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Variants search result for Homo sapiens
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22 records found for search term Snx6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156177772CV2201537single nucleotide variantNM_152233.4(SNX6):c.-12C>Tnot specified [RCV004080028]uncertain significance143463012834630128Humanname
329373239CV2434155single nucleotide variantNM_152233.4(SNX6):c.-15C>Tnot specified [RCV004250051]uncertain significance143463013134630131Humanname
405733892CV3322733single nucleotide variantNM_152233.4(SNX6):c.-18C>Gnot specified [RCV004464695]uncertain significance143463013434630134Humanname
405733899CV3322734single nucleotide variantNM_152233.4(SNX6):c.-30G>Tnot specified [RCV004464696]uncertain significance143463014634630146Humanname
8635211CV90433single nucleotide variantNM_021249.3(SNX6):c.45-711C>TMalignant melanoma [RCV000070531]not provided143460418234604182Humanname
156075229CV2321763single nucleotide variantNM_152233.3(SNX6):c.4C>T (p.Arg2Cys)not specified [RCV004179756]uncertain significance143463014934630149Humanname
156253109CV2390122single nucleotide variantNM_152233.4(SNX6):c.161G>A (p.Ser54Asn)not specified [RCV004240511]uncertain significance143460813934608139Humanname
598245735CV3911791single nucleotide variantNM_152233.4(SNX6):c.206A>G (p.Gln69Arg)not specified [RCV005277041]uncertain significance143460809434608094Humanname
156318744CV2260737single nucleotide variantNM_152233.4(SNX6):c.721G>A (p.Ala241Thr)not specified [RCV004125662]uncertain significance143458630334586303Humanname
156301817CV2307107single nucleotide variantNM_152233.4(SNX6):c.598G>A (p.Val200Ile)not specified [RCV004159589]uncertain significance143459756434597564Humanname
401719294CV2679486single nucleotide variantNM_152233.4(SNX6):c.823G>A (p.Asp275Asn)not specified [RCV004287791]uncertain significance143458157234581572Humanname
401891031CV2778607single nucleotide variantNM_152233.4(SNX6):c.779C>G (p.Ser260Cys)not specified [RCV004344255]uncertain significance143458624534586245Humanname
407504102CV3484863single nucleotide variantNM_152233.4(SNX6):c.622G>T (p.Asp208Tyr)not specified [RCV004670431]uncertain significance143459314134593141Humanname
407525329CV3484864single nucleotide variantNM_152233.4(SNX6):c.623A>T (p.Asp208Val)not specified [RCV004679151]uncertain significance143459314034593140Humanname
597755525CV3607370single nucleotide variantNM_152233.4(SNX6):c.722C>G (p.Ala241Gly)not specified [RCV004868196]uncertain significance143458630234586302Humanname
597755528CV3607372single nucleotide variantNM_152233.4(SNX6):c.627C>A (p.Phe209Leu)not specified [RCV004868197]uncertain significance143459313634593136Humanname
598172381CV3911790single nucleotide variantNM_152233.4(SNX6):c.815A>G (p.Glu272Gly)not specified [RCV005285018]uncertain significance143458158034581580Humanname
598245744CV3911792single nucleotide variantNM_152233.4(SNX6):c.916G>A (p.Ala306Thr)not specified [RCV005277042]uncertain significance143457576134575761Humanname
156328694CV2213664single nucleotide variantNM_152233.4(SNX6):c.1001A>G (p.Asn334Ser)not specified [RCV004089741]uncertain significance143456793434567934Humanname
401783404CV2723536single nucleotide variantNM_152233.4(SNX6):c.1216A>C (p.Thr406Pro)not specified [RCV004323940]uncertain significance143456312734563127Humanname
407504110CV3484866single nucleotide variantNM_152233.4(SNX6):c.1084C>T (p.Leu362Phe)not specified [RCV004670433]uncertain significance143456776934567769Humanname
597741232CV3607371single nucleotide variantNM_152233.4(SNX6):c.1174C>A (p.Leu392Ile)not specified [RCV004864822]uncertain significance143456316934563169Humanname