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Variants search result for Homo sapiens
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20 records found for search term Hoxc5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15107881CV713612single nucleotide variantNM_018953.4(HOXC5):c.237G>A (p.Ala79=)not provided [RCV000960380]benign125403335954033359Humanname
401858799CV2773636single nucleotide variantNM_018953.4(HOXC5):c.73G>A (p.Gly25Arg)not specified [RCV004356328]uncertain significance125403319554033195Humanname
405798263CV3263433single nucleotide variantNM_018953.4(HOXC5):c.28T>C (p.Tyr10His)not specified [RCV004402072]uncertain significance125403315054033150Humanname
405798254CV3263436single nucleotide variantNM_018953.4(HOXC5):c.49C>A (p.Pro17Thr)not specified [RCV004402075]uncertain significance125403317154033171Humanname
407483813CV3433826single nucleotide variantNM_018953.4(HOXC5):c.61A>G (p.Met21Val)not specified [RCV004633027]uncertain significance125403318354033183Humanname
15135153CV713611single nucleotide variantNM_018953.4(HOXC5):c.33G>C (p.Lys11Asn)not provided [RCV000965241]benign125403315554033155Humanname
156080099CV2226597single nucleotide variantNM_018953.4(HOXC5):c.275C>T (p.Ala92Val)not specified [RCV004101847]uncertain significance125403339754033397Humanname
156122636CV2276112single nucleotide variantNM_018953.4(HOXC5):c.295T>A (p.Tyr99Asn)not specified [RCV004141777]uncertain significance125403341754033417Humanname
405798270CV3263431single nucleotide variantNM_018953.4(HOXC5):c.266A>G (p.Asp89Gly)not specified [RCV004402070]uncertain significance125403338854033388Humanname
405798260CV3263434single nucleotide variantNM_018953.4(HOXC5):c.290G>T (p.Gly97Val)not specified [RCV004402073]uncertain significance125403341254033412Humanname
407483818CV3433827single nucleotide variantNM_018953.4(HOXC5):c.121G>A (p.Gly41Ser)not specified [RCV004633028]uncertain significance125403324354033243Humanname
407483266CV3433828single nucleotide variantNM_018953.4(HOXC5):c.283A>G (p.Asn95Asp)not specified [RCV004626247]uncertain significance125403340554033405Humanname
597695542CV3679725single nucleotide variantNM_018953.4(HOXC5):c.185A>C (p.Asp62Ala)not specified [RCV004928737]uncertain significance125403330754033307Humanname
401746259CV2701415single nucleotide variantNM_018953.4(HOXC5):c.533G>A (p.Arg178His)not specified [RCV004311773]uncertain significance125403435654034356Humanname
401856731CV2756695single nucleotide variantNM_018953.4(HOXC5):c.403C>A (p.Pro135Thr)not specified [RCV004345204]uncertain significance125403352554033525Humanname
405798257CV3263435single nucleotide variantNM_018953.4(HOXC5):c.427T>A (p.Trp143Arg)not specified [RCV004402074]uncertain significance125403354954033549Humanname
597695516CV3679723single nucleotide variantNM_018953.4(HOXC5):c.311C>T (p.Ala104Val)not specified [RCV004928735]uncertain significance125403343354033433Humanname
597695529CV3679724single nucleotide variantNM_018953.4(HOXC5):c.458C>G (p.Thr153Arg)not specified [RCV004928736]uncertain significance125403428154034281Humanname
598192025CV3971782single nucleotide variantNM_018953.4(HOXC5):c.361G>A (p.Glu121Lys)not specified [RCV005354382]uncertain significance125403348354033483Humanname
598192032CV3971783single nucleotide variantNM_018953.4(HOXC5):c.653G>A (p.Ser218Asn)not specified [RCV005354383]uncertain significance125403447654034476Humanname