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Variants search result for Homo sapiens
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16 records found for search term Myl9
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
25321527CV806410deletionNM_006097.5(MYL9):c.184+2_184+10delMegacystis-microcolon-intestinal hypoperistalsis syndrome 4 [RCV001523898]|Visceral myopathy 1 [RCV001009609]|not specified [RCV005372510]pathogenic|likely pathogenic|uncertain significance203654506436545072Human3name
329357387CV2427698single nucleotide variantNM_006097.5(MYL9):c.290C>T (p.Thr97Met)not specified [RCV004252483]uncertain significance203654813736548137Humanname
329370292CV2461665single nucleotide variantNM_006097.5(MYL9):c.134G>A (p.Arg45His)not specified [RCV004269830]uncertain significance203654501836545018Humanname
405726278CV3321088single nucleotide variantNM_006097.5(MYL9):c.213G>C (p.Glu71Asp)not specified [RCV004450459]uncertain significance203654806036548060Humanname
152037434CV1669118single nucleotide variantNM_006097.5(MYL9):c.445G>C (p.Asp149His)not provided [RCV002224170]uncertain significance203654917536549175Humanname
156178497CV2201597single nucleotide variantNM_006097.5(MYL9):c.431G>A (p.Arg144Gln)not specified [RCV004080086]uncertain significance203654916136549161Humanname
156257420CV2219879single nucleotide variantNM_006097.5(MYL9):c.511G>C (p.Asp171His)not specified [RCV004095512]uncertain significance203654924136549241Humanname
156223455CV2232994single nucleotide variantNM_006097.5(MYL9):c.510A>C (p.Lys170Asn)not specified [RCV004103364]uncertain significance203654924036549240Humanname
156275913CV2316492single nucleotide variantNM_006097.5(MYL9):c.326G>C (p.Cys109Ser)not specified [RCV004169966]uncertain significance203654817336548173Humanname
156288697CV2332952single nucleotide variantNM_006097.5(MYL9):c.316G>A (p.Ala106Thr)not specified [RCV004194253]uncertain significance203654816336548163Humanname
156402103CV2367984single nucleotide variantNM_006097.5(MYL9):c.298G>A (p.Glu100Lys)not specified [RCV004223074]uncertain significance203654814536548145Humanname
407515163CV3454548single nucleotide variantNM_006097.5(MYL9):c.426G>A (p.Met142Ile)not specified [RCV004649805]uncertain significance203654915636549156Humanname
407515170CV3454550single nucleotide variantNM_006097.5(MYL9):c.397C>T (p.Arg133Cys)not specified [RCV004649807]uncertain significance203654912736549127Humanname
407515173CV3454551single nucleotide variantNM_006097.5(MYL9):c.331G>A (p.Asp111Asn)not specified [RCV004649808]uncertain significance203654817836548178Humanname
597664508CV3564888single nucleotide variantNM_006097.5(MYL9):c.379C>T (p.Leu127Phe)not specified [RCV004828922]uncertain significance203654910936549109Humanname
597664516CV3564889single nucleotide variantNM_006097.5(MYL9):c.361G>T (p.Asp121Tyr)not specified [RCV004828923]uncertain significance203654909136549091Humanname