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23 records found for search term Fgf11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597751637CV3672655single nucleotide variantNM_004112.4(FGF11):c.5C>A (p.Ala2Glu)not specified [RCV004923766]uncertain significance1774396257439625Humanname
598241522CV3955508single nucleotide variantNM_004112.4(FGF11):c.5C>G (p.Ala2Gly)not specified [RCV005344359]uncertain significance1774396257439625Humanname
401888484CV2761517single nucleotide variantNM_004112.4(FGF11):c.98G>C (p.Arg33Pro)not specified [RCV004334687]uncertain significance1774397187439718Humanname
15174995CV704350single nucleotide variantNM_004112.4(FGF11):c.462C>T (p.Tyr154=)not provided [RCV000950471]benign1774426477442647Humanname
15144860CV741010single nucleotide variantNM_004112.4(FGF11):c.537C>T (p.Gly179=)not provided [RCV000900069]benign1774427227442722Humanname
155912667CV2245614single nucleotide variantNM_004112.4(FGF11):c.283C>G (p.Pro95Ala)not specified [RCV004111508]uncertain significance1774415607441560Humanname
156312586CV2256890single nucleotide variantNM_004112.4(FGF11):c.214G>C (p.Val72Leu)not specified [RCV004599492]uncertain significance1774414917441491Humanname
156059241CV2383519single nucleotide variantNM_004112.4(FGF11):c.110C>T (p.Ser37Phe)not specified [RCV004222526]uncertain significance1774397307439730Humanname
329390563CV2455296single nucleotide variantNM_004112.4(FGF11):c.135C>G (p.Ile45Met)not specified [RCV004274805]uncertain significance1774397557439755Humanname
401724717CV2714943single nucleotide variantNM_004112.4(FGF11):c.239G>A (p.Gly80Asp)not specified [RCV004322268]uncertain significance1774415167441516Humanname
405759675CV3253596single nucleotide variantNM_004112.4(FGF11):c.262G>A (p.Asp88Asn)not specified [RCV004394030]uncertain significance1774415397441539Humanname
597751641CV3672656single nucleotide variantNM_004112.4(FGF11):c.278G>C (p.Gly93Ala)not specified [RCV004923767]uncertain significance1774415557441555Humanname
597751664CV3672660single nucleotide variantNM_004112.4(FGF11):c.208G>A (p.Gly70Ser)not specified [RCV004923771]uncertain significance1774414857441485Humanname
156148658CV2307356single nucleotide variantNM_004112.4(FGF11):c.488G>T (p.Arg163Leu)not specified [RCV004166043]uncertain significance1774426737442673Humanname
401891180CV2774908single nucleotide variantNM_004112.4(FGF11):c.430C>T (p.Arg144Cys)not specified [RCV004346322]uncertain significance1774426157442615Humanname
401898880CV2792080single nucleotide variantNM_004112.4(FGF11):c.520G>A (p.Gly174Ser)not specified [RCV004361310]uncertain significance1774427057442705Humanname
405759684CV3253598single nucleotide variantNM_004112.4(FGF11):c.649G>C (p.Ala217Pro)not specified [RCV004394032]uncertain significance1774431177443117Humanname
407501438CV3439114single nucleotide variantNM_004112.4(FGF11):c.463G>A (p.Val155Ile)not specified [RCV004623256]uncertain significance1774426487442648Humanname
407501443CV3439115single nucleotide variantNM_004112.4(FGF11):c.533A>G (p.Glu178Gly)not specified [RCV004623257]uncertain significance1774427187442718Humanname
597751647CV3672657single nucleotide variantNM_004112.4(FGF11):c.646G>A (p.Glu216Lys)not specified [RCV004923768]uncertain significance1774431147443114Humanname
597751658CV3672659single nucleotide variantNM_004112.4(FGF11):c.407C>T (p.Ser136Leu)not specified [RCV004923770]uncertain significance1774418787441878Humanname
598272021CV3955507single nucleotide variantNM_004112.4(FGF11):c.505C>T (p.Arg169Trp)not specified [RCV005327872]uncertain significance1774426907442690Humanname
8636368CV91591single nucleotide variantNM_004112.3(FGF11):c.521G>A (p.Gly174Asp)Malignant melanoma [RCV000071689]not provided1774427067442706Humanname