Krt24 Variant Search Result - Rat Genome Database

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54 records found for search term Krt24

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15150635	CV740719	single nucleotide variant	NM_019016.3(KRT24):c.27C>T (p.Ser9=)	not provided [RCV000901197]	likely benign	17	40703667	40703667	Human		name
597798031	CV3698453	single nucleotide variant	NM_019016.3(KRT24):c.17G>A (p.Arg6His)	not specified [RCV004935999]	uncertain significance	17	40703677	40703677	Human		name
15119678	CV715431	single nucleotide variant	NM_019016.3(KRT24):c.282C>T (p.Gly94=)	not provided [RCV000962590]	benign	17	40703412	40703412	Human		name
401737040	CV2689551	single nucleotide variant	NM_019016.3(KRT24):c.38G>A (p.Gly13Glu)	not specified [RCV004308381]	uncertain significance	17	40703656	40703656	Human		name
405852841	CV3393267	single nucleotide variant	NM_019016.3(KRT24):c.555C>T (p.Asp185=)	not provided [RCV004545997]	likely benign	17	40703139	40703139	Human		name
15161740	CV727157	single nucleotide variant	NM_019016.3(KRT24):c.552A>G (p.Gly184=)	not provided [RCV000881626]	benign	17	40703142	40703142	Human		name
405817249	CV3273013	single nucleotide variant	NM_019016.3(KRT24):c.185G>A (p.Gly62Asp)	not specified [RCV004412258]	uncertain significance	17	40703509	40703509	Human		name
405817250	CV3273014	single nucleotide variant	NM_019016.3(KRT24):c.250G>A (p.Gly84Arg)	not specified [RCV004412259]	uncertain significance	17	40703444	40703444	Human		name
597798020	CV3698448	single nucleotide variant	NM_019016.3(KRT24):c.160G>T (p.Gly54Trp)	not specified [RCV004935995]	uncertain significance	17	40703534	40703534	Human		name
597798025	CV3698450	single nucleotide variant	NM_019016.3(KRT24):c.233G>A (p.Gly78Glu)	not specified [RCV004935997]	uncertain significance	17	40703461	40703461	Human		name
597794879	CV3698451	single nucleotide variant	NM_019016.3(KRT24):c.200G>T (p.Gly67Val)	not specified [RCV004934658]	uncertain significance	17	40703494	40703494	Human		name
597798028	CV3698452	single nucleotide variant	NM_019016.3(KRT24):c.180T>G (p.Phe60Leu)	not specified [RCV004935998]	uncertain significance	17	40703514	40703514	Human		name
597798037	CV3698455	single nucleotide variant	NM_019016.3(KRT24):c.295T>C (p.Phe99Leu)	not specified [RCV004936001]	uncertain significance	17	40703399	40703399	Human		name
15161725	CV727154	single nucleotide variant	NM_019016.3(KRT24):c.1503T>C (p.Thr501=)	not provided [RCV000881623]	benign	17	40698312	40698312	Human		name
156058331	CV2262884	single nucleotide variant	NM_019016.3(KRT24):c.527A>G (p.Tyr176Cys)	not specified [RCV004125029]	uncertain significance	17	40703167	40703167	Human		name
156014691	CV2272219	single nucleotide variant	NM_019016.3(KRT24):c.870G>T (p.Met290Ile)	not specified [RCV004126900]	uncertain significance	17	40700369	40700369	Human		name
155970411	CV2309183	single nucleotide variant	NM_019016.3(KRT24):c.461A>G (p.Tyr154Cys)	not specified [RCV004171531]	uncertain significance	17	40703233	40703233	Human		name
156047061	CV2340291	single nucleotide variant	NM_019016.3(KRT24):c.817A>T (p.Thr273Ser)	not specified [RCV004194557]	uncertain significance	17	40701178	40701178	Human		name
155923120	CV2347443	single nucleotide variant	NM_019016.3(KRT24):c.556G>A (p.Gly186Ser)	not specified [RCV004200398]	uncertain significance	17	40703138	40703138	Human		name
156191568	CV2388505	single nucleotide variant	NM_019016.3(KRT24):c.727A>G (p.Ser243Gly)	not specified [RCV004237358]	uncertain significance	17	40701268	40701268	Human		name
329362149	CV2448342	single nucleotide variant	NM_019016.3(KRT24):c.829G>C (p.Ala277Pro)	not specified [RCV004256629]	uncertain significance	17	40701166	40701166	Human		name
401736440	CV2688790	single nucleotide variant	NM_019016.3(KRT24):c.684T>A (p.Asp228Glu)	not specified [RCV004303813]	uncertain significance	17	40701865	40701865	Human		name
401734043	CV2697938	single nucleotide variant	NM_019016.3(KRT24):c.853G>A (p.Glu285Lys)	not specified [RCV004302429]	uncertain significance	17	40701142	40701142	Human		name
401874911	CV2756127	single nucleotide variant	NM_019016.3(KRT24):c.448C>T (p.Arg150Cys)	not specified [RCV004338238]	uncertain significance	17	40703246	40703246	Human		name
405817275	CV3273015	single nucleotide variant	NM_019016.3(KRT24):c.319G>A (p.Gly107Arg)	not specified [RCV004412260]	uncertain significance	17	40703375	40703375	Human		name
405817276	CV3273016	single nucleotide variant	NM_019016.3(KRT24):c.370G>A (p.Gly124Ser)	not specified [RCV004412261]	uncertain significance	17	40703324	40703324	Human		name
405817277	CV3273017	single nucleotide variant	NM_019016.3(KRT24):c.416G>T (p.Gly139Val)	not specified [RCV004412262]	uncertain significance	17	40703278	40703278	Human		name
405817278	CV3273018	single nucleotide variant	NM_019016.3(KRT24):c.622G>A (p.Ala208Thr)	not specified [RCV004412263]	likely benign	17	40701927	40701927	Human		name
405817279	CV3273019	single nucleotide variant	NM_019016.3(KRT24):c.664A>G (p.Asn222Asp)	not specified [RCV004412264]	uncertain significance	17	40701885	40701885	Human		name
405817280	CV3273020	single nucleotide variant	NM_019016.3(KRT24):c.721C>T (p.Arg241Trp)	not specified [RCV004412265]	uncertain significance	17	40701274	40701274	Human		name
407499975	CV3445478	single nucleotide variant	NM_019016.3(KRT24):c.626C>T (p.Ala209Val)	not specified [RCV004644453]	uncertain significance	17	40701923	40701923	Human		name
407459919	CV3445480	single nucleotide variant	NM_019016.3(KRT24):c.913G>A (p.Ala305Thr)	not specified [RCV004633709]	uncertain significance	17	40700326	40700326	Human		name
597798034	CV3698454	single nucleotide variant	NM_019016.3(KRT24):c.652T>G (p.Leu218Val)	not specified [RCV004936000]	uncertain significance	17	40701897	40701897	Human		name
598184111	CV3980322	single nucleotide variant	NM_019016.3(KRT24):c.820G>A (p.Glu274Lys)	not specified [RCV005353019]	uncertain significance	17	40701175	40701175	Human		name
598162847	CV3980323	single nucleotide variant	NM_019016.3(KRT24):c.563C>T (p.Ser188Leu)	not specified [RCV005368723]	uncertain significance	17	40703131	40703131	Human		name
598162853	CV3980324	single nucleotide variant	NM_019016.3(KRT24):c.730G>A (p.Val244Met)	not specified [RCV005368724]	uncertain significance	17	40701265	40701265	Human		name
15152446	CV715430	single nucleotide variant	NM_019016.3(KRT24):c.343G>A (p.Ala115Thr)	not provided [RCV000968353]	benign	17	40703351	40703351	Human		name
156309985	CV2249712	single nucleotide variant	NM_019016.3(KRT24):c.1481G>C (p.Ser494Thr)	not specified [RCV004122483]	uncertain significance	17	40698334	40698334	Human		name
156193470	CV2296979	single nucleotide variant	NM_019016.3(KRT24):c.1003C>T (p.Arg335Trp)	not specified [RCV004150909]	uncertain significance	17	40700236	40700236	Human		name
156087079	CV2366352	single nucleotide variant	NM_019016.3(KRT24):c.1214C>T (p.Thr405Met)	not specified [RCV004212405]	likely benign	17	40699591	40699591	Human		name
156185359	CV2377838	single nucleotide variant	NM_019016.3(KRT24):c.1192G>C (p.Ala398Pro)	not specified [RCV004230414]	uncertain significance	17	40699613	40699613	Human		name
329371481	CV2431888	single nucleotide variant	NM_019016.3(KRT24):c.1447T>C (p.Ser483Pro)	not specified [RCV004255023]	uncertain significance	17	40698565	40698565	Human		name
401719233	CV2731256	single nucleotide variant	NM_019016.3(KRT24):c.1454G>A (p.Ser485Asn)	not specified [RCV004332682]	uncertain significance	17	40698558	40698558	Human		name
405817245	CV3273009	single nucleotide variant	NM_019016.3(KRT24):c.1028T>C (p.Leu343Pro)	not specified [RCV004412254]	uncertain significance	17	40700113	40700113	Human		name
405817246	CV3273010	single nucleotide variant	NM_019016.3(KRT24):c.1057G>A (p.Ala353Thr)	not specified [RCV004412255]	uncertain significance	17	40700084	40700084	Human		name
405817247	CV3273011	single nucleotide variant	NM_019016.3(KRT24):c.1234G>A (p.Glu412Lys)	not specified [RCV004412256]	uncertain significance	17	40699571	40699571	Human		name
405817248	CV3273012	single nucleotide variant	NM_019016.3(KRT24):c.1358G>A (p.Gly453Glu)	not specified [RCV004412257]	uncertain significance	17	40699447	40699447	Human		name
407499879	CV3445479	single nucleotide variant	NM_019016.3(KRT24):c.1272G>C (p.Gln424His)	not specified [RCV004644454]	uncertain significance	17	40699533	40699533	Human		name
597798014	CV3698446	single nucleotide variant	NM_019016.3(KRT24):c.1189G>A (p.Val397Met)	not specified [RCV004935993]	likely benign	17	40699616	40699616	Human		name
597798017	CV3698447	single nucleotide variant	NM_019016.3(KRT24):c.1490G>A (p.Arg497Lys)	not specified [RCV004935994]	uncertain significance	17	40698325	40698325	Human		name
597798040	CV3698456	single nucleotide variant	NM_019016.3(KRT24):c.1112T>A (p.Leu371Gln)	not specified [RCV004936002]	uncertain significance	17	40700029	40700029	Human		name
598184121	CV3980325	single nucleotide variant	NM_019016.3(KRT24):c.1123C>A (p.Leu375Ile)	not specified [RCV005353020]	uncertain significance	17	40700018	40700018	Human		name
15161730	CV727155	single nucleotide variant	NM_019016.3(KRT24):c.1252T>C (p.Trp418Arg)	not provided [RCV000881624]	benign	17	40699553	40699553	Human		name
15161735	CV727156	single nucleotide variant	NM_019016.3(KRT24):c.1244G>A (p.Cys415Tyr)	not provided [RCV000881625]	benign	17	40699561	40699561	Human		name

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