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Variants search result for Homo sapiens
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54 records found for search term Narf
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155923830CV2248618single nucleotide variantNM_012336.4(NARF):c.19A>C (p.Thr7Pro)not specified [RCV004121804]uncertain significance178245882282458822Humanname
598159308CV3987271single nucleotide variantNM_012336.4(NARF):c.153C>T (p.Ser51=)not specified [RCV005390127]likely benign178246433182464331Humanname
156198277CV2259341single nucleotide variantNM_012336.4(NARF):c.54T>A (p.Asp18Glu)not specified [RCV004122347]uncertain significance178246001882460018Humanname
401872811CV2793165single nucleotide variantNM_012336.4(NARF):c.91G>C (p.Ala31Pro)not specified [RCV004360474]uncertain significance178246005582460055Humanname
598159301CV3987267single nucleotide variantNM_012336.4(NARF):c.61G>A (p.Glu21Lys)not specified [RCV005390125]uncertain significance178246002582460025Humanname
156151304CV2377546single nucleotide variantNM_012336.4(NARF):c.235G>A (p.Val79Ile)not specified [RCV004225697]uncertain significance178246441382464413Humanname
155934279CV2399484single nucleotide variantNM_012336.4(NARF):c.106G>A (p.Glu36Lys)not specified [RCV004242749]uncertain significance178246007082460070Humanname
329374009CV2447537single nucleotide variantNM_012336.4(NARF):c.206C>G (p.Ser69Cys)not specified [RCV004255895]uncertain significance178246438482464384Humanname
407488105CV3447953single nucleotide variantNM_012336.4(NARF):c.260A>G (p.Asp87Gly)not specified [RCV004641183]uncertain significance178246877182468771Humanname
597654790CV3565209single nucleotide variantNM_012336.4(NARF):c.136G>A (p.Ala46Thr)not specified [RCV004834113]uncertain significance178246431482464314Humanname
598215293CV3987268single nucleotide variantNM_012336.4(NARF):c.232C>T (p.Arg78Cys)not specified [RCV005378724]uncertain significance178246441082464410Humanname
156347110CV2297828single nucleotide variantNM_012336.4(NARF):c.755G>A (p.Cys252Tyr)not specified [RCV004157773]uncertain significance178248119782481197Humanname
156146836CV2357962single nucleotide variantNM_012336.4(NARF):c.809T>A (p.Val270Glu)not provided [RCV004695690]|not specified [RCV004209742]uncertain significance178248375582483755Humanname
156346934CV2375341single nucleotide variantNM_012336.4(NARF):c.743G>A (p.Arg248Gln)not specified [RCV004232742]uncertain significance178248118582481185Humanname
156270194CV2379465single nucleotide variantNM_012336.4(NARF):c.628G>A (p.Ala210Thr)not specified [RCV004217184]uncertain significance178247890782478907Humanname
156205810CV2385255single nucleotide variantNM_012336.4(NARF):c.467G>A (p.Arg156His)not specified [RCV004228497]likely benign178247264582472645Humanname
156166252CV2398914single nucleotide variantNM_012336.4(NARF):c.466C>T (p.Arg156Cys)not specified [RCV004245229]uncertain significance178247264482472644Humanname
329377272CV2435866single nucleotide variantNM_012336.4(NARF):c.554G>A (p.Arg185His)not specified [RCV004255100]likely benign178247883382478833Humanname
329354191CV2437639single nucleotide variantNM_012336.4(NARF):c.962G>A (p.Arg321Gln)not specified [RCV004260957]uncertain significance178248494182484941Humanname
329364740CV2443815single nucleotide variantNM_012336.4(NARF):c.487C>T (p.Arg163Cys)not specified [RCV004258155]uncertain significance178247266582472665Humanname
401726488CV2674157single nucleotide variantNM_012336.4(NARF):c.419C>T (p.Ala140Val)not specified [RCV004295559]uncertain significance178247259782472597Humanname
401737339CV2679287single nucleotide variantNM_012336.4(NARF):c.454G>C (p.Val152Leu)not specified [RCV004285831]uncertain significance178247263282472632Humanname
401760683CV2706048single nucleotide variantNM_012336.4(NARF):c.487C>A (p.Arg163Ser)not specified [RCV004314748]uncertain significance178247266582472665Humanname
401749720CV2710930single nucleotide variantNM_012336.4(NARF):c.502C>G (p.Leu168Val)not specified [RCV004310649]uncertain significance178247268082472680Humanname
405749184CV3328263single nucleotide variantNM_012336.4(NARF):c.866G>A (p.Arg289His)not specified [RCV004466837]uncertain significance178248484582484845Humanname
405765562CV3328326single nucleotide variantNM_012336.4(NARF):c.580G>A (p.Ala194Thr)not specified [RCV004469380]uncertain significance178247885982478859Humanname
405765660CV3328343single nucleotide variantNM_012336.4(NARF):c.826G>C (p.Asp276His)not specified [RCV004469397]uncertain significance178248377282483772Humanname
407520761CV3447948single nucleotide variantNM_012336.4(NARF):c.680C>T (p.Pro227Leu)not specified [RCV004652295]uncertain significance178248112282481122Humanname
407487851CV3447949single nucleotide variantNM_012336.4(NARF):c.410C>T (p.Thr137Met)not specified [RCV004641181]uncertain significance178247258882472588Humanname
407487856CV3447950single nucleotide variantNM_012336.4(NARF):c.823G>A (p.Val275Ile)not specified [RCV004641182]uncertain significance178248376982483769Humanname
407487864CV3447954single nucleotide variantNM_012336.4(NARF):c.770G>T (p.Gly257Val)not specified [RCV004641184]uncertain significance178248371682483716Humanname
597654771CV3565207single nucleotide variantNM_012336.4(NARF):c.377A>G (p.Lys126Arg)not specified [RCV004834111]uncertain significance178246888882468888Humanname
597654797CV3565210single nucleotide variantNM_012336.4(NARF):c.826G>A (p.Asp276Asn)not specified [RCV004834114]uncertain significance178248377282483772Humanname
597655937CV3565211single nucleotide variantNM_012336.4(NARF):c.457C>T (p.Arg153Cys)not specified [RCV004834115]uncertain significance178247263582472635Humanname
597655927CV3565212single nucleotide variantNM_012336.4(NARF):c.739T>C (p.Ser247Pro)not specified [RCV004834116]uncertain significance178248118182481181Humanname
598159305CV3987269single nucleotide variantNM_012336.4(NARF):c.829A>T (p.Thr277Ser)not specified [RCV005390126]uncertain significance178248377582483775Humanname
598215297CV3987270single nucleotide variantNM_012336.4(NARF):c.559A>G (p.Ile187Val)not specified [RCV005378725]likely benign178247883882478838Humanname
598159311CV3987272single nucleotide variantNM_012336.4(NARF):c.721C>A (p.Pro241Thr)not specified [RCV005390128]uncertain significance178248116382481163Humanname
598215302CV3987273single nucleotide variantNM_012336.4(NARF):c.671T>C (p.Ile224Thr)not specified [RCV005378726]uncertain significance178248111382481113Humanname
156069645CV2232246single nucleotide variantNM_012336.4(NARF):c.1114C>T (p.Leu372Phe)not specified [RCV004105031]uncertain significance178248563982485639Humanname
156220665CV2250721single nucleotide variantNM_012336.4(NARF):c.1292C>T (p.Ser431Phe)not specified [RCV004129605]uncertain significance178248807882488078Humanname
156039274CV2261197single nucleotide variantNM_012336.4(NARF):c.1231C>T (p.Arg411Cys)not specified [RCV004128081]uncertain significance178248801782488017Humanname
155920715CV2340329single nucleotide variantNM_012336.4(NARF):c.1040A>G (p.Tyr347Cys)not specified [RCV004195017]uncertain significance178248556582485565Humanname
156181483CV2353083single nucleotide variantNM_012336.4(NARF):c.1235C>T (p.Pro412Leu)not specified [RCV004203565]uncertain significance178248802182488021Humanname
156107764CV2355352single nucleotide variantNM_012336.4(NARF):c.1229G>A (p.Arg410Gln)not specified [RCV004203200]uncertain significance178248801582488015Humanname
156108137CV2355379single nucleotide variantNM_012336.4(NARF):c.1054A>C (p.Ile352Leu)not specified [RCV004205238]uncertain significance178248557982485579Humanname
401748278CV2698336single nucleotide variantNM_012336.4(NARF):c.1289A>G (p.Asn430Ser)not specified [RCV004304878]uncertain significance178248807582488075Humanname
401738394CV2711849single nucleotide variantNM_012336.4(NARF):c.1285A>C (p.Ile429Leu)not specified [RCV004309482]uncertain significance178248807182488071Humanname
405749294CV3328279single nucleotide variantNM_012336.4(NARF):c.1175C>T (p.Ala392Val)not specified [RCV004466853]uncertain significance178248796182487961Humanname
407520764CV3447951single nucleotide variantNM_012336.4(NARF):c.1207A>G (p.Ile403Val)not specified [RCV004652296]uncertain significance178248799382487993Humanname
597654779CV3565208single nucleotide variantNM_012336.4(NARF):c.1244G>A (p.Ser415Asn)not specified [RCV004834112]uncertain significance178248803082488030Humanname
8636401CV91625single nucleotide variantNM_001038618.2(NARF):c.564C>T (p.Ser188=)Malignant melanoma [RCV000071723]not provided178248118382481183Humanname
8635902CV91125single nucleotide variantNM_022493.2(NARFL):c.574+155C>TMalignant melanoma [RCV000071223]not provided16734582734582Humanname
8635903CV91126single nucleotide variantNM_022493.2(NARFL):c.277G>A (p.Glu93Lys)Malignant melanoma [RCV000071224]not provided16737215737215Humanname