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31 records found for search term Rnf208
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156383137CV2361425single nucleotide variantNM_031297.7(RNF208):c.4C>T (p.Pro2Ser)not specified [RCV004221070]uncertain significance9137221209137221209Humanname
405698236CV3313230single nucleotide variantNM_031297.7(RNF208):c.17G>T (p.Gly6Val)not specified [RCV004446606]uncertain significance9137221196137221196Humanname
155922858CV2347396single nucleotide variantNM_031297.7(RNF208):c.94G>A (p.Ala32Thr)not specified [RCV004207236]uncertain significance9137221119137221119Humanname
597687509CV3590369single nucleotide variantNM_031297.7(RNF208):c.49C>T (p.Leu17Phe)not specified [RCV004858501]uncertain significance9137221164137221164Humanname
156152431CV2307630single nucleotide variantNM_031297.7(RNF208):c.287G>A (p.Arg96Gln)not specified [RCV004168048]uncertain significance9137220926137220926Humanname
156051657CV2324133single nucleotide variantNM_031297.7(RNF208):c.281T>A (p.Leu94Gln)not specified [RCV004178416]uncertain significance9137220932137220932Humanname
405698240CV3313231single nucleotide variantNM_031297.7(RNF208):c.283C>A (p.Pro95Thr)not specified [RCV004446607]uncertain significance9137220930137220930Humanname
407486487CV3479692single nucleotide variantNM_031297.7(RNF208):c.295C>T (p.Arg99Cys)not specified [RCV004665469]uncertain significance9137220918137220918Humanname
597755116CV3590367single nucleotide variantNM_031297.7(RNF208):c.160C>T (p.Pro54Ser)not specified [RCV004847538]uncertain significance9137221053137221053Humanname
156050712CV2237833single nucleotide variantNM_031297.7(RNF208):c.389C>T (p.Ser130Leu)not specified [RCV004109072]uncertain significance9137220824137220824Humanname
156243760CV2242981single nucleotide variantNM_031297.7(RNF208):c.569G>T (p.Arg190Leu)not specified [RCV004107861]uncertain significance9137220644137220644Humanname
155972619CV2335818single nucleotide variantNM_031297.7(RNF208):c.401C>T (p.Ser134Leu)not specified [RCV004196053]uncertain significance9137220812137220812Humanname
155969121CV2339386single nucleotide variantNM_031297.7(RNF208):c.759C>A (p.Asn253Lys)not specified [RCV004191609]uncertain significance9137220454137220454Humanname
156387664CV2372816single nucleotide variantNM_031297.7(RNF208):c.682G>A (p.Gly228Arg)not specified [RCV004221999]uncertain significance9137220531137220531Humanname
156146775CV2381809single nucleotide variantNM_031297.7(RNF208):c.769G>A (p.Ala257Thr)not specified [RCV004232255]uncertain significance9137220444137220444Humanname
401768385CV2716509single nucleotide variantNM_031297.7(RNF208):c.571C>G (p.Arg191Gly)not specified [RCV004327596]uncertain significance9137220642137220642Humanname
405698244CV3313232single nucleotide variantNM_031297.7(RNF208):c.326G>A (p.Arg109His)not specified [RCV004446608]uncertain significance9137220887137220887Humanname
405698249CV3313233single nucleotide variantNM_031297.7(RNF208):c.404C>T (p.Ala135Val)not specified [RCV004446609]uncertain significance9137220809137220809Humanname
405698263CV3313235single nucleotide variantNM_031297.7(RNF208):c.599G>A (p.Gly200Asp)not specified [RCV004446611]uncertain significance9137220614137220614Humanname
407508744CV3479691single nucleotide variantNM_031297.7(RNF208):c.370C>T (p.Arg124Trp)not specified [RCV004672142]uncertain significance9137220843137220843Humanname
407486492CV3479693single nucleotide variantNM_031297.7(RNF208):c.331G>T (p.Ala111Ser)not specified [RCV004665470]uncertain significance9137220882137220882Humanname
407486500CV3479694single nucleotide variantNM_031297.7(RNF208):c.412G>A (p.Gly138Ser)not specified [RCV004665471]uncertain significance9137220801137220801Humanname
597687500CV3590368single nucleotide variantNM_031297.7(RNF208):c.754C>T (p.Arg252Trp)not specified [RCV004858500]uncertain significance9137220459137220459Humanname
597755119CV3590370single nucleotide variantNM_031297.7(RNF208):c.718C>G (p.Arg240Gly)not specified [RCV004847539]uncertain significance9137220495137220495Humanname
597755123CV3590371single nucleotide variantNM_031297.7(RNF208):c.452A>C (p.Asn151Thr)not specified [RCV004847540]uncertain significance9137220761137220761Humanname
597755128CV3590372single nucleotide variantNM_031297.7(RNF208):c.314T>C (p.Leu105Pro)not specified [RCV004847541]uncertain significance9137220899137220899Humanname
598204822CV3909588single nucleotide variantNM_031297.7(RNF208):c.328G>A (p.Val110Met)not specified [RCV005269607]uncertain significance9137220885137220885Humanname
598204828CV3909589single nucleotide variantNM_031297.7(RNF208):c.568C>T (p.Arg190Cys)not specified [RCV005269608]uncertain significance9137220645137220645Humanname
598204835CV3909590single nucleotide variantNM_031297.7(RNF208):c.755G>A (p.Arg252Gln)not specified [RCV005269609]uncertain significance9137220458137220458Humanname
598204842CV3909591single nucleotide variantNM_031297.7(RNF208):c.563C>T (p.Thr188Ile)not specified [RCV005269610]uncertain significance9137220650137220650Humanname
598204851CV3909592single nucleotide variantNM_031297.7(RNF208):c.695A>G (p.Glu232Gly)not specified [RCV005269611]uncertain significance9137220518137220518Humanname