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28 records found for search term Gipr
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407456509CV3415910single nucleotide variantNM_000164.4(GIPR):c.280+273A>Cnot provided [RCV004598787]benign194567166545671665Humanname
156224601CV2229827single nucleotide variantNM_000164.4(GIPR):c.22C>G (p.Gln8Glu)not specified [RCV004105398]uncertain significance194566954245669542Humanname
156257771CV2219921single nucleotide variantNM_000164.4(GIPR):c.92C>A (p.Thr31Lys)not specified [RCV004095548]uncertain significance194567065445670654Humanname
156302869CV2319789single nucleotide variantNM_000164.4(GIPR):c.68C>G (p.Ala23Gly)not specified [RCV004187317]uncertain significance194566958845669588Humanname
329357214CV2431282single nucleotide variantNM_000164.4(GIPR):c.47G>A (p.Cys16Tyr)not specified [RCV004250615]uncertain significance194566956745669567Humanname
329398539CV2471165single nucleotide variantNM_000164.4(GIPR):c.49G>A (p.Gly17Arg)not specified [RCV004278413]uncertain significance194566956945669569Humanname
405736842CV3254908single nucleotide variantNM_000164.4(GIPR):c.34C>G (p.Arg12Gly)not specified [RCV004390726]uncertain significance194566955445669554Humanname
597706969CV3684535single nucleotide variantNM_000164.4(GIPR):c.324A>G (p.Gln108=)not specified [RCV004917042]likely benign194567289445672894Humanname
156235019CV2245395single nucleotide variantNM_000164.4(GIPR):c.101A>G (p.Glu34Gly)not specified [RCV004109186]uncertain significance194567066345670663Humanname
405736821CV3254905single nucleotide variantNM_000164.4(GIPR):c.107A>C (p.Tyr36Ser)not specified [RCV004390723]uncertain significance194567066945670669Humanname
405736834CV3254907single nucleotide variantNM_000164.4(GIPR):c.197A>T (p.Asp66Val)not specified [RCV004390725]uncertain significance194567130945671309Humanname
156118100CV2209226single nucleotide variantNM_000164.4(GIPR):c.387C>A (p.Asp129Glu)not specified [RCV004093418]uncertain significance194567407645674076Humanname
156250359CV2232165single nucleotide variantNM_000164.4(GIPR):c.856T>C (p.Cys286Arg)not specified [RCV004104970]uncertain significance194567771145677711Humanname
155916290CV2282012single nucleotide variantNM_000164.4(GIPR):c.898C>T (p.Arg300Trp)not specified [RCV004138769]uncertain significance194567775345677753Humanname
155908630CV2302475single nucleotide variantNM_000164.4(GIPR):c.782T>A (p.Leu261His)not specified [RCV004161202]uncertain significance194567709745677097Humanname
156065423CV2323708single nucleotide variantNM_000164.4(GIPR):c.331C>G (p.Leu111Val)not specified [RCV004174370]uncertain significance194567290145672901Humanname
156274706CV2334134single nucleotide variantNM_000164.4(GIPR):c.419T>C (p.Met140Thr)not specified [RCV004183647]uncertain significance194567410845674108Humanname
156308351CV2369912single nucleotide variantNM_000164.4(GIPR):c.911T>G (p.Leu304Arg)not specified [RCV004208380]uncertain significance194567776645677766Humanname
405736851CV3254909single nucleotide variantNM_000164.4(GIPR):c.913A>G (p.Met305Val)not specified [RCV004390727]uncertain significance194567776845677768Humanname
597706978CV3684536single nucleotide variantNM_000164.4(GIPR):c.754G>A (p.Glu252Lys)not specified [RCV004917043]uncertain significance194567706945677069Humanname
8628351CV83495single nucleotide variantNM_000164.2(GIPR):c.616C>T (p.Leu206Phe)Malignant melanoma [RCV000063576]not provided194567480945674809Humanname
155902579CV2274711single nucleotide variantNM_000164.4(GIPR):c.1243A>G (p.Ser415Gly)not specified [RCV004139079]uncertain significance194568177745681777Humanname
156027363CV2278426single nucleotide variantNM_000164.4(GIPR):c.1067T>C (p.Val356Ala)not specified [RCV004132880]uncertain significance194567814145678141Humanname
156201954CV2313184single nucleotide variantNM_000164.4(GIPR):c.1339T>A (p.Ser447Thr)not specified [RCV004161443]uncertain significance194568187345681873Humanname
156210451CV2378143single nucleotide variantNM_000164.4(GIPR):c.1244G>T (p.Ser415Ile)not specified [RCV004233060]uncertain significance194568177845681778Humanname
156153892CV2395029single nucleotide variantNM_000164.4(GIPR):c.1108C>A (p.Arg370Ser)not specified [RCV004236719]uncertain significance194567818245678182Humanname
401729814CV2731753single nucleotide variantNM_000164.4(GIPR):c.1210C>A (p.Arg404Ser)not specified [RCV004332242]uncertain significance194568174445681744Humanname
405736829CV3254906single nucleotide variantNM_000164.4(GIPR):c.1231C>T (p.Arg411Cys)not specified [RCV004390724]uncertain significance194568176545681765Humanname