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Variants search result for Homo sapiens
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23 records found for search term Ifnb1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597763866CV3679849single nucleotide variantNM_002176.4(IFNB1):c.9C>G (p.Asn3Lys)not specified [RCV004926391]uncertain significance92107786121077861Humanname
598268257CV3979265single nucleotide variantNM_002176.4(IFNB1):c.14G>A (p.Cys5Tyr)not specified [RCV005349666]uncertain significance92107785621077856Humanname
15165880CV711924single nucleotide variantNM_002176.4(IFNB1):c.232T>C (p.Leu78=)not provided [RCV000971047]benign92107763821077638Humanname
15197209CV723532single nucleotide variantNM_002176.4(IFNB1):c.228C>T (p.Ala76=)not provided [RCV000889992]benign92107764221077642Humanname
156195013CV2347406single nucleotide variantNM_002176.4(IFNB1):c.70T>C (p.Tyr24His)not specified [RCV004207244]uncertain significance92107780021077800Humanname
407466341CV3440600single nucleotide variantNM_002176.4(IFNB1):c.80T>C (p.Leu27Pro)not specified [RCV004635604]uncertain significance92107779021077790Humanname
407466346CV3440601single nucleotide variantNM_002176.4(IFNB1):c.68G>C (p.Ser23Thr)not specified [RCV004635605]uncertain significance92107780221077802Humanname
156210676CV2259821single nucleotide variantNM_002176.4(IFNB1):c.178G>A (p.Asp60Asn)not specified [RCV004117086]uncertain significance92107769221077692Humanname
401863644CV2777043single nucleotide variantNM_002176.4(IFNB1):c.157C>G (p.Leu53Val)not specified [RCV004351838]uncertain significance92107771321077713Humanname
597763876CV3679847single nucleotide variantNM_002176.4(IFNB1):c.266C>T (p.Ala89Val)not specified [RCV004926389]uncertain significance92107760421077604Humanname
597763870CV3679848single nucleotide variantNM_002176.4(IFNB1):c.129G>C (p.Trp43Cys)not specified [RCV004926390]uncertain significance92107774121077741Humanname
598268263CV3979266single nucleotide variantNM_002176.4(IFNB1):c.278A>G (p.Gln93Arg)not specified [RCV005349667]likely benign92107759221077592Humanname
15115836CV711925single nucleotide variantNM_002176.4(IFNB1):c.180C>A (p.Asp60Glu)not provided [RCV000961922]benign92107769021077690Humanname
150534776CV1311608single nucleotide variantNM_002176.4(IFNB1):c.403G>T (p.Gly135Ter)Multisystem inflammatory syndrome in children [RCV001779418]|not provided [RCV003992548]risk factor|uncertain significance92107746721077467Human1name
156340568CV2229528single nucleotide variantNM_002176.4(IFNB1):c.424C>A (p.His142Asn)not specified [RCV004103068]uncertain significance92107744621077446Humanname
156299727CV2306879single nucleotide variantNM_002176.4(IFNB1):c.322C>T (p.Leu108Phe)not specified [RCV004157409]uncertain significance92107754821077548Humanname
155934930CV2372575single nucleotide variantNM_002176.4(IFNB1):c.461T>G (p.Leu154Arg)not specified [RCV004219367]uncertain significance92107740921077409Humanname
329387725CV2446700single nucleotide variantNM_002176.4(IFNB1):c.341A>G (p.His114Arg)not specified [RCV004253747]uncertain significance92107752921077529Humanname
329373065CV2455855single nucleotide variantNM_002176.4(IFNB1):c.413T>C (p.Met138Thr)not specified [RCV004279137]uncertain significance92107745721077457Humanname
407466349CV3440602single nucleotide variantNM_002176.4(IFNB1):c.422T>G (p.Leu141Arg)not specified [RCV004635606]uncertain significance92107744821077448Humanname
597763649CV3679846single nucleotide variantNM_002176.4(IFNB1):c.446G>A (p.Arg149Lys)not specified [RCV004926388]uncertain significance92107742421077424Humanname
597763863CV3679850single nucleotide variantNM_002176.4(IFNB1):c.421C>G (p.Leu141Val)not specified [RCV004926392]uncertain significance92107744921077449Humanname
15202179CV723531single nucleotide variantNM_002176.4(IFNB1):c.498A>G (p.Ile166Met)not provided [RCV000891401]benign92107737221077372Humanname