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Variants search result for Homo sapiens
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30 records found for search term Cldn6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15161390CV703633single nucleotide variantNM_021195.5(CLDN6):c.42A>G (p.Thr14=)not provided [RCV000947664]benign1630159803015980Humanname
598243014CV3944541single nucleotide variantNM_021195.5(CLDN6):c.31G>A (p.Val11Ile)not specified [RCV005321839]likely benign1630159913015991Humanname
156279885CV2224028single nucleotide variantNM_021195.5(CLDN6):c.259G>A (p.Ala87Thr)not specified [RCV004095903]likely benign1630157633015763Humanname
329368736CV2428120single nucleotide variantNM_021195.5(CLDN6):c.215C>T (p.Ala72Val)not specified [RCV004254492]uncertain significance1630158073015807Humanname
401781947CV2722352single nucleotide variantNM_021195.5(CLDN6):c.121G>T (p.Val41Leu)not specified [RCV004322763]uncertain significance1630159013015901Humanname
407462808CV3419384single nucleotide variantNM_021195.5(CLDN6):c.241C>T (p.Arg81Cys)not specified [RCV004612919]uncertain significance1630157813015781Humanname
597782629CV3660329single nucleotide variantNM_021195.5(CLDN6):c.295C>G (p.Leu99Val)not specified [RCV004900039]uncertain significance1630157273015727Humanname
597782642CV3660333single nucleotide variantNM_021195.5(CLDN6):c.139T>A (p.Trp47Arg)not specified [RCV004900043]uncertain significance1630158833015883Humanname
598243006CV3944540single nucleotide variantNM_021195.5(CLDN6):c.202G>A (p.Asp68Asn)not specified [RCV005321838]uncertain significance1630158203015820Humanname
156178912CV2258277single nucleotide variantNM_021195.5(CLDN6):c.404C>G (p.Pro135Arg)not specified [RCV004121644]uncertain significance1630156183015618Humanname
156103825CV2310824single nucleotide variantNM_021195.5(CLDN6):c.614C>T (p.Pro205Leu)not specified [RCV004163872]uncertain significance1630154083015408Humanname
156175708CV2327045single nucleotide variantNM_021195.5(CLDN6):c.484G>T (p.Ala162Ser)not specified [RCV004178633]uncertain significance1630155383015538Humanname
155977907CV2339871single nucleotide variantNM_021195.5(CLDN6):c.506C>T (p.Ala169Val)not specified [RCV004189977]uncertain significance1630155163015516Humanname
156155495CV2359734single nucleotide variantNM_021195.5(CLDN6):c.434G>A (p.Arg145Gln)not specified [RCV004210551]likely benign1630155883015588Humanname
329365521CV2440836single nucleotide variantNM_021195.5(CLDN6):c.443A>G (p.Tyr148Cys)not specified [RCV004261233]uncertain significance1630155793015579Humanname
329379142CV2443314single nucleotide variantNM_021195.5(CLDN6):c.326A>G (p.Glu109Gly)not specified [RCV004260115]uncertain significance1630156963015696Humanname
401761926CV2699459single nucleotide variantNM_021195.5(CLDN6):c.632C>T (p.Pro211Leu)not specified [RCV004299678]uncertain significance1630153903015390Humanname
405685960CV3306642single nucleotide variantNM_021195.5(CLDN6):c.346C>T (p.Arg116Cys)not specified [RCV004444360]uncertain significance1630156763015676Humanname
405685860CV3306643single nucleotide variantNM_021195.5(CLDN6):c.379A>G (p.Ile127Val)not specified [RCV004444361]uncertain significance1630156433015643Humanname
405685780CV3306644single nucleotide variantNM_021195.5(CLDN6):c.591G>A (p.Met197Ile)not specified [RCV004444362]uncertain significance1630154313015431Humanname
407462804CV3419385single nucleotide variantNM_021195.5(CLDN6):c.406G>A (p.Val136Met)not specified [RCV004612920]uncertain significance1630156163015616Humanname
597782621CV3660327single nucleotide variantNM_021195.5(CLDN6):c.532G>A (p.Gly178Arg)not specified [RCV004900037]uncertain significance1630154903015490Humanname
597782625CV3660328single nucleotide variantNM_021195.5(CLDN6):c.301G>A (p.Gly101Arg)not specified [RCV004900038]uncertain significance1630157213015721Humanname
597782631CV3660330single nucleotide variantNM_021195.5(CLDN6):c.595C>T (p.Arg199Cys)not specified [RCV004900040]uncertain significance1630154273015427Humanname
597782635CV3660331single nucleotide variantNM_021195.5(CLDN6):c.395C>T (p.Thr132Met)not specified [RCV004900041]uncertain significance1630156273015627Humanname
597782638CV3660332single nucleotide variantNM_021195.5(CLDN6):c.320G>C (p.Cys107Ser)not specified [RCV004900042]uncertain significance1630157023015702Humanname
597782645CV3660334single nucleotide variantNM_021195.5(CLDN6):c.463G>A (p.Ala155Thr)not specified [RCV004900044]uncertain significance1630155593015559Humanname
597782649CV3660335single nucleotide variantNM_021195.5(CLDN6):c.643C>A (p.Pro215Thr)not specified [RCV004900045]uncertain significance1630153793015379Humanname
597782653CV3660336single nucleotide variantNM_021195.5(CLDN6):c.637G>A (p.Glu213Lys)not specified [RCV004900046]uncertain significance1630153853015385Humanname
598264576CV3944542single nucleotide variantNM_021195.5(CLDN6):c.565G>T (p.Gly189Trp)not specified [RCV005326161]uncertain significance1630154573015457Humanname