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Variants search result for Homo sapiens
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19 records found for search term Gipc2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401732698CV2708944single nucleotide variantNM_017655.6(GIPC2):c.5C>A (p.Pro2His)not specified [RCV004309911]uncertain significance17804609978046099Humanname
597759455CV3684524single nucleotide variantNM_017655.6(GIPC2):c.47C>T (p.Thr16Ile)not specified [RCV004925508]uncertain significance17804614178046141Humanname
156178781CV2229410single nucleotide variantNM_017655.6(GIPC2):c.293G>A (p.Gly98Glu)not specified [RCV004101185]uncertain significance17808072778080727Humanname
329388353CV2437332single nucleotide variantNM_017655.6(GIPC2):c.164G>A (p.Gly55Asp)not specified [RCV004256209]uncertain significance17804625878046258Humanname
405736798CV3254901single nucleotide variantNM_017655.6(GIPC2):c.236C>G (p.Ser79Trp)not specified [RCV004390719]uncertain significance17804633078046330Humanname
597706939CV3684521single nucleotide variantNM_017655.6(GIPC2):c.134A>G (p.His45Arg)not specified [RCV004917039]uncertain significance17804622878046228Humanname
156117726CV2209188single nucleotide variantNM_017655.6(GIPC2):c.755A>G (p.Asp252Gly)not specified [RCV004093392]uncertain significance17812592178125921Humanname
156059552CV2305336single nucleotide variantNM_017655.6(GIPC2):c.632G>C (p.Gly211Ala)not specified [RCV004171247]uncertain significance17811941778119417Humanname
156264725CV2329467single nucleotide variantNM_017655.6(GIPC2):c.676C>T (p.Arg226Cys)not specified [RCV004187469]uncertain significance17811946178119461Humanname
156193283CV2397977single nucleotide variantNM_017655.6(GIPC2):c.382G>C (p.Gly128Arg)not specified [RCV004241585]uncertain significance17808081678080816Humanname
401724722CV2714945single nucleotide variantNM_017655.6(GIPC2):c.749T>G (p.Ile250Ser)not specified [RCV004322270]uncertain significance17812591578125915Humanname
401880428CV2783206single nucleotide variantNM_017655.6(GIPC2):c.596A>G (p.Lys199Arg)not specified [RCV004363546]uncertain significance17809512178095121Humanname
405736808CV3254903single nucleotide variantNM_017655.6(GIPC2):c.875A>G (p.Asp292Gly)not specified [RCV004390721]uncertain significance17813567078135670Humanname
597706920CV3684518single nucleotide variantNM_017655.6(GIPC2):c.829G>A (p.Val277Ile)not specified [RCV004917037]uncertain significance17813562478135624Humanname
597759450CV3684519single nucleotide variantNM_017655.6(GIPC2):c.892G>A (p.Glu298Lys)not specified [RCV004925507]uncertain significance17813568778135687Humanname
597706930CV3684520single nucleotide variantNM_017655.6(GIPC2):c.839A>G (p.Asp280Gly)not specified [RCV004917038]uncertain significance17813563478135634Humanname
597706947CV3684522single nucleotide variantNM_017655.6(GIPC2):c.889G>T (p.Asp297Tyr)not specified [RCV004917040]uncertain significance17813568478135684Humanname
597706958CV3684523single nucleotide variantNM_017655.6(GIPC2):c.908T>A (p.Val303Asp)not specified [RCV004917041]uncertain significance17813570378135703Humanname
598251658CV3977672single nucleotide variantNM_017655.6(GIPC2):c.511G>A (p.Val171Ile)not specified [RCV005345938]uncertain significance17809503678095036Humanname