| 597775698 | CV3619985 | single nucleotide variant | NM_003268.6(TLR5):c.10C>T (p.His4Tyr) | not specified [RCV004872603] | uncertain significance | 1 | 223113022 | 223113022 | Human | | name |
| 329395678 | CV2454459 | single nucleotide variant | NM_003268.6(TLR5):c.68C>G (p.Ser23Cys) | not specified [RCV004267962] | uncertain significance | 1 | 223112964 | 223112964 | Human | | name |
| 401936772 | CV2816064 | single nucleotide variant | NM_003268.6(TLR5):c.456A>C (p.Leu152=) | not provided [RCV003414790] | likely benign | 1 | 223112576 | 223112576 | Human | | name |
| 405290037 | CV3214034 | single nucleotide variant | NM_003268.6(TLR5):c.333T>C (p.His111=) | TLR5-related disorder [RCV003926878] | likely benign | 1 | 223112699 | 223112699 | Human | | name , trait , alternate_id |
| 405783831 | CV3342946 | single nucleotide variant | NM_003268.6(TLR5):c.29G>A (p.Gly10Glu) | not specified [RCV004472431] | uncertain significance | 1 | 223113003 | 223113003 | Human | | name |
| 15159335 | CV718681 | single nucleotide variant | NM_003268.6(TLR5):c.867A>C (p.Ser289=) | not provided [RCV000881176] | benign | 1 | 223112165 | 223112165 | Human | | name |
| 155955557 | CV2274473 | single nucleotide variant | NM_003268.6(TLR5):c.236G>C (p.Ser79Thr) | not specified [RCV004136830] | likely benign | 1 | 223112796 | 223112796 | Human | | name |
| 401783228 | CV2703894 | single nucleotide variant | NM_003268.6(TLR5):c.151C>G (p.Leu51Val) | not specified [RCV004306752] | uncertain significance | 1 | 223112881 | 223112881 | Human | | name |
| 405293377 | CV3207381 | single nucleotide variant | NM_003268.6(TLR5):c.1857T>A (p.Val619=) | TLR5-related disorder [RCV003931763] | likely benign | 1 | 223111175 | 223111175 | Human | | name , trait , alternate_id |
| 15195240 | CV696488 | single nucleotide variant | NM_003268.6(TLR5):c.1332C>T (p.Leu444=) | not provided [RCV000955868] | benign | 1 | 223111700 | 223111700 | Human | | name |
| 15149354 | CV707116 | single nucleotide variant | NM_003268.6(TLR5):c.2493A>G (p.Lys831=) | not provided [RCV000967738] | benign|likely benign | 1 | 223110539 | 223110539 | Human | | name |
| 15115911 | CV707118 | single nucleotide variant | NM_003268.6(TLR5):c.1368T>C (p.Asn456=) | not provided [RCV000961938] | benign | 1 | 223111664 | 223111664 | Human | | name |
| 15181872 | CV707119 | single nucleotide variant | NM_003268.6(TLR5):c.245C>T (p.Thr82Ile) | not provided [RCV000974498] | benign | 1 | 223112787 | 223112787 | Human | | name |
| 155984969 | CV2247817 | single nucleotide variant | NM_003268.6(TLR5):c.932T>C (p.Leu311Pro) | not specified [RCV004121281] | uncertain significance | 1 | 223112100 | 223112100 | Human | | name |
| 156191794 | CV2289373 | single nucleotide variant | NM_003268.6(TLR5):c.610G>A (p.Ala204Thr) | not specified [RCV004152339] | uncertain significance | 1 | 223112422 | 223112422 | Human | | name |
| 155962853 | CV2388311 | single nucleotide variant | NM_003268.6(TLR5):c.571G>A (p.Glu191Lys) | not specified [RCV004234763] | likely benign | 1 | 223112461 | 223112461 | Human | | name |
| 329376748 | CV2428530 | single nucleotide variant | NM_003268.6(TLR5):c.917G>A (p.Arg306Gln) | not specified [RCV004253315] | uncertain significance | 1 | 223112115 | 223112115 | Human | | name |
| 401747839 | CV2696805 | single nucleotide variant | NM_003268.6(TLR5):c.322T>C (p.Tyr108His) | not specified [RCV004290775] | uncertain significance | 1 | 223112710 | 223112710 | Human | | name |
| 401752643 | CV2723304 | single nucleotide variant | NM_003268.6(TLR5):c.484C>T (p.Leu162Phe) | not specified [RCV004329527] | uncertain significance | 1 | 223112548 | 223112548 | Human | | name |
| 405783837 | CV3342947 | single nucleotide variant | NM_003268.6(TLR5):c.472C>T (p.Arg158Cys) | not specified [RCV004472432] | uncertain significance | 1 | 223112560 | 223112560 | Human | | name |
| 405783842 | CV3342948 | single nucleotide variant | NM_003268.6(TLR5):c.716C>T (p.Thr239Ile) | not specified [RCV004472433] | uncertain significance | 1 | 223112316 | 223112316 | Human | | name |
| 407452670 | CV3475934 | single nucleotide variant | NM_003268.6(TLR5):c.614C>A (p.Ala205Asp) | not specified [RCV004684161] | uncertain significance | 1 | 223112418 | 223112418 | Human | | name |
| 407452673 | CV3475936 | single nucleotide variant | NM_003268.6(TLR5):c.955C>T (p.Leu319Phe) | not specified [RCV004684163] | uncertain significance | 1 | 223112077 | 223112077 | Human | | name |
| 597775682 | CV3610476 | single nucleotide variant | NM_003268.6(TLR5):c.460A>C (p.Lys154Gln) | not specified [RCV004872599] | uncertain significance | 1 | 223112572 | 223112572 | Human | | name |
| 597775686 | CV3610477 | single nucleotide variant | NM_003268.6(TLR5):c.866C>T (p.Ser289Leu) | not specified [RCV004872600] | uncertain significance | 1 | 223112166 | 223112166 | Human | | name |
| 597775700 | CV3619986 | single nucleotide variant | NM_003268.6(TLR5):c.655T>G (p.Cys219Gly) | not specified [RCV004872604] | uncertain significance | 1 | 223112377 | 223112377 | Human | | name |
| 597775724 | CV3619993 | single nucleotide variant | NM_003268.6(TLR5):c.638C>T (p.Ser213Leu) | not specified [RCV004872610] | uncertain significance | 1 | 223112394 | 223112394 | Human | | name |
| 598124058 | CV3884117 | duplication | NM_003268.6(TLR5):c.603dup (p.Ser202Ter) | Systemic lupus erythematosus, susceptibility to, 1 [RCV005234885] | likely pathogenic | 1 | 223112428 | 223112429 | Human | 1 | name |
| 598199732 | CV3920742 | single nucleotide variant | NM_003268.6(TLR5):c.815A>G (p.His272Arg) | not specified [RCV005289889] | uncertain significance | 1 | 223112217 | 223112217 | Human | | name |
| 15195245 | CV696489 | single nucleotide variant | NM_003268.6(TLR5):c.428A>C (p.Asn143Thr) | not provided [RCV000955869] | benign | 1 | 223112604 | 223112604 | Human | | name |
| 15159340 | CV718682 | single nucleotide variant | NM_003268.6(TLR5):c.334C>G (p.Pro112Ala) | not provided [RCV000881177] | benign | 1 | 223112698 | 223112698 | Human | | name |
| 8629317 | CV84462 | single nucleotide variant | NM_003268.5(TLR5):c.445C>T (p.Arg149Cys) | Malignant melanoma [RCV000064544] | not provided | 1 | 223112587 | 223112587 | Human | | name |
| 8559475 | CV21697 | single nucleotide variant | NM_003268.6(TLR5):c.1174C>T (p.Arg392Ter) | Legionnaire disease, susceptibility to [RCV000007037]|Melioidosis, resistance to [RCV000074501]|Systemic lupus erythematosus, resistance to, 1 [RCV000007038] | pathogenic|risk factor|protective | 1 | 223111858 | 223111858 | Human | 6 | name |
| 8559475 | CV21697 | single nucleotide variant | NM_003268.6(TLR5):c.1174C>T (p.Arg392Ter) | Legionnaire disease, susceptibility to [RCV000007037]|Melioidosis, resistance to [RCV000074501]|Systemic lupus erythematosus, resistance to, 1 [RCV000007038] | pathogenic|risk factor|protective | 1 | 223111858 | 223111859 | Human | 6 | name |
| 8559476 | CV21698 | single nucleotide variant | NM_003268.6(TLR5):c.1775A>G (p.Asn592Ser) | Legionnaire disease, susceptibility to [RCV000007039]|TLR5-related disorder [RCV003974802] | risk factor|benign | 1 | 223111257 | 223111257 | Human | 1 | name , trait , alternate_id |
| 156267857 | CV2198857 | single nucleotide variant | NM_003268.6(TLR5):c.1582T>G (p.Leu528Val) | not specified [RCV004077892] | uncertain significance | 1 | 223111450 | 223111450 | Human | | name |
| 156362495 | CV2265543 | single nucleotide variant | NM_003268.6(TLR5):c.1114A>T (p.Ile372Phe) | not specified [RCV004124287] | uncertain significance | 1 | 223111918 | 223111918 | Human | | name |
| 155904758 | CV2276133 | single nucleotide variant | NM_003268.6(TLR5):c.1204A>T (p.Ile402Phe) | not specified [RCV004141796] | uncertain significance | 1 | 223111828 | 223111828 | Human | | name |
| 155921201 | CV2276263 | single nucleotide variant | NM_003268.6(TLR5):c.2324C>G (p.Ala775Gly) | not specified [RCV004144022] | uncertain significance | 1 | 223110708 | 223110708 | Human | | name |
| 156170772 | CV2277032 | single nucleotide variant | NM_003268.6(TLR5):c.2317A>G (p.Ser773Gly) | not specified [RCV004140352] | uncertain significance | 1 | 223110715 | 223110715 | Human | | name |
| 156295123 | CV2303021 | single nucleotide variant | NM_003268.6(TLR5):c.2405A>G (p.Lys802Arg) | not specified [RCV004156813] | uncertain significance | 1 | 223110627 | 223110627 | Human | | name |
| 155905454 | CV2303115 | single nucleotide variant | NM_003268.6(TLR5):c.1783A>C (p.Asn595His) | not specified [RCV004156891] | uncertain significance | 1 | 223111249 | 223111249 | Human | | name |
| 156246598 | CV2310639 | single nucleotide variant | NM_003268.6(TLR5):c.1822A>G (p.Ile608Val) | not specified [RCV004157300] | uncertain significance | 1 | 223111210 | 223111210 | Human | | name |
| 156175454 | CV2327148 | single nucleotide variant | NM_003268.6(TLR5):c.1991G>A (p.Arg664Gln) | not specified [RCV004178712] | uncertain significance | 1 | 223111041 | 223111041 | Human | | name |
| 156066227 | CV2348998 | single nucleotide variant | NM_003268.6(TLR5):c.2552T>C (p.Leu851Ser) | not specified [RCV004203425] | uncertain significance | 1 | 223110480 | 223110480 | Human | | name |
| 155981627 | CV2351387 | single nucleotide variant | NM_003268.6(TLR5):c.1960C>T (p.Leu654Phe) | not specified [RCV004193079] | uncertain significance | 1 | 223111072 | 223111072 | Human | | name |
| 156037559 | CV2374083 | single nucleotide variant | NM_003268.6(TLR5):c.1516G>T (p.Val506Phe) | not specified [RCV004227200] | uncertain significance | 1 | 223111516 | 223111516 | Human | | name |
| 156348489 | CV2383127 | single nucleotide variant | NM_003268.6(TLR5):c.1393G>A (p.Gly465Arg) | not specified [RCV004219742] | uncertain significance | 1 | 223111639 | 223111639 | Human | | name |
| 329387002 | CV2436198 | single nucleotide variant | NM_003268.6(TLR5):c.2204T>C (p.Val735Ala) | not specified [RCV004249831] | uncertain significance | 1 | 223110828 | 223110828 | Human | | name |
| 11525852 | CV246874 | single nucleotide variant | NM_003268.6(TLR5):c.2537A>G (p.Asp846Gly) | not provided [RCV003417853]|not specified [RCV000238959] | benign|likely benign | 1 | 223110495 | 223110495 | Human | | name |
| 11525715 | CV246875 | single nucleotide variant | NM_003268.6(TLR5):c.1930A>T (p.Ile644Phe) | not provided [RCV003417852]|not specified [RCV000238768] | benign|likely benign | 1 | 223111102 | 223111102 | Human | | name |
| 11526038 | CV246876 | single nucleotide variant | NM_003268.6(TLR5):c.1459C>A (p.Leu487Ile) | not provided [RCV000967739]|not specified [RCV000239239] | benign|likely benign | 1 | 223111573 | 223111573 | Human | | name |
| 401736402 | CV2683012 | single nucleotide variant | NM_003268.6(TLR5):c.1019T>G (p.Val340Gly) | not specified [RCV004283795] | uncertain significance | 1 | 223112013 | 223112013 | Human | | name |
| 401763522 | CV2703927 | single nucleotide variant | NM_003268.6(TLR5):c.1536C>A (p.Asn512Lys) | not specified [RCV004308825] | uncertain significance | 1 | 223111496 | 223111496 | Human | | name |
| 401889490 | CV2758146 | single nucleotide variant | NM_003268.6(TLR5):c.2098A>G (p.Ser700Gly) | not specified [RCV004341522] | uncertain significance | 1 | 223110934 | 223110934 | Human | | name |
| 401874137 | CV2772776 | single nucleotide variant | NM_003268.6(TLR5):c.1398T>G (p.Asp466Glu) | not specified [RCV004357575] | uncertain significance | 1 | 223111634 | 223111634 | Human | | name |
| 405280876 | CV3190606 | single nucleotide variant | NM_003268.6(TLR5):c.2160T>A (p.Ser720Arg) | TLR5-related disorder [RCV003907044] | likely benign | 1 | 223110872 | 223110872 | Human | | name , trait , alternate_id |
| 405276884 | CV3193518 | single nucleotide variant | NM_003268.6(TLR5):c.1846T>C (p.Phe616Leu) | TLR5-related disorder [RCV003974686] | benign | 1 | 223111186 | 223111186 | Human | | name , trait , alternate_id |
| 405783762 | CV3342934 | single nucleotide variant | NM_003268.6(TLR5):c.1000G>A (p.Gly334Arg) | not specified [RCV004472419] | uncertain significance | 1 | 223112032 | 223112032 | Human | | name |
| 405783767 | CV3342935 | single nucleotide variant | NM_003268.6(TLR5):c.1017A>T (p.Gln339His) | not specified [RCV004472420] | uncertain significance | 1 | 223112015 | 223112015 | Human | | name |
| 405783772 | CV3342936 | single nucleotide variant | NM_003268.6(TLR5):c.1357C>G (p.Leu453Val) | not specified [RCV004472421] | uncertain significance | 1 | 223111675 | 223111675 | Human | | name |
| 405783779 | CV3342937 | single nucleotide variant | NM_003268.6(TLR5):c.1409C>T (p.Ser470Leu) | not specified [RCV004472422] | uncertain significance | 1 | 223111623 | 223111623 | Human | | name |
| 405783783 | CV3342938 | single nucleotide variant | NM_003268.6(TLR5):c.1429C>G (p.Gln477Glu) | not specified [RCV004472423] | uncertain significance | 1 | 223111603 | 223111603 | Human | | name |
| 405783794 | CV3342940 | single nucleotide variant | NM_003268.6(TLR5):c.1651G>C (p.Glu551Gln) | not specified [RCV004472425] | uncertain significance | 1 | 223111381 | 223111381 | Human | | name |
| 405783800 | CV3342941 | single nucleotide variant | NM_003268.6(TLR5):c.1685C>T (p.Ala562Val) | not specified [RCV004472426] | uncertain significance | 1 | 223111347 | 223111347 | Human | | name |
| 405783807 | CV3342942 | single nucleotide variant | NM_003268.6(TLR5):c.1852G>A (p.Gly618Arg) | not specified [RCV004472427] | uncertain significance | 1 | 223111180 | 223111180 | Human | | name |
| 405783812 | CV3342943 | single nucleotide variant | NM_003268.6(TLR5):c.2119G>A (p.Val707Met) | not specified [RCV004472428] | uncertain significance | 1 | 223110913 | 223110913 | Human | | name |
| 405783818 | CV3342944 | single nucleotide variant | NM_003268.6(TLR5):c.2237A>C (p.Asp746Ala) | not specified [RCV004472429] | likely benign | 1 | 223110795 | 223110795 | Human | | name |
| 405783824 | CV3342945 | single nucleotide variant | NM_003268.6(TLR5):c.2263G>A (p.Val755Ile) | not specified [RCV004472430] | uncertain significance | 1 | 223110769 | 223110769 | Human | | name |
| 407452660 | CV3475928 | single nucleotide variant | NM_003268.6(TLR5):c.2360T>C (p.Leu787Pro) | not specified [RCV004684155] | uncertain significance | 1 | 223110672 | 223110672 | Human | | name |
| 407452661 | CV3475929 | single nucleotide variant | NM_003268.6(TLR5):c.1336C>T (p.Arg446Trp) | not specified [RCV004684156] | uncertain significance | 1 | 223111696 | 223111696 | Human | | name |
| 407452664 | CV3475930 | single nucleotide variant | NM_003268.6(TLR5):c.1645A>G (p.Asn549Asp) | not specified [RCV004684157] | uncertain significance | 1 | 223111387 | 223111387 | Human | | name |
| 407452666 | CV3475932 | single nucleotide variant | NM_003268.6(TLR5):c.2531A>G (p.Lys844Arg) | not specified [RCV004684159] | uncertain significance | 1 | 223110501 | 223110501 | Human | | name |
| 407452668 | CV3475933 | single nucleotide variant | NM_003268.6(TLR5):c.1965G>A (p.Met655Ile) | not specified [RCV004684160] | uncertain significance | 1 | 223111067 | 223111067 | Human | | name |
| 407452672 | CV3475935 | single nucleotide variant | NM_003268.6(TLR5):c.2512A>G (p.Lys838Glu) | not specified [RCV004684162] | uncertain significance | 1 | 223110520 | 223110520 | Human | | name |
| 597775678 | CV3610475 | single nucleotide variant | NM_003268.6(TLR5):c.1762A>G (p.Ser588Gly) | not specified [RCV004872598] | uncertain significance | 1 | 223111270 | 223111270 | Human | | name |
| 597795187 | CV3610478 | single nucleotide variant | NM_003268.6(TLR5):c.2219G>A (p.Arg740His) | not specified [RCV004878106] | likely benign | 1 | 223110813 | 223110813 | Human | | name |
| 597775690 | CV3619983 | single nucleotide variant | NM_003268.6(TLR5):c.1924C>A (p.Leu642Ile) | not specified [RCV004872601] | uncertain significance | 1 | 223111108 | 223111108 | Human | | name |
| 597775694 | CV3619984 | single nucleotide variant | NM_003268.6(TLR5):c.1732C>T (p.His578Tyr) | not specified [RCV004872602] | uncertain significance | 1 | 223111300 | 223111300 | Human | | name |
| 597775704 | CV3619987 | single nucleotide variant | NM_003268.6(TLR5):c.1589G>T (p.Gly530Val) | not specified [RCV004872605] | uncertain significance | 1 | 223111443 | 223111443 | Human | | name |
| 597775712 | CV3619989 | single nucleotide variant | NM_003268.6(TLR5):c.1094T>C (p.Ile365Thr) | not specified [RCV004872607] | uncertain significance | 1 | 223111938 | 223111938 | Human | | name |
| 597775716 | CV3619990 | single nucleotide variant | NM_003268.6(TLR5):c.2438A>G (p.Gln813Arg) | not specified [RCV004872608] | likely benign | 1 | 223110594 | 223110594 | Human | | name |
| 597795188 | CV3619991 | single nucleotide variant | NM_003268.6(TLR5):c.1945A>C (p.Thr649Pro) | not specified [RCV004878107] | uncertain significance | 1 | 223111087 | 223111087 | Human | | name |
| 597775720 | CV3619992 | single nucleotide variant | NM_003268.6(TLR5):c.1865T>C (p.Phe622Ser) | not specified [RCV004872609] | uncertain significance | 1 | 223111167 | 223111167 | Human | | name |
| 598199725 | CV3920741 | single nucleotide variant | NM_003268.6(TLR5):c.1313T>C (p.Leu438Pro) | not specified [RCV005289888] | uncertain significance | 1 | 223111719 | 223111719 | Human | | name |
| 598199737 | CV3920743 | single nucleotide variant | NM_003268.6(TLR5):c.1036A>G (p.Asn346Asp) | not specified [RCV005289890] | uncertain significance | 1 | 223111996 | 223111996 | Human | | name |
| 598199744 | CV3920744 | single nucleotide variant | NM_003268.6(TLR5):c.1093A>G (p.Ile365Val) | not specified [RCV005289891] | uncertain significance | 1 | 223111939 | 223111939 | Human | | name |
| 15183497 | CV707117 | single nucleotide variant | NM_003268.6(TLR5):c.2254A>G (p.Arg752Gly) | not provided [RCV000974889] | benign | 1 | 223110778 | 223110778 | Human | | name |
| 15128854 | CV732178 | single nucleotide variant | NM_003268.6(TLR5):c.1661A>G (p.Asp554Gly) | not provided [RCV000897344] | likely benign | 1 | 223111371 | 223111371 | Human | | name |
| 15128860 | CV732179 | single nucleotide variant | NM_003268.6(TLR5):c.1643C>T (p.Ala548Val) | not provided [RCV000897345] | likely benign | 1 | 223111389 | 223111389 | Human | | name |
| 8624901 | CV80017 | single nucleotide variant | NM_003268.5(TLR5):c.2193A>T (p.Glu731Asp) | Malignant melanoma [RCV000060093] | not provided | 1 | 223110839 | 223110839 | Human | | name |
