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Variants search result for Homo sapiens
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16 records found for search term Insig2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156188257CV2395399single nucleotide variantNM_016133.4(INSIG2):c.40T>A (p.Cys14Ser)not specified [RCV004241276]uncertain significance2118096596118096596Humanname
407522702CV3444881single nucleotide variantNM_016133.4(INSIG2):c.29G>A (p.Gly10Glu)not specified [RCV004630779]uncertain significance2118096585118096585Humanname
597784452CV3683508single nucleotide variantNM_016133.4(INSIG2):c.92G>A (p.Arg31Gln)not specified [RCV004931704]uncertain significance2118096648118096648Humanname
15171738CV696987single nucleotide variantNM_016133.4(INSIG2):c.345T>C (p.Phe115=)not provided [RCV000949887]benign2118103297118103297Humanname
15116104CV707690single nucleotide variantNM_016133.4(INSIG2):c.627A>G (p.Gln209=)not provided [RCV000961976]benign2118107180118107180Humanname
405784799CV3267875single nucleotide variantNM_016133.4(INSIG2):c.118G>T (p.Val40Leu)not specified [RCV004398249]uncertain significance2118096674118096674Humanname
405784803CV3267876single nucleotide variantNM_016133.4(INSIG2):c.167C>T (p.Thr56Met)not specified [RCV004398250]uncertain significance2118096723118096723Humanname
407511301CV3444880single nucleotide variantNM_016133.4(INSIG2):c.100G>A (p.Val34Met)not specified [RCV004626415]uncertain significance2118096656118096656Humanname
156220905CV2222424single nucleotide variantNM_016133.4(INSIG2):c.403C>G (p.Leu135Val)not specified [RCV004099282]uncertain significance2118106770118106770Humanname
156219713CV2225982single nucleotide variantNM_016133.4(INSIG2):c.425T>C (p.Ile142Thr)not specified [RCV004105145]uncertain significance2118106792118106792Humanname
155959768CV2313947single nucleotide variantNM_016133.4(INSIG2):c.356A>G (p.Asn119Ser)not specified [RCV004164251]uncertain significance2118103308118103308Humanname
401752550CV2723273single nucleotide variantNM_016133.4(INSIG2):c.403C>T (p.Leu135Phe)not specified [RCV004329500]uncertain significance2118106770118106770Humanname
407522696CV3444878single nucleotide variantNM_016133.4(INSIG2):c.652A>T (p.Ile218Phe)not specified [RCV004630777]uncertain significance2118108296118108296Humanname
407522699CV3444879single nucleotide variantNM_016133.4(INSIG2):c.601A>G (p.Ile201Val)not specified [RCV004630778]uncertain significance2118107154118107154Humanname
407522705CV3444882single nucleotide variantNM_016133.4(INSIG2):c.634A>G (p.Met212Val)not specified [RCV004630780]uncertain significance2118107187118107187Humanname
597784448CV3683507single nucleotide variantNM_016133.4(INSIG2):c.382G>A (p.Asp128Asn)not specified [RCV004931703]uncertain significance2118106749118106749Humanname