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29 records found for search term Ankrd13c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156397566CV2197259single nucleotide variantNM_030816.5(ANKRD13C):c.76G>A (p.Gly26Arg)not specified [RCV004079035]uncertain significance17035433370354333Humanname
401780356CV2673987single nucleotide variantNM_030816.5(ANKRD13C):c.58G>C (p.Gly20Arg)not specified [RCV004293356]uncertain significance17035435170354351Humanname
597648697CV3703135single nucleotide variantNM_030816.5(ANKRD13C):c.97G>C (p.Ala33Pro)not specified [RCV004942834]uncertain significance17035431270354312Humanname
156251369CV2286838single nucleotide variantNM_030816.5(ANKRD13C):c.238C>G (p.Leu80Val)not specified [RCV004142640]uncertain significance17035417170354171Humanname
329355787CV2430487single nucleotide variantNM_030816.5(ANKRD13C):c.212A>G (p.Asn71Ser)not specified [RCV004252073]uncertain significance17035419770354197Humanname
329378159CV2446876single nucleotide variantNM_030816.5(ANKRD13C):c.215C>T (p.Pro72Leu)not specified [RCV004257727]uncertain significance17035419470354194Humanname
329396524CV2459690single nucleotide variantNM_030816.5(ANKRD13C):c.253G>T (p.Val85Leu)not specified [RCV004277115]uncertain significance17035415670354156Humanname
405811424CV3284936single nucleotide variantNM_030816.5(ANKRD13C):c.1296A>G (p.Lys432=)not specified [RCV004408472]likely benign17027481870274818Humanname
405811457CV3284951single nucleotide variantNM_030816.5(ANKRD13C):c.173A>G (p.His58Arg)not specified [RCV004408487]uncertain significance17035423670354236Humanname
407475654CV3447231single nucleotide variantNM_030816.5(ANKRD13C):c.134A>G (p.Lys45Arg)not specified [RCV004638400]uncertain significance17035427570354275Humanname
407475664CV3447235single nucleotide variantNM_030816.5(ANKRD13C):c.229G>A (p.Ala77Thr)not specified [RCV004638402]uncertain significance17035418070354180Humanname
407506921CV3447248single nucleotide variantNM_030816.5(ANKRD13C):c.226C>A (p.Pro76Thr)not specified [RCV004646607]uncertain significance17035418370354183Humanname
598236624CV3984408single nucleotide variantNM_030816.5(ANKRD13C):c.289G>A (p.Gly97Ser)not specified [RCV005363903]uncertain significance17035412070354120Humanname
156316217CV2250882single nucleotide variantNM_030816.5(ANKRD13C):c.340T>C (p.Tyr114His)not specified [RCV004123472]uncertain significance17035406970354069Humanname
401866117CV2786148single nucleotide variantNM_030816.5(ANKRD13C):c.545C>T (p.Ala182Val)not specified [RCV004359954]uncertain significance17032488570324885Humanname
405811501CV3284972single nucleotide variantNM_030816.5(ANKRD13C):c.844A>T (p.Asn282Tyr)not specified [RCV004408508]uncertain significance17030084170300841Humanname
405811508CV3284975single nucleotide variantNM_030816.5(ANKRD13C):c.918T>G (p.His306Gln)not specified [RCV004408511]uncertain significance17030076770300767Humanname
407475649CV3447229single nucleotide variantNM_030816.5(ANKRD13C):c.407A>G (p.Asn136Ser)not specified [RCV004638399]uncertain significance17035400270354002Humanname
407506918CV3447242single nucleotide variantNM_030816.5(ANKRD13C):c.310G>T (p.Val104Phe)not specified [RCV004646606]uncertain significance17035409970354099Humanname
597648627CV3703126single nucleotide variantNM_030816.5(ANKRD13C):c.897A>C (p.Lys299Asn)not specified [RCV004942825]uncertain significance17030078870300788Humanname
598236599CV3984399single nucleotide variantNM_030816.5(ANKRD13C):c.725G>A (p.Arg242Gln)not specified [RCV005363898]uncertain significance17030627570306275Humanname
156399254CV2205011single nucleotide variantNM_030816.5(ANKRD13C):c.1331A>C (p.Glu444Ala)not specified [RCV004077628]uncertain significance17027478370274783Humanname
155927866CV2349831single nucleotide variantNM_030816.5(ANKRD13C):c.1417G>A (p.Val473Ile)not specified [RCV004206255]likely benign17027093470270934Humanname
405811417CV3284933single nucleotide variantNM_030816.5(ANKRD13C):c.1195A>G (p.Ile399Val)not specified [RCV004408469]uncertain significance17029240870292408Humanname
405811448CV3284947single nucleotide variantNM_030816.5(ANKRD13C):c.1556A>C (p.Glu519Ala)not specified [RCV004408483]uncertain significance17026278770262787Humanname
597648954CV3703105single nucleotide variantNM_030816.5(ANKRD13C):c.1235T>A (p.Leu412His)not specified [RCV004942804]uncertain significance17027682570276825Humanname
597648884CV3703115single nucleotide variantNM_030816.5(ANKRD13C):c.1229A>G (p.Gln410Arg)not specified [RCV004942814]uncertain significance17027683170276831Humanname
597648766CV3703144single nucleotide variantNM_030816.5(ANKRD13C):c.1462A>G (p.Met488Val)not specified [RCV004942843]uncertain significance17027088970270889Humanname
598236580CV3984389single nucleotide variantNM_030816.5(ANKRD13C):c.1143G>T (p.Glu381Asp)not specified [RCV005363894]uncertain significance17029246070292460Humanname