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22 records found for search term Cacng7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156045454CV2319025single nucleotide variantNM_031896.5(CACNG7):c.22G>C (p.Ala8Pro)not specified [RCV004178112]uncertain significance195391285353912853Humanname
405752983CV3302368single nucleotide variantNM_031896.5(CACNG7):c.78C>G (p.Ile26Met)not specified [RCV004432399]uncertain significance195391290953912909Humanname
405752990CV3302369single nucleotide variantNM_031896.5(CACNG7):c.80C>T (p.Ala27Val)not specified [RCV004432400]uncertain significance195391291153912911Humanname
8637016CV92241single nucleotide variantNM_031896.4(CACNG7):c.369C>T (p.Ile123=)Malignant melanoma [RCV000072339]not provided195391545053915450Humanname
156261514CV2216458single nucleotide variantNM_031896.5(CACNG7):c.242C>T (p.Pro81Leu)not specified [RCV004097272]uncertain significance195391454553914545Humanname
155984084CV2247724single nucleotide variantNM_031896.5(CACNG7):c.147G>T (p.Glu49Asp)not specified [RCV004119409]uncertain significance195391297853912978Humanname
155999394CV2296191single nucleotide variantNM_031896.5(CACNG7):c.200G>A (p.Arg67Gln)not specified [RCV004154111]uncertain significance195391450353914503Humanname
329371731CV2442878single nucleotide variantNM_031896.5(CACNG7):c.199C>T (p.Arg67Trp)not specified [RCV004253486]uncertain significance195391450253914502Humanname
405752966CV3302365single nucleotide variantNM_031896.5(CACNG7):c.100C>G (p.Leu34Val)not specified [RCV004432396]uncertain significance195391293153912931Humanname
405752971CV3302366single nucleotide variantNM_031896.5(CACNG7):c.106A>G (p.Met36Val)not specified [RCV004432397]uncertain significance195391293753912937Humanname
405752978CV3302367single nucleotide variantNM_031896.5(CACNG7):c.200G>T (p.Arg67Leu)not specified [RCV004432398]uncertain significance195391450353914503Humanname
597763137CV3637615single nucleotide variantNM_031896.5(CACNG7):c.244G>A (p.Glu82Lys)not specified [RCV004895318]uncertain significance195391454753914547Humanname
598202752CV3946674single nucleotide variantNM_031896.5(CACNG7):c.166G>A (p.Ala56Thr)not specified [RCV005314515]uncertain significance195391299753912997Humanname
156194994CV2223389single nucleotide variantNM_031896.5(CACNG7):c.726C>G (p.Ser242Arg)not specified [RCV004105979]uncertain significance195394219153942191Humanname
155935417CV2225586single nucleotide variantNM_031896.5(CACNG7):c.797A>G (p.Asp266Gly)not specified [RCV004100961]uncertain significance195394226253942262Humanname
401723567CV2724948single nucleotide variantNM_031896.5(CACNG7):c.380G>A (p.Arg127Lys)not specified [RCV004319712]uncertain significance195391546153915461Humanname
401877478CV2790184single nucleotide variantNM_031896.5(CACNG7):c.698A>G (p.Gln233Arg)not specified [RCV004364107]uncertain significance195394216353942163Humanname
597763142CV3637616single nucleotide variantNM_031896.5(CACNG7):c.640C>G (p.Pro214Ala)not specified [RCV004895319]uncertain significance195394210553942105Humanname
598202739CV3946672single nucleotide variantNM_031896.5(CACNG7):c.629A>G (p.Tyr210Cys)not specified [RCV005314513]uncertain significance195394209453942094Humanname
598202745CV3946673single nucleotide variantNM_031896.5(CACNG7):c.748G>T (p.Val250Leu)not specified [RCV005314514]uncertain significance195394221353942213Humanname
8637017CV92242single nucleotide variantNM_031896.4(CACNG7):c.370C>T (p.Arg124Cys)Malignant melanoma [RCV000072340]not provided195391545153915451Humanname
42723294CV984439single nucleotide variantNM_031896.5(CACNG7):c.784A>G (p.Ile262Val)Intellectual disability [RCV001291077]likely pathogenic195394224953942249Human2name