Krt80 Variant Search Result - Rat Genome Database

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60 records found for search term Krt80

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329365343	CV2444810	single nucleotide variant	NM_182507.3(KRT80):c.26G>A (p.Gly9Asp)	not specified [RCV004259054]	uncertain significance	12	52191877	52191877	Human		name
401898888	CV2792088	single nucleotide variant	NM_182507.3(KRT80):c.13T>C (p.Ser5Pro)	not specified [RCV004361317]	uncertain significance	12	52191890	52191890	Human		name
156224567	CV2355669	single nucleotide variant	NM_182507.3(KRT80):c.73C>T (p.Arg25Trp)	not specified [RCV004198625]	uncertain significance	12	52191830	52191830	Human		name
401892939	CV2758273	single nucleotide variant	NM_182507.3(KRT80):c.74G>A (p.Arg25Gln)	KRT80-related disorder [RCV003901019]\|not specified [RCV004341630]	likely benign\|uncertain significance	12	52191829	52191829	Human		name , trait , alternate_id
405653346	CV3269491	single nucleotide variant	NM_182507.3(KRT80):c.35G>A (p.Ser12Asn)	not specified [RCV004414555]	uncertain significance	12	52191868	52191868	Human		name
156064077	CV2200056	single nucleotide variant	NM_182507.3(KRT80):c.143G>A (p.Gly48Asp)	not specified [RCV004069639]	uncertain significance	12	52191760	52191760	Human		name
156387289	CV2221466	single nucleotide variant	NM_182507.3(KRT80):c.232C>A (p.Gln78Lys)	not specified [RCV004096748]	uncertain significance	12	52191671	52191671	Human		name
401757387	CV2675274	single nucleotide variant	NM_182507.3(KRT80):c.134G>C (p.Ser45Thr)	not specified [RCV004290041]	uncertain significance	12	52191769	52191769	Human		name
401750141	CV2701019	single nucleotide variant	NM_182507.3(KRT80):c.273T>G (p.Asn91Lys)	not specified [RCV004309626]	uncertain significance	12	52191630	52191630	Human		name
401884611	CV2761925	single nucleotide variant	NM_182507.3(KRT80):c.233A>T (p.Gln78Leu)	not specified [RCV004339554]	uncertain significance	12	52191670	52191670	Human		name
407500427	CV3445659	single nucleotide variant	NM_182507.3(KRT80):c.252G>T (p.Lys84Asn)	not specified [RCV004644597]	uncertain significance	12	52191651	52191651	Human		name
598172655	CV3980573	single nucleotide variant	NM_182507.3(KRT80):c.116C>T (p.Pro39Leu)	not specified [RCV005370807]	likely benign	12	52191787	52191787	Human		name
156369023	CV2263248	single nucleotide variant	NM_182507.3(KRT80):c.449G>A (p.Arg150Gln)	not specified [RCV004131747]	uncertain significance	12	52185439	52185439	Human		name
155963035	CV2282694	single nucleotide variant	NM_182507.3(KRT80):c.898G>A (p.Ala300Thr)	not specified [RCV004141562]	uncertain significance	12	52173097	52173097	Human		name
156296635	CV2297595	single nucleotide variant	NM_182507.3(KRT80):c.716G>A (p.Gly239Asp)	not specified [RCV004155294]	uncertain significance	12	52173715	52173715	Human		name
156187924	CV2302823	single nucleotide variant	NM_182507.3(KRT80):c.383T>C (p.Leu128Pro)	not specified [RCV004162727]	uncertain significance	12	52185505	52185505	Human		name
156209189	CV2304436	single nucleotide variant	NM_182507.3(KRT80):c.553T>C (p.Phe185Leu)	not specified [RCV004164533]	uncertain significance	12	52180920	52180920	Human		name
155920539	CV2343366	single nucleotide variant	NM_182507.3(KRT80):c.379G>A (p.Asp127Asn)	not specified [RCV004194980]	uncertain significance	12	52185509	52185509	Human		name
156341078	CV2348157	single nucleotide variant	NM_182507.3(KRT80):c.314A>T (p.Glu105Val)	not specified [RCV004197829]	uncertain significance	12	52185574	52185574	Human		name
155921698	CV2350711	single nucleotide variant	NM_182507.3(KRT80):c.320G>A (p.Arg107His)	not specified [RCV004207057]	uncertain significance	12	52185568	52185568	Human		name
156254697	CV2358848	single nucleotide variant	NM_182507.3(KRT80):c.596G>A (p.Arg199Gln)	not specified [RCV004212195]	uncertain significance	12	52180583	52180583	Human		name
155930361	CV2366736	single nucleotide variant	NM_182507.3(KRT80):c.886C>T (p.Arg296Cys)	not specified [RCV004210735]	uncertain significance	12	52173109	52173109	Human		name
156045662	CV2397268	single nucleotide variant	NM_182507.3(KRT80):c.891C>A (p.Ser297Arg)	not specified [RCV004238801]	uncertain significance	12	52173104	52173104	Human		name
329382500	CV2424411	single nucleotide variant	NM_182507.3(KRT80):c.524T>C (p.Ile175Thr)	not specified [RCV004252307]	uncertain significance	12	52180949	52180949	Human		name
329377910	CV2460830	single nucleotide variant	NM_182507.3(KRT80):c.853T>A (p.Ser285Thr)	not specified [RCV004271143]	uncertain significance	12	52173142	52173142	Human		name
401743193	CV2677790	single nucleotide variant	NM_182507.3(KRT80):c.431G>A (p.Arg144His)	not specified [RCV004291860]	uncertain significance	12	52185457	52185457	Human		name
401873327	CV2761427	single nucleotide variant	NM_182507.3(KRT80):c.486G>T (p.Glu162Asp)	not specified [RCV004334606]	uncertain significance	12	52185402	52185402	Human		name
405653348	CV3269492	single nucleotide variant	NM_182507.3(KRT80):c.607G>C (p.Glu203Gln)	not specified [RCV004414556]	uncertain significance	12	52180572	52180572	Human		name
405653350	CV3269493	single nucleotide variant	NM_182507.3(KRT80):c.754G>A (p.Val252Met)	not specified [RCV004414557]	uncertain significance	12	52173677	52173677	Human		name
405653351	CV3269494	single nucleotide variant	NM_182507.3(KRT80):c.793C>T (p.Arg265Cys)	not specified [RCV004414558]	uncertain significance	12	52173638	52173638	Human		name
405653353	CV3269495	single nucleotide variant	NM_182507.3(KRT80):c.894G>C (p.Glu298Asp)	not specified [RCV004414559]	uncertain significance	12	52173101	52173101	Human		name
405653355	CV3269496	single nucleotide variant	NM_182507.3(KRT80):c.913C>T (p.Arg305Cys)	not specified [RCV004414560]	uncertain significance	12	52173082	52173082	Human		name
407500417	CV3445656	single nucleotide variant	NM_182507.3(KRT80):c.728G>A (p.Arg243His)	not specified [RCV004644594]	uncertain significance	12	52173703	52173703	Human		name
407500420	CV3445657	single nucleotide variant	NM_182507.3(KRT80):c.850C>A (p.Arg284Ser)	not specified [RCV004644595]	uncertain significance	12	52173145	52173145	Human		name
407500424	CV3445658	single nucleotide variant	NM_182507.3(KRT80):c.788C>T (p.Ala263Val)	not specified [RCV004644596]	uncertain significance	12	52173643	52173643	Human		name
407500431	CV3445660	single nucleotide variant	NM_182507.3(KRT80):c.929G>A (p.Arg310Gln)	not specified [RCV004644598]	uncertain significance	12	52173066	52173066	Human		name
597624678	CV3695715	single nucleotide variant	NM_182507.3(KRT80):c.704C>T (p.Ser235Leu)	not specified [RCV004937699]	uncertain significance	12	52173727	52173727	Human		name
597624681	CV3695718	single nucleotide variant	NM_182507.3(KRT80):c.715G>A (p.Gly239Ser)	not specified [RCV004937702]	uncertain significance	12	52173716	52173716	Human		name
597624682	CV3695719	single nucleotide variant	NM_182507.3(KRT80):c.502C>G (p.Arg168Gly)	not specified [RCV004937703]	uncertain significance	12	52185386	52185386	Human		name
597624684	CV3695721	single nucleotide variant	NM_182507.3(KRT80):c.746G>A (p.Ser249Asn)	not specified [RCV004937705]	uncertain significance	12	52173685	52173685	Human		name
598222111	CV3980572	single nucleotide variant	NM_182507.3(KRT80):c.811G>A (p.Glu271Lys)	not specified [RCV005360932]	uncertain significance	12	52173620	52173620	Human		name
598222117	CV3980574	single nucleotide variant	NM_182507.3(KRT80):c.599C>A (p.Thr200Asn)	not specified [RCV005360933]	uncertain significance	12	52180580	52180580	Human		name
598195933	CV3980575	single nucleotide variant	NM_182507.3(KRT80):c.796A>G (p.Ser266Gly)	not specified [RCV005355090]	uncertain significance	12	52173635	52173635	Human		name
15125470	CV713576	single nucleotide variant	NM_182507.3(KRT80):c.727C>T (p.Arg243Cys)	not provided [RCV000963584]	benign	12	52173704	52173704	Human		name
15147072	CV713577	single nucleotide variant	NM_182507.3(KRT80):c.712G>A (p.Val238Ile)	not provided [RCV000967268]	benign	12	52173719	52173719	Human		name
15193938	CV725146	single nucleotide variant	NM_182507.3(KRT80):c.430C>T (p.Arg144Cys)	not provided [RCV000889082]	benign	12	52185458	52185458	Human		name
156398968	CV2194901	single nucleotide variant	NM_182507.3(KRT80):c.1210G>A (p.Ala404Thr)	not specified [RCV004075431]	uncertain significance	12	52171682	52171682	Human		name
156252195	CV2196692	single nucleotide variant	NM_182507.3(KRT80):c.1081C>T (p.Arg361Trp)	not specified [RCV004073951]	uncertain significance	12	52172295	52172295	Human		name
156381969	CV2212510	single nucleotide variant	NM_182507.3(KRT80):c.1036G>T (p.Ala346Ser)	not specified [RCV004091394]	uncertain significance	12	52172340	52172340	Human		name
156011332	CV2291133	single nucleotide variant	NM_182507.3(KRT80):c.1331T>G (p.Phe444Cys)	not specified [RCV004151656]	uncertain significance	12	52171426	52171426	Human		name
156167065	CV2345250	single nucleotide variant	NM_182507.3(KRT80):c.1330T>G (p.Phe444Val)	not specified [RCV004195988]	uncertain significance	12	52171427	52171427	Human		name
156337056	CV2360870	single nucleotide variant	NM_182507.3(KRT80):c.1182G>A (p.Met394Ile)	not specified [RCV004213641]	uncertain significance	12	52171710	52171710	Human		name
401760302	CV2694995	single nucleotide variant	NM_182507.3(KRT80):c.1235C>T (p.Ala412Val)	not specified [RCV004301371]	uncertain significance	12	52171522	52171522	Human		name
401876301	CV2774453	single nucleotide variant	NM_182507.3(KRT80):c.1082G>A (p.Arg361Gln)	not specified [RCV004347788]	uncertain significance	12	52172294	52172294	Human		name
405653344	CV3269490	single nucleotide variant	NM_182507.3(KRT80):c.1297G>A (p.Val433Met)	not specified [RCV004414554]	uncertain significance	12	52171460	52171460	Human		name
597624679	CV3695716	single nucleotide variant	NM_182507.3(KRT80):c.1337A>G (p.Gln446Arg)	not specified [RCV004937700]	uncertain significance	12	52171420	52171420	Human		name
597624680	CV3695717	single nucleotide variant	NM_182507.3(KRT80):c.1052C>T (p.Ala351Val)	not specified [RCV004937701]	uncertain significance	12	52172324	52172324	Human		name
597624683	CV3695720	single nucleotide variant	NM_182507.3(KRT80):c.1317G>C (p.Met439Ile)	not specified [RCV004937704]	uncertain significance	12	52171440	52171440	Human		name
597624685	CV3695722	single nucleotide variant	NM_182507.3(KRT80):c.1318T>A (p.Ser440Thr)	not specified [RCV004937706]	uncertain significance	12	52171439	52171439	Human		name
598222125	CV3980576	single nucleotide variant	NM_182507.3(KRT80):c.1175G>A (p.Gly392Asp)	not specified [RCV005360934]	uncertain significance	12	52172201	52172201	Human		name

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