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28 records found for search term Gmcl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15178270CV777305single nucleotide variantNM_178439.5(GMCL1):c.758+10T>Cnot provided [RCV000951239]benign26984420669844206Humanname
405755249CV3261945single nucleotide variantNM_178439.5(GMCL1):c.38G>A (p.Arg13Lys)not specified [RCV004393354]uncertain significance26982993069829930Humanname
597788329CV3678086single nucleotide variantNM_178439.5(GMCL1):c.46C>G (p.Leu16Val)not specified [RCV004932691]uncertain significance26982993869829938Humanname
597788335CV3678088single nucleotide variantNM_178439.5(GMCL1):c.49G>T (p.Ala17Ser)not specified [RCV004932692]uncertain significance26982994169829941Humanname
597729834CV3678090single nucleotide variantNM_178439.5(GMCL1):c.43G>A (p.Ala15Thr)not specified [RCV004919755]uncertain significance26982993569829935Humanname
598263934CV3978048single nucleotide variantNM_178439.5(GMCL1):c.83C>T (p.Ser28Leu)not specified [RCV005348710]uncertain significance26982997569829975Humanname
155990454CV2285260single nucleotide variantNM_178439.5(GMCL1):c.142G>A (p.Gly48Ser)not specified [RCV004145454]uncertain significance26983003469830034Humanname
401746773CV2691979single nucleotide variantNM_178439.5(GMCL1):c.231G>C (p.Glu77Asp)not specified [RCV004301708]uncertain significance26983012369830123Humanname
405755241CV3261944single nucleotide variantNM_178439.5(GMCL1):c.200A>G (p.Glu67Gly)not specified [RCV004393353]uncertain significance26983009269830092Humanname
8630412CV85567single nucleotide variantNM_178439.3(GMCL1):c.1377T>G (p.Ala459=)Malignant melanoma [RCV000065650]not provided26987175769871757Humanname
156072026CV2376806single nucleotide variantNM_178439.5(GMCL1):c.619A>G (p.Thr207Ala)not specified [RCV004227467]uncertain significance26984318869843188Humanname
155963059CV2388338single nucleotide variantNM_178439.5(GMCL1):c.566G>A (p.Cys189Tyr)not specified [RCV004234789]uncertain significance26984102669841026Humanname
401770742CV2726246single nucleotide variantNM_178439.5(GMCL1):c.970G>A (p.Gly324Arg)not specified [RCV004326702]uncertain significance26985485869854858Humanname
407519871CV3443502single nucleotide variantNM_178439.5(GMCL1):c.791C>T (p.Ser264Phe)not specified [RCV004629819]uncertain significance26984757569847575Humanname
597729825CV3678089single nucleotide variantNM_178439.5(GMCL1):c.331A>G (p.Lys111Glu)not specified [RCV004919754]uncertain significance26983761769837617Humanname
598232590CV3978049single nucleotide variantNM_178439.5(GMCL1):c.908A>G (p.Asp303Gly)not specified [RCV005342621]uncertain significance26984971669849716Humanname
156326484CV2219619single nucleotide variantNM_178439.5(GMCL1):c.1214G>A (p.Gly405Asp)not specified [RCV004093734]uncertain significance26986497169864971Humanname
155918293CV2236789single nucleotide variantNM_178439.5(GMCL1):c.1318T>G (p.Cys440Gly)not specified [RCV004112556]uncertain significance26986981869869818Humanname
401735020CV2690748single nucleotide variantNM_178439.5(GMCL1):c.1387A>G (p.Ser463Gly)not specified [RCV004298469]uncertain significance26987176769871767Humanname
401773816CV2702450single nucleotide variantNM_178439.5(GMCL1):c.1402A>T (p.Ile468Leu)not specified [RCV004316962]uncertain significance26987178269871782Humanname
401749140CV2713780single nucleotide variantNM_178439.5(GMCL1):c.1523A>G (p.Tyr508Cys)not specified [RCV004321124]uncertain significance26987897969878979Humanname
405755216CV3261941single nucleotide variantNM_178439.5(GMCL1):c.1229G>A (p.Arg410His)not specified [RCV004393350]uncertain significance26986972969869729Humanname
405755227CV3261942single nucleotide variantNM_178439.5(GMCL1):c.1261C>G (p.Leu421Val)not specified [RCV004393351]uncertain significance26986976169869761Humanname
405755234CV3261943single nucleotide variantNM_178439.5(GMCL1):c.1424A>G (p.Tyr475Cys)not specified [RCV004393352]uncertain significance26987180469871804Humanname
598263932CV3978047single nucleotide variantNM_178439.5(GMCL1):c.1321A>T (p.Ser441Cys)not specified [RCV005348709]uncertain significance26986982169869821Humanname
598263937CV3978050single nucleotide variantNM_178439.5(GMCL1):c.1328C>G (p.Ser443Cys)not specified [RCV005348711]uncertain significance26986982869869828Humanname
15183594CV708341single nucleotide variantNM_178439.5(GMCL1):c.1346G>A (p.Arg449Gln)not provided [RCV000974912]benign26986984669869846Humanname
8630411CV85566single nucleotide variantNM_178439.3(GMCL1):c.1276A>G (p.Asn426Asp)Malignant melanoma [RCV000065649]not provided26986977669869776Humanname