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43 records found for search term Calhm1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598203489CV3942872single nucleotide variantNM_001001412.4(CALHM1):c.17G>A (p.Arg6Gln)not specified [RCV005314633]uncertain significance10103458735103458735Humanname
598203496CV3942873single nucleotide variantNM_001001412.4(CALHM1):c.21G>T (p.Met7Ile)not specified [RCV005314634]uncertain significance10103458731103458731Humanname
598203502CV3942874single nucleotide variantNM_001001412.4(CALHM1):c.23T>A (p.Ile8Asn)not specified [RCV005314635]uncertain significance10103458729103458729Humanname
155916823CV2336214single nucleotide variantNM_001001412.4(CALHM1):c.266G>A (p.Arg89Gln)not specified [RCV004191970]uncertain significance10103458486103458486Humanname
329384964CV2454415single nucleotide variantNM_001001412.4(CALHM1):c.290G>A (p.Arg97His)not specified [RCV004267925]uncertain significance10103458462103458462Humanname
329390393CV2459177single nucleotide variantNM_001001412.4(CALHM1):c.100A>T (p.Met34Leu)not specified [RCV004272622]uncertain significance10103458652103458652Humanname
401907754CV2809593single nucleotide variantNM_001001412.4(CALHM1):c.175G>A (p.Ala59Thr)not provided [RCV003422854]uncertain significance10103458577103458577Humanname
405766472CV3302516single nucleotide variantNM_001001412.4(CALHM1):c.149C>T (p.Ala50Val)not specified [RCV004434530]uncertain significance10103458603103458603Humanname
407501057CV3424423single nucleotide variantNM_001001412.4(CALHM1):c.160G>A (p.Ala54Thr)not specified [RCV004607288]uncertain significance10103458592103458592Humanname
597763681CV3647338single nucleotide variantNM_001001412.4(CALHM1):c.265C>T (p.Arg89Trp)not specified [RCV004895425]uncertain significance10103458487103458487Humanname
598203509CV3942875single nucleotide variantNM_001001412.4(CALHM1):c.213G>T (p.Met71Ile)not specified [RCV005314636]uncertain significance10103458539103458539Humanname
156031772CV2209701single nucleotide variantNM_001001412.4(CALHM1):c.955G>A (p.Glu319Lys)not specified [RCV004083026]uncertain significance10103455348103455348Humanname
155915189CV2264961single nucleotide variantNM_001001412.4(CALHM1):c.475G>A (p.Val159Met)not specified [RCV004134692]uncertain significance10103458277103458277Humanname
155903397CV2274870single nucleotide variantNM_001001412.4(CALHM1):c.416G>C (p.Gly139Ala)not specified [RCV004133062]uncertain significance10103458336103458336Humanname
155991583CV2276608single nucleotide variantNM_001001412.4(CALHM1):c.932C>T (p.Pro311Leu)not specified [RCV004146094]uncertain significance10103455371103455371Humanname
156029768CV2278659single nucleotide variantNM_001001412.4(CALHM1):c.848C>T (p.Ala283Val)not specified [RCV004134862]uncertain significance10103455455103455455Humanname
156254467CV2311540single nucleotide variantNM_001001412.4(CALHM1):c.514G>C (p.Ala172Pro)not specified [RCV004168365]uncertain significance10103458238103458238Humanname
156161277CV2323435single nucleotide variantNM_001001412.4(CALHM1):c.814G>A (p.Ala272Thr)not specified [RCV004165654]uncertain significance10103455489103455489Humanname
156085706CV2340472single nucleotide variantNM_001001412.4(CALHM1):c.976G>A (p.Gly326Ser)not specified [RCV004197197]uncertain significance10103455327103455327Humanname
155983243CV2371249single nucleotide variantNM_001001412.4(CALHM1):c.871C>T (p.Arg291Cys)not specified [RCV004220986]uncertain significance10103455432103455432Humanname
329383166CV2441943single nucleotide variantNM_001001412.4(CALHM1):c.961C>A (p.Pro321Thr)not specified [RCV004262120]uncertain significance10103455342103455342Humanname
401727311CV2684568single nucleotide variantNM_001001412.4(CALHM1):c.701C>T (p.Thr234Met)not specified [RCV004293677]uncertain significance10103455602103455602Humanname
401765031CV2701739single nucleotide variantNM_001001412.4(CALHM1):c.601G>A (p.Val201Met)not specified [RCV004314143]uncertain significance10103455702103455702Humanname
401774220CV2702652single nucleotide variantNM_001001412.4(CALHM1):c.982G>T (p.Ala328Ser)not specified [RCV004318918]uncertain significance10103455321103455321Humanname
401878600CV2770702single nucleotide variantNM_001001412.4(CALHM1):c.353C>T (p.Thr118Met)not specified [RCV004349748]uncertain significance10103458399103458399Humanname
405766478CV3302517single nucleotide variantNM_001001412.4(CALHM1):c.319G>A (p.Ala107Thr)not specified [RCV004434531]uncertain significance10103458433103458433Humanname
405766484CV3302518single nucleotide variantNM_001001412.4(CALHM1):c.329C>T (p.Ala110Val)not specified [RCV004434532]uncertain significance10103458423103458423Humanname
405766489CV3302519single nucleotide variantNM_001001412.4(CALHM1):c.403G>A (p.Val135Met)not specified [RCV004434533]uncertain significance10103458349103458349Humanname
405766496CV3302520single nucleotide variantNM_001001412.4(CALHM1):c.485C>T (p.Pro162Leu)not specified [RCV004434534]uncertain significance10103458267103458267Humanname
405766501CV3302521single nucleotide variantNM_001001412.4(CALHM1):c.617G>A (p.Arg206Gln)not specified [RCV004434535]uncertain significance10103455686103455686Humanname
405766506CV3302522single nucleotide variantNM_001001412.4(CALHM1):c.638C>T (p.Ala213Val)not specified [RCV004434536]uncertain significance10103455665103455665Humanname
405766511CV3302523single nucleotide variantNM_001001412.4(CALHM1):c.682C>A (p.Arg228Ser)not specified [RCV004434537]uncertain significance10103455621103455621Humanname
405766517CV3302524single nucleotide variantNM_001001412.4(CALHM1):c.889G>T (p.Gly297Cys)not specified [RCV004434538]uncertain significance10103455414103455414Humanname
407474364CV3424424single nucleotide variantNM_001001412.4(CALHM1):c.305C>T (p.Ser102Phe)not specified [RCV004600594]uncertain significance10103458447103458447Humanname
597763665CV3637779single nucleotide variantNM_001001412.4(CALHM1):c.322C>T (p.Leu108Phe)not specified [RCV004895421]uncertain significance10103458430103458430Humanname
597763669CV3637780single nucleotide variantNM_001001412.4(CALHM1):c.557C>T (p.Ala186Val)not specified [RCV004895422]uncertain significance10103455746103455746Humanname
597763673CV3637781single nucleotide variantNM_001001412.4(CALHM1):c.353C>A (p.Thr118Lys)not specified [RCV004895423]uncertain significance10103458399103458399Humanname
597763677CV3647337single nucleotide variantNM_001001412.4(CALHM1):c.725T>A (p.Phe242Tyr)not specified [RCV004895424]uncertain significance10103455578103455578Humanname
12849110CV371133single nucleotide variantNM_001001412.4(CALHM1):c.461G>A (p.Arg154His)not provided [RCV000424150]likely pathogenic10103458291103458291Humanname
598203478CV3942870single nucleotide variantNM_001001412.4(CALHM1):c.608G>A (p.Arg203His)not specified [RCV005314631]uncertain significance10103455695103455695Humanname
598203483CV3942871single nucleotide variantNM_001001412.4(CALHM1):c.607C>T (p.Arg203Cys)not specified [RCV005314632]uncertain significance10103455696103455696Humanname
15118700CV712135single nucleotide variantNM_001001412.4(CALHM1):c.457G>A (p.Ala153Thr)not provided [RCV000962424]benign10103458295103458295Humanname
405766464CV3302515single nucleotide variantNM_001001412.4(CALHM1):c.1012G>A (p.Glu338Lys)not specified [RCV004434529]uncertain significance10103455291103455291Humanname