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Variants search result for Homo sapiens
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31 records found for search term Mageb4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15149629CV729558single nucleotide variantNM_002367.4(MAGEB4):c.75C>T (p.Leu25=)not provided [RCV000879205]benignX3024221030242210Humanname
156076415CV2251311single nucleotide variantNM_002367.4(MAGEB4):c.28C>T (p.Arg10Cys)not specified [RCV004115523]uncertain significanceX3024216330242163Humanname
156395711CV2325880single nucleotide variantNM_002367.4(MAGEB4):c.49C>G (p.Arg17Gly)not specified [RCV004174061]uncertain significanceX3024218430242184Humanname
407484340CV3449591single nucleotide variantNM_002367.4(MAGEB4):c.83G>A (p.Gly28Asp)not specified [RCV004640510]uncertain significanceX3024221830242218Humanname
598164775CV3992321single nucleotide variantNM_002367.4(MAGEB4):c.88C>T (p.Pro30Ser)not specified [RCV005369059]uncertain significanceX3024222330242223Humanname
598183922CV3992324single nucleotide variantNM_002367.4(MAGEB4):c.80T>A (p.Val27Asp)not specified [RCV005373005]uncertain significanceX3024221530242215Humanname
15175104CV706204single nucleotide variantNM_002367.4(MAGEB4):c.354G>A (p.Gln118=)not provided [RCV000950498]benignX3024248930242489Humanname
15101015CV729557single nucleotide variantNM_002367.4(MAGEB4):c.56G>A (p.Arg19His)not provided [RCV000892209]benignX3024219130242191Humanname
15189022CV743292single nucleotide variantNM_002367.4(MAGEB4):c.705C>T (p.His235=)not provided [RCV000909532]likely benignX3024284030242840Humanname
8637842CV93068single nucleotide variantNM_002367.3(MAGEB4):c.601C>T (p.Leu201=)Malignant melanoma [RCV000073166]not providedX3024273630242736Humanname
155924366CV2248760single nucleotide variantNM_002367.4(MAGEB4):c.236G>T (p.Gly79Val)not specified [RCV004121915]uncertain significanceX3024237130242371Humanname
155965711CV2395990single nucleotide variantNM_002367.4(MAGEB4):c.206C>T (p.Thr69Ile)not specified [RCV004237538]uncertain significanceX3024234130242341Humanname
407468777CV3449594single nucleotide variantNM_002367.4(MAGEB4):c.203C>T (p.Thr68Ile)not specified [RCV004636403]uncertain significanceX3024233830242338Humanname
407484352CV3449595single nucleotide variantNM_002367.4(MAGEB4):c.281C>T (p.Ser94Phe)not specified [RCV004640512]uncertain significanceX3024241630242416Humanname
598164782CV3992322single nucleotide variantNM_002367.4(MAGEB4):c.235G>A (p.Gly79Arg)not specified [RCV005369060]likely benignX3024237030242370Humanname
8637841CV93067single nucleotide variantNM_002367.3(MAGEB4):c.142G>A (p.Asp48Asn)Malignant melanoma [RCV000073165]not providedX3024227730242277Humanname
155974949CV2221243single nucleotide variantNM_002367.4(MAGEB4):c.698A>G (p.Lys233Arg)not specified [RCV004094680]uncertain significanceX3024283330242833Humanname
401926594CV2821417single nucleotide variantNM_002367.4(MAGEB4):c.959G>C (p.Arg320Thr)not provided [RCV003438001]likely benignX3024309430243094Humanname
405651239CV3277543single nucleotide variantNM_002367.4(MAGEB4):c.316A>G (p.Lys106Glu)not specified [RCV004413521]uncertain significanceX3024245130242451Humanname
405651241CV3277544single nucleotide variantNM_002367.4(MAGEB4):c.725G>A (p.Arg242Gln)not specified [RCV004413522]uncertain significanceX3024286030242860Humanname
405651243CV3277545single nucleotide variantNM_002367.4(MAGEB4):c.833C>A (p.Ala278Glu)not specified [RCV004413523]uncertain significanceX3024296830242968Humanname
405651245CV3277546single nucleotide variantNM_002367.4(MAGEB4):c.983C>T (p.Thr328Ile)not specified [RCV004413524]uncertain significanceX3024311830243118Humanname
407468774CV3449593single nucleotide variantNM_002367.4(MAGEB4):c.709A>G (p.Ile237Val)not specified [RCV004636402]uncertain significanceX3024284430242844Humanname
597623674CV3694090single nucleotide variantNM_002367.4(MAGEB4):c.338C>T (p.Thr113Met)not specified [RCV004936691]uncertain significanceX3024247330242473Humanname
597623675CV3694091single nucleotide variantNM_002367.4(MAGEB4):c.325C>G (p.Leu109Val)not specified [RCV004936692]uncertain significanceX3024246030242460Humanname
597623677CV3694093single nucleotide variantNM_002367.4(MAGEB4):c.733A>C (p.Ile245Leu)not specified [RCV004936694]uncertain significanceX3024286830242868Humanname
598164788CV3992323single nucleotide variantNM_002367.4(MAGEB4):c.437A>G (p.His146Arg)not specified [RCV005369061]uncertain significanceX3024257230242572Humanname
15179775CV729559single nucleotide variantNM_002367.4(MAGEB4):c.799C>A (p.Arg267Ser)not provided [RCV000885366]benignX3024293430242934Humanname
15163912CV729560single nucleotide variantNM_002367.4(MAGEB4):c.989T>C (p.Met330Thr)not provided [RCV000882078]benignX3024312430243124Humanname
151661780CV1330011single nucleotide variantNM_002367.4(MAGEB4):c.1041A>T (p.Ter347Cys)not provided [RCV001823422]uncertain significanceX3024317630243176Humanname
405651237CV3277542single nucleotide variantNM_002367.4(MAGEB4):c.1019G>A (p.Ser340Asn)not specified [RCV004413520]uncertain significanceX3024315430243154Humanname