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Variants search result for Homo sapiens
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58 records found for search term Marco
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15201947CV719205single nucleotide variantNM_006770.4(MARCO):c.30C>T (p.Asp10=)not provided [RCV000891340]likely benign2118942330118942330Humanname
155946505CV2266193single nucleotide variantNM_006770.4(MARCO):c.19C>A (p.Leu7Ile)not specified [RCV004128770]uncertain significance2118942319118942319Humanname
405658263CV3281564single nucleotide variantNM_006770.4(MARCO):c.25G>A (p.Glu9Lys)not specified [RCV004416385]uncertain significance2118942325118942325Humanname
156130578CV2210055single nucleotide variantNM_006770.4(MARCO):c.95A>G (p.Asn32Ser)not specified [RCV004076484]likely benign2118942395118942395Humanname
405853058CV3393489single nucleotide variantNM_006770.4(MARCO):c.495T>A (p.Pro165=)not provided [RCV004546219]likely benign2118974367118974367Humanname
15183643CV707691single nucleotide variantNM_006770.4(MARCO):c.924T>C (p.Val308=)not provided [RCV000974924]benign2118982178118982178Humanname
15150220CV732730single nucleotide variantNM_006770.4(MARCO):c.417G>A (p.Gln139=)not provided [RCV000901103]likely benign2118970331118970331Humanname
156214999CV2257533single nucleotide variantNM_006770.4(MARCO):c.114G>T (p.Arg38Ser)not specified [RCV004125588]uncertain significance2118969176118969176Humanname
155917648CV2332852single nucleotide variantNM_006770.4(MARCO):c.202C>G (p.Leu68Val)not specified [RCV004192116]uncertain significance2118970116118970116Humanname
155932524CV2364410single nucleotide variantNM_006770.4(MARCO):c.260C>T (p.Ala87Val)not specified [RCV004223621]uncertain significance2118970174118970174Humanname
156003257CV2399642single nucleotide variantNM_006770.4(MARCO):c.142G>A (p.Val48Met)not specified [RCV004244158]uncertain significance2118969204118969204Humanname
405658260CV3281563single nucleotide variantNM_006770.4(MARCO):c.172G>A (p.Ala58Thr)not specified [RCV004416384]uncertain significance2118969234118969234Humanname
405853083CV3393514single nucleotide variantNM_006770.4(MARCO):c.1026A>T (p.Pro342=)not provided [RCV004546244]likely benign2118982373118982373Humanname
597636353CV3697569single nucleotide variantNM_006770.4(MARCO):c.197A>T (p.Gln66Leu)not specified [RCV004940766]uncertain significance2118969259118969259Humanname
597636364CV3697571single nucleotide variantNM_006770.4(MARCO):c.178G>A (p.Ala60Thr)not specified [RCV004940768]uncertain significance2118969240118969240Humanname
598176865CV3985470single nucleotide variantNM_006770.4(MARCO):c.224G>A (p.Arg75Gln)not specified [RCV005371493]uncertain significance2118970138118970138Humanname
8625114CV80233single nucleotide variantNM_006770.3(MARCO):c.1440G>A (p.Gln480=)Malignant melanoma [RCV000060309]not provided2118994397118994397Humanname
156276462CV2209779single nucleotide variantNM_006770.4(MARCO):c.492G>A (p.Met164Ile)not specified [RCV004083090]uncertain significance2118974364118974364Humanname
156245094CV2218942single nucleotide variantNM_006770.4(MARCO):c.512C>T (p.Pro171Leu)not specified [RCV004087126]uncertain significance2118974384118974384Humanname
155953168CV2264313single nucleotide variantNM_006770.4(MARCO):c.464T>A (p.Leu155His)not specified [RCV004138232]uncertain significance2118974336118974336Humanname
155904522CV2298818single nucleotide variantNM_006770.4(MARCO):c.746A>G (p.Lys249Arg)not specified [RCV004156370]uncertain significance2118977915118977915Humanname
155909109CV2307216single nucleotide variantNM_006770.4(MARCO):c.364T>C (p.Trp122Arg)not specified [RCV004159680]uncertain significance2118970278118970278Humanname
156285563CV2317645single nucleotide variantNM_006770.4(MARCO):c.926C>T (p.Pro309Leu)not specified [RCV004172581]uncertain significance2118982180118982180Humanname
155920862CV2340354single nucleotide variantNM_006770.4(MARCO):c.509C>G (p.Pro170Arg)not specified [RCV004197086]uncertain significance2118974381118974381Humanname
156261076CV2381289single nucleotide variantNM_006770.4(MARCO):c.425G>A (p.Gly142Glu)not specified [RCV004227350]likely benign2118971499118971499Humanname
329382643CV2449280single nucleotide variantNM_006770.4(MARCO):c.454G>A (p.Ala152Thr)not specified [RCV004257413]uncertain significance2118971528118971528Humanname
329369551CV2461154single nucleotide variantNM_006770.4(MARCO):c.934C>T (p.Pro312Ser)not specified [RCV004265569]uncertain significance2118982188118982188Humanname
401892999CV2758348single nucleotide variantNM_006770.4(MARCO):c.509C>T (p.Pro170Leu)not specified [RCV004341698]likely benign2118974381118974381Humanname
401857058CV2762424single nucleotide variantNM_006770.4(MARCO):c.608A>T (p.Glu203Val)not specified [RCV004335526]uncertain significance2118974560118974560Humanname
405658265CV3281565single nucleotide variantNM_006770.4(MARCO):c.328G>A (p.Ala110Thr)not specified [RCV004416386]uncertain significance2118970242118970242Humanname
405658270CV3281567single nucleotide variantNM_006770.4(MARCO):c.554G>A (p.Arg185Gln)not specified [RCV004416388]uncertain significance2118974426118974426Humanname
405658272CV3281568single nucleotide variantNM_006770.4(MARCO):c.829G>A (p.Gly277Arg)not specified [RCV004416389]uncertain significance2118981471118981471Humanname
405658275CV3281569single nucleotide variantNM_006770.4(MARCO):c.843C>A (p.Asp281Glu)not specified [RCV004416390]uncertain significance2118981485118981485Humanname
405658277CV3281570single nucleotide variantNM_006770.4(MARCO):c.917A>C (p.Gln306Pro)not specified [RCV004416391]uncertain significance2118982171118982171Humanname
405658279CV3281571single nucleotide variantNM_006770.4(MARCO):c.953C>G (p.Pro318Arg)not specified [RCV004416392]uncertain significance2118982207118982207Humanname
405658281CV3281572single nucleotide variantNM_006770.4(MARCO):c.992G>A (p.Gly331Glu)not specified [RCV004416393]uncertain significance2118982246118982246Humanname
407494772CV3456871single nucleotide variantNM_006770.4(MARCO):c.500C>G (p.Ala167Gly)not specified [RCV004643067]uncertain significance2118974372118974372Humanname
407494777CV3456872single nucleotide variantNM_006770.4(MARCO):c.650G>A (p.Gly217Glu)not specified [RCV004643068]uncertain significance2118977507118977507Humanname
407494781CV3456874single nucleotide variantNM_006770.4(MARCO):c.449A>C (p.Gln150Pro)not specified [RCV004643069]uncertain significance2118971523118971523Humanname
597636359CV3697570single nucleotide variantNM_006770.4(MARCO):c.520C>T (p.Pro174Ser)not specified [RCV004940767]uncertain significance2118974392118974392Humanname
597636370CV3697572single nucleotide variantNM_006770.4(MARCO):c.897T>A (p.Asp299Glu)not specified [RCV004940769]uncertain significance2118981652118981652Humanname
597636376CV3697573single nucleotide variantNM_006770.4(MARCO):c.614G>A (p.Gly205Asp)not specified [RCV004940770]uncertain significance2118977471118977471Humanname
598198808CV3985474single nucleotide variantNM_006770.4(MARCO):c.601A>C (p.Lys201Gln)not specified [RCV005375607]uncertain significance2118974553118974553Humanname
156373134CV2204819single nucleotide variantNM_006770.4(MARCO):c.1198G>A (p.Gly400Arg)not specified [RCV004075073]uncertain significance2118991866118991866Humanname
156198463CV2237436single nucleotide variantNM_006770.4(MARCO):c.1199G>T (p.Gly400Val)not specified [RCV004106400]uncertain significance2118991867118991867Humanname
156277423CV2287852single nucleotide variantNM_006770.4(MARCO):c.1496C>T (p.Thr499Ile)not specified [RCV004143293]uncertain significance2118994453118994453Humanname
156386786CV2364842single nucleotide variantNM_006770.4(MARCO):c.1348G>A (p.Glu450Lys)not specified [RCV004219704]uncertain significance2118993219118993219Humanname
156308868CV2366487single nucleotide variantNM_006770.4(MARCO):c.1466G>A (p.Arg489Gln)not specified [RCV004208464]likely benign2118994423118994423Humanname
329357896CV2453803single nucleotide variantNM_006770.4(MARCO):c.1172G>A (p.Gly391Glu)not specified [RCV004271211]uncertain significance2118991840118991840Humanname
401875796CV2777533single nucleotide variantNM_006770.4(MARCO):c.1295G>A (p.Arg432Gln)not specified [RCV004343393]uncertain significance2118993166118993166Humanname
405658257CV3281562single nucleotide variantNM_006770.4(MARCO):c.1049G>A (p.Ser350Asn)not specified [RCV004416383]uncertain significance2118982396118982396Humanname
597636380CV3697574single nucleotide variantNM_006770.4(MARCO):c.1382G>A (p.Arg461His)not specified [RCV004940771]uncertain significance2118993253118993253Humanname
598198785CV3985471single nucleotide variantNM_006770.4(MARCO):c.1270G>A (p.Val424Ile)not specified [RCV005375604]uncertain significance2118993141118993141Humanname
598198793CV3985472single nucleotide variantNM_006770.4(MARCO):c.1187A>G (p.Lys396Arg)not specified [RCV005375605]uncertain significance2118991855118991855Humanname
598198800CV3985473single nucleotide variantNM_006770.4(MARCO):c.1233G>T (p.Lys411Asn)not specified [RCV005375606]uncertain significance2118992457118992457Humanname
8625113CV80232single nucleotide variantNM_006770.3(MARCO):c.1045G>A (p.Gly349Arg)Malignant melanoma [RCV000060308]not provided2118982392118982392Humanname
8629808CV84955single nucleotide variantNM_006770.3(MARCO):c.1166C>T (p.Ala389Val)Malignant melanoma [RCV000065037]not provided2118991834118991834Humanname
401944184CV2840551single nucleotide variantNM_001363511.2(MARCOL):c.762A>G (p.Gln254=)not provided [RCV003457132]likely benign5148243158148243158Humanname