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43 records found for search term Calhm2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156298901CV2241010single nucleotide variantNM_015916.5(CALHM2):c.76G>A (p.Gly26Ser)not specified [RCV004102276]uncertain significance10103449866103449866Humanname
401777983CV2718409single nucleotide variantNM_015916.5(CALHM2):c.31T>G (p.Phe11Val)not specified [RCV004318232]uncertain significance10103449911103449911Humanname
405766536CV3302527single nucleotide variantNM_015916.5(CALHM2):c.29G>A (p.Arg10His)not specified [RCV004434541]uncertain significance10103449913103449913Humanname
329387078CV2463312single nucleotide variantNM_015916.5(CALHM2):c.169G>A (p.Gly57Arg)not specified [RCV004275372]uncertain significance10103449773103449773Humanname
401899757CV2762168single nucleotide variantNM_015916.5(CALHM2):c.176C>T (p.Ala59Val)not specified [RCV004341982]uncertain significance10103449766103449766Humanname
401890679CV2778288single nucleotide variantNM_015916.5(CALHM2):c.155G>A (p.Arg52Gln)not specified [RCV004350343]uncertain significance10103449787103449787Humanname
405766523CV3302525single nucleotide variantNM_015916.5(CALHM2):c.110A>C (p.Glu37Ala)not specified [RCV004434539]uncertain significance10103449832103449832Humanname
405766530CV3302526single nucleotide variantNM_015916.5(CALHM2):c.253G>C (p.Glu85Gln)not specified [RCV004434540]uncertain significance10103449689103449689Humanname
407474371CV3424426single nucleotide variantNM_015916.5(CALHM2):c.253G>A (p.Glu85Lys)not specified [RCV004600596]uncertain significance10103449689103449689Humanname
597763693CV3647341single nucleotide variantNM_015916.5(CALHM2):c.289G>A (p.Ala97Thr)not specified [RCV004895428]uncertain significance10103449653103449653Humanname
598203537CV3942880single nucleotide variantNM_015916.5(CALHM2):c.184G>C (p.Gly62Arg)not specified [RCV005314641]uncertain significance10103449758103449758Humanname
155972557CV2214324single nucleotide variantNM_015916.5(CALHM2):c.593T>C (p.Leu198Pro)not specified [RCV004086311]uncertain significance10103447531103447531Humanname
156020327CV2230321single nucleotide variantNM_015916.5(CALHM2):c.329C>T (p.Ala110Val)not specified [RCV004099929]uncertain significance10103449613103449613Humanname
156237726CV2235709single nucleotide variantNM_015916.5(CALHM2):c.940G>A (p.Asp314Asn)not specified [RCV004111847]uncertain significance10103447184103447184Humanname
156071637CV2254930single nucleotide variantNM_015916.5(CALHM2):c.326G>A (p.Arg109His)not specified [RCV004117167]uncertain significance10103449616103449616Humanname
156181118CV2255050single nucleotide variantNM_015916.5(CALHM2):c.613C>T (p.Leu205Phe)not specified [RCV004115691]uncertain significance10103447511103447511Humanname
156251410CV2286840single nucleotide variantNM_015916.5(CALHM2):c.658T>C (p.Trp220Arg)not specified [RCV004142642]uncertain significance10103447466103447466Humanname
155941308CV2294229single nucleotide variantNM_015916.5(CALHM2):c.413C>T (p.Pro138Leu)not specified [RCV004149581]uncertain significance10103449529103449529Humanname
155990595CV2374768single nucleotide variantNM_015916.5(CALHM2):c.533G>A (p.Arg178His)not specified [RCV004225373]uncertain significance10103449409103449409Humanname
156258078CV2383693single nucleotide variantNM_015916.5(CALHM2):c.382T>C (p.Tyr128His)not specified [RCV004231581]uncertain significance10103449560103449560Humanname
329362027CV2456657single nucleotide variantNM_015916.5(CALHM2):c.532C>T (p.Arg178Cys)not specified [RCV004277840]uncertain significance10103449410103449410Humanname
401726842CV2674568single nucleotide variantNM_015916.5(CALHM2):c.325C>T (p.Arg109Cys)not specified [RCV004291444]uncertain significance10103449617103449617Humanname
401733609CV2682585single nucleotide variantNM_015916.5(CALHM2):c.444C>G (p.Phe148Leu)not specified [RCV004292638]uncertain significance10103449498103449498Humanname
401857857CV2766045single nucleotide variantNM_015916.5(CALHM2):c.850G>A (p.Val284Ile)not specified [RCV004340505]uncertain significance10103447274103447274Humanname
401864461CV2784875single nucleotide variantNM_015916.5(CALHM2):c.811G>A (p.Gly271Ser)not specified [RCV004352654]uncertain significance10103447313103447313Humanname
405766542CV3302528single nucleotide variantNM_015916.5(CALHM2):c.351G>T (p.Trp117Cys)not specified [RCV004434542]uncertain significance10103449591103449591Humanname
405766548CV3302529single nucleotide variantNM_015916.5(CALHM2):c.406G>A (p.Val136Met)not specified [RCV004434543]uncertain significance10103449536103449536Humanname
405766553CV3302530single nucleotide variantNM_015916.5(CALHM2):c.492G>C (p.Glu164Asp)not specified [RCV004434544]uncertain significance10103449450103449450Humanname
405766558CV3302531single nucleotide variantNM_015916.5(CALHM2):c.643C>T (p.Arg215Cys)not specified [RCV004434545]uncertain significance10103447481103447481Humanname
405766565CV3302532single nucleotide variantNM_015916.5(CALHM2):c.698G>C (p.Arg233Pro)not specified [RCV004434546]uncertain significance10103447426103447426Humanname
405766571CV3302533single nucleotide variantNM_015916.5(CALHM2):c.710T>A (p.Val237Glu)not specified [RCV004434547]uncertain significance10103447414103447414Humanname
405766578CV3302534single nucleotide variantNM_015916.5(CALHM2):c.727G>A (p.Ala243Thr)not specified [RCV004434548]uncertain significance10103447397103447397Humanname
405766583CV3302535single nucleotide variantNM_015916.5(CALHM2):c.946G>C (p.Val316Leu)not specified [RCV004434549]uncertain significance10103447178103447178Humanname
407474368CV3424425single nucleotide variantNM_015916.5(CALHM2):c.670C>T (p.Arg224Cys)not specified [RCV004600595]uncertain significance10103447454103447454Humanname
407474376CV3424428single nucleotide variantNM_015916.5(CALHM2):c.815C>T (p.Thr272Met)not specified [RCV004600597]uncertain significance10103447309103447309Humanname
597763685CV3647339single nucleotide variantNM_015916.5(CALHM2):c.932C>T (p.Ala311Val)not specified [RCV004895426]uncertain significance10103447192103447192Humanname
597763689CV3647340single nucleotide variantNM_015916.5(CALHM2):c.516C>G (p.Phe172Leu)not specified [RCV004895427]uncertain significance10103449426103449426Humanname
597763697CV3647342single nucleotide variantNM_015916.5(CALHM2):c.635T>C (p.Leu212Pro)not specified [RCV004895429]uncertain significance10103447489103447489Humanname
598203513CV3942876single nucleotide variantNM_015916.5(CALHM2):c.600C>A (p.Phe200Leu)not specified [RCV005314637]uncertain significance10103447524103447524Humanname
598203519CV3942877single nucleotide variantNM_015916.5(CALHM2):c.806T>C (p.Val269Ala)not specified [RCV005314638]uncertain significance10103447318103447318Humanname
598203525CV3942878single nucleotide variantNM_015916.5(CALHM2):c.706G>A (p.Glu236Lys)not specified [RCV005314639]uncertain significance10103447418103447418Humanname
598203531CV3942879single nucleotide variantNM_015916.5(CALHM2):c.961C>T (p.Leu321Phe)not specified [RCV005314640]uncertain significance10103447163103447163Humanname
8626762CV81906single nucleotide variantNM_015916.4(CALHM2):c.440A>G (p.His147Arg)Malignant melanoma [RCV000061985]not provided10103449502103449502Humanname