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Variants search result for Homo sapiens
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10 records found for search term Commd3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329399991CV2444265single nucleotide variantNM_012071.4(COMMD3):c.426T>G (p.His142Gln)not specified [RCV004263033]uncertain significance102231882022318820Humanname
407477405CV3423287single nucleotide variantNM_012071.4(COMMD3):c.487T>C (p.Tyr163His)not specified [RCV004608318]likely benign102231897722318977Humanname
598233514CV3948805single nucleotide variantNM_012071.4(COMMD3):c.403C>G (p.Gln135Glu)not specified [RCV005319944]uncertain significance102231870522318705Humanname
401752858CV2682960single nucleotide variantNM_001204062.2(COMMD3-BMI1):c.6G>T (p.Glu2Asp)not specified [RCV004283750]uncertain significance102231642322316423Humanname
8633578CV88793single nucleotide variantNM_001204062.1(COMMD3-BMI1):c.293A>G (p.Glu98Gly)Malignant melanoma [RCV000068888]not provided102231814622318146Humanname
156142346CV2383769single nucleotide variantNM_001204062.2(COMMD3-BMI1):c.356T>C (p.Leu119Pro)not specified [RCV004231647]uncertain significance102231896422318964Humanname
405656982CV3305465single nucleotide variantNM_001204062.2(COMMD3-BMI1):c.418T>C (p.Tyr140His)not specified [RCV004437746]uncertain significance102232643822326438Humanname
597648266CV3654079single nucleotide variantNM_001204062.2(COMMD3-BMI1):c.992C>T (p.Thr331Ile)not specified [RCV004910225]uncertain significance102232869122328691Humanname
38461800CV919264single nucleotide variantNM_001204062.2(COMMD3-BMI1):c.541T>G (p.Phe181Val)See cases [RCV001197934]uncertain significance102232656122326561Humanname
8626799CV81943single nucleotide variantNM_001204062.1(COMMD3-BMI1):c.1373C>T (p.Ser458Leu)Malignant melanoma [RCV000062022]not provided102232950522329505Humanname