uncertain significance16673934866739348Humanname
597673072CV3595725single nucleotide variantNM_032291.4(SGIP1):c.1432G>C (p.Val478Leu)not specified [RCV004856641]uncertain significance16668926466689264Humanname
598166826CV3921216single nucleotide variantNM_032291.4(SGIP1):c.1591G>A (p.Val531Ile)not specified [RCV005283727]uncertain significance16669545466695454Humanname
598166832CV3921217single nucleotide variantNM_032291.4(SGIP1):c.1301C>T (p.Pro434Leu)not specified [RCV005283728]uncertain significance16668235566682355Humanname
598166843CV3921219single nucleotide variantNM_032291.4(SGIP1):c.1229C>G (p.Thr410Ser)not specified [RCV005283730]uncertain significance16668228366682283Humanname
598198605CV3921222single nucleotide variantNM_032291.4(SGIP1):c.2258T>C (p.Leu753Ser)not specified [RCV005268271]uncertain significance16674068166740681Humanname
598198612CV3921223single nucleotide variantNM_032291.4(SGIP1):c.1734C>A (p.Asp578Glu)not specified [RCV005268272]uncertain significance16671939766719397Humanname