Krt34 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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58 records found for search term Krt34

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156033436	CV2236244	single nucleotide variant	NM_001386014.1(KRT34):c.-59A>C	not specified [RCV004107945]	uncertain significance	17	41382305	41382305	Human		name
329376602	CV2472252	single nucleotide variant	NM_001386014.1(KRT34):c.-18A>G	not specified [RCV004283358]	uncertain significance	17	41382264	41382264	Human		name
597794918	CV3698547	single nucleotide variant	NM_001386014.1(KRT34):c.-14C>A	not specified [RCV004934671]	uncertain significance	17	41382260	41382260	Human		name
8636145	CV91369	single nucleotide variant	NM_021013.3(KRT34):c.621C>T (p.Ile207=)	Malignant melanoma [RCV000071467]	not provided	17	41381149	41381149	Human		name
405817351	CV3269257	single nucleotide variant	NM_001386014.1(KRT34):c.26G>A (p.Ser9Asn)	not specified [RCV004412336]	likely benign	17	41382221	41382221	Human		name
405817352	CV3269258	single nucleotide variant	NM_001386014.1(KRT34):c.53C>T (p.Ser18Phe)	not specified [RCV004412337]	uncertain significance	17	41382194	41382194	Human		name
407499981	CV3445533	single nucleotide variant	NM_001386014.1(KRT34):c.44G>C (p.Ser15Thr)	not specified [RCV004644500]	uncertain significance	17	41382203	41382203	Human		name
156270946	CV2195202	single nucleotide variant	NM_001386014.1(KRT34):c.271C>T (p.Arg91Trp)	not specified [RCV004080142]	likely benign	17	41381976	41381976	Human		name
155925838	CV2287753	single nucleotide variant	NM_001386014.1(KRT34):c.157A>G (p.Asn53Asp)	not specified [RCV004143208]	uncertain significance	17	41382090	41382090	Human		name
401935766	CV2811342	single nucleotide variant	NM_001386014.1(KRT34):c.1116C>T (p.Cys372=)	not provided [RCV003413227]	likely benign	17	41378128	41378128	Human		name
597798231	CV3698538	single nucleotide variant	NM_001386014.1(KRT34):c.196C>T (p.Arg66Cys)	not specified [RCV004936069]	uncertain significance	17	41382051	41382051	Human		name
597798249	CV3698548	single nucleotide variant	NM_001386014.1(KRT34):c.286G>A (p.Glu96Lys)	not specified [RCV004936075]	uncertain significance	17	41381961	41381961	Human		name
598163013	CV3980385	single nucleotide variant	NM_001386014.1(KRT34):c.259C>A (p.Leu87Ile)	not specified [RCV005368750]	uncertain significance	17	41381988	41381988	Human		name
156194976	CV2214428	single nucleotide variant	NM_001386014.1(KRT34):c.947G>A (p.Ser316Asn)	not specified [RCV004088187]	uncertain significance	17	41379106	41379106	Human		name
156251848	CV2232346	single nucleotide variant	NM_001386014.1(KRT34):c.538G>A (p.Val180Met)	not specified [RCV004098982]	uncertain significance	17	41381106	41381106	Human		name
156299628	CV2244778	single nucleotide variant	NM_001386014.1(KRT34):c.945G>C (p.Gln315His)	not specified [RCV004102761]	uncertain significance	17	41379108	41379108	Human		name
156208619	CV2250135	single nucleotide variant	NM_001386014.1(KRT34):c.977C>T (p.Ala326Val)	not specified [RCV004116944]	uncertain significance	17	41379076	41379076	Human		name
156186864	CV2346652	single nucleotide variant	NM_001386014.1(KRT34):c.910G>A (p.Glu304Lys)	not specified [RCV004199677]	uncertain significance	17	41379143	41379143	Human		name
156226892	CV2352789	single nucleotide variant	NM_001386014.1(KRT34):c.985C>T (p.Arg329Cys)	not specified [RCV004198803]	uncertain significance	17	41379068	41379068	Human		name
156061973	CV2353696	single nucleotide variant	NM_001386014.1(KRT34):c.367G>C (p.Glu123Gln)	not specified [RCV004201712]	uncertain significance	17	41381777	41381777	Human		name
156385698	CV2364543	single nucleotide variant	NM_001386014.1(KRT34):c.631G>C (p.Val211Leu)	not specified [RCV004217402]	uncertain significance	17	41379689	41379689	Human		name
156200696	CV2392425	single nucleotide variant	NM_001386014.1(KRT34):c.488G>A (p.Arg163His)	not specified [RCV004244006]	uncertain significance	17	41381156	41381156	Human		name
401735907	CV2672773	single nucleotide variant	NM_001386014.1(KRT34):c.470C>T (p.Ser157Leu)	not specified [RCV004281557]	uncertain significance	17	41381174	41381174	Human		name
401766584	CV2676215	single nucleotide variant	NM_001386014.1(KRT34):c.487C>T (p.Arg163Cys)	not specified [RCV004286262]	uncertain significance	17	41381157	41381157	Human		name
401770011	CV2710814	single nucleotide variant	NM_001386014.1(KRT34):c.986G>A (p.Arg329His)	not specified [RCV004308737]	uncertain significance	17	41379067	41379067	Human		name
401877260	CV2764564	single nucleotide variant	NM_001386014.1(KRT34):c.757G>C (p.Glu253Gln)	not specified [RCV004339119]	uncertain significance	17	41379472	41379472	Human		name
401899663	CV2764566	single nucleotide variant	NM_001386014.1(KRT34):c.758A>T (p.Glu253Val)	not specified [RCV004339121]	uncertain significance	17	41379471	41379471	Human		name
401883076	CV2788717	single nucleotide variant	NM_001386014.1(KRT34):c.728T>G (p.Val243Gly)	not specified [RCV004361193]	uncertain significance	17	41379592	41379592	Human		name
405817354	CV3269260	single nucleotide variant	NM_001386014.1(KRT34):c.371A>G (p.Asn124Ser)	not specified [RCV004412339]	uncertain significance	17	41381773	41381773	Human		name
405817355	CV3269261	single nucleotide variant	NM_001386014.1(KRT34):c.577A>C (p.Asn193His)	not specified [RCV004412340]	uncertain significance	17	41381067	41381067	Human		name
405817356	CV3269262	single nucleotide variant	NM_001386014.1(KRT34):c.607T>C (p.Ser203Pro)	not specified [RCV004412341]	uncertain significance	17	41379713	41379713	Human		name
407499980	CV3445532	single nucleotide variant	NM_001386014.1(KRT34):c.499G>A (p.Asp167Asn)	not specified [RCV004644499]	uncertain significance	17	41381145	41381145	Human		name
407499985	CV3445534	single nucleotide variant	NM_001386014.1(KRT34):c.392T>C (p.Ile131Thr)	not specified [RCV004644501]	uncertain significance	17	41381752	41381752	Human		name
407499997	CV3445537	single nucleotide variant	NM_001386014.1(KRT34):c.325A>C (p.Thr109Pro)	not specified [RCV004644504]	uncertain significance	17	41381922	41381922	Human		name
597794912	CV3698539	single nucleotide variant	NM_001386014.1(KRT34):c.604C>T (p.Arg202Cys)	not specified [RCV004934669]	uncertain significance	17	41379716	41379716	Human		name
597798234	CV3698542	single nucleotide variant	NM_001386014.1(KRT34):c.643A>G (p.Thr215Ala)	not specified [RCV004936070]	likely benign	17	41379677	41379677	Human		name
597798240	CV3698544	single nucleotide variant	NM_001386014.1(KRT34):c.754G>A (p.Glu252Lys)	not specified [RCV004936072]	uncertain significance	17	41379475	41379475	Human		name
597798243	CV3698545	single nucleotide variant	NM_001386014.1(KRT34):c.742G>A (p.Ala248Thr)	not specified [RCV004936073]	likely benign	17	41379578	41379578	Human		name
597798246	CV3698546	single nucleotide variant	NM_001386014.1(KRT34):c.718C>T (p.Arg240Cys)	not specified [RCV004936074]	uncertain significance	17	41379602	41379602	Human		name
597798254	CV3698549	single nucleotide variant	NM_001386014.1(KRT34):c.769C>A (p.Gln257Lys)	not specified [RCV004936076]	uncertain significance	17	41379460	41379460	Human		name
597798255	CV3698550	single nucleotide variant	NM_001386014.1(KRT34):c.616G>A (p.Gly206Arg)	not specified [RCV004936077]	uncertain significance	17	41379704	41379704	Human		name
597798259	CV3698551	single nucleotide variant	NM_001386014.1(KRT34):c.486A>G (p.Ile162Met)	not specified [RCV004936078]	uncertain significance	17	41381158	41381158	Human		name
597798261	CV3698553	single nucleotide variant	NM_001386014.1(KRT34):c.373G>A (p.Ala125Thr)	not specified [RCV004936079]	uncertain significance	17	41381771	41381771	Human		name
598163006	CV3980384	single nucleotide variant	NM_001386014.1(KRT34):c.803G>A (p.Cys268Tyr)	not specified [RCV005368749]	likely benign	17	41379426	41379426	Human		name
598221962	CV3980387	single nucleotide variant	NM_001386014.1(KRT34):c.647C>A (p.Ala216Asp)	not specified [RCV005360903]	uncertain significance	17	41379673	41379673	Human		name
598163019	CV3980388	single nucleotide variant	NM_001386014.1(KRT34):c.727G>C (p.Val243Leu)	not specified [RCV005368751]	uncertain significance	17	41379593	41379593	Human		name
598163025	CV3980389	single nucleotide variant	NM_001386014.1(KRT34):c.752C>T (p.Thr251Ile)	not specified [RCV005368752]	uncertain significance	17	41379477	41379477	Human		name
598163037	CV3980391	single nucleotide variant	NM_001386014.1(KRT34):c.576G>C (p.Lys192Asn)	not specified [RCV005368754]	uncertain significance	17	41381068	41381068	Human		name
156332652	CV2339816	single nucleotide variant	NM_001386014.1(KRT34):c.1133G>C (p.Ser378Thr)	not specified [RCV004196506]	uncertain significance	17	41378111	41378111	Human		name
401721303	CV2673670	single nucleotide variant	NM_001386014.1(KRT34):c.1079T>A (p.Leu360Gln)	not specified [RCV004282401]	uncertain significance	17	41378974	41378974	Human		name
401740328	CV2683326	single nucleotide variant	NM_001386014.1(KRT34):c.1042C>T (p.Arg348Trp)	not specified [RCV004288102]	uncertain significance	17	41379011	41379011	Human		name
401753777	CV2685056	single nucleotide variant	NM_001386014.1(KRT34):c.1064C>T (p.Thr355Met)	not specified [RCV004289635]	uncertain significance	17	41378989	41378989	Human		name
401884988	CV2766384	single nucleotide variant	NM_001386014.1(KRT34):c.1116C>G (p.Cys372Trp)	not specified [RCV004342628]	uncertain significance	17	41378128	41378128	Human		name
405817350	CV3269256	single nucleotide variant	NM_001386014.1(KRT34):c.1037G>C (p.Arg346Pro)	not specified [RCV004412335]	uncertain significance	17	41379016	41379016	Human		name
407499989	CV3445535	single nucleotide variant	NM_001386014.1(KRT34):c.1070G>A (p.Arg357Gln)	not specified [RCV004644502]	uncertain significance	17	41378983	41378983	Human		name
407499993	CV3445536	single nucleotide variant	NM_001386014.1(KRT34):c.1142C>A (p.Ser381Tyr)	not specified [RCV004644503]	uncertain significance	17	41378102	41378102	Human		name
597798237	CV3698543	single nucleotide variant	NM_001386014.1(KRT34):c.1126A>G (p.Asn376Asp)	not specified [RCV004936071]	uncertain significance	17	41378118	41378118	Human		name
598163030	CV3980390	single nucleotide variant	NM_001386014.1(KRT34):c.1172G>T (p.Gly391Val)	not specified [RCV005368753]	uncertain significance	17	41378072	41378072	Human		name

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