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55 records found for search term Slc39a3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156223778CV2355607single nucleotide variantNM_144564.5(SLC39A3):c.64G>A (p.Gly22Ser)not specified [RCV004205449]uncertain significance1927371942737194Humanname
407514779CV3484603single nucleotide variantNM_144564.5(SLC39A3):c.48C>G (p.Phe16Leu)not specified [RCV004674697]uncertain significance1927372102737210Humanname
597703333CV3599997single nucleotide variantNM_144564.5(SLC39A3):c.86T>C (p.Ile29Thr)not specified [RCV004860185]uncertain significance1927371722737172Humanname
156261102CV2322349single nucleotide variantNM_144564.5(SLC39A3):c.112C>T (p.His38Tyr)not specified [RCV004176103]uncertain significance1927371462737146Humanname
401879496CV2773133single nucleotide variantNM_144564.5(SLC39A3):c.116G>C (p.Arg39Pro)not specified [RCV004351557]uncertain significance1927371422737142Humanname
405709355CV3329155single nucleotide variantNM_144564.5(SLC39A3):c.115C>T (p.Arg39Cys)not specified [RCV004461543]uncertain significance1927371432737143Humanname
405709362CV3329156single nucleotide variantNM_144564.5(SLC39A3):c.146C>T (p.Thr49Ile)not specified [RCV004461544]uncertain significance1927371122737112Humanname
407514775CV3484602single nucleotide variantNM_144564.5(SLC39A3):c.164T>G (p.Phe55Cys)not specified [RCV004674696]uncertain significance1927370942737094Humanname
597703342CV3599998single nucleotide variantNM_144564.5(SLC39A3):c.220G>A (p.Val74Ile)not specified [RCV004860186]uncertain significance1927334762733476Humanname
598244015CV3915022single nucleotide variantNM_144564.5(SLC39A3):c.160G>T (p.Val54Leu)not specified [RCV005276792]uncertain significance1927370982737098Humanname
155959733CV2194002single nucleotide variantNM_144564.5(SLC39A3):c.679C>T (p.Arg227Trp)not specified [RCV004076770]uncertain significance1927330172733017Humanname
155927483CV2230795single nucleotide variantNM_144564.5(SLC39A3):c.367G>A (p.Ala123Thr)not specified [RCV004092012]uncertain significance1927333292733329Humanname
156055904CV2243237single nucleotide variantNM_144564.5(SLC39A3):c.488C>T (p.Ser163Leu)not specified [RCV004110125]uncertain significance1927332082733208Humanname
156025216CV2273952single nucleotide variantNM_144564.5(SLC39A3):c.505C>T (p.Arg169Cys)not specified [RCV004134355]uncertain significance1927331912733191Humanname
156134710CV2284681single nucleotide variantNM_144564.5(SLC39A3):c.811G>A (p.Gly271Ser)not specified [RCV004140834]uncertain significance1927328852732885Humanname
156189036CV2292597single nucleotide variantNM_144564.5(SLC39A3):c.922G>A (p.Gly308Arg)not specified [RCV004150363]uncertain significance1927327742732774Humanname
155969584CV2309087single nucleotide variantNM_144564.5(SLC39A3):c.756C>G (p.Ser252Arg)not specified [RCV004171448]uncertain significance1927329402732940Humanname
156250740CV2311244single nucleotide variantNM_144564.5(SLC39A3):c.533C>T (p.Ser178Leu)not specified [RCV004166328]uncertain significance1927331632733163Humanname
156157971CV2314494single nucleotide variantNM_144564.5(SLC39A3):c.672G>A (p.Met224Ile)not specified [RCV004168594]uncertain significance1927330242733024Humanname
156046942CV2315644single nucleotide variantNM_144564.5(SLC39A3):c.422C>T (p.Ala141Val)not specified [RCV004169677]uncertain significance1927332742733274Humanname
155913685CV2341837single nucleotide variantNM_144564.5(SLC39A3):c.325C>T (p.Arg109Cys)not specified [RCV004184790]uncertain significance1927333712733371Humanname
156062880CV2353879single nucleotide variantNM_144564.5(SLC39A3):c.374C>T (p.Ser125Leu)not specified [RCV004201878]uncertain significance1927333222733322Humanname
156096304CV2375350single nucleotide variantNM_144564.5(SLC39A3):c.770C>T (p.Pro257Leu)not specified [RCV004232751]uncertain significance1927329262732926Humanname
156199262CV2392240single nucleotide variantNM_144564.5(SLC39A3):c.706G>A (p.Val236Ile)not specified [RCV004243851]uncertain significance1927329902732990Humanname
156000318CV2396564single nucleotide variantNM_144564.5(SLC39A3):c.433G>A (p.Ala145Thr)not specified [RCV004242265]uncertain significance1927332632733263Humanname
329375672CV2431604single nucleotide variantNM_144564.5(SLC39A3):c.787G>A (p.Val263Met)not specified [RCV004254752]uncertain significance1927329092732909Humanname
329374955CV2470851single nucleotide variantNM_144564.5(SLC39A3):c.476T>C (p.Val159Ala)not specified [RCV004276060]uncertain significance1927332202733220Humanname
401780300CV2673961single nucleotide variantNM_144564.5(SLC39A3):c.806C>T (p.Ala269Val)not specified [RCV004293332]uncertain significance1927328902732890Humanname
401757446CV2675310single nucleotide variantNM_144564.5(SLC39A3):c.482G>A (p.Gly161Asp)not specified [RCV004290074]uncertain significance1927332142733214Humanname
401740905CV2679831single nucleotide variantNM_144564.5(SLC39A3):c.370G>A (p.Gly124Arg)not specified [RCV004282287]uncertain significance1927333262733326Humanname
401748305CV2698345single nucleotide variantNM_144564.5(SLC39A3):c.673C>T (p.Pro225Ser)not specified [RCV004304887]uncertain significance1927330232733023Humanname
401764031CV2700357single nucleotide variantNM_144564.5(SLC39A3):c.914T>C (p.Val305Ala)not specified [RCV004311013]uncertain significance1927327822732782Humanname
401775682CV2710668single nucleotide variantNM_144564.5(SLC39A3):c.755G>A (p.Ser252Asn)not specified [RCV004319573]uncertain significance1927329412732941Humanname
401892332CV2777445single nucleotide variantNM_144564.5(SLC39A3):c.673C>A (p.Pro225Thr)not specified [RCV004356225]uncertain significance1927330232733023Humanname
405709374CV3329158single nucleotide variantNM_144564.5(SLC39A3):c.493G>A (p.Ala165Thr)not specified [RCV004461546]uncertain significance1927332032733203Humanname
405709381CV3329159single nucleotide variantNM_144564.5(SLC39A3):c.527C>T (p.Ala176Val)not specified [RCV004461547]uncertain significance1927331692733169Humanname
405709387CV3329160single nucleotide variantNM_144564.5(SLC39A3):c.637G>A (p.Val213Met)not specified [RCV004461548]uncertain significance1927330592733059Humanname
405709394CV3329161single nucleotide variantNM_144564.5(SLC39A3):c.684C>G (p.Asp228Glu)not specified [RCV004461549]uncertain significance1927330122733012Humanname
407514764CV3484597single nucleotide variantNM_144564.5(SLC39A3):c.757G>A (p.Ala253Thr)not specified [RCV004674692]uncertain significance1927329392732939Humanname
407514767CV3484598single nucleotide variantNM_144564.5(SLC39A3):c.379G>C (p.Val127Leu)not specified [RCV004674693]uncertain significance1927333172733317Humanname
407451676CV3484599single nucleotide variantNM_144564.5(SLC39A3):c.473G>A (p.Ser158Asn)not specified [RCV004683738]uncertain significance1927332232733223Humanname
407514771CV3484600single nucleotide variantNM_144564.5(SLC39A3):c.421G>A (p.Ala141Thr)not specified [RCV004674694]uncertain significance1927332752733275Humanname
407514781CV3484604single nucleotide variantNM_144564.5(SLC39A3):c.460G>T (p.Gly154Cys)not specified [RCV004674698]uncertain significance1927332362733236Humanname
597765986CV3599988single nucleotide variantNM_144564.5(SLC39A3):c.388G>A (p.Asp130Asn)not specified [RCV004870521]uncertain significance1927333082733308Humanname
597765988CV3599989single nucleotide variantNM_144564.5(SLC39A3):c.680G>A (p.Arg227Gln)not specified [RCV004870522]uncertain significance1927330162733016Humanname
597765992CV3599990single nucleotide variantNM_144564.5(SLC39A3):c.616G>A (p.Val206Ile)not specified [RCV004870523]likely benign1927330802733080Humanname
597765997CV3599991single nucleotide variantNM_144564.5(SLC39A3):c.424C>T (p.Arg142Trp)not specified [RCV004870524]uncertain significance1927332722733272Humanname
597766002CV3599992single nucleotide variantNM_144564.5(SLC39A3):c.434C>T (p.Ala145Val)not specified [RCV004870525]uncertain significance1927332622733262Humanname
597766006CV3599993single nucleotide variantNM_144564.5(SLC39A3):c.712G>A (p.Ala238Thr)not specified [RCV004870526]uncertain significance1927329842732984Humanname
597766013CV3599995single nucleotide variantNM_144564.5(SLC39A3):c.686C>T (p.Ala229Val)not specified [RCV004870528]uncertain significance1927330102733010Humanname
597766017CV3599996single nucleotide variantNM_144564.5(SLC39A3):c.863A>G (p.Glu288Gly)not specified [RCV004870529]uncertain significance1927328332732833Humanname
598244001CV3915019single nucleotide variantNM_144564.5(SLC39A3):c.622G>A (p.Glu208Lys)not specified [RCV005276790]uncertain significance1927330742733074Humanname
598244009CV3915020single nucleotide variantNM_144564.5(SLC39A3):c.328A>G (p.Lys110Glu)not specified [RCV005276791]uncertain significance1927333682733368Humanname
598237271CV3915021single nucleotide variantNM_144564.5(SLC39A3):c.389A>T (p.Asp130Val)not specified [RCV005275623]uncertain significance1927333072733307Humanname
15171439CV704894single nucleotide variantNM_144564.5(SLC39A3):c.506G>A (p.Arg169His)not provided [RCV000949834]benign1927331902733190Humanname