Tmprss5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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111 records found for search term Tmprss5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150539331	CV1308667	single nucleotide variant	NM_030770.4(TMPRSS5):c.-51G>A	not provided [RCV001766171]	likely benign	11	113706275	113706275	Human		name
150532598	CV1309305	single nucleotide variant	NM_030770.4(TMPRSS5):c.*92C>T	not provided [RCV001752986]	likely benign	11	113688168	113688168	Human		name
405267789	CV3220689	deletion	NM_030770.4(TMPRSS5):c.3+6del	TMPRSS5-related disorder [RCV003947414]	likely benign	11	113706216	113706216	Human		name , trait , alternate_id
150331099	CV1169433	single nucleotide variant	NM_030770.4(TMPRSS5):c.*137C>T	not provided [RCV001536327]	benign	11	113688123	113688123	Human		name
150458503	CV1248945	single nucleotide variant	NM_030770.4(TMPRSS5):c.3+12T>C	not provided [RCV001669121]	benign	11	113706210	113706210	Human		name
150541643	CV1306484	single nucleotide variant	NM_030770.4(TMPRSS5):c.3+42C>G	not provided [RCV001768106]	likely benign	11	113706180	113706180	Human		name
405265712	CV3220845	single nucleotide variant	NM_030770.4(TMPRSS5):c.786-4G>A	TMPRSS5-related disorder [RCV003969016]	likely benign	11	113693253	113693253	Human		name , trait , alternate_id
13539404	CV504057	single nucleotide variant	NM_030770.4(TMPRSS5):c.465-6G>A	TMPRSS5-related disorder [RCV003980167]\|not provided [RCV000895865]\|not specified [RCV000613229]	benign	11	113696977	113696977	Human		name , trait , alternate_id
150331087	CV1172189	single nucleotide variant	NM_030770.4(TMPRSS5):c.579-42G>T	not provided [RCV001538469]	benign	11	113695485	113695485	Human		name
150470740	CV1248061	single nucleotide variant	NM_030770.4(TMPRSS5):c.328+52A>C	not provided [RCV001671097]	benign	11	113698853	113698853	Human		name
150487988	CV1262820	single nucleotide variant	NM_030770.4(TMPRSS5):c.107-75A>G	not provided [RCV001687218]	benign	11	113699768	113699768	Human		name
150441612	CV1287594	single nucleotide variant	NM_030770.4(TMPRSS5):c.579-40G>A	not provided [RCV001725314]	benign	11	113695483	113695483	Human		name
150533846	CV1305937	single nucleotide variant	NM_030770.4(TMPRSS5):c.107-55T>C	not provided [RCV001755339]	likely benign	11	113699748	113699748	Human		name
14744558	CV664932	single nucleotide variant	NM_030770.4(TMPRSS5):c.786-41C>T	not provided [RCV000842837]	benign	11	113693290	113693290	Human		name
14744560	CV665600	single nucleotide variant	NM_030770.4(TMPRSS5):c.965-66C>T	not provided [RCV000842838]	benign	11	113691005	113691005	Human		name
150502756	CV1212312	deletion	NM_030770.4(TMPRSS5):c.1063+81del	not provided [RCV001595186]	benign	11	113690760	113690760	Human		name
150446165	CV1215615	single nucleotide variant	NM_030770.4(TMPRSS5):c.206-233A>G	not provided [RCV001611208]	benign	11	113699260	113699260	Human		name
150454244	CV1232236	single nucleotide variant	NM_030770.4(TMPRSS5):c.206-188G>C	not provided [RCV001648249]	benign	11	113699215	113699215	Human		name
150488957	CV1250462	single nucleotide variant	NM_030770.4(TMPRSS5):c.964+105T>C	not provided [RCV001674424]	benign	11	113692966	113692966	Human		name
150473648	CV1252441	single nucleotide variant	NM_030770.4(TMPRSS5):c.206-184C>G	not provided [RCV001671643]	benign	11	113699211	113699211	Human		name
150455528	CV1259880	single nucleotide variant	NM_030770.4(TMPRSS5):c.579-162G>T	not provided [RCV001681359]	benign	11	113695605	113695605	Human		name
150473701	CV1262946	single nucleotide variant	NM_030770.4(TMPRSS5):c.964+233G>C	not provided [RCV001684762]	benign	11	113692838	113692838	Human		name
150475894	CV1263567	single nucleotide variant	NM_030770.4(TMPRSS5):c.205+109G>A	not provided [RCV001685090]	benign	11	113699486	113699486	Human		name
150492443	CV1266655	single nucleotide variant	NM_030770.4(TMPRSS5):c.1206+47T>G	not provided [RCV001687977]	benign	11	113690184	113690184	Human		name
150440696	CV1266955	single nucleotide variant	NM_030770.4(TMPRSS5):c.206-210G>C	not provided [RCV001690391]	benign	11	113699237	113699237	Human		name
150493590	CV1267177	single nucleotide variant	NM_030770.4(TMPRSS5):c.964+219A>T	not provided [RCV001688205]	benign	11	113692852	113692852	Human		name
150495067	CV1267459	single nucleotide variant	NM_030770.4(TMPRSS5):c.965-119G>A	not provided [RCV001688487]	benign	11	113691058	113691058	Human		name
150457533	CV1269503	duplication	NM_030770.4(TMPRSS5):c.785+216dup	not provided [RCV001693043]	benign	11	113694244	113694245	Human		name
150463630	CV1273180	single nucleotide variant	NM_030770.4(TMPRSS5):c.206-219A>G	not provided [RCV001693937]	benign	11	113699246	113699246	Human		name
150454235	CV1276963	single nucleotide variant	NM_030770.4(TMPRSS5):c.964+234G>T	not provided [RCV001708754]	benign	11	113692837	113692837	Human		name
150541735	CV1306523	single nucleotide variant	NM_030770.4(TMPRSS5):c.106+109G>A	not provided [RCV001768146]	likely benign	11	113699957	113699957	Human		name
150543084	CV1306709	single nucleotide variant	NM_030770.4(TMPRSS5):c.1360-55C>T	not provided [RCV001769773]	likely benign	11	113688329	113688329	Human		name
150532820	CV1308143	single nucleotide variant	NM_030770.4(TMPRSS5):c.107-100G>A	not provided [RCV001753133]	likely benign	11	113699793	113699793	Human		name
13537940	CV503455	single nucleotide variant	NM_030770.4(TMPRSS5):c.1359+10G>A	not provided [RCV000957003]\|not specified [RCV000611107]	benign	11	113689755	113689755	Human		name
14727595	CV664923	single nucleotide variant	NM_030770.4(TMPRSS5):c.1206+41T>G	not provided [RCV000834389]	benign	11	113690190	113690190	Human		name
14744746	CV665796	single nucleotide variant	NM_030770.4(TMPRSS5):c.1206+35T>G	not provided [RCV000842949]	benign	11	113690196	113690196	Human		name
150485108	CV1250159	single nucleotide variant	NM_030770.4(TMPRSS5):c.1064-161C>T	not provided [RCV001673772]	benign	11	113690534	113690534	Human		name
150485062	CV1262016	single nucleotide variant	NM_030770.4(TMPRSS5):c.1064-152A>G	not provided [RCV001686707]	benign	11	113690525	113690525	Human		name
150498041	CV1281736	single nucleotide variant	NM_030770.4(TMPRSS5):c.1063+142T>G	not provided [RCV001717949]	benign	11	113690699	113690699	Human		name
150501696	CV1238468	microsatellite	NM_030770.4(TMPRSS5):c.206-186GACA[2]	not provided [RCV001656898]	benign	11	113699202	113699205	Human		name
13541115	CV503716	single nucleotide variant	NM_030770.4(TMPRSS5):c.42G>A (p.Gln14=)	not provided [RCV004707362]\|not specified [RCV000615695]	benign	11	113700130	113700130	Human		name
598228390	CV3934961	single nucleotide variant	NM_030770.4(TMPRSS5):c.25C>T (p.Pro9Ser)	not specified [RCV005294736]	uncertain significance	11	113700147	113700147	Human		name
13529388	CV503468	single nucleotide variant	NM_030770.4(TMPRSS5):c.162C>T (p.Ala54=)	not provided [RCV000959232]\|not specified [RCV000600291]	benign	11	113699638	113699638	Human		name
13526542	CV503712	single nucleotide variant	NM_030770.4(TMPRSS5):c.117A>G (p.Ala39=)	not provided [RCV004707363]\|not specified [RCV000604263]	benign	11	113699683	113699683	Human		name
150502573	CV1254566	deletion	NM_030770.4(TMPRSS5):c.206-184_206-179del	not provided [RCV001677268]	benign	11	113699206	113699211	Human		name
329396116	CV2451894	single nucleotide variant	NM_030770.4(TMPRSS5):c.31A>G (p.Met11Val)	not specified [RCV004276567]	likely benign	11	113700141	113700141	Human		name
597801362	CV3620490	single nucleotide variant	NM_030770.4(TMPRSS5):c.64C>A (p.Pro22Thr)	not specified [RCV004880593]	uncertain significance	11	113700108	113700108	Human		name
13538389	CV503150	single nucleotide variant	NM_030770.4(TMPRSS5):c.747G>A (p.Ala249=)	not provided [RCV004707368]\|not specified [RCV000611768]	benign	11	113694516	113694516	Human		name
13541500	CV503152	single nucleotide variant	NM_030770.4(TMPRSS5):c.663G>T (p.Gly221=)	not provided [RCV004707365]\|not specified [RCV000616243]	benign	11	113694600	113694600	Human		name
150550484	CV1308209	single nucleotide variant	NM_030770.4(TMPRSS5):c.139C>T (p.Arg47Cys)	not provided [RCV001753200]	likely benign	11	113699661	113699661	Human		name
155926678	CV2395774	single nucleotide variant	NM_030770.4(TMPRSS5):c.178G>A (p.Gly60Ser)	not specified [RCV004235303]	uncertain significance	11	113699622	113699622	Human		name
329374368	CV2434792	single nucleotide variant	NM_030770.4(TMPRSS5):c.127C>T (p.Arg43Cys)	not specified [RCV004248487]	likely benign	11	113699673	113699673	Human		name
405258142	CV3208228	single nucleotide variant	NM_030770.4(TMPRSS5):c.1092G>C (p.Thr364=)	TMPRSS5-related disorder [RCV003941665]	likely benign	11	113690345	113690345	Human		name , trait , alternate_id
405272633	CV3210104	single nucleotide variant	NM_030770.4(TMPRSS5):c.1260G>A (p.Val420=)	TMPRSS5-related disorder [RCV003914353]	likely benign	11	113689864	113689864	Human		name , trait , alternate_id
405773843	CV3343531	single nucleotide variant	NM_030770.4(TMPRSS5):c.194C>T (p.Ser65Leu)	not specified [RCV004470758]	uncertain significance	11	113699606	113699606	Human		name
405773851	CV3343532	single nucleotide variant	NM_030770.4(TMPRSS5):c.220C>T (p.Pro74Ser)	not specified [RCV004470759]	uncertain significance	11	113699013	113699013	Human		name
597801358	CV3620492	single nucleotide variant	NM_030770.4(TMPRSS5):c.136C>G (p.Arg46Gly)	not specified [RCV004880595]	uncertain significance	11	113699664	113699664	Human		name
13536915	CV503461	single nucleotide variant	NM_030770.4(TMPRSS5):c.1134C>T (p.Cys378=)	not provided [RCV004707367]\|not specified [RCV000609666]	benign	11	113690303	113690303	Human		name
13525610	CV503466	single nucleotide variant	NM_030770.4(TMPRSS5):c.1017C>T (p.Gly339=)	not provided [RCV004704113]\|not specified [RCV000603308]	likely benign	11	113690887	113690887	Human		name
13540856	CV503472	single nucleotide variant	NM_030770.4(TMPRSS5):c.137G>A (p.Arg46Gln)	TMPRSS5-related disorder [RCV003980141]\|not provided [RCV004707364]\|not specified [RCV000615302]	benign	11	113699663	113699663	Human		name , trait , alternate_id
13532082	CV504041	single nucleotide variant	NM_030770.4(TMPRSS5):c.1158C>T (p.Pro386=)	not provided [RCV000884735]\|not specified [RCV000606685]	benign\|likely benign	11	113690279	113690279	Human		name
13538824	CV504043	single nucleotide variant	NM_030770.4(TMPRSS5):c.1102T>C (p.Leu368=)	not provided [RCV004708967]\|not specified [RCV000612407]	benign	11	113690335	113690335	Human		name
15151894	CV712605	single nucleotide variant	NM_030770.4(TMPRSS5):c.1143C>T (p.Ser381=)	not provided [RCV000968238]	benign	11	113690294	113690294	Human		name
15123538	CV737731	deletion	NM_030770.4(TMPRSS5):c.517del (p.Gln173fs)	not provided [RCV000896430]	benign	11	113696919	113696919	Human		name
156378743	CV2207791	single nucleotide variant	NM_030770.4(TMPRSS5):c.928G>A (p.Ala310Thr)	not specified [RCV004084227]	uncertain significance	11	113693107	113693107	Human		name
156292344	CV2246630	single nucleotide variant	NM_030770.4(TMPRSS5):c.706G>A (p.Ala236Thr)	not specified [RCV004110372]	uncertain significance	11	113694557	113694557	Human		name
156099641	CV2250689	single nucleotide variant	NM_030770.4(TMPRSS5):c.536C>T (p.Ser179Phe)	not specified [RCV004129311]	uncertain significance	11	113696900	113696900	Human		name
156311134	CV2260132	single nucleotide variant	NM_030770.4(TMPRSS5):c.348C>A (p.Ser116Arg)	not specified [RCV004119129]	uncertain significance	11	113697399	113697399	Human		name
155957247	CV2304133	single nucleotide variant	NM_030770.4(TMPRSS5):c.821A>G (p.His274Arg)	not specified [RCV004170167]	uncertain significance	11	113693214	113693214	Human		name
156073043	CV2331553	single nucleotide variant	NM_030770.4(TMPRSS5):c.847G>A (p.Val283Ile)	not specified [RCV004182154]	uncertain significance	11	113693188	113693188	Human		name
329385758	CV2462289	single nucleotide variant	NM_030770.4(TMPRSS5):c.489C>A (p.Asn163Lys)	not specified [RCV004266281]	uncertain significance	11	113696947	113696947	Human		name
401749879	CV2719434	single nucleotide variant	NM_030770.4(TMPRSS5):c.839A>C (p.His280Pro)	not specified [RCV004326836]	uncertain significance	11	113693196	113693196	Human		name
401778907	CV2732969	single nucleotide variant	NM_030770.4(TMPRSS5):c.887C>T (p.Pro296Leu)	not specified [RCV004331145]	uncertain significance	11	113693148	113693148	Human		name
405773856	CV3343533	single nucleotide variant	NM_030770.4(TMPRSS5):c.388C>T (p.Arg130Cys)	not specified [RCV004470760]	uncertain significance	11	113697359	113697359	Human		name
405773862	CV3343534	single nucleotide variant	NM_030770.4(TMPRSS5):c.448A>G (p.Ser150Gly)	not specified [RCV004470761]	uncertain significance	11	113697299	113697299	Human		name
405773868	CV3343535	single nucleotide variant	NM_030770.4(TMPRSS5):c.538C>T (p.Pro180Ser)	not specified [RCV004470762]	uncertain significance	11	113696898	113696898	Human		name
405773874	CV3343536	single nucleotide variant	NM_030770.4(TMPRSS5):c.880A>T (p.Ile294Phe)	not specified [RCV004470763]	uncertain significance	11	113693155	113693155	Human		name
407527235	CV3483000	single nucleotide variant	NM_030770.4(TMPRSS5):c.953T>G (p.Leu318Arg)	not specified [RCV004679967]	uncertain significance	11	113693082	113693082	Human		name
407458879	CV3483001	single nucleotide variant	NM_030770.4(TMPRSS5):c.501C>G (p.Ile167Met)	not specified [RCV004686976]	uncertain significance	11	113696935	113696935	Human		name
597801372	CV3620484	single nucleotide variant	NM_030770.4(TMPRSS5):c.526G>C (p.Ala176Pro)	not specified [RCV004880588]	uncertain significance	11	113696910	113696910	Human		name
597801370	CV3620485	single nucleotide variant	NM_030770.4(TMPRSS5):c.891C>A (p.His297Gln)	not specified [RCV004880589]	uncertain significance	11	113693144	113693144	Human		name
597801366	CV3620488	single nucleotide variant	NM_030770.4(TMPRSS5):c.589A>C (p.Thr197Pro)	not specified [RCV004880591]	uncertain significance	11	113695433	113695433	Human		name
598253011	CV3934958	single nucleotide variant	NM_030770.4(TMPRSS5):c.652A>T (p.Ile218Leu)	not specified [RCV005278178]	uncertain significance	11	113694611	113694611	Human		name
598228384	CV3934959	single nucleotide variant	NM_030770.4(TMPRSS5):c.749C>T (p.Pro250Leu)	not specified [RCV005294735]	uncertain significance	11	113694514	113694514	Human		name
598253018	CV3934960	single nucleotide variant	NM_030770.4(TMPRSS5):c.404G>A (p.Cys135Tyr)	not specified [RCV005278179]	uncertain significance	11	113697343	113697343	Human		name
598228407	CV3934963	single nucleotide variant	NM_030770.4(TMPRSS5):c.991G>T (p.Ala331Ser)	not specified [RCV005294738]	uncertain significance	11	113690913	113690913	Human		name
598228415	CV3934965	single nucleotide variant	NM_030770.4(TMPRSS5):c.713G>T (p.Gly238Val)	not specified [RCV005294739]	uncertain significance	11	113694550	113694550	Human		name
13531021	CV503144	single nucleotide variant	NM_030770.4(TMPRSS5):c.976G>T (p.Ala326Ser)	not provided [RCV001697374]	benign\|likely benign	11	113690928	113690928	Human		name
14742286	CV656030	single nucleotide variant	NM_030770.4(TMPRSS5):c.733G>A (p.Gly245Ser)	not provided [RCV000841276]\|not specified [RCV004029230]	likely benign\|uncertain significance	11	113694530	113694530	Human		name
14739860	CV656031	single nucleotide variant	NM_030770.4(TMPRSS5):c.725C>T (p.Thr242Met)	not provided [RCV000840074]	likely benign	11	113694538	113694538	Human		name
14729921	CV656032	single nucleotide variant	NM_030770.4(TMPRSS5):c.601G>A (p.Val201Ile)	not provided [RCV000835439]	likely benign	11	113695421	113695421	Human		name
14731475	CV656033	single nucleotide variant	NM_030770.4(TMPRSS5):c.373G>A (p.Val125Met)	not provided [RCV000836142]	benign	11	113697374	113697374	Human	2	name
14731475	CV656033	single nucleotide variant	NM_030770.4(TMPRSS5):c.373G>A (p.Val125Met)	not provided [RCV000836142]	benign	11	113697374	113697375	Human	2	name
15118820	CV712606	single nucleotide variant	NM_030770.4(TMPRSS5):c.751C>T (p.Arg251Cys)	not provided [RCV000962444]	benign	11	113694512	113694512	Human		name
15183800	CV724195	single nucleotide variant	NM_030770.4(TMPRSS5):c.632C>T (p.Ala211Val)	not provided [RCV000886304]	benign\|likely benign	11	113694631	113694631	Human		name
15171203	CV737730	single nucleotide variant	NM_030770.4(TMPRSS5):c.592T>A (p.Ser198Thr)	not provided [RCV000905419]	likely benign	11	113695430	113695430	Human		name
8633853	CV89069	single nucleotide variant	NM_030770.3(TMPRSS5):c.608C>T (p.Ser203Phe)	Malignant melanoma [RCV000069166]	not provided	11	113695414	113695414	Human		name
150553846	CV1306712	single nucleotide variant	NM_030770.4(TMPRSS5):c.1171G>T (p.Ala391Ser)	not provided [RCV001769776]	likely benign	11	113690266	113690266	Human		name
150550323	CV1309236	single nucleotide variant	NM_030770.4(TMPRSS5):c.1159C>T (p.Arg387Cys)	not provided [RCV001752917]\|not specified [RCV005288541]	likely benign\|uncertain significance	11	113690278	113690278	Human		name
156133758	CV2350399	single nucleotide variant	NM_030770.4(TMPRSS5):c.1265T>G (p.Val422Gly)	not specified [RCV004202341]	uncertain significance	11	113689859	113689859	Human		name
156134126	CV2361967	single nucleotide variant	NM_030770.4(TMPRSS5):c.1021C>T (p.Arg341Trp)	not specified [RCV004207734]	uncertain significance	11	113690883	113690883	Human		name
329361607	CV2455784	single nucleotide variant	NM_030770.4(TMPRSS5):c.1080G>A (p.Met360Ile)	not specified [RCV004279076]	uncertain significance	11	113690357	113690357	Human		name
405773830	CV3343529	single nucleotide variant	NM_030770.4(TMPRSS5):c.1112C>G (p.Thr371Ser)	not specified [RCV004470756]	uncertain significance	11	113690325	113690325	Human		name
405773838	CV3343530	single nucleotide variant	NM_030770.4(TMPRSS5):c.1253G>A (p.Arg418His)	not specified [RCV004470757]	likely benign	11	113689871	113689871	Human		name
597801373	CV3620483	single nucleotide variant	NM_030770.4(TMPRSS5):c.1175G>T (p.Gly392Val)	not specified [RCV004880587]	uncertain significance	11	113690262	113690262	Human		name
597801364	CV3620489	single nucleotide variant	NM_030770.4(TMPRSS5):c.1325C>T (p.Ala442Val)	not specified [RCV004880592]	uncertain significance	11	113689799	113689799	Human		name
597801360	CV3620491	single nucleotide variant	NM_030770.4(TMPRSS5):c.1159C>G (p.Arg387Gly)	not specified [RCV004880594]	uncertain significance	11	113690278	113690278	Human		name
598228398	CV3934962	single nucleotide variant	NM_030770.4(TMPRSS5):c.1036G>A (p.Gly346Ser)	not specified [RCV005294737]	uncertain significance	11	113690868	113690868	Human		name
598253024	CV3934964	single nucleotide variant	NM_030770.4(TMPRSS5):c.1003C>T (p.His335Tyr)	not specified [RCV005278180]	uncertain significance	11	113690901	113690901	Human		name
13531084	CV503143	single nucleotide variant	NM_030770.4(TMPRSS5):c.1105T>C (p.Phe369Leu)	not provided [RCV004708968]\|not specified [RCV000600933]	benign	11	113690332	113690332	Human		name
13536727	CV503702	single nucleotide variant	NM_030770.4(TMPRSS5):c.1190G>A (p.Arg397Lys)	not provided [RCV004705701]\|not specified [RCV000609410]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	113690247	113690247	Human		name

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