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Variants search result for Homo sapiens
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29 records found for search term Myl6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405866950CV2842467single nucleotide variantNM_021019.5(MYL6):c.*16+4C>TEBV-positive nodal T- and NK-cell lymphoma [RCV004557824]likely benign125616067456160674Humanname
156148564CV2212927single nucleotide variantNM_021019.5(MYL6):c.4T>C (p.Cys2Arg)not specified [RCV004091561]uncertain significance125615868456158684Humanname
156246700CV2310670single nucleotide variantNM_021019.5(MYL6):c.7G>A (p.Asp3Asn)not specified [RCV004157329]uncertain significance125615868756158687Humanname
598273647CV3994063single nucleotide variantNM_021019.5(MYL6):c.7G>T (p.Asp3Tyr)not specified [RCV005389759]uncertain significance125615868756158687Humanname
329363208CV2464962single nucleotide variantNM_021019.5(MYL6):c.95G>A (p.Cys32Tyr)not specified [RCV004284880]uncertain significance125615965056159650Humanname
598190144CV3994062single nucleotide variantNM_021019.5(MYL6):c.62G>A (p.Arg21Gln)not specified [RCV005373996]uncertain significance125615961756159617Humanname
598273650CV3994065single nucleotide variantNM_021019.5(MYL6):c.61C>G (p.Arg21Gly)not specified [RCV005389760]uncertain significance125615961656159616Humanname
156110846CV2207740single nucleotide variantNM_021019.5(MYL6):c.340G>C (p.Val114Leu)not specified [RCV004084181]uncertain significance125616013956160139Humanname
156173270CV2380898single nucleotide variantNM_021019.5(MYL6):c.431T>C (p.Phe144Ser)not specified [RCV004218444]uncertain significance125616062956160629Humanname
401746379CV2695557single nucleotide variantNM_021019.5(MYL6):c.350G>A (p.Gly117Asp)not specified [RCV004305729]uncertain significance125616024356160243Humanname
597664444CV3564880single nucleotide variantNM_021019.5(MYL6):c.449C>T (p.Ser150Leu)not specified [RCV004828914]uncertain significance125616064756160647Humanname
598190151CV3994064single nucleotide variantNM_021019.5(MYL6):c.328C>T (p.Arg110Trp)not specified [RCV005373997]uncertain significance125616012756160127Humanname
156152447CV2209366single nucleotide variantNM_002475.5(MYL6B):c.267T>G (p.Cys89Trp)not specified [RCV004093539]uncertain significance125615511956155119Humanname
156020621CV2270348single nucleotide variantNM_002475.5(MYL6B):c.277A>G (p.Met93Val)not specified [RCV004135549]uncertain significance125615512956155129Humanname
155966073CV2284192single nucleotide variantNM_002475.5(MYL6B):c.209A>G (p.Lys70Arg)not specified [RCV004146566]uncertain significance125615506156155061Humanname
329382677CV2424520single nucleotide variantNM_002475.5(MYL6B):c.239G>A (p.Gly80Glu)not specified [RCV004252404]uncertain significance125615509156155091Humanname
405725238CV3320975single nucleotide variantNM_002475.5(MYL6B):c.265T>C (p.Cys89Arg)not specified [RCV004450346]uncertain significance125615511756155117Humanname
598190167CV3994067single nucleotide variantNM_002475.5(MYL6B):c.148C>T (p.Pro50Ser)not specified [RCV005373999]uncertain significance125615406656154066Humanname
155948606CV2242517single nucleotide variantNM_002475.5(MYL6B):c.317T>C (p.Leu106Pro)not specified [RCV004113591]uncertain significance125615516956155169Humanname
156003366CV2254174single nucleotide variantNM_002475.5(MYL6B):c.533C>G (p.Thr178Ser)not specified [RCV004129856]uncertain significance125615748056157480Humanname
155988176CV2285323single nucleotide variantNM_002475.5(MYL6B):c.307G>A (p.Ala103Thr)not specified [RCV004139201]uncertain significance125615515956155159Humanname
155992405CV2286196single nucleotide variantNM_002475.5(MYL6B):c.388A>T (p.Met130Leu)not specified [RCV004146162]uncertain significance125615546056155460Humanname
156281921CV2348816single nucleotide variantNM_002475.5(MYL6B):c.334C>T (p.Pro112Ser)not specified [RCV004203261]uncertain significance125615518656155186Humanname
405725500CV3321004single nucleotide variantNM_002475.5(MYL6B):c.451C>T (p.Arg151Cys)not specified [RCV004450375]uncertain significance125615552356155523Humanname
405725599CV3321015single nucleotide variantNM_002475.5(MYL6B):c.475G>A (p.Gly159Ser)not specified [RCV004450386]uncertain significance125615554756155547Humanname
405725676CV3321023single nucleotide variantNM_002475.5(MYL6B):c.475G>C (p.Gly159Arg)not specified [RCV004450394]uncertain significance125615554756155547Humanname
407515156CV3454546single nucleotide variantNM_002475.5(MYL6B):c.622G>A (p.Val208Ile)not specified [RCV004649803]uncertain significance125615772156157721Humanname
598190159CV3994066single nucleotide variantNM_002475.5(MYL6B):c.527A>C (p.Lys176Thr)not specified [RCV005373998]uncertain significance125615747456157474Humanname
598190180CV3994069single nucleotide variantNM_002475.5(MYL6B):c.409A>T (p.Asn137Tyr)not specified [RCV005374001]uncertain significance125615548156155481Humanname