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Variants search result for Homo sapiens
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52 records found for search term Zswim3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329363523CV2471717single nucleotide variantNM_080752.4(ZSWIM3):c.74G>A (p.Arg25Lys)not specified [RCV004286995]uncertain significance204585789945857899Humanname
598276455CV3938366single nucleotide variantNM_080752.4(ZSWIM3):c.32A>G (p.Glu11Gly)not specified [RCV005305589]uncertain significance204585785745857857Humanname
401879172CV2778212single nucleotide variantNM_080752.4(ZSWIM3):c.211C>T (p.Arg71Trp)not specified [RCV004349932]uncertain significance204587676945876769Humanname
405688902CV3355247single nucleotide variantNM_080752.4(ZSWIM3):c.225G>A (p.Met75Ile)not specified [RCV004490352]uncertain significance204587678345876783Humanname
405688909CV3355248single nucleotide variantNM_080752.4(ZSWIM3):c.240G>T (p.Leu80Phe)not specified [RCV004490353]uncertain significance204587679845876798Humanname
405688913CV3355249single nucleotide variantNM_080752.4(ZSWIM3):c.260G>A (p.Arg87Lys)not specified [RCV004490354]likely benign204587681845876818Humanname
407488046CV3421095single nucleotide variantNM_080752.4(ZSWIM3):c.206G>A (p.Arg69Lys)not specified [RCV004603902]uncertain significance204587676445876764Humanname
597758263CV3646388single nucleotide variantNM_080752.4(ZSWIM3):c.212G>A (p.Arg71Gln)not specified [RCV004894288]likely benign204587677045876770Humanname
597758295CV3646394single nucleotide variantNM_080752.4(ZSWIM3):c.270A>T (p.Arg90Ser)not specified [RCV004894294]uncertain significance204587682845876828Humanname
598276453CV3938364single nucleotide variantNM_080752.4(ZSWIM3):c.116A>C (p.His39Pro)not specified [RCV005305587]uncertain significance204585794145857941Humanname
156400506CV2199226single nucleotide variantNM_080752.4(ZSWIM3):c.605G>A (p.Arg202Gln)not specified [RCV004082587]uncertain significance204587716345877163Humanname
155981218CV2272826single nucleotide variantNM_080752.4(ZSWIM3):c.320T>C (p.Val107Ala)not specified [RCV004135733]uncertain significance204587687845876878Humanname
156251477CV2273406single nucleotide variantNM_080752.4(ZSWIM3):c.784G>C (p.Val262Leu)not specified [RCV004132170]uncertain significance204587734245877342Humanname
156150599CV2307490single nucleotide variantNM_080752.4(ZSWIM3):c.565A>G (p.Met189Val)not specified [RCV004166145]uncertain significance204587712345877123Humanname
156109125CV2313931single nucleotide variantNM_080752.4(ZSWIM3):c.890T>A (p.Ile297Asn)not specified [RCV004164238]uncertain significance204587744845877448Humanname
329392373CV2438904single nucleotide variantNM_080752.4(ZSWIM3):c.317A>T (p.Lys106Ile)not specified [RCV004264432]uncertain significance204587687545876875Humanname
405688917CV3355250single nucleotide variantNM_080752.4(ZSWIM3):c.325A>C (p.Ser109Arg)not specified [RCV004490355]uncertain significance204587688345876883Humanname
405688920CV3355251single nucleotide variantNM_080752.4(ZSWIM3):c.823G>A (p.Asp275Asn)not specified [RCV004490356]uncertain significance204587738145877381Humanname
405688924CV3355252single nucleotide variantNM_080752.4(ZSWIM3):c.959G>A (p.Arg320His)not specified [RCV004490357]uncertain significance204587751745877517Humanname
407488051CV3421096single nucleotide variantNM_080752.4(ZSWIM3):c.935G>T (p.Arg312Leu)not specified [RCV004603903]uncertain significance204587749345877493Humanname
407499724CV3421098single nucleotide variantNM_080752.4(ZSWIM3):c.419C>G (p.Thr140Ser)not specified [RCV004606945]uncertain significance204587697745876977Humanname
597758269CV3646389single nucleotide variantNM_080752.4(ZSWIM3):c.647G>A (p.Arg216His)not specified [RCV004894289]uncertain significance204587720545877205Humanname
597758273CV3646390single nucleotide variantNM_080752.4(ZSWIM3):c.821C>A (p.Ser274Tyr)not specified [RCV004894290]uncertain significance204587737945877379Humanname
597758285CV3646392single nucleotide variantNM_080752.4(ZSWIM3):c.469G>A (p.Val157Met)not specified [RCV004894292]uncertain significance204587702745877027Humanname
598201001CV3938361single nucleotide variantNM_080752.4(ZSWIM3):c.446C>T (p.Ser149Leu)not specified [RCV005314153]uncertain significance204587700445877004Humanname
156019481CV2230024single nucleotide variantNM_080752.4(ZSWIM3):c.1495C>T (p.His499Tyr)not specified [RCV004105824]uncertain significance204587805345878053Humanname
155914552CV2242757single nucleotide variantNM_080752.4(ZSWIM3):c.1727G>A (p.Gly576Asp)not specified [RCV004113783]uncertain significance204587828545878285Humanname
156201914CV2256200single nucleotide variantNM_080752.4(ZSWIM3):c.1844G>A (p.Arg615Gln)not specified [RCV004116464]uncertain significance204587840245878402Humanname
156232626CV2273763single nucleotide variantNM_080752.4(ZSWIM3):c.1576A>C (p.Met526Leu)not specified [RCV004132406]uncertain significance204587813445878134Humanname
156285855CV2289108single nucleotide variantNM_080752.4(ZSWIM3):c.1949A>C (p.Asp650Ala)not specified [RCV004150044]uncertain significance204587850745878507Humanname
156067935CV2289446single nucleotide variantNM_080752.4(ZSWIM3):c.1937G>A (p.Arg646His)not specified [RCV004152395]uncertain significance204587849545878495Humanname
156101242CV2313468single nucleotide variantNM_080752.4(ZSWIM3):c.2018G>A (p.Arg673His)not specified [RCV004163780]uncertain significance204587857645878576Humanname
156052296CV2320294single nucleotide variantNM_080752.4(ZSWIM3):c.1046A>G (p.Asn349Ser)not specified [RCV004178462]uncertain significance204587760445877604Humanname
156264991CV2329489single nucleotide variantNM_080752.4(ZSWIM3):c.1721C>T (p.Pro574Leu)not specified [RCV004180628]uncertain significance204587827945878279Humanname
156090983CV2384606single nucleotide variantNM_080752.4(ZSWIM3):c.1006C>T (p.Arg336Trp)not specified [RCV004232389]uncertain significance204587756445877564Humanname
401720837CV2673508single nucleotide variantNM_080752.4(ZSWIM3):c.1597G>A (p.Val533Ile)not specified [RCV004288476]likely benign204587815545878155Humanname
401774586CV2691789single nucleotide variantNM_080752.4(ZSWIM3):c.1791G>C (p.Glu597Asp)not specified [RCV004299240]uncertain significance204587834945878349Humanname
401782625CV2697127single nucleotide variantNM_080752.4(ZSWIM3):c.1565A>G (p.His522Arg)not specified [RCV004302123]uncertain significance204587812345878123Humanname
401859970CV2765228single nucleotide variantNM_080752.4(ZSWIM3):c.1315C>T (p.Pro439Ser)not specified [RCV004339755]uncertain significance204587787345877873Humanname
401877658CV2779899single nucleotide variantNM_080752.4(ZSWIM3):c.1039C>G (p.Leu347Val)not specified [RCV004353513]uncertain significance204587759745877597Humanname
405688877CV3355242single nucleotide variantNM_080752.4(ZSWIM3):c.1034C>T (p.Ala345Val)not specified [RCV004490347]uncertain significance204587759245877592Humanname
405688882CV3355243single nucleotide variantNM_080752.4(ZSWIM3):c.1342A>C (p.Ser448Arg)not specified [RCV004490348]uncertain significance204587790045877900Humanname
405688892CV3355245single nucleotide variantNM_080752.4(ZSWIM3):c.1744C>T (p.Arg582Cys)not specified [RCV004490350]uncertain significance204587830245878302Humanname
407488041CV3421094single nucleotide variantNM_080752.4(ZSWIM3):c.1426G>A (p.Ala476Thr)not specified [RCV004603901]uncertain significance204587798445877984Humanname
407488056CV3421097single nucleotide variantNM_080752.4(ZSWIM3):c.1921C>T (p.Arg641Cys)not specified [RCV004603904]uncertain significance204587847945878479Humanname
597758258CV3646387single nucleotide variantNM_080752.4(ZSWIM3):c.1768T>C (p.Tyr590His)not specified [RCV004894287]likely benign204587832645878326Humanname
597758279CV3646391single nucleotide variantNM_080752.4(ZSWIM3):c.1553A>G (p.Gln518Arg)not specified [RCV004894291]uncertain significance204587811145878111Humanname
597758290CV3646393single nucleotide variantNM_080752.4(ZSWIM3):c.2057G>A (p.Gly686Glu)not specified [RCV004894293]uncertain significance204587861545878615Humanname
598276452CV3938362single nucleotide variantNM_080752.4(ZSWIM3):c.2077G>C (p.Val693Leu)not specified [RCV005305586]uncertain significance204587863545878635Humanname
598201007CV3938363single nucleotide variantNM_080752.4(ZSWIM3):c.1745G>A (p.Arg582His)not specified [RCV005314154]uncertain significance204587830345878303Humanname
598276454CV3938365single nucleotide variantNM_080752.4(ZSWIM3):c.1946T>C (p.Val649Ala)not specified [RCV005305588]uncertain significance204587850445878504Humanname
598276456CV3938367single nucleotide variantNM_080752.4(ZSWIM3):c.1394C>T (p.Thr465Ile)not specified [RCV005305590]uncertain significance204587795245877952Humanname