Irak1 Variant Search Result - Rat Genome Database

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104 records found for search term Irak1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405283972	CV3213504	single nucleotide variant	NM_001569.4(IRAK1):c.137-8C>A	IRAK1-related disorder [RCV003922085]	likely benign	X	154019606	154019606	Human		name , trait , alternate_id
405266892	CV3220179	single nucleotide variant	NM_001569.4(IRAK1):c.909+9A>G	IRAK1-related disorder [RCV003969440]	likely benign	X	154017997	154017997	Human		name , trait , alternate_id
405270831	CV3212164	single nucleotide variant	NM_001569.4(IRAK1):c.729+10G>A	IRAK1-related disorder [RCV003949527]	likely benign	X	154018589	154018589	Human		name , trait , alternate_id
40816255	CV969256	single nucleotide variant	NM_001569.4(IRAK1):c.1303-2A>G	not provided [RCV001260500]	uncertain significance	X	154014280	154014280	Human		name
404983204	CV2849254	single nucleotide variant	NM_001569.4(IRAK1):c.2080+91G>A	not specified [RCV003489126]	benign	X	154012438	154012438	Human		name
155976058	CV2231564	single nucleotide variant	NM_001569.4(IRAK1):c.26A>C (p.Glu9Ala)	not specified [RCV004096619]	uncertain significance	X	154019787	154019787	Human		name
151235551	CV1318888	single nucleotide variant	NM_001569.4(IRAK1):c.792C>A (p.Ser264=)	not provided [RCV001795704]	likely benign	X	154018293	154018293	Human		name
404982472	CV2849109	single nucleotide variant	NM_001569.4(IRAK1):c.483C>T (p.Val161=)	not specified [RCV003488981]	benign	X	154019032	154019032	Human	3	name
405261763	CV3194284	single nucleotide variant	NM_001569.4(IRAK1):c.639G>A (p.Ser213=)	IRAK1-related disorder [RCV003896319]	likely benign	X	154018689	154018689	Human		name , trait , alternate_id
405269821	CV3197969	single nucleotide variant	NM_001569.4(IRAK1):c.726G>A (p.Lys242=)	IRAK1-related disorder [RCV003899781]	likely benign	X	154018602	154018602	Human		name , trait , alternate_id
401929869	CV2824350	single nucleotide variant	NM_001569.4(IRAK1):c.1128C>T (p.Ser376=)	IRAK1-related disorder [RCV003939042]\|not provided [RCV003440027]	likely benign	X	154016545	154016545	Human		name , trait , alternate_id
405271944	CV3203051	single nucleotide variant	NM_001569.4(IRAK1):c.1641C>T (p.Tyr547=)	IRAK1-related disorder [RCV003914103]	likely benign	X	154013332	154013332	Human		name , trait , alternate_id
405289899	CV3213995	single nucleotide variant	NM_001569.4(IRAK1):c.1098C>T (p.Arg366=)	IRAK1-related disorder [RCV003926845]	likely benign	X	154016575	154016575	Human		name , trait , alternate_id
596948073	CV3547665	single nucleotide variant	NM_001569.4(IRAK1):c.1920A>G (p.Thr640=)	not provided [RCV004811970]	likely benign	X	154013053	154013053	Human		name
598128396	CV3887600	single nucleotide variant	NM_001569.4(IRAK1):c.1854C>T (p.Ala618=)	not provided [RCV005243773]	likely benign	X	154013119	154013119	Human		name
15172472	CV706155	single nucleotide variant	NM_001569.4(IRAK1):c.1104C>T (p.Ala368=)	IRAK1-related disorder [RCV003960608]\|not provided [RCV000950035]	benign\|likely benign	X	154016569	154016569	Human		name , trait , alternate_id
15133877	CV743236	single nucleotide variant	NM_001569.4(IRAK1):c.1140G>A (p.Arg380=)	not provided [RCV000898198]	likely benign	X	154016533	154016533	Human		name
15184609	CV773886	single nucleotide variant	NM_001569.4(IRAK1):c.1701A>G (p.Pro567=)	not provided [RCV000930848]	likely benign	X	154013272	154013272	Human		name
156290946	CV2226257	single nucleotide variant	NM_001569.4(IRAK1):c.628C>T (p.His210Tyr)	not specified [RCV004099504]	uncertain significance	X	154018700	154018700	Human		name
156360992	CV2326298	single nucleotide variant	NM_001569.4(IRAK1):c.524C>A (p.Ala175Asp)	not specified [RCV004180847]	uncertain significance	X	154018991	154018991	Human		name
156089706	CV2359400	single nucleotide variant	NM_001569.4(IRAK1):c.844G>A (p.Gly282Ser)	not specified [RCV004214725]	uncertain significance	X	154018071	154018071	Human		name
156105408	CV2400367	single nucleotide variant	NM_001569.4(IRAK1):c.455C>G (p.Thr152Ser)	not specified [RCV004244419]	uncertain significance	X	154019060	154019060	Human		name
329376249	CV2438055	single nucleotide variant	NM_001569.4(IRAK1):c.476G>A (p.Gly159Asp)	not specified [RCV004256847]	uncertain significance	X	154019039	154019039	Human		name
329400198	CV2440722	single nucleotide variant	NM_001569.4(IRAK1):c.421A>C (p.Thr141Pro)	not specified [RCV004258670]	uncertain significance	X	154019212	154019212	Human		name
401724381	CV2677861	single nucleotide variant	NM_001569.4(IRAK1):c.494C>T (p.Ala165Val)	not specified [RCV004294356]	uncertain significance	X	154019021	154019021	Human		name
401772793	CV2712908	single nucleotide variant	NM_001569.4(IRAK1):c.395C>T (p.Pro132Leu)	not specified [RCV004314310]	uncertain significance	X	154019238	154019238	Human		name
401875332	CV2789020	single nucleotide variant	NM_001569.4(IRAK1):c.904T>A (p.Cys302Ser)	not specified [RCV004363328]	uncertain significance	X	154018011	154018011	Human		name
401929871	CV2824351	single nucleotide variant	NM_001569.4(IRAK1):c.530C>T (p.Ser177Phe)	not provided [RCV003440028]	likely benign	X	154018985	154018985	Human		name
404982416	CV2849097	single nucleotide variant	NM_001569.4(IRAK1):c.587T>C (p.Phe196Ser)	not specified [RCV003488969]	benign	X	154018741	154018741	Human		name
405282828	CV3213049	single nucleotide variant	NM_001569.4(IRAK1):c.338C>T (p.Thr113Ile)	IRAK1-related disorder [RCV003957143]	benign	X	154019295	154019295	Human		name , trait , alternate_id
405293371	CV3221375	single nucleotide variant	NM_001569.4(IRAK1):c.390G>C (p.Trp130Cys)	IRAK1-related disorder [RCV003966875]	uncertain significance	X	154019243	154019243	Human		name , trait , alternate_id
405800903	CV3275236	single nucleotide variant	NM_001569.4(IRAK1):c.325C>T (p.Pro109Ser)	not specified [RCV004403183]	uncertain significance	X	154019308	154019308	Human		name
405800905	CV3275237	single nucleotide variant	NM_001569.4(IRAK1):c.538A>C (p.Lys180Gln)	not specified [RCV004403184]	uncertain significance	X	154018977	154018977	Human		name
407523492	CV3455308	single nucleotide variant	NM_001569.4(IRAK1):c.373G>A (p.Ala125Thr)	not specified [RCV004631086]	uncertain significance	X	154019260	154019260	Human		name
407523498	CV3455310	single nucleotide variant	NM_001569.4(IRAK1):c.484C>T (p.Pro162Ser)	not specified [RCV004631088]	uncertain significance	X	154019031	154019031	Human		name
596946491	CV3548313	single nucleotide variant	NM_001569.4(IRAK1):c.361A>G (p.Ile121Val)	not provided [RCV004810138]	likely benign	X	154019272	154019272	Human		name
597765357	CV3680681	single nucleotide variant	NM_001569.4(IRAK1):c.709G>T (p.Ala237Ser)	not specified [RCV004926762]	uncertain significance	X	154018619	154018619	Human		name
598170460	CV3979588	single nucleotide variant	NM_001569.4(IRAK1):c.520C>G (p.Pro174Ala)	not specified [RCV005370341]	uncertain significance	X	154018995	154018995	Human		name
13446291	CV438472	single nucleotide variant	NM_001569.4(IRAK1):c.712G>A (p.Val238Met)	not provided [RCV000513528]	uncertain significance	X	154018616	154018616	Human		name
15121051	CV717718	single nucleotide variant	NM_001569.4(IRAK1):c.607T>A (p.Cys203Ser)	not provided [RCV000962822]	benign	X	154018721	154018721	Human		name
15154851	CV717719	single nucleotide variant	NM_001569.4(IRAK1):c.581G>A (p.Arg194His)	not provided [RCV000968813]	benign	X	154018747	154018747	Human		name
15153203	CV717720	single nucleotide variant	NM_001569.4(IRAK1):c.361A>C (p.Ile121Leu)	IRAK1-related disorder [RCV003916260]\|not provided [RCV000968501]\|not specified [RCV001702870]	benign\|likely benign	X	154019272	154019272	Human		name , trait , alternate_id
155798246	CV1859661	single nucleotide variant	NM_001569.4(IRAK1):c.1138C>T (p.Arg380Trp)	Inguinal hernia [RCV002465453]	uncertain significance	X	154016535	154016535	Human	2	name
156237370	CV2193555	single nucleotide variant	NM_001569.4(IRAK1):c.1417A>T (p.Ile473Phe)	not specified [RCV004073030]	uncertain significance	X	154014164	154014164	Human		name
156250882	CV2232235	single nucleotide variant	NM_001569.4(IRAK1):c.1924G>A (p.Val642Met)	IRAK1-related disorder [RCV003946362]\|not specified [RCV004599463]	likely benign\|uncertain significance	X	154013049	154013049	Human		name , trait , alternate_id
156155236	CV2328742	single nucleotide variant	NM_001569.4(IRAK1):c.1408G>A (p.Ala470Thr)	not specified [RCV004177972]	uncertain significance	X	154014173	154014173	Human		name
156031241	CV2380959	single nucleotide variant	NM_001569.4(IRAK1):c.1459C>G (p.Pro487Ala)	not specified [RCV004220537]	uncertain significance	X	154014122	154014122	Human		name
156031253	CV2380960	single nucleotide variant	NM_001569.4(IRAK1):c.1460C>G (p.Pro487Arg)	not specified [RCV004220538]	uncertain significance	X	154014121	154014121	Human		name
156031270	CV2380961	single nucleotide variant	NM_001569.4(IRAK1):c.1463A>G (p.Glu488Gly)	not specified [RCV004220539]	uncertain significance	X	154014118	154014118	Human		name
156031293	CV2380962	single nucleotide variant	NM_001569.4(IRAK1):c.1472T>C (p.Leu491Pro)	not specified [RCV004220540]	uncertain significance	X	154014109	154014109	Human		name
329364590	CV2443722	single nucleotide variant	NM_001569.4(IRAK1):c.2072C>T (p.Ser691Phe)	not specified [RCV004256022]	uncertain significance	X	154012537	154012537	Human		name
329386432	CV2456004	single nucleotide variant	NM_001569.4(IRAK1):c.1294A>G (p.Lys432Glu)	not specified [RCV004272911]	uncertain significance	X	154016040	154016040	Human		name
329393862	CV2472172	single nucleotide variant	NM_001569.4(IRAK1):c.2003A>G (p.Lys668Arg)	not specified [RCV004283295]	uncertain significance	X	154012606	154012606	Human		name
401726344	CV2674108	single nucleotide variant	NM_001569.4(IRAK1):c.1277C>T (p.Thr426Met)	not specified [RCV004295514]	likely benign	X	154016057	154016057	Human		name
401722410	CV2676974	single nucleotide variant	NM_001569.4(IRAK1):c.1798C>T (p.Arg600Cys)	not specified [RCV004293576]	uncertain significance	X	154013175	154013175	Human		name
401768008	CV2727351	single nucleotide variant	NM_001569.4(IRAK1):c.1823G>T (p.Cys608Phe)	not specified [RCV004327455]	uncertain significance	X	154013150	154013150	Human		name
401767509	CV2729710	single nucleotide variant	NM_001569.4(IRAK1):c.1588G>A (p.Gly530Arg)	not specified [RCV004331965]	uncertain significance	X	154013385	154013385	Human		name
401929867	CV2824349	single nucleotide variant	NM_001569.4(IRAK1):c.1855G>A (p.Gly619Ser)	IRAK1-related disorder [RCV003929196]\|not provided [RCV003440026]	likely benign	X	154013118	154013118	Human		name , trait , alternate_id
404982469	CV2849108	single nucleotide variant	NM_001569.4(IRAK1):c.1595C>T (p.Ser532Leu)	not specified [RCV003488980]	benign	X	154013378	154013378	Human		name
405263819	CV3189755	single nucleotide variant	NM_001569.4(IRAK1):c.1195G>C (p.Gly399Arg)	IRAK1-related disorder [RCV003896804]	uncertain significance	X	154016478	154016478	Human		name , trait , alternate_id
405269342	CV3195756	single nucleotide variant	NM_001569.4(IRAK1):c.1096C>T (p.Arg366Cys)	IRAK1-related disorder [RCV003912321]	likely benign	X	154016577	154016577	Human		name , trait , alternate_id
405800893	CV3275231	single nucleotide variant	NM_001569.4(IRAK1):c.1642G>A (p.Val548Met)	not specified [RCV004403178]	likely benign	X	154013331	154013331	Human		name
405800895	CV3275232	single nucleotide variant	NM_001569.4(IRAK1):c.1672G>A (p.Ala558Thr)	not specified [RCV004403179]	uncertain significance	X	154013301	154013301	Human		name
405800897	CV3275233	single nucleotide variant	NM_001569.4(IRAK1):c.1681T>C (p.Trp561Arg)	not specified [RCV004403180]	uncertain significance	X	154013292	154013292	Human		name
405800899	CV3275234	single nucleotide variant	NM_001569.4(IRAK1):c.2074C>G (p.Leu692Val)	not specified [RCV004403181]	uncertain significance	X	154012535	154012535	Human		name
405800901	CV3275235	single nucleotide variant	NM_001569.4(IRAK1):c.2087G>A (p.Gly696Asp)	not specified [RCV004403182]	uncertain significance	X	154011911	154011911	Human		name
408367080	CV3512122	single nucleotide variant	NM_001569.4(IRAK1):c.1106G>A (p.Gly369Glu)	IRAK1-related disorder [RCV004757776]\|not provided [RCV005242583]	likely benign	X	154016567	154016567	Human		name , trait , alternate_id
597765014	CV3680680	single nucleotide variant	NM_001569.4(IRAK1):c.1973C>T (p.Pro658Leu)	not specified [RCV004926761]	uncertain significance	X	154012636	154012636	Human		name
597765362	CV3680682	single nucleotide variant	NM_001569.4(IRAK1):c.1111A>C (p.Ser371Arg)	not specified [RCV004926763]	uncertain significance	X	154016562	154016562	Human		name
598170452	CV3979583	single nucleotide variant	NM_001569.4(IRAK1):c.1904C>G (p.Pro635Arg)	not specified [RCV005370339]	uncertain significance	X	154013069	154013069	Human		name
598194772	CV3979584	single nucleotide variant	NM_001569.4(IRAK1):c.1109C>G (p.Ser370Cys)	not specified [RCV005354881]	uncertain significance	X	154016564	154016564	Human		name
598194777	CV3979585	single nucleotide variant	NM_001569.4(IRAK1):c.1328A>G (p.Glu443Gly)	not specified [RCV005354882]	uncertain significance	X	154014253	154014253	Human		name
598170456	CV3979586	single nucleotide variant	NM_001569.4(IRAK1):c.1919C>T (p.Thr640Ile)	not specified [RCV005370340]	uncertain significance	X	154013054	154013054	Human		name
598210861	CV3979587	single nucleotide variant	NM_001569.4(IRAK1):c.1823G>A (p.Cys608Tyr)	not specified [RCV005358594]	uncertain significance	X	154013150	154013150	Human		name
15160312	CV717717	single nucleotide variant	NM_001569.4(IRAK1):c.1874C>T (p.Thr625Met)	not provided [RCV000969876]	benign	X	154013099	154013099	Human		name
15150823	CV758375	single nucleotide variant	NM_001569.4(IRAK1):c.1799G>A (p.Arg600His)	not provided [RCV000923548]	benign	X	154013174	154013174	Human		name
405112308	CV2938849	insertion	NM_001010844.4(IRAK1BP1):c.381+11_381+12insTCTTA	not provided [RCV003666411]	benign	6	78885450	78885451	Human		name
405800907	CV3275238	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.5C>G (p.Ser2Cys)	not specified [RCV004403185]	uncertain significance	6	78867581	78867581	Human		name
329365586	CV2440909	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.19C>T (p.Pro7Ser)	not specified [RCV004261300]	uncertain significance	6	78867595	78867595	Human		name
156148841	CV2265306	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.93A>C (p.Arg31Ser)	not specified [RCV004128198]	uncertain significance	6	78867669	78867669	Human		name
401899244	CV2783772	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.70G>C (p.Glu24Gln)	not specified [RCV004360686]	uncertain significance	6	78867646	78867646	Human		name
405800914	CV3275241	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.68G>A (p.Arg23Gln)	not specified [RCV004403188]	uncertain significance	6	78867644	78867644	Human		name
407523506	CV3455312	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.62G>C (p.Arg21Pro)	not specified [RCV004631090]	uncertain significance	6	78867638	78867638	Human		name
596946418	CV3548239	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.723T>C (p.Ala241=)	not provided [RCV004810064]	likely benign	6	78898274	78898274	Human		name
597765028	CV3680683	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.34T>G (p.Phe12Val)	not specified [RCV004926764]	uncertain significance	6	78867610	78867610	Human		name
401743581	CV2715515	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.173C>T (p.Thr58Ile)	not specified [RCV004326609]	uncertain significance	6	78867749	78867749	Human		name
597765032	CV3680684	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.256A>G (p.Lys86Glu)	not specified [RCV004926765]	uncertain significance	6	78867832	78867832	Human		name
597765036	CV3680685	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.236A>C (p.Glu79Ala)	not specified [RCV004926766]	uncertain significance	6	78867812	78867812	Human		name
156305774	CV2252653	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.551G>A (p.Arg184His)	not specified [RCV004118518]	uncertain significance	6	78898102	78898102	Human		name
156135445	CV2256900	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.301C>A (p.Gln101Lys)	not specified [RCV004121103]	uncertain significance	6	78867877	78867877	Human		name
156055911	CV2308836	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.422T>C (p.Ile141Thr)	not specified [RCV004169140]	uncertain significance	6	78897869	78897869	Human		name
156353899	CV2324166	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.305A>G (p.Gln102Arg)	not specified [RCV004176911]	uncertain significance	6	78867881	78867881	Human		name
156391332	CV2385286	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.343T>C (p.Phe115Leu)	not specified [RCV004230571]	uncertain significance	6	78885405	78885405	Human		name
329377509	CV2435942	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.714A>G (p.Ile238Met)	not specified [RCV004255166]	uncertain significance	6	78898265	78898265	Human		name
329392491	CV2468166	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.754G>A (p.Gly252Arg)	not specified [RCV004275753]	uncertain significance	6	78898305	78898305	Human		name
401855835	CV2757524	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.317C>T (p.Ala106Val)	not specified [RCV004340901]	uncertain significance	6	78885379	78885379	Human		name
401890651	CV2778273	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.577G>A (p.Val193Ile)	not specified [RCV004350331]	uncertain significance	6	78898128	78898128	Human		name
405800909	CV3275239	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.613G>C (p.Glu205Gln)	not specified [RCV004403186]	uncertain significance	6	78898164	78898164	Human		name
405800912	CV3275240	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.667C>T (p.Leu223Phe)	not specified [RCV004403187]	uncertain significance	6	78898218	78898218	Human		name
407523503	CV3455311	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.577G>T (p.Val193Phe)	not specified [RCV004631089]	uncertain significance	6	78898128	78898128	Human		name
598210869	CV3979589	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.335C>A (p.Thr112Lys)	not specified [RCV005358595]	uncertain significance	6	78885397	78885397	Human		name
598194783	CV3979590	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.307G>C (p.Gly103Arg)	not specified [RCV005354883]	uncertain significance	6	78867883	78867883	Human		name
598170464	CV3979591	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.549G>T (p.Trp183Cys)	not specified [RCV005370342]	uncertain significance	6	78898100	78898100	Human		name
598194788	CV3979592	single nucleotide variant	NM_001010844.4(IRAK1BP1):c.413T>G (p.Met138Arg)	not specified [RCV005354884]	uncertain significance	6	78897860	78897860	Human		name

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