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Variants search result for All species
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54 records found for search term Wdr43
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15098196CV777306single nucleotide variantNM_015131.3(WDR43):c.364-10T>Anot provided [RCV000958499]benign22890645028906450Humanname
597791487CV3633622single nucleotide variantNM_015131.3(WDR43):c.22A>G (p.Ser8Gly)not specified [RCV004876677]uncertain significance22889472028894720Humanname
401726724CV2677322single nucleotide variantNM_015131.3(WDR43):c.95C>T (p.Ala32Val)not specified [RCV004295938]uncertain significance22889479328894793Humanname
407523946CV3489798single nucleotide variantNM_015131.3(WDR43):c.46G>A (p.Gly16Arg)not specified [RCV004678245]uncertain significance22889474428894744Humanname
155926288CV2284847single nucleotide variantNM_015131.3(WDR43):c.145C>T (p.His49Tyr)not specified [RCV004143307]uncertain significance22889484328894843Humanname
405807015CV3356211single nucleotide variantNM_015131.3(WDR43):c.107G>A (p.Gly36Asp)not specified [RCV004480471]uncertain significance22889480528894805Humanname
405807021CV3356214single nucleotide variantNM_015131.3(WDR43):c.136A>T (p.Asn46Tyr)not specified [RCV004480474]uncertain significance22889483428894834Humanname
597791493CV3633625single nucleotide variantNM_015131.3(WDR43):c.135C>A (p.Asn45Lys)not specified [RCV004876679]uncertain significance22889483328894833Humanname
598219775CV3933221single nucleotide variantNM_015131.3(WDR43):c.226G>A (p.Glu76Lys)not specified [RCV005293374]uncertain significance22890198728901987Humanname
598219795CV3933227single nucleotide variantNM_015131.3(WDR43):c.1266C>T (p.Thr422=)not specified [RCV005293377]likely benign22892766128927661Humanname
598257623CV3933230single nucleotide variantNM_015131.3(WDR43):c.223A>G (p.Lys75Glu)not specified [RCV005299863]uncertain significance22889492128894921Humanname
156290576CV2226201single nucleotide variantNM_015131.3(WDR43):c.658A>G (p.Arg220Gly)not specified [RCV004105599]uncertain significance22891412028914120Humanname
156035313CV2246730single nucleotide variantNM_015131.3(WDR43):c.404A>C (p.His135Pro)not specified [RCV004112272]uncertain significance22890650028906500Humanname
155976285CV2342754single nucleotide variantNM_015131.3(WDR43):c.505A>G (p.Ser169Gly)not specified [RCV004189798]uncertain significance22891260928912609Humanname
156168878CV2345484single nucleotide variantNM_015131.3(WDR43):c.346T>G (p.Leu116Val)not specified [RCV004198251]uncertain significance22890210728902107Humanname
156014091CV2368662single nucleotide variantNM_015131.3(WDR43):c.463G>A (p.Val155Ile)not specified [RCV004214558]uncertain significance22890655928906559Humanname
401880496CV2763061single nucleotide variantNM_015131.3(WDR43):c.474C>G (p.Cys158Trp)not specified [RCV004336116]uncertain significance22890657028906570Humanname
405807028CV3356218single nucleotide variantNM_015131.3(WDR43):c.506G>A (p.Ser169Asn)not specified [RCV004480478]uncertain significance22891261028912610Humanname
405807030CV3356219single nucleotide variantNM_015131.3(WDR43):c.543G>T (p.Lys181Asn)not specified [RCV004480479]uncertain significance22891264728912647Humanname
405807032CV3356220single nucleotide variantNM_015131.3(WDR43):c.750G>C (p.Gln250His)not specified [RCV004480480]uncertain significance22891789628917896Humanname
597791478CV3633619single nucleotide variantNM_015131.3(WDR43):c.815A>G (p.Tyr272Cys)not specified [RCV004876674]uncertain significance22891796128917961Humanname
597791490CV3633623single nucleotide variantNM_015131.3(WDR43):c.514A>G (p.Ser172Gly)not specified [RCV004876678]uncertain significance22891261828912618Humanname
597791498CV3633628single nucleotide variantNM_015131.3(WDR43):c.614C>T (p.Thr205Ile)not specified [RCV004876681]uncertain significance22891407628914076Humanname
598219789CV3933224single nucleotide variantNM_015131.3(WDR43):c.980A>G (p.Lys327Arg)not specified [RCV005293376]uncertain significance22892504728925047Humanname
598257609CV3933226single nucleotide variantNM_015131.3(WDR43):c.563G>A (p.Arg188Gln)not specified [RCV005299860]uncertain significance22891266728912667Humanname
598257614CV3933228single nucleotide variantNM_015131.3(WDR43):c.786G>A (p.Met262Ile)not specified [RCV005299861]uncertain significance22891793228917932Humanname
598257618CV3933229single nucleotide variantNM_015131.3(WDR43):c.724C>T (p.His242Tyr)not specified [RCV005299862]uncertain significance22891418628914186Humanname
155919800CV2209717single nucleotide variantNM_015131.3(WDR43):c.1321C>T (p.Arg441Cys)not specified [RCV004083042]uncertain significance22892959428929594Humanname
155981351CV2233070single nucleotide variantNM_015131.3(WDR43):c.1826A>G (p.Asp609Gly)not specified [RCV004103700]uncertain significance22894647128946471Humanname
155983530CV2240745single nucleotide variantNM_015131.3(WDR43):c.1553A>G (p.Asn518Ser)not specified [RCV004119357]uncertain significance22893695028936950Humanname
156041111CV2310864single nucleotide variantNM_015131.3(WDR43):c.1336G>C (p.Asp446His)not specified [RCV004163907]uncertain significance22892960928929609Humanname
156181006CV2327785single nucleotide variantNM_015131.3(WDR43):c.1084G>T (p.Val362Leu)not specified [RCV004179130]uncertain significance22892515128925151Humanname
156175816CV2331124single nucleotide variantNM_015131.3(WDR43):c.1681A>G (p.Thr561Ala)not specified [RCV004181736]uncertain significance22894152128941521Humanname
156271032CV2333813single nucleotide variantNM_015131.3(WDR43):c.1771C>G (p.Pro591Ala)not specified [RCV004181313]uncertain significance22894234828942348Humanname
156079816CV2341286single nucleotide variantNM_015131.3(WDR43):c.1076T>C (p.Ile359Thr)not specified [RCV004186696]uncertain significance22892514328925143Humanname
329368231CV2442664single nucleotide variantNM_015131.3(WDR43):c.1231C>T (p.His411Tyr)not specified [RCV004265016]uncertain significance22892762628927626Humanname
329392834CV2468983single nucleotide variantNM_015131.3(WDR43):c.1271A>G (p.Gln424Arg)not specified [RCV004274246]uncertain significance22892766628927666Humanname
401726349CV2674110single nucleotide variantNM_015131.3(WDR43):c.1390G>A (p.Val464Ile)not specified [RCV004295516]uncertain significance22892966328929663Humanname
401753918CV2716932single nucleotide variantNM_015131.3(WDR43):c.1993G>A (p.Asp665Asn)not specified [RCV004330022]uncertain significance22894673828946738Humanname
405807013CV3356210single nucleotide variantNM_015131.3(WDR43):c.1012G>T (p.Ala338Ser)not specified [RCV004480470]uncertain significance22892507928925079Humanname
405807017CV3356212single nucleotide variantNM_015131.3(WDR43):c.1235A>C (p.His412Pro)not specified [RCV004480472]uncertain significance22892763028927630Humanname
405807019CV3356213single nucleotide variantNM_015131.3(WDR43):c.1322G>A (p.Arg441His)not specified [RCV004480473]uncertain significance22892959528929595Humanname
405807022CV3356215single nucleotide variantNM_015131.3(WDR43):c.1468A>G (p.Ile490Val)not specified [RCV004480475]uncertain significance22893555128935551Humanname
405807024CV3356216single nucleotide variantNM_015131.3(WDR43):c.1637C>A (p.Pro546His)not specified [RCV004480476]uncertain significance22894147728941477Humanname
405807026CV3356217single nucleotide variantNM_015131.3(WDR43):c.1813G>A (p.Glu605Lys)not specified [RCV004480477]uncertain significance22894645828946458Humanname
597791481CV3633620single nucleotide variantNM_015131.3(WDR43):c.1967C>T (p.Thr656Ile)not specified [RCV004876675]likely benign22894671228946712Humanname
597791484CV3633621single nucleotide variantNM_015131.3(WDR43):c.1504A>G (p.Ile502Val)not specified [RCV004876676]likely benign22893558728935587Humanname
597739459CV3633624single nucleotide variantNM_015131.3(WDR43):c.1118T>C (p.Leu373Ser)not specified [RCV004890271]uncertain significance22892649928926499Humanname
597791496CV3633626single nucleotide variantNM_015131.3(WDR43):c.1045C>A (p.Leu349Ile)not specified [RCV004876680]uncertain significance22892511228925112Humanname
597739455CV3633629single nucleotide variantNM_015131.3(WDR43):c.1973G>C (p.Ser658Thr)not specified [RCV004890272]uncertain significance22894671828946718Humanname
597791501CV3633630single nucleotide variantNM_015131.3(WDR43):c.1678A>C (p.Lys560Gln)not specified [RCV004876682]uncertain significance22894151828941518Humanname
598219770CV3933219single nucleotide variantNM_015131.3(WDR43):c.1351A>C (p.Lys451Gln)not specified [RCV005293373]uncertain significance22892962428929624Humanname
598257595CV3933220single nucleotide variantNM_015131.3(WDR43):c.1387C>G (p.Pro463Ala)not specified [RCV005299857]uncertain significance22892966028929660Humanname
598257605CV3933225single nucleotide variantNM_015131.3(WDR43):c.1376C>T (p.Thr459Met)not specified [RCV005299859]uncertain significance22892964928929649Humanname