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Variants search result for Homo sapiens
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18 records found for search term Cldn4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
152103409CV1667445single nucleotide variantNM_001305.5(CLDN4):c.33C>T (p.Ile11=)not provided [RCV002214432]likely benign77383123473831234Humanname
597782605CV3660320single nucleotide variantNM_001305.5(CLDN4):c.61G>A (p.Val21Ile)not specified [RCV004900033]uncertain significance77383126273831262Humanname
156244437CV2283347single nucleotide variantNM_001305.5(CLDN4):c.218T>A (p.Leu73Gln)not specified [RCV004146003]uncertain significance77383141973831419Humanname
156178153CV2287907single nucleotide variantNM_001305.5(CLDN4):c.190T>C (p.Cys64Arg)not specified [RCV004147691]uncertain significance77383139173831391Humanname
156325146CV2335173single nucleotide variantNM_001305.5(CLDN4):c.242G>A (p.Arg81His)not specified [RCV004184702]uncertain significance77383144373831443Humanname
401754605CV2682249single nucleotide variantNM_001305.5(CLDN4):c.244G>A (p.Ala82Thr)not specified [RCV004297207]uncertain significance77383144573831445Humanname
407462819CV3419381single nucleotide variantNM_001305.5(CLDN4):c.268G>A (p.Val90Met)not specified [RCV004612916]uncertain significance77383146973831469Humanname
597782609CV3660321single nucleotide variantNM_001305.5(CLDN4):c.284T>C (p.Val95Ala)not specified [RCV004900034]uncertain significance77383148573831485Humanname
598264571CV3944536single nucleotide variantNM_001305.5(CLDN4):c.221C>T (p.Pro74Leu)not specified [RCV005326160]uncertain significance77383142273831422Humanname
598242991CV3944538single nucleotide variantNM_001305.5(CLDN4):c.128C>T (p.Ser43Leu)not specified [RCV005321836]uncertain significance77383132973831329Humanname
156400240CV2199057single nucleotide variantNM_001305.5(CLDN4):c.518T>C (p.Leu173Pro)not specified [RCV004080458]uncertain significance77383171973831719Humanname
156267467CV2329683single nucleotide variantNM_001305.5(CLDN4):c.397A>T (p.Ile133Leu)not specified [RCV004180794]uncertain significance77383159873831598Humanname
401742103CV2722115single nucleotide variantNM_001305.5(CLDN4):c.560C>A (p.Pro187His)not specified [RCV004328375]uncertain significance77383176173831761Humanname
401729602CV2733183single nucleotide variantNM_001305.5(CLDN4):c.337G>A (p.Ala113Thr)not specified [RCV004332108]uncertain significance77383153873831538Humanname
405686334CV3306639single nucleotide variantNM_001305.5(CLDN4):c.500G>T (p.Gly167Val)not specified [RCV004444357]uncertain significance77383170173831701Humanname
597782613CV3660323single nucleotide variantNM_001305.5(CLDN4):c.568G>A (p.Asp190Asn)not specified [RCV004900035]uncertain significance77383176973831769Humanname
597782617CV3660324single nucleotide variantNM_001305.5(CLDN4):c.399A>G (p.Ile133Met)not specified [RCV004900036]likely benign77383160073831600Humanname
598242985CV3944537single nucleotide variantNM_001305.5(CLDN4):c.463G>A (p.Gly155Arg)not specified [RCV005321835]uncertain significance77383166473831664Humanname