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Variants search result for Homo sapiens
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26 records found for search term Tmem184b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
596941320CV3542475single nucleotide variantNM_012264.5(TMEM184B):c.787+1G>ANeuromuscular disease [RCV004797721]uncertain significance223822542338225423Human1name
597753579CV3613588single nucleotide variantNM_012264.5(TMEM184B):c.8T>C (p.Val3Ala)not specified [RCV004867400]uncertain significance223824795438247954Humanname
401739829CV2683180single nucleotide variantNM_012264.5(TMEM184B):c.11G>A (p.Arg4Lys)not specified [RCV004286177]uncertain significance223824795138247951Humanname
407453509CV3486478single nucleotide variantNM_012264.5(TMEM184B):c.16G>A (p.Asp6Asn)not specified [RCV004684568]uncertain significance223824794638247946Humanname
598213577CV3917537single nucleotide variantNM_012264.5(TMEM184B):c.16G>T (p.Asp6Tyr)not specified [RCV005292342]uncertain significance223824794638247946Humanname
329358893CV2425430single nucleotide variantNM_012264.5(TMEM184B):c.70G>A (p.Val24Ile)not specified [RCV004251085]uncertain significance223824789238247892Humanname
405753056CV3336172single nucleotide variantNM_012264.5(TMEM184B):c.38C>T (p.Ala13Val)not specified [RCV004467399]likely benign223824792438247924Humanname
156040517CV2261303single nucleotide variantNM_012264.5(TMEM184B):c.133G>T (p.Ala45Ser)not specified [RCV004128165]uncertain significance223824782938247829Humanname
401774746CV2728258single nucleotide variantNM_012264.5(TMEM184B):c.274G>A (p.Ala92Thr)not specified [RCV004326066]uncertain significance223824601938246019Humanname
597753583CV3613589single nucleotide variantNM_012264.5(TMEM184B):c.107A>G (p.Glu36Gly)not specified [RCV004867401]uncertain significance223824785538247855Humanname
598213573CV3917536single nucleotide variantNM_012264.5(TMEM184B):c.101C>T (p.Ala34Val)not specified [RCV005292341]uncertain significance223824786138247861Humanname
156231933CV2273619single nucleotide variantNM_012264.5(TMEM184B):c.602G>A (p.Arg201Gln)not specified [RCV004132293]uncertain significance223822679438226794Humanname
156356103CV2320723single nucleotide variantNM_012264.5(TMEM184B):c.998T>C (p.Met333Thr)not specified [RCV004179076]uncertain significance223822169538221695Humanname
329390590CV2437104single nucleotide variantNM_012264.5(TMEM184B):c.619G>A (p.Val207Ile)not specified [RCV004262911]uncertain significance223822559238225592Humanname
401771916CV2722990single nucleotide variantNM_012264.5(TMEM184B):c.991G>T (p.Ala331Ser)not specified [RCV004327164]uncertain significance223822170238221702Humanname
407453511CV3486479single nucleotide variantNM_012264.5(TMEM184B):c.731G>T (p.Ser244Ile)not specified [RCV004684569]uncertain significance223822548038225480Humanname
597753575CV3613587single nucleotide variantNM_012264.5(TMEM184B):c.844C>T (p.Arg282Cys)not specified [RCV004867399]uncertain significance223822492338224923Humanname
598213565CV3917533single nucleotide variantNM_012264.5(TMEM184B):c.991G>A (p.Ala331Thr)not specified [RCV005292339]uncertain significance223822170238221702Humanname
598178553CV3917534single nucleotide variantNM_012264.5(TMEM184B):c.363G>C (p.Leu121Phe)not specified [RCV005285993]uncertain significance223823133038231330Humanname
598213569CV3917535single nucleotide variantNM_012264.5(TMEM184B):c.570C>G (p.Ser190Arg)not specified [RCV005292340]uncertain significance223822682638226826Humanname
156374856CV2194882single nucleotide variantNM_012264.5(TMEM184B):c.1130G>A (p.Arg377His)not specified [RCV004075414]uncertain significance223822156338221563Humanname
156250152CV2215630single nucleotide variantNM_012264.5(TMEM184B):c.1144G>A (p.Gly382Ser)not specified [RCV004089383]likely benign223822154938221549Humanname
155942323CV2225676single nucleotide variantNM_012264.5(TMEM184B):c.1039C>T (p.His347Tyr)not specified [RCV004103099]uncertain significance223822165438221654Humanname
401740363CV2706004single nucleotide variantNM_012264.5(TMEM184B):c.1174G>A (p.Ala392Thr)not specified [RCV004320915]uncertain significance223822151938221519Humanname
401873220CV2776250single nucleotide variantNM_012264.5(TMEM184B):c.1106C>A (p.Thr369Asn)not specified [RCV004353618]uncertain significance223822158738221587Humanname
405753050CV3336171single nucleotide variantNM_012264.5(TMEM184B):c.1037C>T (p.Pro346Leu)not specified [RCV004467398]uncertain significance223822165638221656Humanname