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Variants search result for Homo sapiens
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12 records found for search term Cmtm3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401885142CV2759619single nucleotide variantNM_181553.4(CMTM3):c.85G>A (p.Ala29Thr)not specified [RCV004338590]uncertain significance166660489066604890Humanname
405662970CV3305122single nucleotide variantNM_181553.4(CMTM3):c.40C>A (p.Pro14Thr)not specified [RCV004439644]uncertain significance166660484566604845Humanname
405662976CV3305123single nucleotide variantNM_181553.4(CMTM3):c.82C>T (p.Arg28Cys)not specified [RCV004439645]uncertain significance166660488766604887Humanname
156073146CV2299156single nucleotide variantNM_181553.4(CMTM3):c.182C>T (p.Ala61Val)not specified [RCV004152499]uncertain significance166660834366608343Humanname
407469710CV3429437single nucleotide variantNM_181553.4(CMTM3):c.144G>C (p.Glu48Asp)not specified [RCV004615269]uncertain significance166660494966604949Humanname
597798555CV3653652single nucleotide variantNM_181553.4(CMTM3):c.182C>G (p.Ala61Gly)not specified [RCV004904748]uncertain significance166660834366608343Humanname
598256742CV3941064single nucleotide variantNM_181553.4(CMTM3):c.181G>C (p.Ala61Pro)not specified [RCV005324266]uncertain significance166660834266608342Humanname
156234210CV2223942single nucleotide variantNM_181553.4(CMTM3):c.352A>G (p.Ile118Val)not specified [RCV004094202]uncertain significance166660948366609483Humanname
156303731CV2359428single nucleotide variantNM_181553.4(CMTM3):c.422T>C (p.Ile141Thr)not specified [RCV004214750]uncertain significance166660990566609905Humanname
401898150CV2781004single nucleotide variantNM_181553.4(CMTM3):c.371A>G (p.Tyr124Cys)not specified [RCV004354533]uncertain significance166660950266609502Humanname
407469704CV3429435single nucleotide variantNM_181553.4(CMTM3):c.499A>C (p.Thr167Pro)not specified [RCV004615267]uncertain significance166660998266609982Humanname
407469713CV3429438single nucleotide variantNM_181553.4(CMTM3):c.536C>T (p.Ser179Leu)not specified [RCV004615270]uncertain significance166661262466612624Humanname