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38 records found for search term Tmem186
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401855970CV2754177single nucleotide variantNM_015421.4(TMEM186):c.8C>T (p.Ala3Val)not specified [RCV004334367]uncertain significance1687965868796586Humanname
15106914CV693951single nucleotide variantNM_015421.4(TMEM186):c.1A>G (p.Met1Val)not provided [RCV000871399]|not specified [RCV001817006]benign|likely benign1687976148797614Humanname
405655152CV3228428single nucleotide variantNM_015421.4(TMEM186):c.204C>T (p.Phe68=)not specified [RCV003995163]likely benign1687963908796390Humanname
597753625CV3613600single nucleotide variantNM_015421.4(TMEM186):c.26G>A (p.Arg9His)not specified [RCV004867411]uncertain significance1687965688796568Humanname
405753116CV3336181single nucleotide variantNM_015421.4(TMEM186):c.29G>C (p.Arg10Thr)not specified [RCV004467408]uncertain significance1687965658796565Humanname
597753621CV3613599single nucleotide variantNM_015421.4(TMEM186):c.34C>T (p.Arg12Trp)not specified [RCV004867410]uncertain significance1687965608796560Humanname
156162268CV2272672single nucleotide variantNM_015421.4(TMEM186):c.195C>G (p.Ile65Met)not specified [RCV004133545]uncertain significance1687963998796399Humanname
401773604CV2709403single nucleotide variantNM_015421.4(TMEM186):c.233A>G (p.Gln78Arg)not specified [RCV004316539]uncertain significance1687963618796361Humanname
405753100CV3336179single nucleotide variantNM_015421.4(TMEM186):c.171G>C (p.Trp57Cys)not specified [RCV004467406]uncertain significance1687964238796423Humanname
405753110CV3336180single nucleotide variantNM_015421.4(TMEM186):c.278A>G (p.Tyr93Cys)not specified [RCV004467407]uncertain significance1687963168796316Humanname
597753616CV3613597single nucleotide variantNM_015421.4(TMEM186):c.140A>G (p.Lys47Arg)not specified [RCV004867409]uncertain significance1687964548796454Humanname
597753629CV3613601single nucleotide variantNM_015421.4(TMEM186):c.205G>C (p.Gly69Arg)not specified [RCV004867412]uncertain significance1687963898796389Humanname
598178618CV3917556single nucleotide variantNM_015421.4(TMEM186):c.200C>T (p.Thr67Ile)not specified [RCV005286002]likely benign1687963948796394Humanname
156054550CV2243099single nucleotide variantNM_015421.4(TMEM186):c.321T>A (p.Ser107Arg)not specified [RCV004110010]uncertain significance1687962738796273Humanname
156148899CV2292839single nucleotide variantNM_015421.4(TMEM186):c.425T>G (p.Val142Gly)not specified [RCV004148354]uncertain significance1687961698796169Humanname
156092980CV2300183single nucleotide variantNM_015421.4(TMEM186):c.444G>C (p.Trp148Cys)not specified [RCV004151372]uncertain significance1687961508796150Humanname
155963570CV2308289single nucleotide variantNM_015421.4(TMEM186):c.626A>G (p.His209Arg)not specified [RCV004164781]uncertain significance1687959688795968Humanname
156396686CV2330213single nucleotide variantNM_015421.4(TMEM186):c.583C>T (p.Arg195Cys)not specified [RCV004187672]uncertain significance1687960118796011Humanname
155964603CV2330469single nucleotide variantNM_015421.4(TMEM186):c.498A>C (p.Glu166Asp)not specified [RCV004181038]uncertain significance1687960968796096Humanname
156282575CV2334599single nucleotide variantNM_015421.4(TMEM186):c.307G>A (p.Val103Met)not specified [RCV004188588]uncertain significance1687962878796287Humanname
155916600CV2336173single nucleotide variantNM_015421.4(TMEM186):c.421C>T (p.Arg141Trp)not specified [RCV004189766]uncertain significance1687961738796173Humanname
156030314CV2379592single nucleotide variantNM_015421.4(TMEM186):c.633G>A (p.Met211Ile)not specified [RCV004217292]uncertain significance1687959618795961Humanname
155992829CV2381610single nucleotide variantNM_015421.4(TMEM186):c.398T>G (p.Leu133Arg)not specified [RCV004232083]uncertain significance1687961968796196Humanname
155964209CV2395811single nucleotide variantNM_015421.4(TMEM186):c.427G>T (p.Ala143Ser)not specified [RCV004235335]uncertain significance1687961678796167Humanname
155997977CV2396167single nucleotide variantNM_015421.4(TMEM186):c.500C>G (p.Thr167Ser)not specified [RCV004240131]likely benign1687960948796094Humanname
329391056CV2447665single nucleotide variantNM_015421.4(TMEM186):c.329C>T (p.Ser110Leu)not specified [RCV004258462]uncertain significance1687962658796265Humanname
329398409CV2464981single nucleotide variantNM_015421.4(TMEM186):c.424G>C (p.Val142Leu)not specified [RCV004284896]uncertain significance1687961708796170Humanname
401742730CV2697850single nucleotide variantNM_015421.4(TMEM186):c.338C>A (p.Ala113Asp)not specified [RCV004300563]uncertain significance1687962568796256Humanname
401746835CV2731989single nucleotide variantNM_015421.4(TMEM186):c.452G>A (p.Arg151Gln)not specified [RCV004333224]uncertain significance1687961428796142Humanname
405753121CV3336182single nucleotide variantNM_015421.4(TMEM186):c.527T>C (p.Val176Ala)not specified [RCV004467409]uncertain significance1687960678796067Humanname
405753509CV3336183single nucleotide variantNM_015421.4(TMEM186):c.539G>A (p.Arg180Gln)not specified [RCV004467410]likely benign1687960558796055Humanname
407458703CV3486484single nucleotide variantNM_015421.4(TMEM186):c.530G>A (p.Arg177His)not specified [RCV004686909]uncertain significance1687960648796064Humanname
597795227CV3613598single nucleotide variantNM_015421.4(TMEM186):c.472A>G (p.Met158Val)not specified [RCV004878144]likely benign1687961228796122Humanname
598178587CV3917550single nucleotide variantNM_015421.4(TMEM186):c.346A>C (p.Met116Leu)not specified [RCV005285998]uncertain significance1687962488796248Humanname
598178596CV3917551single nucleotide variantNM_015421.4(TMEM186):c.374G>A (p.Arg125Gln)not specified [RCV005285999]uncertain significance1687962208796220Humanname
598178604CV3917553single nucleotide variantNM_015421.4(TMEM186):c.413C>G (p.Thr138Ser)not specified [RCV005286000]uncertain significance1687961818796181Humanname
598178610CV3917554single nucleotide variantNM_015421.4(TMEM186):c.386G>T (p.Gly129Val)not specified [RCV005286001]uncertain significance1687962088796208Humanname
598213623CV3917555single nucleotide variantNM_015421.4(TMEM186):c.581G>A (p.Gly194Glu)not specified [RCV005292352]uncertain significance1687960138796013Humanname