Muc5b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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1001 records found for search term Muc5b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401909684	CV2806493	single nucleotide variant	NM_002458.3(MUC5B):c.70+8C>T	not provided [RCV003424590]	likely benign	11	1223201	1223201	Human		name
9687870	CV175375	single nucleotide variant	NM_002458.3(MUC5B):c.576+9G>T	not provided [RCV004718047]\|not specified [RCV000151036]	benign	11	1227154	1227154	Human		name
15202192	CV730742	single nucleotide variant	NM_002458.3(MUC5B):c.977-5C>T	not provided [RCV000891405]	benign\|likely benign	11	1229165	1229165	Human		name
15101774	CV777916	single nucleotide variant	NM_002458.3(MUC5B):c.127+9C>T	not provided [RCV000959158]	benign	11	1225746	1225746	Human		name
150471428	CV1259113	single nucleotide variant	NM_002458.3(MUC5B):c.977-16A>G	not provided [RCV001684358]	benign	11	1229154	1229154	Human		name
150435858	CV1270870	single nucleotide variant	NM_002458.3(MUC5B):c.667+95C>T	not provided [RCV001689420]	benign	11	1227493	1227493	Human		name
150475335	CV1271178	single nucleotide variant	NM_002458.3(MUC5B):c.462-64G>T	not provided [RCV001696001]	benign	11	1226967	1226967	Human		name
150491284	CV1280280	single nucleotide variant	NM_002458.3(MUC5B):c.577-47T>G	not provided [RCV001716617]	benign	11	1227261	1227261	Human		name
9689923	CV175801	single nucleotide variant	NM_002458.3(MUC5B):c.2631-9C>G	not provided [RCV004718075]\|not specified [RCV000155558]	benign	11	1235076	1235076	Human		name
11093218	CV230010	single nucleotide variant	NM_002458.3(MUC5B):c.1541-5G>A	not provided [RCV004718104]\|not specified [RCV000219499]	benign	11	1231418	1231418	Human		name
11093051	CV230012	single nucleotide variant	NM_002458.3(MUC5B):c.2478+8C>A	not specified [RCV000219303]	likely benign	11	1234313	1234313	Human		name
11096419	CV230013	single nucleotide variant	NM_002458.3(MUC5B):c.2769+4C>T	not provided [RCV000957630]\|not specified [RCV000223555]	benign	11	1235227	1235227	Human		name
405262613	CV3184992	single nucleotide variant	NM_002458.3(MUC5B):c.3454+7C>T	not provided [RCV003885556]	likely benign	11	1239034	1239034	Human		name
407507902	CV3457900	single nucleotide variant	NM_002458.3(MUC5B):c.2066-3C>G	not specified [RCV004646951]	uncertain significance	11	1233010	1233010	Human		name
13529495	CV497368	single nucleotide variant	NM_002458.3(MUC5B):c.200-12C>T	not specified [RCV000605761]	likely benign	11	1226603	1226603	Human		name
15138512	CV775641	single nucleotide variant	NM_002458.3(MUC5B):c.2769+8G>A	not provided [RCV000943407]	likely benign	11	1235231	1235231	Human		name
150511967	CV1212882	single nucleotide variant	NM_002458.3(MUC5B):c.977-179G>A	not provided [RCV001598114]	benign	11	1228991	1228991	Human		name
150515783	CV1216327	single nucleotide variant	NM_002458.3(MUC5B):c.1102+78G>C	not provided [RCV001608518]	benign	11	1229373	1229373	Human		name
150465935	CV1218104	single nucleotide variant	NM_002458.3(MUC5B):c.2322-83G>A	not provided [RCV001614230]	benign	11	1233710	1233710	Human		name
150446896	CV1232170	single nucleotide variant	NM_002458.3(MUC5B):c.3057+75T>C	not provided [RCV001646078]	benign	11	1236637	1236637	Human		name
150444738	CV1233060	single nucleotide variant	NM_002458.3(MUC5B):c.775-258G>T	not provided [RCV001645733]	benign	11	1228306	1228306	Human		name
150435541	CV1233882	single nucleotide variant	NM_002458.3(MUC5B):c.2065+38G>A	not provided [RCV001644009]	benign	11	1232808	1232808	Human		name
150472738	CV1235108	single nucleotide variant	NM_002458.3(MUC5B):c.3058-94C>T	not provided [RCV001651477]	benign	11	1236831	1236831	Human		name
150494461	CV1238870	single nucleotide variant	NM_002458.3(MUC5B):c.3970+35C>T	not provided [RCV001655414]	benign	11	1240410	1240410	Human		name
150490681	CV1239157	single nucleotide variant	NM_002458.3(MUC5B):c.667+103A>G	not provided [RCV001654725]	benign	11	1227501	1227501	Human		name
150430461	CV1242999	single nucleotide variant	NM_002458.3(MUC5B):c.977-158G>T	not provided [RCV001662932]	benign	11	1229012	1229012	Human		name
150467362	CV1255894	single nucleotide variant	NM_002458.3(MUC5B):c.1939-18T>C	not provided [RCV001670528]	benign	11	1232626	1232626	Human		name
150489257	CV1265388	single nucleotide variant	NM_002458.3(MUC5B):c.976+188A>G	not provided [RCV001687424]	benign	11	1228953	1228953	Human		name
150456282	CV1269056	single nucleotide variant	NM_002458.3(MUC5B):c.1102+58C>T	not provided [RCV001692880]	benign	11	1229353	1229353	Human		name
150475967	CV1279163	single nucleotide variant	NM_002458.3(MUC5B):c.1679-90C>T	not provided [RCV001713916]	benign	11	1231906	1231906	Human		name
150489680	CV1279184	single nucleotide variant	NM_002458.3(MUC5B):c.775-193C>G	not provided [RCV001716341]	benign	11	1228371	1228371	Human		name
150437702	CV1286587	single nucleotide variant	NM_002458.3(MUC5B):c.976+180G>A	not provided [RCV001724666]	benign	11	1228945	1228945	Human		name
9689920	CV175099	single nucleotide variant	NM_002458.3(MUC5B):c.1103-11G>C	not provided [RCV004718073]\|not specified [RCV000155555]	benign	11	1229679	1229679	Human		name
9687872	CV175799	single nucleotide variant	NM_002458.3(MUC5B):c.1843+11C>G	not provided [RCV001651013]\|not specified [RCV000151038]	benign	11	1232171	1232171	Human		name
9689924	CV175803	single nucleotide variant	NM_002458.3(MUC5B):c.15218-4G>A	not provided [RCV004718076]\|not specified [RCV000155559]	benign	11	1254088	1254088	Human		name
9688491	CV175809	single nucleotide variant	NM_002458.3(MUC5B):c.16137-7C>T	not provided [RCV004718056]\|not specified [RCV000151050]	benign	11	1256664	1256664	Human		name
9689927	CV175811	single nucleotide variant	NM_002458.3(MUC5B):c.16450+8G>C	not provided [RCV004718082]\|not specified [RCV000155566]	benign	11	1257718	1257718	Human		name
598224197	CV3894098	single nucleotide variant	NM_002458.3(MUC5B):c.1103-27G>A	not provided [RCV005257341]	benign	11	1229663	1229663	Human		name
13538771	CV497178	single nucleotide variant	NM_002458.3(MUC5B):c.3584-10C>T	not provided [RCV004707356]\|not specified [RCV000612325]	likely benign	11	1239789	1239789	Human		name
15110301	CV730746	single nucleotide variant	NM_002458.3(MUC5B):c.16924-5A>C	not provided [RCV000894034]	benign	11	1260346	1260346	Human		name
15101802	CV777937	single nucleotide variant	NM_002458.3(MUC5B):c.16450+9C>G	not provided [RCV000959163]	benign	11	1257719	1257719	Human		name
15101785	CV778129	single nucleotide variant	NM_002458.3(MUC5B):c.2769+10C>G	not provided [RCV000959160]	benign	11	1235233	1235233	Human		name
150511292	CV1212697	single nucleotide variant	NM_002458.3(MUC5B):c.1102+171C>T	not provided [RCV001597928]	benign	11	1229466	1229466	Human		name
150454412	CV1219978	single nucleotide variant	NM_002458.3(MUC5B):c.2631-198G>A	not provided [RCV001612360]	benign	11	1234887	1234887	Human		name
150500513	CV1224805	single nucleotide variant	NM_002458.3(MUC5B):c.2321+101T>C	not provided [RCV001620637]	benign	11	1233369	1233369	Human		name
150445572	CV1233201	single nucleotide variant	NM_002458.3(MUC5B):c.1103-117G>A	not provided [RCV001645874]	benign	11	1229573	1229573	Human		name
150462796	CV1253712	single nucleotide variant	NM_002458.3(MUC5B):c.1471-119T>C	not provided [RCV001669754]	benign	11	1230817	1230817	Human		name
150505600	CV1255515	single nucleotide variant	NM_002458.3(MUC5B):c.1102+154C>T	not provided [RCV001677962]	benign	11	1229449	1229449	Human		name
150454851	CV1261049	single nucleotide variant	NM_002458.3(MUC5B):c.16801-59T>C	not provided [RCV001681246]	benign	11	1259904	1259904	Human		name
150447105	CV1261475	single nucleotide variant	NM_002458.3(MUC5B):c.15045+79T>C	not provided [RCV001680149]	benign	11	1252603	1252603	Human		name
150464066	CV1263899	single nucleotide variant	NM_002458.3(MUC5B):c.15477+71C>T	not provided [RCV001682600]	benign	11	1254422	1254422	Human		name
150476608	CV1279287	single nucleotide variant	NM_002458.3(MUC5B):c.2881-157G>A	not provided [RCV001714008]	benign	11	1236229	1236229	Human		name
150480958	CV1279622	single nucleotide variant	NM_002458.3(MUC5B):c.16555+53A>G	not provided [RCV001714750]	benign	11	1258256	1258256	Human		name
150473625	CV1281544	single nucleotide variant	NM_002458.3(MUC5B):c.3058-180G>A	not provided [RCV001713560]	benign	11	1236745	1236745	Human		name
9689926	CV175664	single nucleotide variant	NM_002458.3(MUC5B):c.15477+12C>A	not provided [RCV004718078]\|not specified [RCV000155561]	benign	11	1254363	1254363	Human		name
9687877	CV175804	single nucleotide variant	NM_002458.3(MUC5B):c.15477+11G>A	not provided [RCV004718051]\|not specified [RCV000151044]	benign	11	1254362	1254362	Human		name
9688487	CV175805	single nucleotide variant	NM_002458.3(MUC5B):c.15478-13T>C	not provided [RCV004718052]\|not specified [RCV000151045]	benign	11	1254681	1254681	Human		name
9687881	CV175812	single nucleotide variant	NM_002458.3(MUC5B):c.16713+10G>A	not provided [RCV001534087]\|not specified [RCV000151054]	benign	11	1259071	1259071	Human		name
11092521	CV230020	single nucleotide variant	NM_002458.3(MUC5B):c.16593+15G>C	not provided [RCV004718106]\|not specified [RCV000218644]	benign	11	1258382	1258382	Human		name
150464756	CV1241370	single nucleotide variant	NM_002458.3(MUC5B):c.15218-304C>A	not provided [RCV001649881]	benign	11	1253788	1253788	Human		name
150459034	CV1248391	single nucleotide variant	NM_002458.3(MUC5B):c.15218-216G>A	not provided [RCV001669212]	benign	11	1253876	1253876	Human		name
150443813	CV1249329	single nucleotide variant	NM_002458.3(MUC5B):c.16450+116C>T	not provided [RCV001666761]	benign	11	1257826	1257826	Human		name
150447918	CV1253473	single nucleotide variant	NM_002458.3(MUC5B):c.15217+278G>A	not provided [RCV001667401]	benign	11	1253258	1253258	Human		name
12895907	CV389907	microsatellite	NM_002458.3(MUC5B):c.2377+12CCCTG[3]	not specified [RCV000454620]	benign	11	1233860	1233864	Human		name
15103929	CV768278	single nucleotide variant	NM_002458.3(MUC5B):c.144G>A (p.Ser48=)	not provided [RCV000937288]	likely benign	11	1226221	1226221	Human		name
9689916	CV175097	single nucleotide variant	NM_002458.3(MUC5B):c.723G>A (p.Thr241=)	not provided [RCV001636699]\|not specified [RCV000155551]	benign	11	1227730	1227730	Human	3	name
9689916	CV175097	single nucleotide variant	NM_002458.3(MUC5B):c.723G>A (p.Thr241=)	not provided [RCV001636699]\|not specified [RCV000155551]	benign	11	1227730	1227731	Human	3	name
9689918	CV175098	single nucleotide variant	NM_002458.3(MUC5B):c.933C>T (p.His311=)	not specified [RCV000155553]	benign	11	1228722	1228722	Human		name
9687868	CV175374	single nucleotide variant	NM_002458.3(MUC5B):c.324C>T (p.Arg108=)	not provided [RCV000950196]\|not specified [RCV000151034]	benign\|likely benign	11	1226739	1226739	Human		name
401909687	CV2806495	single nucleotide variant	NM_002458.3(MUC5B):c.642G>A (p.Pro214=)	not provided [RCV003424592]	likely benign	11	1227373	1227373	Human		name
15108845	CV724269	single nucleotide variant	NM_002458.3(MUC5B):c.492C>T (p.Leu164=)	not provided [RCV000893747]	benign	11	1227061	1227061	Human		name
15194944	CV768279	single nucleotide variant	NM_002458.3(MUC5B):c.450C>T (p.Ile150=)	not provided [RCV000933791]	likely benign	11	1226865	1226865	Human		name
9687867	CV175095	single nucleotide variant	NM_002458.3(MUC5B):c.151C>T (p.Arg51Trp)	not provided [RCV001538966]\|not specified [RCV000151033]	benign	11	1226228	1226228	Human		name
9687871	CV175100	single nucleotide variant	NM_002458.3(MUC5B):c.1596G>C (p.Leu532=)	not provided [RCV001689695]\|not specified [RCV000151037]	benign	11	1231478	1231478	Human		name
9687866	CV175373	single nucleotide variant	NM_002458.3(MUC5B):c.101A>G (p.Glu34Gly)	not provided [RCV001618304]\|not specified [RCV000151032]	benign	11	1225711	1225711	Human		name
9689919	CV175377	single nucleotide variant	NM_002458.3(MUC5B):c.1065C>T (p.Cys355=)	not provided [RCV001540491]\|not specified [RCV000155554]	benign	11	1229258	1229258	Human		name
9689921	CV175378	single nucleotide variant	NM_002458.3(MUC5B):c.1287C>T (p.Gly429=)	not provided [RCV004718074]\|not specified [RCV000155556]	benign	11	1230071	1230071	Human		name
9687873	CV175659	single nucleotide variant	NM_002458.3(MUC5B):c.2007T>C (p.Tyr669=)	not provided [RCV004718048]\|not specified [RCV000151039]	benign	11	1232712	1232712	Human		name
9687874	CV175660	single nucleotide variant	NM_002458.3(MUC5B):c.2493C>T (p.Cys831=)	not provided [RCV001723711]\|not specified [RCV000151040]	benign	11	1234543	1234543	Human		name
156118694	CV2228732	single nucleotide variant	NM_002458.3(MUC5B):c.226G>T (p.Val76Leu)	not specified [RCV004093208]	uncertain significance	11	1226641	1226641	Human		name
11094756	CV230009	single nucleotide variant	NM_002458.3(MUC5B):c.1440G>A (p.Ala480=)	not provided [RCV004718103]\|not specified [RCV000221454]	benign	11	1230570	1230570	Human		name
11095426	CV230014	single nucleotide variant	NM_002458.3(MUC5B):c.2925G>A (p.Ala975=)	not provided [RCV004705047]\|not specified [RCV000222297]	likely benign	11	1236430	1236430	Human		name
156044494	CV2308008	single nucleotide variant	NM_002458.3(MUC5B):c.211G>A (p.Ala71Thr)	not specified [RCV004170437]	uncertain significance	11	1226626	1226626	Human		name
401898818	CV2782725	single nucleotide variant	NM_002458.3(MUC5B):c.196A>G (p.Ser66Gly)	not specified [RCV004359729]	uncertain significance	11	1226273	1226273	Human		name
401909691	CV2806497	single nucleotide variant	NM_002458.3(MUC5B):c.1422C>T (p.Asn474=)	not provided [RCV003424594]	likely benign	11	1230552	1230552	Human		name
401909693	CV2806498	single nucleotide variant	NM_002458.3(MUC5B):c.1611G>A (p.Leu537=)	not provided [RCV003424595]	likely benign	11	1231493	1231493	Human		name
401909695	CV2806499	single nucleotide variant	NM_002458.3(MUC5B):c.1923C>G (p.Pro641=)	not provided [RCV003424596]	likely benign	11	1232529	1232529	Human		name
401909697	CV2806500	single nucleotide variant	NM_002458.3(MUC5B):c.2139C>T (p.Arg713=)	not provided [RCV003424597]	likely benign	11	1233086	1233086	Human		name
401909699	CV2806501	single nucleotide variant	NM_002458.3(MUC5B):c.2463G>A (p.Thr821=)	not provided [RCV003424598]	likely benign	11	1234290	1234290	Human		name
405657603	CV3314911	single nucleotide variant	NM_002458.3(MUC5B):c.178A>G (p.Thr60Ala)	not specified [RCV004437912]	uncertain significance	11	1226255	1226255	Human		name
407453951	CV3416426	single nucleotide variant	NM_002458.3(MUC5B):c.1974C>T (p.Ser658=)	not provided [RCV004597684]	likely benign	11	1232679	1232679	Human		name
407476576	CV3457883	single nucleotide variant	NM_002458.3(MUC5B):c.175G>T (p.Val59Phe)	not specified [RCV004638616]	uncertain significance	11	1226252	1226252	Human		name
407507912	CV3457904	single nucleotide variant	NM_002458.3(MUC5B):c.130G>A (p.Ala44Thr)	not specified [RCV004646954]	uncertain significance	11	1226207	1226207	Human		name
597643880	CV3557775	single nucleotide variant	NM_002458.3(MUC5B):c.2817C>T (p.Thr939=)	not specified [RCV004825876]	likely benign	11	1235350	1235350	Human		name
597644153	CV3557831	single nucleotide variant	NM_002458.3(MUC5B):c.142T>A (p.Ser48Thr)	not specified [RCV004825920]	uncertain significance	11	1226219	1226219	Human		name
597643380	CV3561582	single nucleotide variant	NM_002458.3(MUC5B):c.274G>A (p.Val92Ile)	not specified [RCV004825817]	uncertain significance	11	1226689	1226689	Human		name
12896794	CV389906	single nucleotide variant	NM_002458.3(MUC5B):c.2034A>G (p.Val678=)	not specified [RCV000455831]	benign	11	1232739	1232739	Human		name
13526403	CV496968	single nucleotide variant	NM_002458.3(MUC5B):c.1497C>T (p.Gly499=)	not provided [RCV000891523]\|not specified [RCV000604116]	benign\|likely benign	11	1230962	1230962	Human		name
15101778	CV701637	single nucleotide variant	NM_002458.3(MUC5B):c.2331G>A (p.Thr777=)	not provided [RCV000959159]	benign	11	1233802	1233802	Human		name
15160320	CV724275	single nucleotide variant	NM_002458.3(MUC5B):c.2271C>T (p.His757=)	not provided [RCV000881360]	benign	11	1233218	1233218	Human		name
15203159	CV752504	single nucleotide variant	NM_002458.3(MUC5B):c.2208G>A (p.Ala736=)	not provided [RCV000913754]	likely benign	11	1233155	1233155	Human		name
15127211	CV752505	single nucleotide variant	NM_002458.3(MUC5B):c.2316C>T (p.Ala772=)	not provided [RCV000919457]	likely benign	11	1233263	1233263	Human		name
126742321	CV1020825	single nucleotide variant	NM_002458.3(MUC5B):c.9849G>A (p.Thr3283=)	Interstitial lung disease 2 [RCV001336472]	uncertain significance	11	1246729	1246729	Human	1	name
126911009	CV1038034	single nucleotide variant	NM_002458.3(MUC5B):c.854C>T (p.Ala285Val)	not provided [RCV001354908]	uncertain significance	11	1228643	1228643	Human		name
150469163	CV1219028	single nucleotide variant	NM_002458.3(MUC5B):c.5577C>T (p.Asn1859=)	not provided [RCV001614780]	benign	11	1242457	1242457	Human		name
9687869	CV175096	single nucleotide variant	NM_002458.3(MUC5B):c.442G>A (p.Val148Ile)	not provided [RCV004718046]\|not specified [RCV000151035]	benign\|likely benign	11	1226857	1226857	Human		name
9689917	CV175376	single nucleotide variant	NM_002458.3(MUC5B):c.757G>A (p.Gly253Ser)	not provided [RCV004718072]\|not specified [RCV000155552]	benign	11	1227764	1227764	Human		name
9691814	CV175661	single nucleotide variant	NM_002458.3(MUC5B):c.3198A>G (p.Ala1066=)	not specified [RCV000151041]	likely benign	11	1237065	1237065	Human		name
10048590	CV193842	single nucleotide variant	NM_002458.3(MUC5B):c.4389C>T (p.Thr1463=)	not provided [RCV004718090]\|not specified [RCV000177536]	benign	11	1241269	1241269	Human		name
10048591	CV193843	single nucleotide variant	NM_002458.3(MUC5B):c.4797T>C (p.Ser1599=)	not provided [RCV001668341]\|not specified [RCV000177537]	benign	11	1241677	1241677	Human		name
156180610	CV2201751	single nucleotide variant	NM_002458.3(MUC5B):c.391C>T (p.Arg131Cys)	not specified [RCV004082194]	uncertain significance	11	1226806	1226806	Human		name
156035679	CV2208217	single nucleotide variant	NM_002458.3(MUC5B):c.826G>A (p.Ala276Thr)	not provided [RCV005242319]\|not specified [RCV004088675]	uncertain significance	11	1228615	1228615	Human		name
156330197	CV2210570	single nucleotide variant	NM_002458.3(MUC5B):c.845C>T (p.Ala282Val)	not specified [RCV004083725]	uncertain significance	11	1228634	1228634	Human		name
156329572	CV2213856	single nucleotide variant	NM_002458.3(MUC5B):c.934G>A (p.Ala312Thr)	not specified [RCV004089907]	uncertain significance	11	1228723	1228723	Human		name
156025081	CV2242198	single nucleotide variant	NM_002458.3(MUC5B):c.428C>G (p.Ala143Gly)	not specified [RCV004109408]	uncertain significance	11	1226843	1226843	Human		name
156240327	CV2265518	single nucleotide variant	NM_002458.3(MUC5B):c.436G>A (p.Gly146Ser)	not specified [RCV004124270]	uncertain significance	11	1226851	1226851	Human		name
155901283	CV2274487	single nucleotide variant	NM_002458.3(MUC5B):c.703C>A (p.Gln235Lys)	not specified [RCV004137116]	uncertain significance	11	1227710	1227710	Human		name
156356023	CV2320711	single nucleotide variant	NM_002458.3(MUC5B):c.870C>A (p.Asp290Glu)	not specified [RCV004179066]	uncertain significance	11	1228659	1228659	Human		name
156294730	CV2321436	single nucleotide variant	NM_002458.3(MUC5B):c.928G>A (p.Ala310Thr)	not specified [RCV004177418]	uncertain significance	11	1228717	1228717	Human		name
329382526	CV2465244	single nucleotide variant	NM_002458.3(MUC5B):c.547T>C (p.Phe183Leu)	not specified [RCV004281046]	uncertain significance	11	1227116	1227116	Human		name
401734430	CV2688506	single nucleotide variant	NM_002458.3(MUC5B):c.941G>T (p.Gly314Val)	not specified [RCV004301478]	uncertain significance	11	1228730	1228730	Human		name
401744381	CV2696990	single nucleotide variant	NM_002458.3(MUC5B):c.328G>A (p.Ala110Thr)	not specified [RCV004292982]	uncertain significance	11	1226743	1226743	Human		name
401898504	CV2787962	single nucleotide variant	NM_002458.3(MUC5B):c.304G>A (p.Val102Met)	not specified [RCV004358620]	uncertain significance	11	1226719	1226719	Human		name
401909686	CV2806494	single nucleotide variant	NM_002458.3(MUC5B):c.356G>A (p.Arg119His)	not provided [RCV003424591]	benign	11	1226771	1226771	Human		name
401909688	CV2806496	single nucleotide variant	NM_002458.3(MUC5B):c.976C>T (p.Pro326Ser)	not provided [RCV003424593]	likely benign	11	1228765	1228765	Human		name
401909700	CV2806502	single nucleotide variant	NM_002458.3(MUC5B):c.3069C>T (p.Cys1023=)	not provided [RCV003424599]	likely benign	11	1236936	1236936	Human		name
401909702	CV2806503	single nucleotide variant	NM_002458.3(MUC5B):c.3087C>T (p.Phe1029=)	not provided [RCV003424600]	benign	11	1236954	1236954	Human		name
401909704	CV2806504	single nucleotide variant	NM_002458.3(MUC5B):c.3216G>A (p.Thr1072=)	not provided [RCV003424601]	likely benign	11	1237083	1237083	Human		name
401909706	CV2806505	single nucleotide variant	NM_002458.3(MUC5B):c.3381G>A (p.Thr1127=)	not provided [RCV003424602]	likely benign	11	1238954	1238954	Human		name
401909708	CV2806506	single nucleotide variant	NM_002458.3(MUC5B):c.3436C>A (p.Arg1146=)	not provided [RCV003424603]	likely benign	11	1239009	1239009	Human		name
401909710	CV2806507	single nucleotide variant	NM_002458.3(MUC5B):c.3768T>G (p.Leu1256=)	not provided [RCV003424604]	likely benign	11	1240084	1240084	Human		name
401909714	CV2806509	single nucleotide variant	NM_002458.3(MUC5B):c.4005C>T (p.Arg1335=)	not provided [RCV003424606]	likely benign	11	1240885	1240885	Human		name
401909716	CV2806510	single nucleotide variant	NM_002458.3(MUC5B):c.4053C>T (p.Pro1351=)	not provided [RCV003424607]	likely benign	11	1240933	1240933	Human		name
401909720	CV2806512	single nucleotide variant	NM_002458.3(MUC5B):c.4264C>T (p.Leu1422=)	not provided [RCV003424609]	likely benign	11	1241144	1241144	Human		name
401909722	CV2806513	single nucleotide variant	NM_002458.3(MUC5B):c.4287C>T (p.Tyr1429=)	not provided [RCV003424610]	likely benign	11	1241167	1241167	Human		name
401909725	CV2806515	single nucleotide variant	NM_002458.3(MUC5B):c.4830G>A (p.Pro1610=)	not provided [RCV003424612]	likely benign	11	1241710	1241710	Human		name
401909727	CV2806516	single nucleotide variant	NM_002458.3(MUC5B):c.5385C>T (p.Asp1795=)	not provided [RCV003424613]	likely benign	11	1242265	1242265	Human		name
401909731	CV2806518	single nucleotide variant	NM_002458.3(MUC5B):c.5496G>A (p.Ala1832=)	not provided [RCV003424615]	likely benign	11	1242376	1242376	Human		name
401909732	CV2806519	single nucleotide variant	NM_002458.3(MUC5B):c.5538G>A (p.Val1846=)	not provided [RCV003424616]	likely benign	11	1242418	1242418	Human		name
401909734	CV2806520	single nucleotide variant	NM_002458.3(MUC5B):c.5631T>C (p.Leu1877=)	not provided [RCV003424617]	likely benign	11	1242511	1242511	Human		name
401909735	CV2806521	single nucleotide variant	NM_002458.3(MUC5B):c.5703G>A (p.Pro1901=)	not provided [RCV003424618]	likely benign	11	1242583	1242583	Human		name
401909739	CV2806523	single nucleotide variant	NM_002458.3(MUC5B):c.5709G>A (p.Thr1903=)	not provided [RCV003424620]	likely benign	11	1242589	1242589	Human		name
401909741	CV2806524	single nucleotide variant	NM_002458.3(MUC5B):c.5754G>A (p.Ala1918=)	not provided [RCV003424621]	likely benign	11	1242634	1242634	Human		name
401909742	CV2806525	single nucleotide variant	NM_002458.3(MUC5B):c.5832C>G (p.Thr1944=)	not provided [RCV003424622]	likely benign	11	1242712	1242712	Human		name
401909744	CV2806526	single nucleotide variant	NM_002458.3(MUC5B):c.6078G>A (p.Thr2026=)	not provided [RCV003424623]	likely benign	11	1242958	1242958	Human		name
401909747	CV2806527	single nucleotide variant	NM_002458.3(MUC5B):c.6156A>G (p.Pro2052=)	not provided [RCV003424624]	likely benign	11	1243036	1243036	Human		name
401909750	CV2806529	single nucleotide variant	NM_002458.3(MUC5B):c.6216G>T (p.Thr2072=)	not provided [RCV003424626]	likely benign	11	1243096	1243096	Human		name
401909755	CV2806531	single nucleotide variant	NM_002458.3(MUC5B):c.6357A>C (p.Thr2119=)	not provided [RCV003424628]	likely benign	11	1243237	1243237	Human		name
401909757	CV2806532	single nucleotide variant	NM_002458.3(MUC5B):c.6450C>G (p.Ser2150=)	not provided [RCV003424629]	likely benign	11	1243330	1243330	Human		name
401909758	CV2806533	single nucleotide variant	NM_002458.3(MUC5B):c.6459T>A (p.Pro2153=)	not provided [RCV003424630]	likely benign	11	1243339	1243339	Human		name
401909768	CV2806538	single nucleotide variant	NM_002458.3(MUC5B):c.6831G>A (p.Thr2277=)	not provided [RCV003424635]	likely benign	11	1243711	1243711	Human		name
401909776	CV2806542	single nucleotide variant	NM_002458.3(MUC5B):c.7005C>G (p.Gly2335=)	not provided [RCV003424639]	likely benign	11	1243885	1243885	Human		name
401909779	CV2806544	single nucleotide variant	NM_002458.3(MUC5B):c.7356G>T (p.Thr2452=)	not provided [RCV003424641]	likely benign	11	1244236	1244236	Human		name
401909781	CV2806545	single nucleotide variant	NM_002458.3(MUC5B):c.7626C>T (p.Ser2542=)	not provided [RCV003424642]	likely benign	11	1244506	1244506	Human		name
401909783	CV2806546	single nucleotide variant	NM_002458.3(MUC5B):c.7665C>T (p.Thr2555=)	not provided [RCV003424643]	likely benign	11	1244545	1244545	Human		name
401909786	CV2806547	single nucleotide variant	NM_002458.3(MUC5B):c.7719T>C (p.Thr2573=)	not provided [RCV003424644]	likely benign	11	1244599	1244599	Human		name
401909790	CV2806549	single nucleotide variant	NM_002458.3(MUC5B):c.7827G>A (p.Leu2609=)	not provided [RCV003424646]	likely benign	11	1244707	1244707	Human		name
401909793	CV2806551	single nucleotide variant	NM_002458.3(MUC5B):c.8139A>T (p.Thr2713=)	not provided [RCV003424648]	likely benign	11	1245019	1245019	Human		name
401909795	CV2806552	single nucleotide variant	NM_002458.3(MUC5B):c.8193C>T (p.Ser2731=)	not provided [RCV003424649]	likely benign	11	1245073	1245073	Human		name
401909797	CV2806553	single nucleotide variant	NM_002458.3(MUC5B):c.8271A>G (p.Arg2757=)	not provided [RCV003424650]	likely benign	11	1245151	1245151	Human		name
401909799	CV2806554	single nucleotide variant	NM_002458.3(MUC5B):c.8328A>G (p.Ser2776=)	not provided [RCV003424651]	benign\|likely benign	11	1245208	1245208	Human		name
401909801	CV2806555	single nucleotide variant	NM_002458.3(MUC5B):c.8343C>G (p.Thr2781=)	not provided [RCV003424652]	likely benign	11	1245223	1245223	Human		name
401909803	CV2806556	single nucleotide variant	NM_002458.3(MUC5B):c.8367G>A (p.Thr2789=)	not provided [RCV003424653]	likely benign	11	1245247	1245247	Human		name
401909805	CV2806557	single nucleotide variant	NM_002458.3(MUC5B):c.8496C>T (p.His2832=)	not provided [RCV003424654]	likely benign	11	1245376	1245376	Human		name
401909809	CV2806559	single nucleotide variant	NM_002458.3(MUC5B):c.8745C>G (p.Leu2915=)	not provided [RCV003424656]	likely benign	11	1245625	1245625	Human		name
401909816	CV2806563	single nucleotide variant	NM_002458.3(MUC5B):c.9075G>A (p.Leu3025=)	not provided [RCV003424660]	likely benign	11	1245955	1245955	Human		name
401909818	CV2806564	single nucleotide variant	NM_002458.3(MUC5B):c.9084G>C (p.Thr3028=)	not provided [RCV003424661]	likely benign	11	1245964	1245964	Human		name
401909821	CV2806565	single nucleotide variant	NM_002458.3(MUC5B):c.9213C>T (p.Ser3071=)	not provided [RCV003424662]	likely benign	11	1246093	1246093	Human		name
401909823	CV2806566	single nucleotide variant	NM_002458.3(MUC5B):c.9387G>A (p.Pro3129=)	not provided [RCV003424663]	likely benign	11	1246267	1246267	Human		name
401909826	CV2806568	single nucleotide variant	NM_002458.3(MUC5B):c.9660C>T (p.Thr3220=)	not provided [RCV003424665]	likely benign	11	1246540	1246540	Human		name
401909832	CV2806571	single nucleotide variant	NM_002458.3(MUC5B):c.9819T>C (p.Thr3273=)	not provided [RCV003424668]	likely benign	11	1246699	1246699	Human		name
401909834	CV2806572	single nucleotide variant	NM_002458.3(MUC5B):c.9837G>A (p.Val3279=)	not provided [RCV003424669]	likely benign	11	1246717	1246717	Human		name
401909836	CV2806573	single nucleotide variant	NM_002458.3(MUC5B):c.9918C>T (p.Thr3306=)	not provided [RCV003424670]	likely benign	11	1246798	1246798	Human		name
401909840	CV2806575	single nucleotide variant	NM_002458.3(MUC5B):c.9927G>A (p.Pro3309=)	not provided [RCV003424672]	likely benign	11	1246807	1246807	Human		name
401943038	CV2839955	single nucleotide variant	NM_002458.3(MUC5B):c.8520G>A (p.Thr2840=)	not provided [RCV003456742]	likely benign	11	1245400	1245400	Human		name
405669265	CV3308442	single nucleotide variant	NM_002458.3(MUC5B):c.933C>A (p.His311Gln)	not specified [RCV004440914]	uncertain significance	11	1228722	1228722	Human		name
405667341	CV3311951	single nucleotide variant	NM_002458.3(MUC5B):c.659A>G (p.Tyr220Cys)	not specified [RCV004440530]	uncertain significance	11	1227390	1227390	Human		name
407507833	CV3457869	single nucleotide variant	NM_002458.3(MUC5B):c.947C>T (p.Pro316Leu)	not specified [RCV004646931]	uncertain significance	11	1228736	1228736	Human		name
407507850	CV3457878	single nucleotide variant	NM_002458.3(MUC5B):c.532C>T (p.Arg178Trp)	not specified [RCV004646936]	uncertain significance	11	1227101	1227101	Human		name
407507950	CV3457919	single nucleotide variant	NM_002458.3(MUC5B):c.979C>T (p.Arg327Trp)	not specified [RCV004646965]	uncertain significance	11	1229172	1229172	Human		name
408384589	CV3504225	single nucleotide variant	NM_002458.3(MUC5B):c.670G>T (p.Ala224Ser)	MUC5B-related disorder [RCV004731885]	uncertain significance	11	1227677	1227677	Human		name , trait , alternate_id
408367685	CV3511745	single nucleotide variant	NM_002458.3(MUC5B):c.5619C>T (p.Asn1873=)	MUC5B-related disorder [RCV004759091]	likely benign	11	1242499	1242499	Human		name , trait , alternate_id
408367710	CV3512197	single nucleotide variant	NM_002458.3(MUC5B):c.3552G>A (p.Gly1184=)	MUC5B-related disorder [RCV004759125]	likely benign	11	1239535	1239535	Human		name , trait , alternate_id
408367711	CV3512221	single nucleotide variant	NM_002458.3(MUC5B):c.5124A>G (p.Thr1708=)	MUC5B-related disorder [RCV004759126]	benign	11	1242004	1242004	Human		name , trait , alternate_id
408367715	CV3512434	single nucleotide variant	NM_002458.3(MUC5B):c.3519A>G (p.Ala1173=)	MUC5B-related disorder [RCV004759138]	likely benign	11	1239502	1239502	Human		name , trait , alternate_id
596946929	CV3546986	single nucleotide variant	NM_002458.3(MUC5B):c.9345G>A (p.Thr3115=)	not provided [RCV004810792]	likely benign	11	1246225	1246225	Human		name
596947664	CV3547244	single nucleotide variant	NM_002458.3(MUC5B):c.6756T>G (p.Leu2252=)	not provided [RCV004811548]	likely benign	11	1243636	1243636	Human		name
596947771	CV3547354	single nucleotide variant	NM_002458.3(MUC5B):c.8700C>T (p.Asn2900=)	not provided [RCV004811658]	likely benign	11	1245580	1245580	Human		name
596945200	CV3547724	single nucleotide variant	NM_002458.3(MUC5B):c.3513C>T (p.Cys1171=)	not provided [RCV004809055]	likely benign	11	1239496	1239496	Human		name
597644098	CV3557821	single nucleotide variant	NM_002458.3(MUC5B):c.481C>T (p.Arg161Cys)	not specified [RCV004825912]	uncertain significance	11	1227050	1227050	Human		name
597639940	CV3557830	single nucleotide variant	NM_002458.3(MUC5B):c.559G>A (p.Gly187Arg)	not specified [RCV004825209]	uncertain significance	11	1227128	1227128	Human		name
597639615	CV3561606	single nucleotide variant	NM_002458.3(MUC5B):c.315G>C (p.Glu105Asp)	not specified [RCV004825175]	uncertain significance	11	1226730	1226730	Human		name
597639643	CV3561623	single nucleotide variant	NM_002458.3(MUC5B):c.933C>G (p.His311Gln)	not specified [RCV004825180]	uncertain significance	11	1228722	1228722	Human		name
598128870	CV3886669	single nucleotide variant	NM_002458.3(MUC5B):c.4749C>T (p.Gly1583=)	not provided [RCV005244329]	likely benign	11	1241629	1241629	Human		name
598129559	CV3886975	single nucleotide variant	NM_002458.3(MUC5B):c.7404G>A (p.Pro2468=)	not provided [RCV005245035]	likely benign	11	1244284	1244284	Human		name
598224886	CV3894177	single nucleotide variant	NM_002458.3(MUC5B):c.980G>A (p.Arg327Gln)	not provided [RCV005257420]	likely benign	11	1229173	1229173	Human		name
12896209	CV389852	single nucleotide variant	NM_002458.3(MUC5B):c.6780A>G (p.Arg2260=)	not provided [RCV001662410]\|not specified [RCV000455039]	benign	11	1243660	1243660	Human		name
12895770	CV389861	single nucleotide variant	NM_002458.3(MUC5B):c.8886T>C (p.Arg2962=)	not provided [RCV004707289]\|not specified [RCV000454430]	likely benign	11	1245766	1245766	Human		name
12896065	CV389878	single nucleotide variant	NM_002458.3(MUC5B):c.9603C>G (p.Thr3201=)	not provided [RCV004718670]\|not specified [RCV000454835]	benign	11	1246483	1246483	Human		name
12896391	CV389909	single nucleotide variant	NM_002458.3(MUC5B):c.3186G>A (p.Pro1062=)	not specified [RCV000455283]	benign	11	1237053	1237053	Human		name
12896186	CV389916	single nucleotide variant	NM_002458.3(MUC5B):c.6600A>G (p.Arg2200=)	not provided [RCV001692116]\|not specified [RCV000455008]	benign	11	1243480	1243480	Human		name
12895953	CV389932	single nucleotide variant	NM_002458.3(MUC5B):c.9048G>A (p.Pro3016=)	not provided [RCV004718666]\|not specified [RCV000454679]	benign	11	1245928	1245928	Human		name
12896758	CV389967	single nucleotide variant	NM_002458.3(MUC5B):c.3189C>T (p.Asp1063=)	not specified [RCV000455784]	benign	11	1237056	1237056	Human		name
12896156	CV389968	single nucleotide variant	NM_002458.3(MUC5B):c.6252A>G (p.Thr2084=)	not provided [RCV001637024]\|not specified [RCV000454960]	benign	11	1243132	1243132	Human		name
12896439	CV389977	single nucleotide variant	NM_002458.3(MUC5B):c.8586A>C (p.Pro2862=)	not provided [RCV001683495]\|not specified [RCV000455341]	benign	11	1245466	1245466	Human		name
12896584	CV389979	single nucleotide variant	NM_002458.3(MUC5B):c.8709G>A (p.Ala2903=)	not provided [RCV003424005]\|not specified [RCV000455549]	benign\|likely benign	11	1245589	1245589	Human		name
12896805	CV389984	single nucleotide variant	NM_002458.3(MUC5B):c.6855G>A (p.Thr2285=)	not provided [RCV001618696]\|not specified [RCV000455846]	benign	11	1243735	1243735	Human		name
12896090	CV390001	single nucleotide variant	NM_002458.3(MUC5B):c.9501C>G (p.Pro3167=)	not provided [RCV004718667]\|not specified [RCV000454868]	benign	11	1246381	1246381	Human		name
12896187	CV390004	single nucleotide variant	NM_002458.3(MUC5B):c.9807T>C (p.Ser3269=)	not provided [RCV001643154]\|not specified [RCV000455009]	benign	11	1246687	1246687	Human		name
12895844	CV390007	single nucleotide variant	NM_002458.3(MUC5B):c.9954C>T (p.Ala3318=)	not provided [RCV001672768]\|not specified [RCV000454535]	benign	11	1246834	1246834	Human		name
598228677	CV3986706	single nucleotide variant	NM_002458.3(MUC5B):c.598G>A (p.Ala200Thr)	not specified [RCV005380911]	uncertain significance	11	1227329	1227329	Human		name
598228843	CV3986737	single nucleotide variant	NM_002458.3(MUC5B):c.950G>A (p.Arg317Gln)	not specified [RCV005380931]	likely benign	11	1228739	1228739	Human		name
598229090	CV3986781	single nucleotide variant	NM_002458.3(MUC5B):c.7269G>A (p.Thr2423=)	not specified [RCV005380965]	likely benign	11	1244149	1244149	Human		name
598229193	CV3986797	single nucleotide variant	NM_002458.3(MUC5B):c.581A>G (p.Glu194Gly)	not specified [RCV005380979]	uncertain significance	11	1227312	1227312	Human		name
617152780	CV4020996	single nucleotide variant	NM_002458.3(MUC5B):c.6882G>A (p.Ser2294=)	not provided [RCV005428749]	likely benign	11	1243762	1243762	Human		name
617153076	CV4021049	single nucleotide variant	NM_002458.3(MUC5B):c.7791C>T (p.Ser2597=)	not provided [RCV005428802]	likely benign	11	1244671	1244671	Human		name
617151192	CV4021823	single nucleotide variant	NM_002458.3(MUC5B):c.8553G>A (p.Ser2851=)	not provided [RCV005426784]	likely benign	11	1245433	1245433	Human		name
13541049	CV496560	single nucleotide variant	NM_002458.3(MUC5B):c.845C>A (p.Ala282Glu)	not specified [RCV000615594]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	1228634	1228634	Human		name
13526784	CV496562	single nucleotide variant	NM_002458.3(MUC5B):c.3846C>T (p.Gly1282=)	not provided [RCV000966221]\|not specified [RCV000604604]	likely benign	11	1240251	1240251	Human		name
13541302	CV497369	single nucleotide variant	NM_002458.3(MUC5B):c.3834C>T (p.Thr1278=)	Interstitial lung disease 2 [RCV002506450]\|not provided [RCV000947311]\|not specified [RCV000615977]	benign\|likely benign	11	1240239	1240239	Human	1	name
14703359	CV654651	single nucleotide variant	NM_002458.3(MUC5B):c.3483T>C (p.His1161=)	not specified [RCV000825189]	likely benign	11	1239466	1239466	Human		name
15101788	CV701642	single nucleotide variant	NM_002458.3(MUC5B):c.3945C>T (p.Thr1315=)	not provided [RCV000959161]	benign	11	1240350	1240350	Human		name
15169677	CV724277	single nucleotide variant	NM_002458.3(MUC5B):c.3765C>T (p.Ser1255=)	not provided [RCV000883317]	benign	11	1240081	1240081	Human		name
126726716	CV1017397	single nucleotide variant	NM_002458.3(MUC5B):c.2725G>A (p.Asp909Asn)	Interstitial lung disease 2 [RCV001332134]	uncertain significance	11	1235179	1235179	Human	1	name
126910091	CV1038035	single nucleotide variant	NM_002458.3(MUC5B):c.1994C>T (p.Ala665Val)	not provided [RCV001354356]	uncertain significance	11	1232699	1232699	Human		name
126913575	CV1038039	single nucleotide variant	NM_002458.3(MUC5B):c.10059G>A (p.Pro3353=)	not provided [RCV001357497]	uncertain significance	11	1246939	1246939	Human		name
126911693	CV1038040	single nucleotide variant	NM_002458.3(MUC5B):c.12243C>A (p.Ser4081=)	not provided [RCV001355645]	uncertain significance	11	1249123	1249123	Human		name
126914850	CV1038041	single nucleotide variant	NM_002458.3(MUC5B):c.13164G>T (p.Thr4388=)	Interstitial lung disease 2 [RCV002486493]\|not provided [RCV001358620]	uncertain significance	11	1250044	1250044	Human	1	name
127233461	CV1053825	single nucleotide variant	NM_002458.3(MUC5B):c.2045A>G (p.Asp682Gly)	Interstitial lung disease 2 [RCV001376074]	likely benign	11	1232750	1232750	Human	1	name
127233462	CV1053826	single nucleotide variant	NM_002458.3(MUC5B):c.2041A>G (p.Ser681Gly)	Interstitial lung disease 2 [RCV001376075]	likely benign	11	1232746	1232746	Human	1	name
150460657	CV1264205	single nucleotide variant	NM_002458.3(MUC5B):c.13929G>A (p.Pro4643=)	not provided [RCV001682122]	benign	11	1250809	1250809	Human		name
150467311	CV1277549	single nucleotide variant	NM_002458.3(MUC5B):c.10371G>A (p.Arg3457=)	not provided [RCV001710844]	benign	11	1247251	1247251	Human		name
152034363	CV1669499	single nucleotide variant	NM_002458.3(MUC5B):c.2029G>A (p.Gly677Ser)	not provided [RCV002223490]	uncertain significance	11	1232734	1232734	Human		name
9687876	CV175662	single nucleotide variant	NM_002458.3(MUC5B):c.14937T>C (p.Ile4979=)	not provided [RCV004718050]\|not specified [RCV000151043]	benign	11	1252416	1252416	Human		name
9689925	CV175663	single nucleotide variant	NM_002458.3(MUC5B):c.15450C>T (p.Thr5150=)	not provided [RCV004718077]\|not specified [RCV000155560]	benign	11	1254324	1254324	Human		name
9693577	CV175666	single nucleotide variant	NM_002458.3(MUC5B):c.15861A>G (p.Pro5287=)	not provided [RCV004706605]\|not specified [RCV000155562]	benign\|likely benign\|conflicting interpretations of pathogenicity	11	1255237	1255237	Human		name
9693579	CV175667	single nucleotide variant	NM_002458.3(MUC5B):c.16014C>T (p.Cys5338=)	not provided [RCV004718080]\|not specified [RCV000155564]	benign	11	1255506	1255506	Human		name
9693580	CV175668	single nucleotide variant	NM_002458.3(MUC5B):c.16110C>A (p.Pro5370=)	not provided [RCV004718081]\|not specified [RCV000155565]	benign	11	1256199	1256199	Human		name
9687882	CV175672	single nucleotide variant	NM_002458.3(MUC5B):c.17043C>T (p.Cys5681=)	MUC5B-related disorder [RCV004758654]\|not provided [RCV000952687]\|not specified [RCV000151055]	benign\|likely benign	11	1260702	1260702	Human	1	name , alternate_id
9689922	CV175800	single nucleotide variant	NM_002458.3(MUC5B):c.2429C>A (p.Thr810Asn)	not provided [RCV000885543]\|not specified [RCV000155557]	benign\|likely benign	11	1234256	1234256	Human		name
9693578	CV175807	single nucleotide variant	NM_002458.3(MUC5B):c.15972T>C (p.Leu5324=)	not provided [RCV004718079]\|not specified [RCV000155563]	benign	11	1255464	1255464	Human		name
9688490	CV175808	single nucleotide variant	NM_002458.3(MUC5B):c.16053C>T (p.Thr5351=)	not provided [RCV004718055]\|not specified [RCV000151048]	benign	11	1255545	1255545	Human		name
10052391	CV194745	single nucleotide variant	NM_002458.3(MUC5B):c.17016C>T (p.Cys5672=)	not provided [RCV000178649]	conflicting interpretations of pathogenicity\|uncertain significance	11	1260675	1260675	Human		name
156398949	CV2194890	single nucleotide variant	NM_002458.3(MUC5B):c.2213C>A (p.Thr738Asn)	not specified [RCV004075421]	uncertain significance	11	1233160	1233160	Human		name
155917948	CV2195582	single nucleotide variant	NM_002458.3(MUC5B):c.2665C>T (p.Arg889Trp)	not specified [RCV004082793]	uncertain significance	11	1235119	1235119	Human		name
156378787	CV2207804	single nucleotide variant	NM_002458.3(MUC5B):c.2384C>T (p.Ala795Val)	not specified [RCV004084239]	likely benign	11	1234211	1234211	Human		name
156401188	CV2210612	single nucleotide variant	NM_002458.3(MUC5B):c.2449C>T (p.Arg817Trp)	not specified [RCV004083762]	uncertain significance	11	1234276	1234276	Human		name
155979985	CV2211865	single nucleotide variant	NM_002458.3(MUC5B):c.2141G>T (p.Gly714Val)	not specified [RCV004087001]	uncertain significance	11	1233088	1233088	Human		name
156139130	CV2212049	single nucleotide variant	NM_002458.3(MUC5B):c.2758A>C (p.Ile920Leu)	not specified [RCV004088960]	uncertain significance	11	1235212	1235212	Human		name
156147601	CV2212845	single nucleotide variant	NM_002458.3(MUC5B):c.2179G>A (p.Val727Met)	not specified [RCV004091515]	uncertain significance	11	1233126	1233126	Human		name
156360927	CV2269138	single nucleotide variant	NM_002458.3(MUC5B):c.1384G>A (p.Val462Met)	not provided [RCV004695463]\|not specified [RCV004130310]	uncertain significance	11	1230514	1230514	Human		name
156031848	CV2274965	single nucleotide variant	NM_002458.3(MUC5B):c.2059G>A (p.Val687Ile)	not specified [RCV004135013]	uncertain significance	11	1232764	1232764	Human		name
156267834	CV2275577	single nucleotide variant	NM_002458.3(MUC5B):c.1748C>T (p.Thr583Met)	not specified [RCV004137215]	uncertain significance	11	1232065	1232065	Human		name
155927724	CV2285232	single nucleotide variant	NM_002458.3(MUC5B):c.1171G>A (p.Gly391Ser)	not specified [RCV004145433]	uncertain significance	11	1229758	1229758	Human		name
156069644	CV2295751	single nucleotide variant	NM_002458.3(MUC5B):c.2896C>T (p.Leu966Phe)	not specified [RCV004151683]	uncertain significance	11	1236401	1236401	Human		name
11091034	CV230011	single nucleotide variant	NM_002458.3(MUC5B):c.2068A>G (p.Lys690Glu)	not specified [RCV000216809]	uncertain significance	11	1233015	1233015	Human		name
11089522	CV230019	single nucleotide variant	NM_002458.3(MUC5B):c.16476G>A (p.Gln5492=)	not provided [RCV004718105]\|not specified [RCV000214916]	benign	11	1258124	1258124	Human		name
155905949	CV2303214	single nucleotide variant	NM_002458.3(MUC5B):c.2918C>T (p.Ala973Val)	not specified [RCV004156973]	likely benign	11	1236423	1236423	Human		name
155930121	CV2366564	single nucleotide variant	NM_002458.3(MUC5B):c.1456G>A (p.Asp486Asn)	not specified [RCV004208536]	likely benign	11	1230586	1230586	Human		name
329386279	CV2455821	single nucleotide variant	NM_002458.3(MUC5B):c.1213A>C (p.Ser405Arg)	not specified [RCV004279109]	uncertain significance	11	1229800	1229800	Human		name
329396600	CV2462791	single nucleotide variant	NM_002458.3(MUC5B):c.1025G>A (p.Cys342Tyr)	not specified [RCV004278706]	uncertain significance	11	1229218	1229218	Human		name
401751871	CV2672605	single nucleotide variant	NM_002458.3(MUC5B):c.2032G>A (p.Val678Ile)	not specified [RCV004287636]	uncertain significance	11	1232737	1232737	Human		name
401745813	CV2678711	single nucleotide variant	NM_002458.3(MUC5B):c.2245G>A (p.Ala749Thr)	not specified [RCV004292711]	uncertain significance	11	1233192	1233192	Human		name
401739788	CV2684173	single nucleotide variant	NM_002458.3(MUC5B):c.1439C>T (p.Ala480Val)	not specified [RCV004288845]	uncertain significance	11	1230569	1230569	Human		name
401730909	CV2686783	single nucleotide variant	NM_002458.3(MUC5B):c.2110G>A (p.Val704Met)	not specified [RCV004301965]	uncertain significance	11	1233057	1233057	Human		name
401772596	CV2687747	single nucleotide variant	NM_002458.3(MUC5B):c.1228T>G (p.Ser410Ala)	not specified [RCV004302734]	uncertain significance	11	1230012	1230012	Human		name
401769138	CV2693314	single nucleotide variant	NM_002458.3(MUC5B):c.1462G>A (p.Gly488Arg)	not specified [RCV004295277]	uncertain significance	11	1230592	1230592	Human		name
401761796	CV2699416	single nucleotide variant	NM_002458.3(MUC5B):c.2470G>A (p.Val824Met)	MUC5B-related disorder [RCV004758931]\|not specified [RCV004305991]	likely benign\|uncertain significance	11	1234297	1234297	Human	1	name , alternate_id
401750589	CV2701382	single nucleotide variant	NM_002458.3(MUC5B):c.1223C>T (p.Thr408Ile)	not specified [RCV004311747]	uncertain significance	11	1230007	1230007	Human		name
401770017	CV2710818	single nucleotide variant	NM_002458.3(MUC5B):c.2099G>T (p.Arg700Leu)	not specified [RCV004308741]	uncertain significance	11	1233046	1233046	Human		name
401870140	CV2792288	single nucleotide variant	NM_002458.3(MUC5B):c.1970G>A (p.Arg657Gln)	not specified [RCV004361475]	uncertain significance	11	1232675	1232675	Human		name
401909844	CV2806577	single nucleotide variant	NM_002458.3(MUC5B):c.10053C>T (p.Ser3351=)	not provided [RCV003424674]	likely benign	11	1246933	1246933	Human		name
401909846	CV2806578	single nucleotide variant	NM_002458.3(MUC5B):c.10179G>A (p.Thr3393=)	not provided [RCV003424675]	likely benign	11	1247059	1247059	Human		name
401909847	CV2806579	single nucleotide variant	NM_002458.3(MUC5B):c.10239T>A (p.Thr3413=)	not provided [RCV003424676]	likely benign	11	1247119	1247119	Human		name
401909849	CV2806580	single nucleotide variant	NM_002458.3(MUC5B):c.10302T>C (p.Thr3434=)	not provided [RCV003424677]	likely benign	11	1247182	1247182	Human		name
401909854	CV2806583	single nucleotide variant	NM_002458.3(MUC5B):c.10824C>A (p.Val3608=)	not provided [RCV003424680]	benign\|likely benign	11	1247704	1247704	Human		name
401909856	CV2806584	single nucleotide variant	NM_002458.3(MUC5B):c.10882C>A (p.Arg3628=)	not provided [RCV003424681]	likely benign	11	1247762	1247762	Human		name
401909863	CV2806587	single nucleotide variant	NM_002458.3(MUC5B):c.11205C>T (p.Thr3735=)	not provided [RCV003424684]	likely benign	11	1248085	1248085	Human		name
401909865	CV2806588	single nucleotide variant	NM_002458.3(MUC5B):c.11436C>T (p.Thr3812=)	not provided [RCV003424685]	likely benign	11	1248316	1248316	Human		name
401909867	CV2806589	single nucleotide variant	NM_002458.3(MUC5B):c.11490T>C (p.Thr3830=)	not provided [RCV003424686]	likely benign	11	1248370	1248370	Human		name
401909872	CV2806591	single nucleotide variant	NM_002458.3(MUC5B):c.11520G>A (p.Thr3840=)	not provided [RCV003424688]	likely benign	11	1248400	1248400	Human		name
401909876	CV2806593	single nucleotide variant	NM_002458.3(MUC5B):c.11724C>T (p.Ser3908=)	not provided [RCV003424690]	likely benign	11	1248604	1248604	Human		name
401909878	CV2806594	single nucleotide variant	NM_002458.3(MUC5B):c.11859G>A (p.Thr3953=)	not provided [RCV003424691]	likely benign	11	1248739	1248739	Human		name
401909880	CV2806595	single nucleotide variant	NM_002458.3(MUC5B):c.11871C>T (p.Thr3957=)	not provided [RCV003424692]	likely benign	11	1248751	1248751	Human		name
401909882	CV2806596	single nucleotide variant	NM_002458.3(MUC5B):c.12042A>G (p.Arg4014=)	not provided [RCV003424693]	likely benign	11	1248922	1248922	Human		name
401909889	CV2806600	single nucleotide variant	NM_002458.3(MUC5B):c.12516C>G (p.Leu4172=)	not provided [RCV003424697]	likely benign	11	1249396	1249396	Human		name
401909891	CV2806601	single nucleotide variant	NM_002458.3(MUC5B):c.12657T>C (p.Arg4219=)	not provided [RCV003424698]	likely benign	11	1249537	1249537	Human		name
401909897	CV2806604	single nucleotide variant	NM_002458.3(MUC5B):c.12837C>T (p.Pro4279=)	not provided [RCV003424701]	likely benign	11	1249717	1249717	Human		name
401909901	CV2806606	single nucleotide variant	NM_002458.3(MUC5B):c.13248G>A (p.Gly4416=)	not provided [RCV003424703]	likely benign	11	1250128	1250128	Human		name
401909903	CV2806607	single nucleotide variant	NM_002458.3(MUC5B):c.13296G>A (p.Ala4432=)	not provided [RCV003424704]	likely benign	11	1250176	1250176	Human		name
401909905	CV2806608	single nucleotide variant	NM_002458.3(MUC5B):c.13326C>T (p.Ser4442=)	not provided [RCV003424705]	likely benign	11	1250206	1250206	Human		name
401909907	CV2806609	single nucleotide variant	NM_002458.3(MUC5B):c.13359G>C (p.Pro4453=)	not provided [RCV003424706]	likely benign	11	1250239	1250239	Human		name
401909909	CV2806610	single nucleotide variant	NM_002458.3(MUC5B):c.13374C>T (p.Thr4458=)	not provided [RCV003424707]	likely benign	11	1250254	1250254	Human		name
401909911	CV2806611	single nucleotide variant	NM_002458.3(MUC5B):c.13389C>T (p.Thr4463=)	not provided [RCV003424708]	benign	11	1250269	1250269	Human		name
401909913	CV2806612	single nucleotide variant	NM_002458.3(MUC5B):c.13515T>C (p.Thr4505=)	not provided [RCV003424709]	likely benign	11	1250395	1250395	Human		name
401909915	CV2806613	single nucleotide variant	NM_002458.3(MUC5B):c.13542C>T (p.Ala4514=)	not provided [RCV003424710]	likely benign	11	1250422	1250422	Human		name
401909917	CV2806614	single nucleotide variant	NM_002458.3(MUC5B):c.13704G>A (p.Thr4568=)	not provided [RCV003424711]	likely benign	11	1250584	1250584	Human		name
401909919	CV2806615	single nucleotide variant	NM_002458.3(MUC5B):c.13737C>G (p.Ala4579=)	not provided [RCV003424712]	likely benign	11	1250617	1250617	Human		name
401909923	CV2806617	single nucleotide variant	NM_002458.3(MUC5B):c.13842G>T (p.Thr4614=)	not provided [RCV003424714]	likely benign	11	1250722	1250722	Human		name
401909925	CV2806618	single nucleotide variant	NM_002458.3(MUC5B):c.13923C>T (p.Ser4641=)	not provided [RCV003424715]	likely benign	11	1250803	1250803	Human		name
401909927	CV2806619	single nucleotide variant	NM_002458.3(MUC5B):c.14109A>T (p.Thr4703=)	not provided [RCV003424716]	likely benign	11	1250989	1250989	Human		name
401909929	CV2806620	single nucleotide variant	NM_002458.3(MUC5B):c.14439G>A (p.Leu4813=)	not provided [RCV003424717]	likely benign	11	1251319	1251319	Human		name
401909933	CV2806622	single nucleotide variant	NM_002458.3(MUC5B):c.14460T>A (p.Thr4820=)	not provided [RCV003424719]	likely benign	11	1251340	1251340	Human		name
401909935	CV2806623	single nucleotide variant	NM_002458.3(MUC5B):c.14505G>A (p.Thr4835=)	not provided [RCV003424720]	likely benign	11	1251385	1251385	Human		name
401909937	CV2806624	single nucleotide variant	NM_002458.3(MUC5B):c.14598C>T (p.Thr4866=)	not provided [RCV003424721]	likely benign	11	1251478	1251478	Human		name
401909944	CV2806628	single nucleotide variant	NM_002458.3(MUC5B):c.14973G>A (p.Pro4991=)	not provided [RCV003424725]	likely benign	11	1252452	1252452	Human		name
401909947	CV2806629	single nucleotide variant	NM_002458.3(MUC5B):c.14985C>T (p.Ser4995=)	not provided [RCV003424726]	likely benign	11	1252464	1252464	Human		name
401909948	CV2806630	single nucleotide variant	NM_002458.3(MUC5B):c.16104C>T (p.Cys5368=)	not provided [RCV003424727]	likely benign	11	1256193	1256193	Human		name
401909950	CV2806631	single nucleotide variant	NM_002458.3(MUC5B):c.16977A>G (p.Gln5659=)	not provided [RCV003424728]	likely benign	11	1260636	1260636	Human		name
401909952	CV2806632	single nucleotide variant	NM_002458.3(MUC5B):c.17058C>T (p.Pro5686=)	not provided [RCV003424729]	likely benign	11	1260717	1260717	Human		name
405265495	CV3185711	single nucleotide variant	NM_002458.3(MUC5B):c.12483C>T (p.Ala4161=)	not provided [RCV003886275]	likely benign	11	1249363	1249363	Human		name
405258184	CV3208236	single nucleotide variant	NM_002458.3(MUC5B):c.1520C>T (p.Thr507Met)	MUC5B-related disorder [RCV003941671]	likely benign	11	1230985	1230985	Human		name , trait , alternate_id
405657589	CV3314906	single nucleotide variant	NM_002458.3(MUC5B):c.1739T>A (p.Val580Glu)	not specified [RCV004437907]	uncertain significance	11	1232056	1232056	Human		name
405657616	CV3314914	single nucleotide variant	NM_002458.3(MUC5B):c.1883C>T (p.Pro628Leu)	not specified [RCV004437915]	uncertain significance	11	1232489	1232489	Human		name
405657632	CV3314919	single nucleotide variant	NM_002458.3(MUC5B):c.1900C>T (p.Arg634Cys)	not specified [RCV004437920]	uncertain significance	11	1232506	1232506	Human		name
405657635	CV3314920	single nucleotide variant	NM_002458.3(MUC5B):c.1933C>T (p.His645Tyr)	not specified [RCV004437921]	uncertain significance	11	1232539	1232539	Human		name
405657673	CV3314931	single nucleotide variant	NM_002458.3(MUC5B):c.1993G>T (p.Ala665Ser)	not specified [RCV004437932]	uncertain significance	11	1232698	1232698	Human		name
405657681	CV3314933	single nucleotide variant	NM_002458.3(MUC5B):c.2000C>A (p.Ser667Tyr)	not specified [RCV004437934]	uncertain significance	11	1232705	1232705	Human		name
405657763	CV3314962	single nucleotide variant	NM_002458.3(MUC5B):c.2209G>A (p.Gly737Ser)	not specified [RCV004437963]	uncertain significance	11	1233156	1233156	Human		name
405657799	CV3314974	single nucleotide variant	NM_002458.3(MUC5B):c.2266G>A (p.Ala756Thr)	not specified [RCV004437975]	uncertain significance	11	1233213	1233213	Human		name
405657816	CV3314980	single nucleotide variant	NM_002458.3(MUC5B):c.2341C>G (p.Leu781Val)	not specified [RCV004437981]	uncertain significance	11	1233812	1233812	Human		name
405657850	CV3314990	single nucleotide variant	NM_002458.3(MUC5B):c.2539G>T (p.Gly847Trp)	not specified [RCV004437991]	uncertain significance	11	1234589	1234589	Human		name
405657859	CV3314993	single nucleotide variant	NM_002458.3(MUC5B):c.2570G>A (p.Cys857Tyr)	not specified [RCV004437994]	uncertain significance	11	1234620	1234620	Human		name
405657880	CV3315001	single nucleotide variant	NM_002458.3(MUC5B):c.2807G>A (p.Arg936His)	not specified [RCV004438002]	uncertain significance	11	1235340	1235340	Human		name
405657885	CV3315003	single nucleotide variant	NM_002458.3(MUC5B):c.2837C>A (p.Thr946Asn)	not specified [RCV004438004]	uncertain significance	11	1235370	1235370	Human		name
405689071	CV3318359	single nucleotide variant	NM_002458.3(MUC5B):c.1289G>A (p.Gly430Glu)	not specified [RCV004444992]	uncertain significance	11	1230073	1230073	Human		name
405689888	CV3318513	single nucleotide variant	NM_002458.3(MUC5B):c.14148C>T (p.Pro4716=)	not specified [RCV004445146]	likely benign	11	1251028	1251028	Human		name
405690431	CV3318608	single nucleotide variant	NM_002458.3(MUC5B):c.1513A>G (p.Ile505Val)	not specified [RCV004445241]	uncertain significance	11	1230978	1230978	Human		name
405690493	CV3318619	single nucleotide variant	NM_002458.3(MUC5B):c.1535C>T (p.Ser512Leu)	not specified [RCV004445252]	uncertain significance	11	1231000	1231000	Human		name
405672935	CV3377634	single nucleotide variant	NM_002458.3(MUC5B):c.1028C>T (p.Thr343Met)	not specified [RCV004515494]	uncertain significance	11	1229221	1229221	Human		name
407455948	CV3415786	single nucleotide variant	NM_002458.3(MUC5B):c.15108C>T (p.Val5036=)	not provided [RCV004598662]	likely benign	11	1252871	1252871	Human		name
407507804	CV3457857	single nucleotide variant	NM_002458.3(MUC5B):c.2639G>C (p.Arg880Thr)	not specified [RCV004646923]	uncertain significance	11	1235093	1235093	Human		name
407507867	CV3457885	single nucleotide variant	NM_002458.3(MUC5B):c.2330C>T (p.Thr777Met)	not specified [RCV004646941]	uncertain significance	11	1233801	1233801	Human		name
407476587	CV3457889	single nucleotide variant	NM_002458.3(MUC5B):c.1106C>T (p.Thr369Met)	not specified [RCV004638619]	uncertain significance	11	1229693	1229693	Human		name
407476599	CV3457902	single nucleotide variant	NM_002458.3(MUC5B):c.1186C>T (p.Pro396Ser)	not specified [RCV004638622]	uncertain significance	11	1229773	1229773	Human		name
407572671	CV3497153	single nucleotide variant	NM_002458.3(MUC5B):c.1304C>T (p.Thr435Ile)	not provided [RCV004698973]	uncertain significance	11	1230088	1230088	Human		name
408378048	CV3500908	single nucleotide variant	NM_002458.3(MUC5B):c.1969C>T (p.Arg657Trp)	not provided [RCV004722558]	likely benign	11	1232674	1232674	Human		name
408379154	CV3501001	single nucleotide variant	NM_002458.3(MUC5B):c.12198G>T (p.Leu4066=)	not provided [RCV004722651]	likely benign	11	1249078	1249078	Human		name
596947692	CV3547273	single nucleotide variant	NM_002458.3(MUC5B):c.14886C>T (p.Thr4962=)	not provided [RCV004811577]	likely benign	11	1252365	1252365	Human		name
596947871	CV3547458	single nucleotide variant	NM_002458.3(MUC5B):c.12447C>G (p.Gly4149=)	not provided [RCV004811762]	likely benign	11	1249327	1249327	Human		name
596948085	CV3547679	single nucleotide variant	NM_002458.3(MUC5B):c.11532C>T (p.Thr3844=)	not provided [RCV004811984]	likely benign	11	1248412	1248412	Human		name
596946395	CV3548213	single nucleotide variant	NM_002458.3(MUC5B):c.16443G>A (p.Thr5481=)	not provided [RCV004810038]	likely benign	11	1257703	1257703	Human		name
596946675	CV3548504	single nucleotide variant	NM_002458.3(MUC5B):c.16494G>A (p.Pro5498=)	not provided [RCV004810331]	likely benign	11	1258142	1258142	Human		name
597639672	CV3557740	single nucleotide variant	NM_002458.3(MUC5B):c.2875G>A (p.Val959Met)	not specified [RCV004825186]	uncertain significance	11	1235408	1235408	Human		name
597643795	CV3557752	single nucleotide variant	NM_002458.3(MUC5B):c.1319T>C (p.Leu440Pro)	not specified [RCV004825862]	uncertain significance	11	1230103	1230103	Human		name
597639723	CV3557770	single nucleotide variant	NM_002458.3(MUC5B):c.2387C>G (p.Ala796Gly)	not specified [RCV004825196]	uncertain significance	11	1234214	1234214	Human		name
597643874	CV3557774	single nucleotide variant	NM_002458.3(MUC5B):c.2549T>A (p.Ile850Asn)	not specified [RCV004825875]	uncertain significance	11	1234599	1234599	Human		name
597643886	CV3557776	single nucleotide variant	NM_002458.3(MUC5B):c.2773T>C (p.Tyr925His)	not specified [RCV004825877]	uncertain significance	11	1235306	1235306	Human		name
597643897	CV3557778	single nucleotide variant	NM_002458.3(MUC5B):c.1408G>A (p.Gly470Ser)	not specified [RCV004825879]	uncertain significance	11	1230538	1230538	Human		name
597643923	CV3557783	single nucleotide variant	NM_002458.3(MUC5B):c.2711T>A (p.Ile904Asn)	not specified [RCV004825883]	uncertain significance	11	1235165	1235165	Human		name
597639759	CV3557799	single nucleotide variant	NM_002458.3(MUC5B):c.2929G>A (p.Gly977Arg)	not specified [RCV004825202]	uncertain significance	11	1236434	1236434	Human		name
597644009	CV3557801	single nucleotide variant	NM_002458.3(MUC5B):c.2305G>A (p.Asp769Asn)	not specified [RCV004825897]	uncertain significance	11	1233252	1233252	Human		name
597639768	CV3557805	single nucleotide variant	NM_002458.3(MUC5B):c.1898C>T (p.Ser633Leu)	not specified [RCV004825204]	uncertain significance	11	1232504	1232504	Human		name
597639779	CV3557813	single nucleotide variant	NM_002458.3(MUC5B):c.2273G>T (p.Gly758Val)	not specified [RCV004825206]	uncertain significance	11	1233220	1233220	Human		name
597644068	CV3557815	single nucleotide variant	NM_002458.3(MUC5B):c.1660C>T (p.His554Tyr)	not specified [RCV004825907]	likely benign	11	1231542	1231542	Human		name
597644074	CV3557816	single nucleotide variant	NM_002458.3(MUC5B):c.16767C>T (p.Thr5589=)	not specified [RCV004825908]	likely benign	11	1259809	1259809	Human		name
597644085	CV3557819	single nucleotide variant	NM_002458.3(MUC5B):c.2488C>T (p.His830Tyr)	not specified [RCV004825910]	uncertain significance	11	1234538	1234538	Human		name
597644136	CV3557828	single nucleotide variant	NM_002458.3(MUC5B):c.1168G>A (p.Gly390Ser)	not specified [RCV004825918]	likely benign	11	1229755	1229755	Human		name
597644158	CV3557832	single nucleotide variant	NM_002458.3(MUC5B):c.1084G>A (p.Gly362Ser)	not specified [RCV004825921]	uncertain significance	11	1229277	1229277	Human		name
597644173	CV3557834	single nucleotide variant	NM_002458.3(MUC5B):c.2554G>A (p.Glu852Lys)	not specified [RCV004825923]	uncertain significance	11	1234604	1234604	Human		name
597643405	CV3561586	single nucleotide variant	NM_002458.3(MUC5B):c.2140G>A (p.Gly714Ser)	not specified [RCV004825821]	likely benign	11	1233087	1233087	Human		name
597639621	CV3561615	single nucleotide variant	NM_002458.3(MUC5B):c.2423C>T (p.Ala808Val)	not specified [RCV004825176]	uncertain significance	11	1234250	1234250	Human		name
598129016	CV3886819	single nucleotide variant	NM_002458.3(MUC5B):c.13137G>A (p.Thr4379=)	not provided [RCV005244479]	likely benign	11	1250017	1250017	Human		name
598129550	CV3886966	single nucleotide variant	NM_002458.3(MUC5B):c.11175G>A (p.Pro3725=)	not provided [RCV005245026]	likely benign	11	1248055	1248055	Human		name
598128308	CV3887509	single nucleotide variant	NM_002458.3(MUC5B):c.11910A>T (p.Thr3970=)	not provided [RCV005243682]	likely benign	11	1248790	1248790	Human		name
598222289	CV3893861	single nucleotide variant	NM_002458.3(MUC5B):c.1855C>T (p.Arg619Trp)	not provided [RCV005257104]	benign	11	1232461	1232461	Human		name
598224204	CV3894099	single nucleotide variant	NM_002458.3(MUC5B):c.12090G>A (p.Ser4030=)	not provided [RCV005257342]	likely benign	11	1248970	1248970	Human		name
598225167	CV3894212	single nucleotide variant	NM_002458.3(MUC5B):c.14514G>C (p.Leu4838=)	not provided [RCV005257455]	likely benign	11	1251394	1251394	Human		name
12896497	CV389884	single nucleotide variant	NM_002458.3(MUC5B):c.11913T>C (p.Pro3971=)	not provided [RCV004705592]\|not specified [RCV000455426]	likely benign	11	1248793	1248793	Human		name
12895915	CV389951	single nucleotide variant	NM_002458.3(MUC5B):c.11562T>C (p.Ser3854=)	not provided [RCV001692118]\|not specified [RCV000454629]	benign	11	1248442	1248442	Human		name
12896102	CV389972	single nucleotide variant	NM_002458.3(MUC5B):c.14718T>C (p.Pro4906=)	not provided [RCV004707292]\|not specified [RCV000454881]	likely benign	11	1251598	1251598	Human		name
12896569	CV389989	deletion	NM_002458.3(MUC5B):c.7663del (p.Thr2555fs)	not specified [RCV000455530]	uncertain significance	11	1244543	1244543	Human		name
12895818	CV389994	single nucleotide variant	NM_002458.3(MUC5B):c.10527G>T (p.Leu3509=)	not provided [RCV001637025]\|not specified [RCV000454495]	benign	11	1247407	1247407	Human		name
12896279	CV389997	single nucleotide variant	NM_002458.3(MUC5B):c.10572T>C (p.Ser3524=)	not provided [RCV001683497]\|not specified [RCV000455135]	benign	11	1247452	1247452	Human		name
12896780	CV389999	single nucleotide variant	NM_002458.3(MUC5B):c.10821A>C (p.Ala3607=)	not provided [RCV001618697]\|not specified [RCV000455811]	benign	11	1247701	1247701	Human		name
12895943	CV390008	single nucleotide variant	NM_002458.3(MUC5B):c.10845C>T (p.Leu3615=)	not provided [RCV001613278]\|not specified [RCV000454665]	benign	11	1247725	1247725	Human		name
12896741	CV390010	single nucleotide variant	NM_002458.3(MUC5B):c.11517C>T (p.Thr3839=)	not provided [RCV001724009]\|not specified [RCV000455763]	benign	11	1248397	1248397	Human		name
12896647	CV390015	single nucleotide variant	NM_002458.3(MUC5B):c.13398G>A (p.Thr4466=)	not provided [RCV001618698]\|not specified [RCV000455635]	benign	11	1250278	1250278	Human		name
12895998	CV390025	single nucleotide variant	NM_002458.3(MUC5B):c.13674T>C (p.Thr4558=)	not provided [RCV004705594]\|not specified [RCV000454738]	likely benign	11	1250554	1250554	Human		name
12896922	CV390033	single nucleotide variant	NM_002458.3(MUC5B):c.14484A>G (p.Thr4828=)	not provided [RCV003424006]\|not specified [RCV000455997]	likely benign	11	1251364	1251364	Human		name
12895799	CV390035	single nucleotide variant	NM_002458.3(MUC5B):c.14748C>T (p.Phe4916=)	not provided [RCV001683499]\|not specified [RCV000454466]	benign	11	1251628	1251628	Human		name
12896885	CV390046	single nucleotide variant	NM_002458.3(MUC5B):c.14586T>C (p.Gly4862=)	not provided [RCV003884542]\|not specified [RCV000455951]	likely benign	11	1251466	1251466	Human		name
598228635	CV3986697	single nucleotide variant	NM_002458.3(MUC5B):c.1546A>T (p.Ile516Phe)	not specified [RCV005380906]	uncertain significance	11	1231428	1231428	Human		name
598228721	CV3986711	single nucleotide variant	NM_002458.3(MUC5B):c.2875G>T (p.Val959Leu)	not specified [RCV005380916]	likely benign	11	1235408	1235408	Human		name
598228729	CV3986713	single nucleotide variant	NM_002458.3(MUC5B):c.2728C>T (p.Arg910Cys)	not specified [RCV005380917]	uncertain significance	11	1235182	1235182	Human		name
598228801	CV3986727	single nucleotide variant	NM_002458.3(MUC5B):c.2450G>A (p.Arg817Gln)	not specified [RCV005380926]	uncertain significance	11	1234277	1234277	Human		name
598228907	CV3986745	single nucleotide variant	NM_002458.3(MUC5B):c.2960G>A (p.Arg987His)	not specified [RCV005380939]	uncertain significance	11	1236465	1236465	Human		name
598263751	CV3986759	single nucleotide variant	NM_002458.3(MUC5B):c.1255C>G (p.Leu419Val)	not specified [RCV005387554]	uncertain significance	11	1230039	1230039	Human		name
598263772	CV3986780	single nucleotide variant	NM_002458.3(MUC5B):c.1423G>A (p.Glu475Lys)	not specified [RCV005387561]	uncertain significance	11	1230553	1230553	Human		name
598229120	CV3986785	single nucleotide variant	NM_002458.3(MUC5B):c.17022C>T (p.Thr5674=)	not specified [RCV005380969]	likely benign	11	1260681	1260681	Human		name
617152673	CV4020904	single nucleotide variant	NM_002458.3(MUC5B):c.17151G>A (p.Leu5717=)	not provided [RCV005428657]	likely benign	11	1261470	1261470	Human		name
15104546	CV701636	single nucleotide variant	NM_002458.3(MUC5B):c.2230G>A (p.Gly744Ser)	not provided [RCV000959708]	likely benign	11	1233177	1233177	Human		name
15101796	CV701647	single nucleotide variant	NM_002458.3(MUC5B):c.15789G>A (p.Pro5263=)	not provided [RCV000959162]	benign	11	1255165	1255165	Human		name
15110284	CV724276	single nucleotide variant	NM_002458.3(MUC5B):c.2786A>C (p.Asn929Thr)	not provided [RCV000894031]	benign	11	1235319	1235319	Human		name
15110292	CV724290	single nucleotide variant	NM_002458.3(MUC5B):c.16806T>C (p.Asn5602=)	not provided [RCV000894032]	benign	11	1259968	1259968	Human		name
15136516	CV737837	single nucleotide variant	NM_002458.3(MUC5B):c.15939C>T (p.Asn5313=)	MUC5B-related disorder [RCV004758750]\|not provided [RCV000898641]	benign\|likely benign	11	1255431	1255431	Human	1	name , alternate_id
15114896	CV737840	single nucleotide variant	NM_002458.3(MUC5B):c.16272C>T (p.Pro5424=)	not provided [RCV000894933]	benign	11	1257532	1257532	Human		name
15120049	CV783897	single nucleotide variant	NM_002458.3(MUC5B):c.1887C>A (p.Asn629Lys)	not provided [RCV000979222]	likely benign	11	1232493	1232493	Human		name
126726719	CV1017398	single nucleotide variant	NM_002458.3(MUC5B):c.9385C>T (p.Pro3129Ser)	Interstitial lung disease 2 [RCV001332135]	uncertain significance	11	1246265	1246265	Human	1	name
126742312	CV1020823	single nucleotide variant	NM_002458.3(MUC5B):c.9005C>A (p.Thr3002Lys)	Interstitial lung disease 2 [RCV001336470]\|not provided [RCV004692572]	conflicting interpretations of pathogenicity\|uncertain significance	11	1245885	1245885	Human	1	name
126742316	CV1020824	single nucleotide variant	NM_002458.3(MUC5B):c.9355A>G (p.Thr3119Ala)	Interstitial lung disease 2 [RCV001336471]	uncertain significance	11	1246235	1246235	Human	1	name
126914746	CV1038036	single nucleotide variant	NM_002458.3(MUC5B):c.4427C>T (p.Ser1476Leu)	not provided [RCV001358526]\|not specified [RCV004034504]	uncertain significance	11	1241307	1241307	Human		name
150501518	CV1224205	single nucleotide variant	NM_002458.3(MUC5B):c.4415C>T (p.Pro1472Leu)	MUC5B-related disorder [RCV004758819]\|not provided [RCV001620846]	benign	11	1241295	1241295	Human	1	name , alternate_id
150511545	CV1229489	single nucleotide variant	NM_002458.3(MUC5B):c.8668C>T (p.Pro2890Ser)	not provided [RCV001637418]	benign	11	1245548	1245548	Human		name
150434411	CV1230781	single nucleotide variant	NM_002458.3(MUC5B):c.6698T>G (p.Val2233Gly)	not provided [RCV001643728]	benign	11	1243578	1243578	Human		name
150486663	CV1234631	single nucleotide variant	NM_002458.3(MUC5B):c.9392C>T (p.Thr3131Met)	not provided [RCV001654054]	benign	11	1246272	1246272	Human		name
150501173	CV1238331	single nucleotide variant	NM_002458.3(MUC5B):c.7312G>A (p.Glu2438Lys)	not provided [RCV001656761]	benign	11	1244192	1244192	Human		name
150501791	CV1241034	single nucleotide variant	NM_002458.3(MUC5B):c.5413G>A (p.Gly1805Ser)	not provided [RCV001656930]	benign	11	1242293	1242293	Human		name
150511977	CV1242847	single nucleotide variant	NM_002458.3(MUC5B):c.9365T>C (p.Met3122Thr)	not provided [RCV001661201]	benign	11	1246245	1246245	Human		name
150487946	CV1251598	single nucleotide variant	NM_002458.3(MUC5B):c.6997C>T (p.Pro2333Ser)	not provided [RCV001674269]	benign	11	1243877	1243877	Human		name
150437696	CV1286586	single nucleotide variant	NM_002458.3(MUC5B):c.4202G>A (p.Arg1401His)	not provided [RCV001724665]	benign	11	1241082	1241082	Human		name
152033614	CV1669012	single nucleotide variant	NM_002458.3(MUC5B):c.5620G>C (p.Val1874Leu)	not provided [RCV002223355]	uncertain significance	11	1242500	1242500	Human		name
9687875	CV175802	single nucleotide variant	NM_002458.3(MUC5B):c.3928C>T (p.Pro1310Ser)	not provided [RCV004718049]\|not specified [RCV000151042]	benign	11	1240333	1240333	Human		name
156398587	CV2194662	single nucleotide variant	NM_002458.3(MUC5B):c.8540A>C (p.Lys2847Thr)	not specified [RCV004082063]	uncertain significance	11	1245420	1245420	Human		name
156398742	CV2194763	single nucleotide variant	NM_002458.3(MUC5B):c.6236C>A (p.Thr2079Lys)	not provided [RCV004809912]\|not specified [RCV004075311]	likely benign\|uncertain significance	11	1243116	1243116	Human		name
156398951	CV2194891	single nucleotide variant	NM_002458.3(MUC5B):c.8252C>G (p.Thr2751Arg)	not specified [RCV004075422]	uncertain significance	11	1245132	1245132	Human		name
156132421	CV2195879	single nucleotide variant	NM_002458.3(MUC5B):c.6808A>T (p.Thr2270Ser)	not specified [RCV004072143]	uncertain significance	11	1243688	1243688	Human		name
156076536	CV2198172	single nucleotide variant	NM_002458.3(MUC5B):c.9164C>T (p.Thr3055Ile)	not specified [RCV004079760]	uncertain significance	11	1246044	1246044	Human		name
156077609	CV2198244	single nucleotide variant	NM_002458.3(MUC5B):c.3514G>A (p.Gly1172Arg)	not specified [RCV004079822]	uncertain significance	11	1239497	1239497	Human		name
156183311	CV2198503	single nucleotide variant	NM_002458.3(MUC5B):c.9386C>T (p.Pro3129Leu)	not specified [RCV004075535]	uncertain significance	11	1246266	1246266	Human		name
156265791	CV2198691	single nucleotide variant	NM_002458.3(MUC5B):c.7798C>A (p.Pro2600Thr)	not specified [RCV004075701]	uncertain significance	11	1244678	1244678	Human		name
156026745	CV2199173	single nucleotide variant	NM_002458.3(MUC5B):c.7381A>G (p.Thr2461Ala)	not specified [RCV004080562]	uncertain significance	11	1244261	1244261	Human		name
156400627	CV2199310	single nucleotide variant	NM_002458.3(MUC5B):c.6665T>C (p.Leu2222Ser)	not specified [RCV004082658]	likely benign	11	1243545	1243545	Human		name
156371543	CV2200799	single nucleotide variant	NM_002458.3(MUC5B):c.6790T>C (p.Ser2264Pro)	not specified [RCV004081435]	uncertain significance	11	1243670	1243670	Human		name
156178226	CV2201577	single nucleotide variant	NM_002458.3(MUC5B):c.9383C>A (p.Thr3128Asn)	not specified [RCV004080066]	uncertain significance	11	1246263	1246263	Human		name
156181112	CV2201790	single nucleotide variant	NM_002458.3(MUC5B):c.8246A>C (p.Asn2749Thr)	not specified [RCV004082228]	uncertain significance	11	1245126	1245126	Human		name
156030317	CV2202388	single nucleotide variant	NM_002458.3(MUC5B):c.5386G>A (p.Val1796Met)	not specified [RCV004080703]	uncertain significance	11	1242266	1242266	Human		name
156399169	CV2204956	single nucleotide variant	NM_002458.3(MUC5B):c.6407C>T (p.Thr2136Met)	not specified [RCV004077579]	uncertain significance	11	1243287	1243287	Human		name
156399346	CV2205065	single nucleotide variant	NM_002458.3(MUC5B):c.7403C>T (p.Pro2468Leu)	not specified [RCV004077673]	uncertain significance	11	1244283	1244283	Human		name
156082622	CV2205456	single nucleotide variant	NM_002458.3(MUC5B):c.7178T>C (p.Val2393Ala)	not specified [RCV004082399]	uncertain significance	11	1244058	1244058	Human		name
156082837	CV2205474	single nucleotide variant	NM_002458.3(MUC5B):c.8087C>T (p.Thr2696Met)	not specified [RCV004082415]	uncertain significance	11	1244967	1244967	Human		name
156376905	CV2206890	single nucleotide variant	NM_002458.3(MUC5B):c.8722G>A (p.Val2908Ile)	not specified [RCV004083558]	uncertain significance	11	1245602	1245602	Human		name
156098221	CV2207026	single nucleotide variant	NM_002458.3(MUC5B):c.9786G>A (p.Met3262Ile)	not specified [RCV004085640]	uncertain significance	11	1246666	1246666	Human		name
156244817	CV2207355	single nucleotide variant	NM_002458.3(MUC5B):c.4559C>T (p.Ser1520Phe)	not specified [RCV004088062]	uncertain significance	11	1241439	1241439	Human		name
155922450	CV2207498	single nucleotide variant	NM_002458.3(MUC5B):c.4675C>A (p.Leu1559Met)	not specified [RCV004089971]	uncertain significance	11	1241555	1241555	Human		name
156111231	CV2207882	single nucleotide variant	NM_002458.3(MUC5B):c.6830C>G (p.Thr2277Arg)	not specified [RCV004084310]	uncertain significance	11	1243710	1243710	Human		name
156379099	CV2207883	single nucleotide variant	NM_002458.3(MUC5B):c.6833C>G (p.Ala2278Gly)	not specified [RCV004084311]	uncertain significance	11	1243713	1243713	Human		name
155926337	CV2208180	single nucleotide variant	NM_002458.3(MUC5B):c.4931C>T (p.Pro1644Leu)	not specified [RCV004088646]	uncertain significance	11	1241811	1241811	Human		name
156141953	CV2208474	single nucleotide variant	NM_002458.3(MUC5B):c.7865C>T (p.Ser2622Phe)	not specified [RCV004091011]	uncertain significance	11	1244745	1244745	Human		name
156380456	CV2208828	single nucleotide variant	NM_002458.3(MUC5B):c.9983T>G (p.Leu3328Arg)	not specified [RCV004084996]	likely benign	11	1246863	1246863	Human		name
156330764	CV2210697	single nucleotide variant	NM_002458.3(MUC5B):c.5147C>T (p.Thr1716Met)	not specified [RCV004083838]	likely benign	11	1242027	1242027	Human		name
156033686	CV2211588	single nucleotide variant	NM_002458.3(MUC5B):c.8458G>A (p.Glu2820Lys)	not specified [RCV004084486]	uncertain significance	11	1245338	1245338	Human		name
156381903	CV2212459	single nucleotide variant	NM_002458.3(MUC5B):c.7496C>T (p.Thr2499Met)	not specified [RCV004091357]	likely benign	11	1244376	1244376	Human		name
155971725	CV2214171	single nucleotide variant	NM_002458.3(MUC5B):c.9013A>T (p.Thr3005Ser)	not specified [RCV004086169]	uncertain significance	11	1245893	1245893	Human		name
156107802	CV2214271	single nucleotide variant	NM_002458.3(MUC5B):c.5660G>C (p.Ser1887Thr)	not specified [RCV004086263]	uncertain significance	11	1242540	1242540	Human		name
156334329	CV2214750	single nucleotide variant	NM_002458.3(MUC5B):c.5264C>A (p.Thr1755Asn)	not specified [RCV004090559]	uncertain significance	11	1242144	1242144	Human		name
156038686	CV2215011	single nucleotide variant	NM_002458.3(MUC5B):c.7268C>T (p.Thr2423Met)	not specified [RCV004084786]	uncertain significance	11	1244148	1244148	Human		name
156381542	CV2215611	single nucleotide variant	NM_002458.3(MUC5B):c.8545C>T (p.Arg2849Cys)	not specified [RCV004089368]	uncertain significance	11	1245425	1245425	Human		name
156106178	CV2217793	single nucleotide variant	NM_002458.3(MUC5B):c.4351G>C (p.Glu1451Gln)	not specified [RCV004083969]	uncertain significance	11	1241231	1241231	Human		name
156106250	CV2217801	single nucleotide variant	NM_002458.3(MUC5B):c.8801T>A (p.Val2934Glu)	not specified [RCV004083976]	uncertain significance	11	1245681	1245681	Human		name
156106593	CV2217883	single nucleotide variant	NM_002458.3(MUC5B):c.5768C>T (p.Thr1923Met)	not specified [RCV004084052]	uncertain significance	11	1242648	1242648	Human		name
156112333	CV2218044	single nucleotide variant	NM_002458.3(MUC5B):c.9772C>T (p.Pro3258Ser)	not specified [RCV004086484]	uncertain significance	11	1246652	1246652	Human		name
156380581	CV2218826	single nucleotide variant	NM_002458.3(MUC5B):c.8663C>T (p.Pro2888Leu)	not specified [RCV004085069]	uncertain significance	11	1245543	1245543	Human		name
156245180	CV2218952	single nucleotide variant	NM_002458.3(MUC5B):c.3983C>T (p.Pro1328Leu)	not specified [RCV004087135]	uncertain significance	11	1240863	1240863	Human		name
156246970	CV2219162	single nucleotide variant	NM_002458.3(MUC5B):c.6343G>A (p.Gly2115Ser)	not specified [RCV004087317]	uncertain significance	11	1243223	1243223	Human		name
156225179	CV2219541	single nucleotide variant	NM_002458.3(MUC5B):c.5204C>A (p.Thr1735Asn)	not specified [RCV004095279]	uncertain significance	11	1242084	1242084	Human		name
156116684	CV2221759	single nucleotide variant	NM_002458.3(MUC5B):c.9848C>A (p.Thr3283Lys)	not specified [RCV004098516]	uncertain significance	11	1246728	1246728	Human		name
156068431	CV2222050	single nucleotide variant	NM_002458.3(MUC5B):c.8448C>G (p.Ser2816Arg)	not specified [RCV004103032]	uncertain significance	11	1245328	1245328	Human		name
156023257	CV2223444	single nucleotide variant	NM_002458.3(MUC5B):c.9971C>T (p.Pro3324Leu)	not specified [RCV004106021]	uncertain significance	11	1246851	1246851	Human		name
156280178	CV2224097	single nucleotide variant	NM_002458.3(MUC5B):c.5813T>A (p.Val1938Glu)	not specified [RCV004095961]	uncertain significance	11	1242693	1242693	Human		name
155972880	CV2224463	single nucleotide variant	NM_002458.3(MUC5B):c.6874C>G (p.Arg2292Gly)	not specified [RCV004098060]	uncertain significance	11	1243754	1243754	Human		name
155929342	CV2224532	single nucleotide variant	NM_002458.3(MUC5B):c.6874C>T (p.Arg2292Cys)	Interstitial lung disease 2 [RCV004771536]\|not specified [RCV004098114]	uncertain significance	11	1243754	1243754	Human	1	name
156065818	CV2225422	single nucleotide variant	NM_002458.3(MUC5B):c.9397T>C (p.Trp3133Arg)	not specified [RCV004100824]	uncertain significance	11	1246277	1246277	Human		name
156291471	CV2226326	single nucleotide variant	NM_002458.3(MUC5B):c.5530G>C (p.Gly1844Arg)	not specified [RCV004099564]	uncertain significance	11	1242410	1242410	Human		name
156020991	CV2226616	single nucleotide variant	NM_002458.3(MUC5B):c.6266C>T (p.Thr2089Met)	not specified [RCV004101865]	likely benign	11	1243146	1243146	Human		name
156123354	CV2227228	single nucleotide variant	NM_002458.3(MUC5B):c.3955C>A (p.Pro1319Thr)	not specified [RCV004091822]	uncertain significance	11	1240360	1240360	Human		name
156278976	CV2227709	single nucleotide variant	NM_002458.3(MUC5B):c.6838T>A (p.Ser2280Thr)	not specified [RCV004094097]	uncertain significance	11	1243718	1243718	Human		name
156388837	CV2229685	single nucleotide variant	NM_002458.3(MUC5B):c.6177C>A (p.Phe2059Leu)	not specified [RCV004103492]	uncertain significance	11	1243057	1243057	Human		name
156287881	CV2229686	single nucleotide variant	NM_002458.3(MUC5B):c.9948C>A (p.Phe3316Leu)	not specified [RCV004103493]	uncertain significance	11	1246828	1246828	Human		name
156385034	CV2231259	single nucleotide variant	NM_002458.3(MUC5B):c.4015C>T (p.Arg1339Cys)	not specified [RCV004094454]	uncertain significance	11	1240895	1240895	Human		name
155976152	CV2231600	single nucleotide variant	NM_002458.3(MUC5B):c.9496G>A (p.Glu3166Lys)	not specified [RCV004096644]	uncertain significance	11	1246376	1246376	Human		name
155981863	CV2233125	single nucleotide variant	NM_002458.3(MUC5B):c.8924C>T (p.Pro2975Leu)	not specified [RCV004103741]	uncertain significance	11	1245804	1245804	Human		name
155982369	CV2233182	single nucleotide variant	NM_002458.3(MUC5B):c.7517C>T (p.Thr2506Ile)	not specified [RCV004103793]	uncertain significance	11	1244397	1244397	Human		name
156046267	CV2234624	single nucleotide variant	NM_002458.3(MUC5B):c.4901C>T (p.Thr1634Met)	not specified [RCV004102588]	uncertain significance	11	1241781	1241781	Human		name
156204528	CV2234730	single nucleotide variant	NM_002458.3(MUC5B):c.6272C>T (p.Thr2091Ile)	not specified [RCV004102671]	uncertain significance	11	1243152	1243152	Human		name
156230241	CV2235036	single nucleotide variant	NM_002458.3(MUC5B):c.3229C>T (p.Arg1077Cys)	not specified [RCV004113220]	uncertain significance	11	1237096	1237096	Human		name
156157497	CV2235297	single nucleotide variant	NM_002458.3(MUC5B):c.4468C>T (p.Pro1490Ser)	not specified [RCV004107334]	uncertain significance	11	1241348	1241348	Human		name
156033685	CV2236313	single nucleotide variant	NM_002458.3(MUC5B):c.9473C>A (p.Pro3158Gln)	not specified [RCV004108007]	uncertain significance	11	1246353	1246353	Human		name
156200301	CV2237683	single nucleotide variant	NM_002458.3(MUC5B):c.8525C>T (p.Thr2842Met)	not provided [RCV003427604]\|not specified [RCV004106608]	likely benign\|uncertain significance	11	1245405	1245405	Human		name
156060210	CV2239419	single nucleotide variant	NM_002458.3(MUC5B):c.8962G>T (p.Gly2988Trp)	not specified [RCV004114145]	uncertain significance	11	1245842	1245842	Human		name
156089534	CV2241477	single nucleotide variant	NM_002458.3(MUC5B):c.8659A>G (p.Met2887Val)	not specified [RCV004104385]	uncertain significance	11	1245539	1245539	Human		name
155913888	CV2242534	single nucleotide variant	NM_002458.3(MUC5B):c.9679A>G (p.Ser3227Gly)	not specified [RCV004113604]	uncertain significance	11	1246559	1246559	Human		name
156084836	CV2244573	single nucleotide variant	NM_002458.3(MUC5B):c.8078C>T (p.Thr2693Met)	not specified [RCV004102302]	uncertain significance	11	1244958	1244958	Human		name
156266202	CV2247135	single nucleotide variant	NM_002458.3(MUC5B):c.9785T>A (p.Met3262Lys)	not specified [RCV004114665]	uncertain significance	11	1246665	1246665	Human		name
156194838	CV2251781	single nucleotide variant	NM_002458.3(MUC5B):c.7006G>A (p.Gly2336Arg)	not specified [RCV004119773]	uncertain significance	11	1243886	1243886	Human		name
156298469	CV2251954	single nucleotide variant	NM_002458.3(MUC5B):c.8246A>G (p.Asn2749Ser)	not specified [RCV004119919]	likely benign	11	1245126	1245126	Human		name
156310218	CV2260012	single nucleotide variant	NM_002458.3(MUC5B):c.6152T>G (p.Val2051Gly)	not specified [RCV004119026]	uncertain significance	11	1243032	1243032	Human		name
156102648	CV2260440	single nucleotide variant	NM_002458.3(MUC5B):c.7709C>T (p.Thr2570Ile)	not specified [RCV004123236]	uncertain significance	11	1244589	1244589	Human		name
156319758	CV2260886	single nucleotide variant	NM_002458.3(MUC5B):c.6029C>T (p.Pro2010Leu)	not specified [RCV004125780]	uncertain significance	11	1242909	1242909	Human		name
155999293	CV2261074	single nucleotide variant	NM_002458.3(MUC5B):c.3883A>G (p.Ile1295Val)	not specified [RCV004127722]	uncertain significance	11	1240288	1240288	Human		name
155947619	CV2262733	single nucleotide variant	NM_002458.3(MUC5B):c.7652G>A (p.Arg2551His)	not specified [RCV004130918]	uncertain significance	11	1244532	1244532	Human		name
156370335	CV2263520	single nucleotide variant	NM_002458.3(MUC5B):c.5765C>T (p.Ser1922Phe)	not specified [RCV004133751]	uncertain significance	11	1242645	1242645	Human		name
156056644	CV2265852	single nucleotide variant	NM_002458.3(MUC5B):c.9776C>T (p.Thr3259Met)	not specified [RCV004126718]	uncertain significance	11	1246656	1246656	Human		name
156153476	CV2265999	single nucleotide variant	NM_002458.3(MUC5B):c.8099C>T (p.Thr2700Ile)	not specified [RCV004126828]	uncertain significance	11	1244979	1244979	Human		name
156245424	CV2267488	single nucleotide variant	NM_002458.3(MUC5B):c.8261C>T (p.Thr2754Ile)	not specified [RCV004135912]	uncertain significance	11	1245141	1245141	Human		name
155944081	CV2271542	single nucleotide variant	NM_002458.3(MUC5B):c.6455C>T (p.Thr2152Ile)	not specified [RCV004128631]	uncertain significance	11	1243335	1243335	Human		name
156336078	CV2273144	single nucleotide variant	NM_002458.3(MUC5B):c.4340G>C (p.Ser1447Thr)	not specified [RCV004137780]	uncertain significance	11	1241220	1241220	Human		name
155901904	CV2274595	single nucleotide variant	NM_002458.3(MUC5B):c.6743C>T (p.Ser2248Leu)	not specified [RCV004138989]	uncertain significance	11	1243623	1243623	Human		name
156132074	CV2280020	single nucleotide variant	NM_002458.3(MUC5B):c.4853C>T (p.Thr1618Met)	not specified [RCV004146383]	uncertain significance	11	1241733	1241733	Human		name
156060129	CV2280107	single nucleotide variant	NM_002458.3(MUC5B):c.6884C>A (p.Thr2295Asn)	not specified [RCV004146761]	uncertain significance	11	1243764	1243764	Human		name
155992440	CV2281208	single nucleotide variant	NM_002458.3(MUC5B):c.8405C>G (p.Thr2802Ser)	not specified [RCV004147458]	uncertain significance	11	1245285	1245285	Human		name
156005113	CV2281450	single nucleotide variant	NM_002458.3(MUC5B):c.4708G>A (p.Val1570Ile)	not specified [RCV004153778]	uncertain significance	11	1241588	1241588	Human		name
156126792	CV2283740	single nucleotide variant	NM_002458.3(MUC5B):c.9368C>T (p.Ser3123Phe)	not specified [RCV004142261]	uncertain significance	11	1246248	1246248	Human		name
156134014	CV2284627	single nucleotide variant	NM_002458.3(MUC5B):c.7214G>A (p.Arg2405His)	not specified [RCV004140790]	uncertain significance	11	1244094	1244094	Human		name
155962335	CV2285640	single nucleotide variant	NM_002458.3(MUC5B):c.3427G>A (p.Val1143Met)	not specified [RCV004141502]	uncertain significance	11	1239000	1239000	Human		name
156277673	CV2286605	single nucleotide variant	NM_002458.3(MUC5B):c.7772G>A (p.Gly2591Asp)	not specified [RCV004142456]	uncertain significance	11	1244652	1244652	Human		name
156065567	CV2287383	single nucleotide variant	NM_002458.3(MUC5B):c.9605C>T (p.Thr3202Ile)	not specified [RCV004146993]	uncertain significance	11	1246485	1246485	Human		name
156006975	CV2288988	single nucleotide variant	NM_002458.3(MUC5B):c.9332C>T (p.Thr3111Met)	not specified [RCV004149944]	uncertain significance	11	1246212	1246212	Human		name
156007155	CV2289043	single nucleotide variant	NM_002458.3(MUC5B):c.9896C>T (p.Thr3299Ile)	not provided [RCV003427617]\|not specified [RCV004149989]	likely benign\|uncertain significance	11	1246776	1246776	Human		name
156293960	CV2293134	single nucleotide variant	NM_002458.3(MUC5B):c.7889T>C (p.Leu2630Pro)	not specified [RCV004150656]	uncertain significance	11	1244769	1244769	Human		name
155940312	CV2294059	single nucleotide variant	NM_002458.3(MUC5B):c.7442C>T (p.Thr2481Met)	not specified [RCV004149442]	likely benign	11	1244322	1244322	Human		name
156086533	CV2295341	single nucleotide variant	NM_002458.3(MUC5B):c.5249C>A (p.Thr1750Lys)	not specified [RCV004158700]	uncertain significance	11	1242129	1242129	Human		name
156001871	CV2296456	single nucleotide variant	NM_002458.3(MUC5B):c.9782C>T (p.Thr3261Ile)	not specified [RCV004148197]	uncertain significance	11	1246662	1246662	Human		name
156170785	CV2296870	single nucleotide variant	NM_002458.3(MUC5B):c.8053G>C (p.Gly2685Arg)	not specified [RCV004148748]	uncertain significance	11	1244933	1244933	Human		name
156208877	CV2304379	single nucleotide variant	NM_002458.3(MUC5B):c.7168C>T (p.Arg2390Cys)	not specified [RCV004164486]	uncertain significance	11	1244048	1244048	Human		name
156048593	CV2304439	single nucleotide variant	NM_002458.3(MUC5B):c.8270G>T (p.Arg2757Leu)	not specified [RCV004164536]	uncertain significance	11	1245150	1245150	Human		name
156290862	CV2306000	single nucleotide variant	NM_002458.3(MUC5B):c.4282G>A (p.Glu1428Lys)	not specified [RCV004160989]	uncertain significance	11	1241162	1241162	Human		name
155908719	CV2307132	single nucleotide variant	NM_002458.3(MUC5B):c.5135C>T (p.Ser1712Leu)	not specified [RCV004159612]	uncertain significance	11	1242015	1242015	Human		name
156151866	CV2307589	single nucleotide variant	NM_002458.3(MUC5B):c.5779A>G (p.Thr1927Ala)	not specified [RCV004168015]	uncertain significance	11	1242659	1242659	Human		name
155972567	CV2309422	single nucleotide variant	NM_002458.3(MUC5B):c.3688G>A (p.Val1230Ile)	not specified [RCV004165564]	uncertain significance	11	1239903	1239903	Human		name
156241641	CV2310242	single nucleotide variant	NM_002458.3(MUC5B):c.3059G>A (p.Gly1020Asp)	not specified [RCV004163340]	uncertain significance	11	1236926	1236926	Human		name
156249050	CV2314119	single nucleotide variant	NM_002458.3(MUC5B):c.6851C>T (p.Ala2284Val)	not specified [RCV004166209]	uncertain significance	11	1243731	1243731	Human		name
156272333	CV2315924	single nucleotide variant	NM_002458.3(MUC5B):c.5650C>T (p.His1884Tyr)	not specified [RCV004171689]	uncertain significance	11	1242530	1242530	Human		name
156049166	CV2319289	single nucleotide variant	NM_002458.3(MUC5B):c.7741A>G (p.Thr2581Ala)	not specified [RCV004180115]	uncertain significance	11	1244621	1244621	Human		name
156166377	CV2319933	single nucleotide variant	NM_002458.3(MUC5B):c.5246T>A (p.Leu1749His)	not specified [RCV004167811]	uncertain significance	11	1242126	1242126	Human		name
156068377	CV2320414	single nucleotide variant	NM_002458.3(MUC5B):c.9082A>C (p.Thr3028Pro)	not specified [RCV004178566]	uncertain significance	11	1245962	1245962	Human		name
156256143	CV2325839	single nucleotide variant	NM_002458.3(MUC5B):c.3238T>C (p.Trp1080Arg)	not specified [RCV004173716]	uncertain significance	11	1237105	1237105	Human		name
156396384	CV2326249	single nucleotide variant	NM_002458.3(MUC5B):c.9989C>T (p.Pro3330Leu)	not specified [RCV004180505]	likely benign	11	1246869	1246869	Human		name
156363062	CV2330512	single nucleotide variant	NM_002458.3(MUC5B):c.7011C>G (p.Asp2337Glu)	not provided [RCV004585010]\|not specified [RCV004181076]	likely benign\|uncertain significance	11	1243891	1243891	Human		name
156171967	CV2337561	single nucleotide variant	NM_002458.3(MUC5B):c.7393C>T (p.Leu2465Phe)	not specified [RCV004187985]	uncertain significance	11	1244273	1244273	Human		name
156173002	CV2337640	single nucleotide variant	NM_002458.3(MUC5B):c.6100G>A (p.Gly2034Ser)	not specified [RCV004181201]	uncertain significance	11	1242980	1242980	Human		name
156056958	CV2343513	single nucleotide variant	NM_002458.3(MUC5B):c.9547G>A (p.Ala3183Thr)	not specified [RCV004190553]	uncertain significance	11	1246427	1246427	Human		name
156384666	CV2371546	single nucleotide variant	NM_002458.3(MUC5B):c.7433C>T (p.Thr2478Ile)	not specified [RCV004216796]	uncertain significance	11	1244313	1244313	Human		name
156041377	CV2387719	single nucleotide variant	NM_002458.3(MUC5B):c.3571C>T (p.Pro1191Ser)	not specified [RCV004234255]	uncertain significance	11	1239554	1239554	Human		name
156108486	CV2390239	single nucleotide variant	NM_002458.3(MUC5B):c.8546G>A (p.Arg2849His)	not provided [RCV004809965]\|not specified [RCV004240615]	likely benign\|uncertain significance	11	1245426	1245426	Human		name
156005144	CV2393959	single nucleotide variant	NM_002458.3(MUC5B):c.8966C>T (p.Thr2989Met)	not specified [RCV004236188]	uncertain significance	11	1245846	1245846	Human		name
156005395	CV2393987	single nucleotide variant	NM_002458.3(MUC5B):c.7883G>T (p.Arg2628Leu)	not specified [RCV004236210]	uncertain significance	11	1244763	1244763	Human		name
156248606	CV2393988	single nucleotide variant	NM_002458.3(MUC5B):c.9997T>C (p.Trp3333Arg)	not specified [RCV004236211]	likely benign	11	1246877	1246877	Human		name
329400662	CV2438628	single nucleotide variant	NM_002458.3(MUC5B):c.6727G>A (p.Gly2243Ser)	not specified [RCV004261798]	uncertain significance	11	1243607	1243607	Human		name
329366624	CV2441760	single nucleotide variant	NM_002458.3(MUC5B):c.6572C>T (p.Pro2191Leu)	not specified [RCV004261973]	likely benign	11	1243452	1243452	Human		name
329389112	CV2448728	single nucleotide variant	NM_002458.3(MUC5B):c.5075C>G (p.Thr1692Ser)	not specified [RCV004259383]	likely benign	11	1241955	1241955	Human		name
329389261	CV2448841	single nucleotide variant	NM_002458.3(MUC5B):c.9742G>C (p.Ala3248Pro)	not specified [RCV004261526]	uncertain significance	11	1246622	1246622	Human		name
329354778	CV2449016	single nucleotide variant	NM_002458.3(MUC5B):c.5830A>G (p.Thr1944Ala)	not specified [RCV004264093]	uncertain significance	11	1242710	1242710	Human		name
329355026	CV2449222	single nucleotide variant	NM_002458.3(MUC5B):c.9353C>A (p.Ala3118Asp)	not specified [RCV004257362]	uncertain significance	11	1246233	1246233	Human		name
329355040	CV2449236	single nucleotide variant	NM_002458.3(MUC5B):c.9581A>G (p.Lys3194Arg)	not specified [RCV004257375]	uncertain significance	11	1246461	1246461	Human		name
329392970	CV2449414	single nucleotide variant	NM_002458.3(MUC5B):c.9044C>T (p.Thr3015Ile)	not specified [RCV004266574]	uncertain significance	11	1245924	1245924	Human		name
329358990	CV2450786	single nucleotide variant	NM_002458.3(MUC5B):c.4222G>A (p.Ala1408Thr)	not specified [RCV004267711]	uncertain significance	11	1241102	1241102	Human		name
329352499	CV2453106	single nucleotide variant	NM_002458.3(MUC5B):c.3275C>A (p.Thr1092Asn)	not specified [RCV004277711]	uncertain significance	11	1237142	1237142	Human		name
329385110	CV2454711	single nucleotide variant	NM_002458.3(MUC5B):c.5195C>G (p.Thr1732Arg)	not specified [RCV004269948]	uncertain significance	11	1242075	1242075	Human		name
329390895	CV2455574	single nucleotide variant	NM_002458.3(MUC5B):c.6176T>A (p.Phe2059Tyr)	not specified [RCV004276825]	uncertain significance	11	1243056	1243056	Human		name
329401845	CV2457935	single nucleotide variant	NM_002458.3(MUC5B):c.6437C>T (p.Thr2146Ile)	not specified [RCV004271519]	uncertain significance	11	1243317	1243317	Human		name
329386124	CV2458853	single nucleotide variant	NM_002458.3(MUC5B):c.8174C>T (p.Thr2725Ile)	not specified [RCV004270270]	uncertain significance	11	1245054	1245054	Human		name
329371549	CV2458896	single nucleotide variant	NM_002458.3(MUC5B):c.9070G>C (p.Val3024Leu)	not specified [RCV004270305]	uncertain significance	11	1245950	1245950	Human		name
329370535	CV2461753	single nucleotide variant	NM_002458.3(MUC5B):c.9032T>A (p.Ile3011Asn)	not specified [RCV004269900]	uncertain significance	11	1245912	1245912	Human		name
329377312	CV2462535	single nucleotide variant	NM_002458.3(MUC5B):c.3125G>A (p.Arg1042Gln)	not specified [RCV004278491]	likely benign	11	1236992	1236992	Human		name
329382853	CV2465439	single nucleotide variant	NM_002458.3(MUC5B):c.6467C>T (p.Thr2156Ile)	not specified [RCV004281209]	uncertain significance	11	1243347	1243347	Human		name
329389406	CV2467324	single nucleotide variant	NM_002458.3(MUC5B):c.5855A>G (p.Lys1952Arg)	not specified [RCV004285121]	uncertain significance	11	1242735	1242735	Human		name
329394488	CV2469898	single nucleotide variant	NM_002458.3(MUC5B):c.3196G>A (p.Ala1066Thr)	not specified [RCV004285367]	uncertain significance	11	1237063	1237063	Human		name
401755926	CV2675598	single nucleotide variant	NM_002458.3(MUC5B):c.9316T>C (p.Ser3106Pro)	not specified [RCV004297258]	uncertain significance	11	1246196	1246196	Human		name
401746323	CV2678815	single nucleotide variant	NM_002458.3(MUC5B):c.4034A>G (p.Asn1345Ser)	not specified [RCV004292797]	uncertain significance	11	1240914	1240914	Human		name
401744813	CV2681130	single nucleotide variant	NM_002458.3(MUC5B):c.5198C>T (p.Ala1733Val)	not specified [RCV004296185]	uncertain significance	11	1242078	1242078	Human		name
401744818	CV2681131	single nucleotide variant	NM_002458.3(MUC5B):c.8919C>G (p.Ser2973Arg)	not specified [RCV004296186]	uncertain significance	11	1245799	1245799	Human		name
401754745	CV2682291	single nucleotide variant	NM_002458.3(MUC5B):c.9448C>T (p.Pro3150Ser)	not specified [RCV004290333]	likely benign	11	1246328	1246328	Human		name
401755405	CV2682474	single nucleotide variant	NM_002458.3(MUC5B):c.7651C>T (p.Arg2551Cys)	not specified [RCV004290498]	uncertain significance	11	1244531	1244531	Human		name
401755454	CV2682490	single nucleotide variant	NM_002458.3(MUC5B):c.5938G>T (p.Val1980Phe)	not specified [RCV004290512]	likely benign	11	1242818	1242818	Human		name
401755641	CV2682539	single nucleotide variant	NM_002458.3(MUC5B):c.5128C>T (p.Arg1710Cys)	MUC5B-related disorder [RCV004758930]\|not specified [RCV004290553]	likely benign\|uncertain significance	11	1242008	1242008	Human	1	name , alternate_id
401733558	CV2682568	single nucleotide variant	NM_002458.3(MUC5B):c.4103G>A (p.Gly1368Glu)	not specified [RCV004290578]	uncertain significance	11	1240983	1240983	Human		name
401730742	CV2686688	single nucleotide variant	NM_002458.3(MUC5B):c.3016C>T (p.Arg1006Trp)	not specified [RCV004300098]	uncertain significance	11	1236521	1236521	Human		name
401782571	CV2686930	single nucleotide variant	NM_002458.3(MUC5B):c.5044G>A (p.Glu1682Lys)	not provided [RCV003427722]\|not specified [RCV004302100]	likely benign\|uncertain significance	11	1241924	1241924	Human		name
401769787	CV2689938	single nucleotide variant	NM_002458.3(MUC5B):c.9709G>A (p.Val3237Ile)	not specified [RCV004297825]	uncertain significance	11	1246589	1246589	Human		name
401734198	CV2690509	single nucleotide variant	NM_002458.3(MUC5B):c.5047C>T (p.Pro1683Ser)	not specified [RCV004304628]	uncertain significance	11	1241927	1241927	Human		name
401775910	CV2692532	single nucleotide variant	NM_002458.3(MUC5B):c.5850C>G (p.Ser1950Arg)	not specified [RCV004312279]	uncertain significance	11	1242730	1242730	Human		name
401769843	CV2693072	single nucleotide variant	NM_002458.3(MUC5B):c.9242C>T (p.Pro3081Leu)	not specified [RCV004308615]	uncertain significance	11	1246122	1246122	Human		name
401731201	CV2693663	single nucleotide variant	NM_002458.3(MUC5B):c.4159G>A (p.Asp1387Asn)	not specified [RCV004297997]	uncertain significance	11	1241039	1241039	Human		name
401761042	CV2695256	single nucleotide variant	NM_002458.3(MUC5B):c.6512C>A (p.Ala2171Asp)	not specified [RCV004303387]	uncertain significance	11	1243392	1243392	Human		name
401761949	CV2699468	single nucleotide variant	NM_002458.3(MUC5B):c.4735T>G (p.Trp1579Gly)	not specified [RCV004299686]	uncertain significance	11	1241615	1241615	Human		name
401737871	CV2700757	single nucleotide variant	NM_002458.3(MUC5B):c.8120C>A (p.Ser2707Tyr)	not specified [RCV004307045]	uncertain significance	11	1245000	1245000	Human		name
401764855	CV2701453	single nucleotide variant	NM_002458.3(MUC5B):c.9820G>C (p.Val3274Leu)	not specified [RCV004312125]	uncertain significance	11	1246700	1246700	Human		name
401763410	CV2703825	single nucleotide variant	NM_002458.3(MUC5B):c.3531A>T (p.Lys1177Asn)	not specified [RCV004306693]	uncertain significance	11	1239514	1239514	Human		name
401718576	CV2704673	single nucleotide variant	NM_002458.3(MUC5B):c.5581G>A (p.Asp1861Asn)	not specified [RCV004307282]	uncertain significance	11	1242461	1242461	Human		name
401763510	CV2714578	single nucleotide variant	NM_002458.3(MUC5B):c.9722C>T (p.Pro3241Leu)	not specified [RCV004318087]	uncertain significance	11	1246602	1246602	Human		name
401770327	CV2715136	single nucleotide variant	NM_002458.3(MUC5B):c.9101C>T (p.Ala3034Val)	not specified [RCV004322707]	uncertain significance	11	1245981	1245981	Human		name
401777898	CV2718379	single nucleotide variant	NM_002458.3(MUC5B):c.5108C>T (p.Thr1703Met)	not specified [RCV004318208]	uncertain significance	11	1241988	1241988	Human		name
401762041	CV2722617	single nucleotide variant	NM_002458.3(MUC5B):c.8996C>T (p.Ala2999Val)	not specified [RCV004325074]	uncertain significance	11	1245876	1245876	Human		name
401783701	CV2723859	single nucleotide variant	NM_002458.3(MUC5B):c.9259C>G (p.Pro3087Ala)	not specified [RCV004325999]	uncertain significance	11	1246139	1246139	Human		name
401729194	CV2735139	single nucleotide variant	NM_002458.3(MUC5B):c.9941C>T (p.Thr3314Met)	not specified [RCV004333836]	uncertain significance	11	1246821	1246821	Human		name
401876476	CV2761071	single nucleotide variant	NM_002458.3(MUC5B):c.6809C>T (p.Thr2270Met)	not specified [RCV004338732]	uncertain significance	11	1243689	1243689	Human		name
401890429	CV2768223	single nucleotide variant	NM_002458.3(MUC5B):c.6854C>T (p.Thr2285Met)	not specified [RCV004350221]	uncertain significance	11	1243734	1243734	Human		name
401887930	CV2768865	single nucleotide variant	NM_002458.3(MUC5B):c.9727T>A (p.Ser3243Thr)	not specified [RCV004346976]	uncertain significance	11	1246607	1246607	Human		name
401880046	CV2769884	single nucleotide variant	NM_002458.3(MUC5B):c.5206G>A (p.Ala1736Thr)	not specified [RCV004353731]	uncertain significance	11	1242086	1242086	Human		name
401864027	CV2770918	single nucleotide variant	NM_002458.3(MUC5B):c.9539C>T (p.Thr3180Met)	not provided [RCV003427747]\|not specified [RCV004343589]	benign\|uncertain significance	11	1246419	1246419	Human		name
401886693	CV2771373	single nucleotide variant	NM_002458.3(MUC5B):c.9344C>T (p.Thr3115Met)	not specified [RCV004348131]	uncertain significance	11	1246224	1246224	Human		name
401886705	CV2771378	single nucleotide variant	NM_002458.3(MUC5B):c.8333C>A (p.Thr2778Asn)	not specified [RCV004348136]	uncertain significance	11	1245213	1245213	Human		name
401895717	CV2771678	single nucleotide variant	NM_002458.3(MUC5B):c.7220T>C (p.Phe2407Ser)	not specified [RCV004350468]	uncertain significance	11	1244100	1244100	Human		name
401858001	CV2774142	single nucleotide variant	NM_002458.3(MUC5B):c.5231G>C (p.Ser1744Thr)	not specified [RCV004345733]	uncertain significance	11	1242111	1242111	Human		name
401885879	CV2774874	single nucleotide variant	NM_002458.3(MUC5B):c.6818C>T (p.Pro2273Leu)	not specified [RCV004343957]	uncertain significance	11	1243698	1243698	Human		name
401887396	CV2775757	single nucleotide variant	NM_002458.3(MUC5B):c.3539G>A (p.Arg1180Gln)	not specified [RCV004350880]	uncertain significance	11	1239522	1239522	Human		name
401891678	CV2779299	single nucleotide variant	NM_002458.3(MUC5B):c.7094A>G (p.Gln2365Arg)	not specified [RCV004350971]	uncertain significance	11	1243974	1243974	Human		name
401891680	CV2779300	single nucleotide variant	NM_002458.3(MUC5B):c.8765A>G (p.Gln2922Arg)	not specified [RCV004350972]	uncertain significance	11	1245645	1245645	Human		name
401864504	CV2781802	single nucleotide variant	NM_002458.3(MUC5B):c.9556A>G (p.Thr3186Ala)	not specified [RCV004356759]	uncertain significance	11	1246436	1246436	Human		name
401885548	CV2783329	single nucleotide variant	NM_002458.3(MUC5B):c.7922C>T (p.Thr2641Ile)	not specified [RCV004363925]	uncertain significance	11	1244802	1244802	Human		name
401885846	CV2783409	single nucleotide variant	NM_002458.3(MUC5B):c.7798C>T (p.Pro2600Ser)	not specified [RCV004365760]	uncertain significance	11	1244678	1244678	Human		name
401899033	CV2785964	single nucleotide variant	NM_002458.3(MUC5B):c.7899G>T (p.Trp2633Cys)	not specified [RCV004359808]	uncertain significance	11	1244779	1244779	Human		name
401865379	CV2791632	single nucleotide variant	NM_002458.3(MUC5B):c.5689C>A (p.Pro1897Thr)	not specified [RCV004358990]	uncertain significance	11	1242569	1242569	Human		name
401909712	CV2806508	single nucleotide variant	NM_002458.3(MUC5B):c.3974C>T (p.Pro1325Leu)	not provided [RCV003424605]	likely benign	11	1240854	1240854	Human		name
401909718	CV2806511	single nucleotide variant	NM_002458.3(MUC5B):c.4174G>A (p.Glu1392Lys)	not provided [RCV003424608]	uncertain significance	11	1241054	1241054	Human		name
401909723	CV2806514	single nucleotide variant	NM_002458.3(MUC5B):c.4430C>T (p.Thr1477Met)	not provided [RCV003424611]	likely benign	11	1241310	1241310	Human		name
401909729	CV2806517	single nucleotide variant	NM_002458.3(MUC5B):c.5487G>T (p.Glu1829Asp)	not provided [RCV003424614]	uncertain significance	11	1242367	1242367	Human		name
401909737	CV2806522	single nucleotide variant	NM_002458.3(MUC5B):c.5708C>T (p.Thr1903Met)	not provided [RCV003424619]	benign	11	1242588	1242588	Human		name
401909748	CV2806528	single nucleotide variant	NM_002458.3(MUC5B):c.6206C>T (p.Thr2069Met)	not provided [RCV003424625]	benign	11	1243086	1243086	Human		name
401909753	CV2806530	single nucleotide variant	NM_002458.3(MUC5B):c.6218C>T (p.Pro2073Leu)	not provided [RCV003424627]	likely benign	11	1243098	1243098	Human		name
401909760	CV2806534	single nucleotide variant	NM_002458.3(MUC5B):c.6594C>G (p.His2198Gln)	not provided [RCV003424631]	likely benign	11	1243474	1243474	Human		name
401909763	CV2806535	single nucleotide variant	NM_002458.3(MUC5B):c.6599G>A (p.Arg2200Gln)	not provided [RCV003424632]	likely benign	11	1243479	1243479	Human		name
401909764	CV2806536	single nucleotide variant	NM_002458.3(MUC5B):c.6626C>T (p.Thr2209Met)	not provided [RCV003424633]	likely benign	11	1243506	1243506	Human		name
401909766	CV2806537	single nucleotide variant	NM_002458.3(MUC5B):c.6685G>C (p.Glu2229Gln)	not provided [RCV003424634]	benign\|likely benign	11	1243565	1243565	Human		name
401909770	CV2806539	single nucleotide variant	NM_002458.3(MUC5B):c.6916A>G (p.Ile2306Val)	not provided [RCV003424636]	likely benign	11	1243796	1243796	Human		name
401909772	CV2806540	single nucleotide variant	NM_002458.3(MUC5B):c.6917T>C (p.Ile2306Thr)	not provided [RCV003424637]	likely benign	11	1243797	1243797	Human		name
401909774	CV2806541	single nucleotide variant	NM_002458.3(MUC5B):c.6923C>T (p.Thr2308Met)	not provided [RCV003424638]	likely benign	11	1243803	1243803	Human		name
401909778	CV2806543	single nucleotide variant	NM_002458.3(MUC5B):c.7051G>A (p.Val2351Ile)	not provided [RCV003424640]\|not specified [RCV004827960]	benign\|likely benign	11	1243931	1243931	Human		name
401909788	CV2806548	single nucleotide variant	NM_002458.3(MUC5B):c.7748C>T (p.Thr2583Met)	not provided [RCV003424645]	likely benign	11	1244628	1244628	Human		name
401909791	CV2806550	single nucleotide variant	NM_002458.3(MUC5B):c.7929A>T (p.Arg2643Ser)	not provided [RCV003424647]	likely benign	11	1244809	1244809	Human		name
401909808	CV2806558	single nucleotide variant	NM_002458.3(MUC5B):c.8501G>C (p.Arg2834Thr)	not provided [RCV003424655]	likely benign	11	1245381	1245381	Human		name
401909810	CV2806560	single nucleotide variant	NM_002458.3(MUC5B):c.8783G>A (p.Arg2928Gln)	not provided [RCV003424657]	likely benign	11	1245663	1245663	Human		name
401909812	CV2806561	single nucleotide variant	NM_002458.3(MUC5B):c.8905G>A (p.Gly2969Ser)	not provided [RCV003424658]	benign	11	1245785	1245785	Human		name
401909815	CV2806562	single nucleotide variant	NM_002458.3(MUC5B):c.8939C>T (p.Thr2980Met)	not provided [RCV003424659]	likely benign	11	1245819	1245819	Human		name
401909824	CV2806567	single nucleotide variant	NM_002458.3(MUC5B):c.9530C>G (p.Thr3177Ser)	not provided [RCV003424664]	likely benign	11	1246410	1246410	Human		name
401909828	CV2806569	single nucleotide variant	NM_002458.3(MUC5B):c.9734T>C (p.Leu3245Pro)	not provided [RCV003424666]	uncertain significance	11	1246614	1246614	Human		name
401909829	CV2806570	single nucleotide variant	NM_002458.3(MUC5B):c.9742G>A (p.Ala3248Thr)	not provided [RCV003424667]	likely benign	11	1246622	1246622	Human		name
401909838	CV2806574	single nucleotide variant	NM_002458.3(MUC5B):c.9926C>T (p.Pro3309Leu)	not provided [RCV003424671]	likely benign	11	1246806	1246806	Human		name
401909842	CV2806576	single nucleotide variant	NM_002458.3(MUC5B):c.9929C>G (p.Thr3310Ser)	not provided [RCV003424673]	likely benign	11	1246809	1246809	Human		name
401943034	CV2839954	single nucleotide variant	NM_002458.3(MUC5B):c.3280G>A (p.Ala1094Thr)	not provided [RCV003456741]	benign	11	1237147	1237147	Human		name
405264562	CV3185337	single nucleotide variant	NM_002458.3(MUC5B):c.8782C>T (p.Arg2928Trp)	not provided [RCV003885901]	benign\|likely benign	11	1245662	1245662	Human		name
405265295	CV3185567	single nucleotide variant	NM_002458.3(MUC5B):c.8072C>T (p.Thr2691Ile)	not provided [RCV003886131]	likely benign	11	1244952	1244952	Human		name
405265413	CV3185638	single nucleotide variant	NM_002458.3(MUC5B):c.8290C>A (p.Pro2764Thr)	not provided [RCV003886202]	benign\|likely benign	11	1245170	1245170	Human		name
405668188	CV3308229	single nucleotide variant	NM_002458.3(MUC5B):c.7925C>A (p.Thr2642Asn)	not specified [RCV004440701]	uncertain significance	11	1244805	1244805	Human		name
405668202	CV3308232	single nucleotide variant	NM_002458.3(MUC5B):c.7940T>G (p.Val2647Gly)	not specified [RCV004440704]	uncertain significance	11	1244820	1244820	Human		name
405668235	CV3308238	single nucleotide variant	NM_002458.3(MUC5B):c.7945C>T (p.Pro2649Ser)	not specified [RCV004440710]	uncertain significance	11	1244825	1244825	Human		name
405668248	CV3308241	single nucleotide variant	NM_002458.3(MUC5B):c.7976C>T (p.Pro2659Leu)	not specified [RCV004440713]	uncertain significance	11	1244856	1244856	Human		name
405668290	CV3308249	single nucleotide variant	NM_002458.3(MUC5B):c.8126C>T (p.Thr2709Ile)	not specified [RCV004440721]	uncertain significance	11	1245006	1245006	Human		name
405668411	CV3308274	single nucleotide variant	NM_002458.3(MUC5B):c.8353A>T (p.Thr2785Ser)	not specified [RCV004440746]	uncertain significance	11	1245233	1245233	Human		name
405668432	CV3308278	single nucleotide variant	NM_002458.3(MUC5B):c.8356G>A (p.Glu2786Lys)	not specified [RCV004440750]	uncertain significance	11	1245236	1245236	Human		name
405668454	CV3308282	single nucleotide variant	NM_002458.3(MUC5B):c.8384C>T (p.Pro2795Leu)	not specified [RCV004440754]	uncertain significance	11	1245264	1245264	Human		name
405668484	CV3308288	single nucleotide variant	NM_002458.3(MUC5B):c.8432G>A (p.Ser2811Asn)	not specified [RCV004440760]	uncertain significance	11	1245312	1245312	Human		name
405668581	CV3308308	single nucleotide variant	NM_002458.3(MUC5B):c.8480C>T (p.Thr2827Met)	not specified [RCV004440780]	uncertain significance	11	1245360	1245360	Human		name
405668676	CV3308327	single nucleotide variant	NM_002458.3(MUC5B):c.8552C>T (p.Ser2851Leu)	not specified [RCV004440799]	uncertain significance	11	1245432	1245432	Human		name
405668721	CV3308335	single nucleotide variant	NM_002458.3(MUC5B):c.8680G>A (p.Asp2894Asn)	not specified [RCV004440807]	uncertain significance	11	1245560	1245560	Human		name
405668760	CV3308343	single nucleotide variant	NM_002458.3(MUC5B):c.8710G>A (p.Ala2904Thr)	not specified [RCV004440815]	uncertain significance	11	1245590	1245590	Human		name
405668841	CV3308360	single nucleotide variant	NM_002458.3(MUC5B):c.8806T>C (p.Cys2936Arg)	not specified [RCV004440832]	uncertain significance	11	1245686	1245686	Human		name
405668864	CV3308364	single nucleotide variant	NM_002458.3(MUC5B):c.8848G>C (p.Val2950Leu)	not specified [RCV004440836]	uncertain significance	11	1245728	1245728	Human		name
405668994	CV3308390	single nucleotide variant	NM_002458.3(MUC5B):c.9026C>T (p.Thr3009Met)	not specified [RCV004440862]	uncertain significance	11	1245906	1245906	Human		name
405669126	CV3308415	single nucleotide variant	NM_002458.3(MUC5B):c.9122C>T (p.Ser3041Phe)	not specified [RCV004440887]	uncertain significance	11	1246002	1246002	Human		name
405669165	CV3308423	single nucleotide variant	NM_002458.3(MUC5B):c.9232G>A (p.Gly3078Arg)	not specified [RCV004440895]	uncertain significance	11	1246112	1246112	Human		name
405678917	CV3308476	single nucleotide variant	NM_002458.3(MUC5B):c.9504C>G (p.Ser3168Arg)	not specified [RCV004442932]	uncertain significance	11	1246384	1246384	Human		name
405678954	CV3308483	single nucleotide variant	NM_002458.3(MUC5B):c.9554C>T (p.Ser3185Phe)	not specified [RCV004442939]	uncertain significance	11	1246434	1246434	Human		name
405678983	CV3308489	single nucleotide variant	NM_002458.3(MUC5B):c.9559C>T (p.Arg3187Trp)	not specified [RCV004442945]	uncertain significance	11	1246439	1246439	Human		name
405679021	CV3308497	single nucleotide variant	NM_002458.3(MUC5B):c.9583G>A (p.Val3195Met)	not specified [RCV004442953]	uncertain significance	11	1246463	1246463	Human		name
405679178	CV3308500	single nucleotide variant	NM_002458.3(MUC5B):c.9596C>T (p.Thr3199Met)	not specified [RCV004442956]	likely benign	11	1246476	1246476	Human		name
405679216	CV3308507	single nucleotide variant	NM_002458.3(MUC5B):c.9613G>A (p.Val3205Ile)	not specified [RCV004442963]	uncertain significance	11	1246493	1246493	Human		name
405679308	CV3308524	single nucleotide variant	NM_002458.3(MUC5B):c.9751C>T (p.Arg3251Cys)	not specified [RCV004442980]	uncertain significance	11	1246631	1246631	Human		name
405679422	CV3308546	single nucleotide variant	NM_002458.3(MUC5B):c.9821T>C (p.Val3274Ala)	not specified [RCV004443002]	likely benign	11	1246701	1246701	Human		name
405679450	CV3308552	single nucleotide variant	NM_002458.3(MUC5B):c.9857C>A (p.Thr3286Lys)	not specified [RCV004443008]	uncertain significance	11	1246737	1246737	Human		name
405679466	CV3308555	single nucleotide variant	NM_002458.3(MUC5B):c.9860C>T (p.Thr3287Ile)	not specified [RCV004443011]	uncertain significance	11	1246740	1246740	Human		name
405679526	CV3308567	single nucleotide variant	NM_002458.3(MUC5B):c.9953C>T (p.Ala3318Val)	not specified [RCV004443023]	uncertain significance	11	1246833	1246833	Human		name
405679586	CV3308580	single nucleotide variant	NM_002458.3(MUC5B):c.9986C>T (p.Thr3329Met)	not specified [RCV004443036]	uncertain significance	11	1246866	1246866	Human		name
405658475	CV3311687	single nucleotide variant	NM_002458.3(MUC5B):c.4910C>T (p.Pro1637Leu)	not specified [RCV004438199]	likely benign	11	1241790	1241790	Human		name
405658486	CV3311690	single nucleotide variant	NM_002458.3(MUC5B):c.4925C>A (p.Ala1642Asp)	not specified [RCV004438202]	uncertain significance	11	1241805	1241805	Human		name
405658508	CV3311696	single nucleotide variant	NM_002458.3(MUC5B):c.4994C>A (p.Thr1665Asn)	not specified [RCV004438208]	uncertain significance	11	1241874	1241874	Human		name
405658544	CV3311707	single nucleotide variant	NM_002458.3(MUC5B):c.5087G>A (p.Arg1696His)	not specified [RCV004438219]	likely benign	11	1241967	1241967	Human		name
405658614	CV3311731	single nucleotide variant	NM_002458.3(MUC5B):c.5219C>A (p.Pro1740Gln)	not specified [RCV004438243]	uncertain significance	11	1242099	1242099	Human		name
405658659	CV3311746	single nucleotide variant	NM_002458.3(MUC5B):c.5348G>A (p.Arg1783His)	not specified [RCV004438258]	uncertain significance	11	1242228	1242228	Human		name
405658686	CV3311755	single nucleotide variant	NM_002458.3(MUC5B):c.5476A>G (p.Lys1826Glu)	not specified [RCV004438267]	likely benign	11	1242356	1242356	Human		name
405658711	CV3311765	single nucleotide variant	NM_002458.3(MUC5B):c.5491C>T (p.Arg1831Trp)	not specified [RCV004438277]	uncertain significance	11	1242371	1242371	Human		name
405658741	CV3311777	single nucleotide variant	NM_002458.3(MUC5B):c.5654G>A (p.Cys1885Tyr)	not specified [RCV004438289]	uncertain significance	11	1242534	1242534	Human		name
405658769	CV3311788	single nucleotide variant	NM_002458.3(MUC5B):c.5698A>G (p.Thr1900Ala)	not specified [RCV004438300]	uncertain significance	11	1242578	1242578	Human		name
405658784	CV3311793	single nucleotide variant	NM_002458.3(MUC5B):c.5747C>T (p.Thr1916Met)	not specified [RCV004438305]	uncertain significance	11	1242627	1242627	Human		name
405658861	CV3311820	single nucleotide variant	NM_002458.3(MUC5B):c.5825C>T (p.Thr1942Met)	not specified [RCV004438332]	likely benign	11	1242705	1242705	Human		name
405666824	CV3311847	single nucleotide variant	NM_002458.3(MUC5B):c.5864C>T (p.Pro1955Leu)	not specified [RCV004440426]	uncertain significance	11	1242744	1242744	Human		name
405666878	CV3311857	single nucleotide variant	NM_002458.3(MUC5B):c.5921C>T (p.Thr1974Ile)	not specified [RCV004440436]	uncertain significance	11	1242801	1242801	Human		name
405666980	CV3311879	single nucleotide variant	NM_002458.3(MUC5B):c.6061A>T (p.Thr2021Ser)	not specified [RCV004440458]	uncertain significance	11	1242941	1242941	Human		name
405667102	CV3311903	single nucleotide variant	NM_002458.3(MUC5B):c.6239C>A (p.Thr2080Asn)	not specified [RCV004440482]	likely benign	11	1243119	1243119	Human		name
405667165	CV3311915	single nucleotide variant	NM_002458.3(MUC5B):c.6367A>G (p.Ser2123Gly)	not specified [RCV004440494]	uncertain significance	11	1243247	1243247	Human		name
405667175	CV3311917	single nucleotide variant	NM_002458.3(MUC5B):c.6381T>G (p.Ser2127Arg)	not specified [RCV004440496]	uncertain significance	11	1243261	1243261	Human		name
405667213	CV3311924	single nucleotide variant	NM_002458.3(MUC5B):c.6422C>T (p.Thr2141Met)	not specified [RCV004440503]	uncertain significance	11	1243302	1243302	Human		name
405667231	CV3311928	single nucleotide variant	NM_002458.3(MUC5B):c.6428C>T (p.Thr2143Ile)	not specified [RCV004440507]	uncertain significance	11	1243308	1243308	Human		name
405667534	CV3311989	single nucleotide variant	NM_002458.3(MUC5B):c.6830C>T (p.Thr2277Met)	not specified [RCV004440568]	uncertain significance	11	1243710	1243710	Human		name
405667666	CV3312017	single nucleotide variant	NM_002458.3(MUC5B):c.6951G>T (p.Gln2317His)	not specified [RCV004440596]	uncertain significance	11	1243831	1243831	Human		name
405667702	CV3312024	single nucleotide variant	NM_002458.3(MUC5B):c.6956C>T (p.Ala2319Val)	not specified [RCV004440603]	uncertain significance	11	1243836	1243836	Human		name
405667765	CV3312037	single nucleotide variant	NM_002458.3(MUC5B):c.7024T>A (p.Ser2342Thr)	not specified [RCV004440616]	uncertain significance	11	1243904	1243904	Human		name
405667825	CV3312049	single nucleotide variant	NM_002458.3(MUC5B):c.7129G>A (p.Val2377Met)	not specified [RCV004440628]	uncertain significance	11	1244009	1244009	Human		name
405667865	CV3312057	single nucleotide variant	NM_002458.3(MUC5B):c.7289C>T (p.Pro2430Leu)	not specified [RCV004440636]	likely benign	11	1244169	1244169	Human		name
405667970	CV3312077	single nucleotide variant	NM_002458.3(MUC5B):c.7450G>A (p.Ala2484Thr)	not specified [RCV004440656]	uncertain significance	11	1244330	1244330	Human		name
405668019	CV3312087	single nucleotide variant	NM_002458.3(MUC5B):c.7724A>G (p.His2575Arg)	not specified [RCV004440666]	uncertain significance	11	1244604	1244604	Human		name
405668044	CV3312092	single nucleotide variant	NM_002458.3(MUC5B):c.7757C>T (p.Thr2586Ile)	not specified [RCV004440671]	uncertain significance	11	1244637	1244637	Human		name
405657945	CV3315023	single nucleotide variant	NM_002458.3(MUC5B):c.3017G>A (p.Arg1006Gln)	not specified [RCV004438024]	uncertain significance	11	1236522	1236522	Human		name
405658000	CV3315042	single nucleotide variant	NM_002458.3(MUC5B):c.3215C>T (p.Thr1072Met)	not specified [RCV004438043]	uncertain significance	11	1237082	1237082	Human		name
405658055	CV3315060	single nucleotide variant	NM_002458.3(MUC5B):c.3361G>A (p.Asp1121Asn)	not specified [RCV004438061]	uncertain significance	11	1238934	1238934	Human		name
405658075	CV3315067	single nucleotide variant	NM_002458.3(MUC5B):c.3509C>A (p.Pro1170His)	not specified [RCV004438068]	uncertain significance	11	1239492	1239492	Human		name
405658132	CV3315086	single nucleotide variant	NM_002458.3(MUC5B):c.3613C>G (p.Pro1205Ala)	not specified [RCV004438087]	uncertain significance	11	1239828	1239828	Human		name
405658145	CV3315091	single nucleotide variant	NM_002458.3(MUC5B):c.3680A>C (p.Tyr1227Ser)	not specified [RCV004438092]	uncertain significance	11	1239895	1239895	Human		name
405658176	CV3315101	single nucleotide variant	NM_002458.3(MUC5B):c.3907C>T (p.Pro1303Ser)	not specified [RCV004438102]	uncertain significance	11	1240312	1240312	Human		name
405658217	CV3315114	single nucleotide variant	NM_002458.3(MUC5B):c.3956C>T (p.Pro1319Leu)	not specified [RCV004438115]	uncertain significance	11	1240361	1240361	Human		name
405658227	CV3315117	single nucleotide variant	NM_002458.3(MUC5B):c.3965C>T (p.Thr1322Met)	not specified [RCV004438118]	uncertain significance	11	1240370	1240370	Human		name
405658283	CV3315136	single nucleotide variant	NM_002458.3(MUC5B):c.4134C>G (p.Ile1378Met)	not specified [RCV004438137]	uncertain significance	11	1241014	1241014	Human		name
405658346	CV3315156	single nucleotide variant	NM_002458.3(MUC5B):c.4373C>G (p.Thr1458Ser)	not specified [RCV004438157]	uncertain significance	11	1241253	1241253	Human		name
405658356	CV3315159	single nucleotide variant	NM_002458.3(MUC5B):c.4424G>A (p.Arg1475Gln)	not specified [RCV004438160]	likely benign	11	1241304	1241304	Human		name
405658386	CV3315168	single nucleotide variant	NM_002458.3(MUC5B):c.4471G>A (p.Val1491Met)	not specified [RCV004438169]	uncertain significance	11	1241351	1241351	Human		name
405658407	CV3315175	single nucleotide variant	NM_002458.3(MUC5B):c.4475C>T (p.Thr1492Met)	not specified [RCV004438176]	uncertain significance	11	1241355	1241355	Human		name
405658416	CV3315178	single nucleotide variant	NM_002458.3(MUC5B):c.4616A>T (p.His1539Leu)	not specified [RCV004438179]	uncertain significance	11	1241496	1241496	Human		name
405658445	CV3315188	single nucleotide variant	NM_002458.3(MUC5B):c.4835C>T (p.Pro1612Leu)	not specified [RCV004438189]	uncertain significance	11	1241715	1241715	Human		name
405852895	CV3393323	single nucleotide variant	NM_002458.3(MUC5B):c.8507C>T (p.Thr2836Ile)	not provided [RCV004546053]	benign	11	1245387	1245387	Human		name
407425284	CV3409429	single nucleotide variant	NM_002458.3(MUC5B):c.8278T>C (p.Ser2760Pro)	not provided [RCV004585360]	likely benign	11	1245158	1245158	Human		name
407425507	CV3409543	single nucleotide variant	NM_002458.3(MUC5B):c.8303G>C (p.Arg2768Pro)	not provided [RCV004585475]	likely benign	11	1245183	1245183	Human		name
407456030	CV3415712	single nucleotide variant	NM_002458.3(MUC5B):c.8333C>T (p.Thr2778Ile)	not provided [RCV004598588]	likely benign	11	1245213	1245213	Human		name
407453723	CV3416374	single nucleotide variant	NM_002458.3(MUC5B):c.8063C>T (p.Pro2688Leu)	not provided [RCV004597632]	likely benign	11	1244943	1244943	Human		name
407507786	CV3457848	single nucleotide variant	NM_002458.3(MUC5B):c.5041A>G (p.Thr1681Ala)	not specified [RCV004646918]	uncertain significance	11	1241921	1241921	Human		name
407507794	CV3457850	single nucleotide variant	NM_002458.3(MUC5B):c.6587C>A (p.Thr2196Asn)	not specified [RCV004646920]	uncertain significance	11	1243467	1243467	Human		name
407476522	CV3457851	single nucleotide variant	NM_002458.3(MUC5B):c.5846C>T (p.Thr1949Ile)	not specified [RCV004638603]	uncertain significance	11	1242726	1242726	Human		name
407507797	CV3457852	single nucleotide variant	NM_002458.3(MUC5B):c.7649C>T (p.Thr2550Ile)	not specified [RCV004646921]	uncertain significance	11	1244529	1244529	Human		name
407476536	CV3457855	single nucleotide variant	NM_002458.3(MUC5B):c.8398G>A (p.Gly2800Ser)	not specified [RCV004638606]	uncertain significance	11	1245278	1245278	Human		name
407507800	CV3457856	single nucleotide variant	NM_002458.3(MUC5B):c.9458C>A (p.Thr3153Asn)	not specified [RCV004646922]	uncertain significance	11	1246338	1246338	Human		name
407507807	CV3457858	single nucleotide variant	NM_002458.3(MUC5B):c.7295C>T (p.Thr2432Met)	not specified [RCV004646924]	uncertain significance	11	1244175	1244175	Human		name
407476540	CV3457860	single nucleotide variant	NM_002458.3(MUC5B):c.8282C>A (p.Pro2761His)	not specified [RCV004638607]	uncertain significance	11	1245162	1245162	Human		name
407507819	CV3457862	single nucleotide variant	NM_002458.3(MUC5B):c.6015G>C (p.Met2005Ile)	not specified [RCV004646927]	uncertain significance	11	1242895	1242895	Human		name
407476548	CV3457864	single nucleotide variant	NM_002458.3(MUC5B):c.7886C>G (p.Thr2629Arg)	not specified [RCV004638609]	uncertain significance	11	1244766	1244766	Human		name
407507826	CV3457866	single nucleotide variant	NM_002458.3(MUC5B):c.5777C>T (p.Pro1926Leu)	not specified [RCV004646929]	uncertain significance	11	1242657	1242657	Human		name
407476553	CV3457868	single nucleotide variant	NM_002458.3(MUC5B):c.8243C>T (p.Pro2748Leu)	not specified [RCV004638610]	likely benign	11	1245123	1245123	Human		name
407476556	CV3457870	single nucleotide variant	NM_002458.3(MUC5B):c.4816C>T (p.Arg1606Cys)	not specified [RCV004638611]	uncertain significance	11	1241696	1241696	Human		name
407476566	CV3457875	single nucleotide variant	NM_002458.3(MUC5B):c.7550G>A (p.Gly2517Glu)	not specified [RCV004638614]	uncertain significance	11	1244430	1244430	Human		name
407476572	CV3457879	single nucleotide variant	NM_002458.3(MUC5B):c.7682C>T (p.Thr2561Ile)	not specified [RCV004638615]	uncertain significance	11	1244562	1244562	Human		name
407507853	CV3457880	single nucleotide variant	NM_002458.3(MUC5B):c.6692C>G (p.Ser2231Cys)	not specified [RCV004646937]	uncertain significance	11	1243572	1243572	Human		name
407507857	CV3457881	single nucleotide variant	NM_002458.3(MUC5B):c.6398T>C (p.Leu2133Pro)	not specified [RCV004646938]	uncertain significance	11	1243278	1243278	Human		name
407507870	CV3457886	single nucleotide variant	NM_002458.3(MUC5B):c.5938G>A (p.Val1980Ile)	not specified [RCV004646942]	uncertain significance	11	1242818	1242818	Human		name
407476579	CV3457887	single nucleotide variant	NM_002458.3(MUC5B):c.3779C>T (p.Thr1260Ile)	not specified [RCV004638617]	uncertain significance	11	1240184	1240184	Human		name
407476583	CV3457888	single nucleotide variant	NM_002458.3(MUC5B):c.4871C>A (p.Thr1624Asn)	not specified [RCV004638618]	uncertain significance	11	1241751	1241751	Human		name
407507876	CV3457890	single nucleotide variant	NM_002458.3(MUC5B):c.9713C>T (p.Thr3238Ile)	not specified [RCV004646943]	uncertain significance	11	1246593	1246593	Human		name
407507886	CV3457893	single nucleotide variant	NM_002458.3(MUC5B):c.5795C>T (p.Thr1932Ile)	not specified [RCV004646946]	uncertain significance	11	1242675	1242675	Human		name
407507895	CV3457897	single nucleotide variant	NM_002458.3(MUC5B):c.3538C>T (p.Arg1180Trp)	not specified [RCV004646949]	uncertain significance	11	1239521	1239521	Human		name
407507898	CV3457898	single nucleotide variant	NM_002458.3(MUC5B):c.5523C>A (p.Asp1841Glu)	not specified [RCV004646950]	uncertain significance	11	1242403	1242403	Human		name
407476595	CV3457899	single nucleotide variant	NM_002458.3(MUC5B):c.6787G>A (p.Glu2263Lys)	not specified [RCV004638621]	uncertain significance	11	1243667	1243667	Human		name
407507909	CV3457903	single nucleotide variant	NM_002458.3(MUC5B):c.7334C>T (p.Thr2445Met)	not specified [RCV004646953]	uncertain significance	11	1244214	1244214	Human		name
407507915	CV3457905	single nucleotide variant	NM_002458.3(MUC5B):c.5444G>C (p.Arg1815Thr)	not specified [RCV004646955]	uncertain significance	11	1242324	1242324	Human		name
407476603	CV3457907	single nucleotide variant	NM_002458.3(MUC5B):c.9362C>A (p.Ser3121Tyr)	not specified [RCV004638623]	uncertain significance	11	1246242	1246242	Human		name
407507922	CV3457908	single nucleotide variant	NM_002458.3(MUC5B):c.5455G>A (p.Gly1819Ser)	not specified [RCV004646957]	uncertain significance	11	1242335	1242335	Human		name
407503803	CV3457910	single nucleotide variant	NM_002458.3(MUC5B):c.5279C>A (p.Thr1760Asn)	not specified [RCV004645591]	uncertain significance	11	1242159	1242159	Human		name
407507930	CV3457911	single nucleotide variant	NM_002458.3(MUC5B):c.8776C>A (p.Pro2926Thr)	not specified [RCV004646959]	uncertain significance	11	1245656	1245656	Human		name
407503805	CV3457912	single nucleotide variant	NM_002458.3(MUC5B):c.9763A>G (p.Thr3255Ala)	not specified [RCV004645592]	uncertain significance	11	1246643	1246643	Human		name
407507933	CV3457913	single nucleotide variant	NM_002458.3(MUC5B):c.7918C>G (p.Pro2640Ala)	not specified [RCV004646960]	uncertain significance	11	1244798	1244798	Human		name
407507937	CV3457914	single nucleotide variant	NM_002458.3(MUC5B):c.6359C>A (p.Pro2120His)	not specified [RCV004646961]	uncertain significance	11	1243239	1243239	Human		name
407507946	CV3457918	single nucleotide variant	NM_002458.3(MUC5B):c.7324A>G (p.Thr2442Ala)	not specified [RCV004646964]	uncertain significance	11	1244204	1244204	Human		name
407507953	CV3457920	single nucleotide variant	NM_002458.3(MUC5B):c.6596G>A (p.Gly2199Glu)	not specified [RCV004646966]	uncertain significance	11	1243476	1243476	Human		name
407507960	CV3457922	single nucleotide variant	NM_002458.3(MUC5B):c.6683C>T (p.Thr2228Ile)	not specified [RCV004646968]	uncertain significance	11	1243563	1243563	Human		name
407507963	CV3457923	single nucleotide variant	NM_002458.3(MUC5B):c.3293C>T (p.Ser1098Phe)	not specified [RCV004646969]	uncertain significance	11	1237160	1237160	Human		name
596947034	CV3547096	single nucleotide variant	NM_002458.3(MUC5B):c.7796C>T (p.Thr2599Ile)	not provided [RCV004810903]	likely benign	11	1244676	1244676	Human		name
596947035	CV3547097	single nucleotide variant	NM_002458.3(MUC5B):c.7841C>T (p.Thr2614Met)	not provided [RCV004810904]	likely benign	11	1244721	1244721	Human		name
596947055	CV3547118	single nucleotide variant	NM_002458.3(MUC5B):c.7882C>A (p.Arg2628Ser)	not provided [RCV004810926]	likely benign	11	1244762	1244762	Human		name
596947076	CV3547140	single nucleotide variant	NM_002458.3(MUC5B):c.6226T>C (p.Trp2076Arg)	not provided [RCV004810948]	likely benign	11	1243106	1243106	Human		name
596947105	CV3547169	single nucleotide variant	NM_002458.3(MUC5B):c.7888C>A (p.Leu2630Ile)	not provided [RCV004810977]	likely benign	11	1244768	1244768	Human		name
596947745	CV3547328	single nucleotide variant	NM_002458.3(MUC5B):c.6875G>A (p.Arg2292His)	not provided [RCV004811632]	likely benign	11	1243755	1243755	Human		name
596947752	CV3547335	single nucleotide variant	NM_002458.3(MUC5B):c.6077C>T (p.Thr2026Met)	not provided [RCV004811639]	benign	11	1242957	1242957	Human		name
596947898	CV3547486	single nucleotide variant	NM_002458.3(MUC5B):c.6656C>T (p.Ser2219Leu)	not provided [RCV004811790]	likely benign	11	1243536	1243536	Human		name
596947914	CV3547503	single nucleotide variant	NM_002458.3(MUC5B):c.8249C>T (p.Thr2750Ile)	not provided [RCV004811807]	likely benign	11	1245129	1245129	Human		name
596947921	CV3547510	single nucleotide variant	NM_002458.3(MUC5B):c.7609T>G (p.Phe2537Val)	not provided [RCV004811814]	likely benign	11	1244489	1244489	Human		name
596948069	CV3547661	single nucleotide variant	NM_002458.3(MUC5B):c.6212T>G (p.Leu2071Arg)	not provided [RCV004811966]	likely benign	11	1243092	1243092	Human		name
596945341	CV3547841	single nucleotide variant	NM_002458.3(MUC5B):c.6155C>T (p.Pro2052Leu)	not provided [RCV004809172]	likely benign	11	1243035	1243035	Human		name
596945365	CV3547851	single nucleotide variant	NM_002458.3(MUC5B):c.6158C>G (p.Thr2053Ser)	not provided [RCV004809182]	likely benign	11	1243038	1243038	Human		name
596947552	CV3549111	single nucleotide variant	NM_002458.3(MUC5B):c.6590C>G (p.Thr2197Arg)	not provided [RCV004811435]	likely benign	11	1243470	1243470	Human		name
597639658	CV3557732	single nucleotide variant	NM_002458.3(MUC5B):c.5900C>T (p.Ala1967Val)	not specified [RCV004825183]	uncertain significance	11	1242780	1242780	Human		name
597639661	CV3557733	single nucleotide variant	NM_002458.3(MUC5B):c.6946C>T (p.Pro2316Ser)	not specified [RCV004825184]	uncertain significance	11	1243826	1243826	Human		name
597639667	CV3557734	single nucleotide variant	NM_002458.3(MUC5B):c.4892C>T (p.Pro1631Leu)	not specified [RCV004825185]	likely benign	11	1241772	1241772	Human		name
597643571	CV3557735	single nucleotide variant	NM_002458.3(MUC5B):c.9271A>G (p.Met3091Val)	not specified [RCV004825848]	uncertain significance	11	1246151	1246151	Human		name
597643739	CV3557741	single nucleotide variant	NM_002458.3(MUC5B):c.9121T>C (p.Ser3041Pro)	not specified [RCV004825853]	likely benign	11	1246001	1246001	Human		name
597643746	CV3557742	single nucleotide variant	NM_002458.3(MUC5B):c.6631C>T (p.Arg2211Cys)	not specified [RCV004825854]	uncertain significance	11	1243511	1243511	Human		name
597643751	CV3557743	single nucleotide variant	NM_002458.3(MUC5B):c.7114G>A (p.Glu2372Lys)	not specified [RCV004825855]	uncertain significance	11	1243994	1243994	Human		name
597643776	CV3557749	single nucleotide variant	NM_002458.3(MUC5B):c.4085A>G (p.Glu1362Gly)	not specified [RCV004825859]	uncertain significance	11	1240965	1240965	Human		name
597643783	CV3557750	single nucleotide variant	NM_002458.3(MUC5B):c.3065T>C (p.Val1022Ala)	not specified [RCV004825860]	uncertain significance	11	1236932	1236932	Human		name
597643788	CV3557751	single nucleotide variant	NM_002458.3(MUC5B):c.3902C>A (p.Ala1301Glu)	not specified [RCV004825861]	likely benign	11	1240307	1240307	Human		name
597643801	CV3557753	single nucleotide variant	NM_002458.3(MUC5B):c.6710C>A (p.Thr2237Asn)	not specified [RCV004825863]	uncertain significance	11	1243590	1243590	Human		name
597643806	CV3557754	single nucleotide variant	NM_002458.3(MUC5B):c.5305A>G (p.Met1769Val)	not specified [RCV004825864]	uncertain significance	11	1242185	1242185	Human		name
597643813	CV3557755	single nucleotide variant	NM_002458.3(MUC5B):c.9364A>C (p.Met3122Leu)	not specified [RCV004825865]	uncertain significance	11	1246244	1246244	Human		name
597639686	CV3557756	single nucleotide variant	NM_002458.3(MUC5B):c.3817G>A (p.Val1273Ile)	not specified [RCV004825189]	likely benign	11	1240222	1240222	Human		name
597639697	CV3557758	single nucleotide variant	NM_002458.3(MUC5B):c.7739T>C (p.Leu2580Pro)	not specified [RCV004825191]	uncertain significance	11	1244619	1244619	Human		name
597643831	CV3557761	single nucleotide variant	NM_002458.3(MUC5B):c.4484C>T (p.Pro1495Leu)	not specified [RCV004825868]	uncertain significance	11	1241364	1241364	Human		name
597643838	CV3557763	single nucleotide variant	NM_002458.3(MUC5B):c.7871C>G (p.Pro2624Arg)	not specified [RCV004825869]	uncertain significance	11	1244751	1244751	Human		name
597639712	CV3557766	single nucleotide variant	NM_002458.3(MUC5B):c.9803C>A (p.Ser3268Tyr)	not specified [RCV004825194]	uncertain significance	11	1246683	1246683	Human		name
597639729	CV3557771	single nucleotide variant	NM_002458.3(MUC5B):c.7904G>C (p.Ser2635Thr)	not specified [RCV004825197]	uncertain significance	11	1244784	1244784	Human		name
597643868	CV3557773	single nucleotide variant	NM_002458.3(MUC5B):c.7730C>T (p.Ser2577Phe)	not specified [RCV004825874]	uncertain significance	11	1244610	1244610	Human		name
597643933	CV3557786	single nucleotide variant	NM_002458.3(MUC5B):c.4876G>T (p.Ala1626Ser)	not specified [RCV004825885]	uncertain significance	11	1241756	1241756	Human		name
597639746	CV3557789	single nucleotide variant	NM_002458.3(MUC5B):c.8078C>G (p.Thr2693Arg)	not specified [RCV004825200]	uncertain significance	11	1244958	1244958	Human		name
597643950	CV3557790	single nucleotide variant	NM_002458.3(MUC5B):c.8296A>G (p.Thr2766Ala)	not specified [RCV004825888]	uncertain significance	11	1245176	1245176	Human		name
597643969	CV3557794	single nucleotide variant	NM_002458.3(MUC5B):c.6839C>A (p.Ser2280Tyr)	not specified [RCV004825891]	uncertain significance	11	1243719	1243719	Human		name
597643976	CV3557795	single nucleotide variant	NM_002458.3(MUC5B):c.5831C>T (p.Thr1944Ile)	not specified [RCV004825892]	uncertain significance	11	1242711	1242711	Human		name
597643981	CV3557796	single nucleotide variant	NM_002458.3(MUC5B):c.5602A>G (p.Met1868Val)	not specified [RCV004825893]	uncertain significance	11	1242482	1242482	Human		name
597643988	CV3557797	single nucleotide variant	NM_002458.3(MUC5B):c.5849G>C (p.Ser1950Thr)	not specified [RCV004825894]	uncertain significance	11	1242729	1242729	Human		name
597644016	CV3557802	single nucleotide variant	NM_002458.3(MUC5B):c.3698G>A (p.Arg1233Lys)	not specified [RCV004825898]	uncertain significance	11	1239913	1239913	Human		name
597644026	CV3557806	single nucleotide variant	NM_002458.3(MUC5B):c.7973C>T (p.Thr2658Ile)	not specified [RCV004825900]	uncertain significance	11	1244853	1244853	Human		name
597644034	CV3557808	single nucleotide variant	NM_002458.3(MUC5B):c.7748C>G (p.Thr2583Arg)	not specified [RCV004825901]	uncertain significance	11	1244628	1244628	Human		name
597644038	CV3557809	single nucleotide variant	NM_002458.3(MUC5B):c.9226A>T (p.Thr3076Ser)	not specified [RCV004825902]	uncertain significance	11	1246106	1246106	Human		name
597644046	CV3557810	single nucleotide variant	NM_002458.3(MUC5B):c.4469C>T (p.Pro1490Leu)	not specified [RCV004825903]	uncertain significance	11	1241349	1241349	Human		name
597644052	CV3557811	single nucleotide variant	NM_002458.3(MUC5B):c.3299T>A (p.Val1100Asp)	not specified [RCV004825904]	uncertain significance	11	1238872	1238872	Human		name
597644079	CV3557818	single nucleotide variant	NM_002458.3(MUC5B):c.8090T>A (p.Ile2697Asn)	not specified [RCV004825909]	uncertain significance	11	1244970	1244970	Human		name
597644109	CV3557823	single nucleotide variant	NM_002458.3(MUC5B):c.5261C>G (p.Ser1754Cys)	not specified [RCV004825914]	uncertain significance	11	1242141	1242141	Human		name
597644116	CV3557824	single nucleotide variant	NM_002458.3(MUC5B):c.6827C>T (p.Thr2276Ile)	not specified [RCV004825915]	uncertain significance	11	1243707	1243707	Human		name
597639933	CV3557826	single nucleotide variant	NM_002458.3(MUC5B):c.6449C>T (p.Ser2150Phe)	not specified [RCV004825208]	uncertain significance	11	1243329	1243329	Human		name
597644130	CV3557827	single nucleotide variant	NM_002458.3(MUC5B):c.8039G>C (p.Ser2680Thr)	not specified [RCV004825917]	uncertain significance	11	1244919	1244919	Human		name
597643341	CV3561574	single nucleotide variant	NM_002458.3(MUC5B):c.7111C>T (p.Arg2371Trp)	not specified [RCV004825810]	uncertain significance	11	1243991	1243991	Human		name
597643368	CV3561579	single nucleotide variant	NM_002458.3(MUC5B):c.4499C>T (p.Thr1500Ile)	not specified [RCV004825815]	uncertain significance	11	1241379	1241379	Human		name
597643400	CV3561585	single nucleotide variant	NM_002458.3(MUC5B):c.7909A>G (p.Thr2637Ala)	not specified [RCV004825820]	uncertain significance	11	1244789	1244789	Human		name
597639584	CV3561587	single nucleotide variant	NM_002458.3(MUC5B):c.7355C>T (p.Thr2452Met)	not specified [RCV004825169]	uncertain significance	11	1244235	1244235	Human		name
597639590	CV3561589	single nucleotide variant	NM_002458.3(MUC5B):c.7037C>A (p.Ala2346Glu)	not specified [RCV004825170]	uncertain significance	11	1243917	1243917	Human		name
597639602	CV3561591	single nucleotide variant	NM_002458.3(MUC5B):c.4979C>G (p.Pro1660Arg)	not specified [RCV004825172]	uncertain significance	11	1241859	1241859	Human		name
597639606	CV3561593	single nucleotide variant	NM_002458.3(MUC5B):c.7435G>A (p.Gly2479Arg)	not specified [RCV004825173]	uncertain significance	11	1244315	1244315	Human		name
597643443	CV3561597	single nucleotide variant	NM_002458.3(MUC5B):c.9514A>G (p.Thr3172Ala)	not specified [RCV004825827]	uncertain significance	11	1246394	1246394	Human		name
597643479	CV3561603	single nucleotide variant	NM_002458.3(MUC5B):c.9409G>A (p.Glu3137Lys)	not specified [RCV004825833]	uncertain significance	11	1246289	1246289	Human		name
597643485	CV3561605	single nucleotide variant	NM_002458.3(MUC5B):c.4006G>A (p.Glu1336Lys)	not specified [RCV004825834]	uncertain significance	11	1240886	1240886	Human		name
597643492	CV3561607	single nucleotide variant	NM_002458.3(MUC5B):c.8282C>T (p.Pro2761Leu)	not specified [RCV004825835]	uncertain significance	11	1245162	1245162	Human		name
597643509	CV3561610	single nucleotide variant	NM_002458.3(MUC5B):c.8270G>A (p.Arg2757Gln)	not specified [RCV004825838]	uncertain significance	11	1245150	1245150	Human		name
597643527	CV3561613	single nucleotide variant	NM_002458.3(MUC5B):c.9383C>T (p.Thr3128Ile)	not specified [RCV004825841]	uncertain significance	11	1246263	1246263	Human		name
597643534	CV3561614	single nucleotide variant	NM_002458.3(MUC5B):c.7870C>A (p.Pro2624Thr)	not specified [RCV004825842]	uncertain significance	11	1244750	1244750	Human		name
597643540	CV3561616	single nucleotide variant	NM_002458.3(MUC5B):c.8704C>T (p.Arg2902Cys)	not specified [RCV004825843]	uncertain significance	11	1245584	1245584	Human		name
597639625	CV3561617	single nucleotide variant	NM_002458.3(MUC5B):c.5558C>T (p.Thr1853Met)	not specified [RCV004825177]	uncertain significance	11	1242438	1242438	Human		name
597639631	CV3561619	single nucleotide variant	NM_002458.3(MUC5B):c.8942C>T (p.Ala2981Val)	not specified [RCV004825178]	uncertain significance	11	1245822	1245822	Human		name
597643554	CV3561620	single nucleotide variant	NM_002458.3(MUC5B):c.6560C>T (p.Thr2187Ile)	not specified [RCV004825845]	uncertain significance	11	1243440	1243440	Human		name
597639636	CV3561622	single nucleotide variant	NM_002458.3(MUC5B):c.4054G>A (p.Gly1352Ser)	not specified [RCV004825179]	uncertain significance	11	1240934	1240934	Human		name
597643566	CV3561625	single nucleotide variant	NM_002458.3(MUC5B):c.3863T>C (p.Ile1288Thr)	not specified [RCV004825847]	uncertain significance	11	1240268	1240268	Human		name
597675266	CV3723722	single nucleotide variant	NM_002458.3(MUC5B):c.7898G>A (p.Trp2633Ter)	Interstitial lung disease 2 [RCV005044423]	uncertain significance	11	1244778	1244778	Human	1	name
598128783	CV3886581	single nucleotide variant	NM_002458.3(MUC5B):c.4079C>T (p.Thr1360Met)	not provided [RCV005244241]	benign	11	1240959	1240959	Human		name
598128842	CV3886641	single nucleotide variant	NM_002458.3(MUC5B):c.9083C>G (p.Thr3028Arg)	not provided [RCV005244301]	benign	11	1245963	1245963	Human		name
12896264	CV389858	single nucleotide variant	NM_002458.3(MUC5B):c.7826T>C (p.Leu2609Pro)	not provided [RCV004707288]\|not specified [RCV000455113]	likely benign	11	1244706	1244706	Human		name
12896807	CV389859	single nucleotide variant	NM_002458.3(MUC5B):c.7877C>G (p.Thr2626Arg)	not provided [RCV001707695]\|not specified [RCV000455850]	benign	11	1244757	1244757	Human		name
12896792	CV389866	single nucleotide variant	NM_002458.3(MUC5B):c.9010G>A (p.Ala3004Thr)	not provided [RCV004705589]\|not specified [RCV000455829]	likely benign	11	1245890	1245890	Human		name
12896366	CV389867	single nucleotide variant	NM_002458.3(MUC5B):c.9143C>T (p.Ala3048Val)	not provided [RCV004705591]\|not specified [RCV000455248]	likely benign	11	1246023	1246023	Human		name
12896799	CV389872	single nucleotide variant	NM_002458.3(MUC5B):c.9179A>C (p.Lys3060Thr)	not provided [RCV004707290]\|not specified [RCV000455836]	likely benign	11	1246059	1246059	Human		name
12896428	CV389877	single nucleotide variant	NM_002458.3(MUC5B):c.9215T>C (p.Phe3072Ser)	not provided [RCV001672767]\|not specified [RCV000455326]	benign	11	1246095	1246095	Human		name
12896664	CV389881	single nucleotide variant	NM_002458.3(MUC5B):c.9850A>G (p.Thr3284Ala)	not provided [RCV001721493]\|not specified [RCV000455653]	benign	11	1246730	1246730	Human		name
12896884	CV389911	single nucleotide variant	NM_002458.3(MUC5B):c.6182C>T (p.Ala2061Val)	not provided [RCV001618695]\|not specified [RCV000455950]	benign	11	1243062	1243062	Human		name
12895888	CV389921	single nucleotide variant	NM_002458.3(MUC5B):c.6713T>C (p.Leu2238Pro)	not provided [RCV001709651]\|not specified [RCV000454597]	benign	11	1243593	1243593	Human		name
12895766	CV389923	single nucleotide variant	NM_002458.3(MUC5B):c.7676C>T (p.Thr2559Met)	not provided [RCV001692117]\|not specified [RCV000454421]	benign	11	1244556	1244556	Human		name
12896245	CV389924	single nucleotide variant	NM_002458.3(MUC5B):c.7829C>G (p.Thr2610Ser)	not provided [RCV004718665]\|not specified [RCV000455086]	benign	11	1244709	1244709	Human		name
12896773	CV389927	single nucleotide variant	NM_002458.3(MUC5B):c.8606T>C (p.Met2869Thr)	not provided [RCV001613277]\|not specified [RCV000455802]	benign	11	1245486	1245486	Human		name
12896891	CV389934	single nucleotide variant	NM_002458.3(MUC5B):c.9452C>T (p.Thr3151Met)	not provided [RCV001643153]\|not specified [RCV000455958]	benign	11	1246332	1246332	Human		name
12896394	CV389936	single nucleotide variant	NM_002458.3(MUC5B):c.9578T>C (p.Leu3193Pro)	not provided [RCV004718668]\|not specified [RCV000455286]	benign	11	1246458	1246458	Human		name
12896852	CV389941	single nucleotide variant	NM_002458.3(MUC5B):c.9593G>C (p.Ser3198Thr)	not provided [RCV004718669]\|not specified [RCV000455913]	benign	11	1246473	1246473	Human		name
12896689	CV389943	single nucleotide variant	NM_002458.3(MUC5B):c.9617T>C (p.Ile3206Thr)	not provided [RCV004718671]\|not specified [RCV000455687]	benign	11	1246497	1246497	Human		name
12895876	CV389946	single nucleotide variant	NM_002458.3(MUC5B):c.9626G>A (p.Arg3209Lys)	not provided [RCV004718672]\|not specified [RCV000454579]	benign	11	1246506	1246506	Human		name
12896422	CV389966	single nucleotide variant	NM_002458.3(MUC5B):c.5647A>G (p.Ser1883Gly)	not provided [RCV004718663]\|not specified [RCV000455320]	benign	11	1242527	1242527	Human		name
12896879	CV389969	single nucleotide variant	NM_002458.3(MUC5B):c.5666C>T (p.Pro1889Leu)	not provided [RCV001597139]\|not specified [RCV000455944]	benign	11	1242546	1242546	Human		name
12896128	CV389973	single nucleotide variant	NM_002458.3(MUC5B):c.5822C>G (p.Thr1941Ser)	not provided [RCV004718664]\|not specified [RCV000454919]	benign	11	1242702	1242702	Human		name
12896684	CV389974	single nucleotide variant	NM_002458.3(MUC5B):c.6632G>C (p.Arg2211Pro)	not provided [RCV001683494]\|not specified [RCV000455681]	benign	11	1243512	1243512	Human		name
12896454	CV389975	single nucleotide variant	NM_002458.3(MUC5B):c.6073G>A (p.Ala2025Thr)	not provided [RCV001707694]\|not specified [RCV000455362]	benign	11	1242953	1242953	Human		name
12896648	CV389978	single nucleotide variant	NM_002458.3(MUC5B):c.6521A>G (p.Asn2174Ser)	not provided [RCV001613276]\|not specified [RCV000455636]	benign	11	1243401	1243401	Human		name
12895855	CV389982	single nucleotide variant	NM_002458.3(MUC5B):c.6581T>C (p.Met2194Thr)	not provided [RCV001653801]\|not specified [RCV000454547]	benign	11	1243461	1243461	Human		name
12896030	CV389983	single nucleotide variant	NM_002458.3(MUC5B):c.9181T>C (p.Ser3061Pro)	not provided [RCV004707291]\|not specified [RCV000454786]	likely benign	11	1246061	1246061	Human		name
12895946	CV389990	single nucleotide variant	NM_002458.3(MUC5B):c.8489C>T (p.Pro2830Leu)	not provided [RCV001712411]\|not specified [RCV000454670]	benign	11	1245369	1245369	Human		name
12896231	CV389992	single nucleotide variant	NM_002458.3(MUC5B):c.8900A>G (p.Asn2967Ser)	not provided [RCV004705588]\|not specified [RCV000455071]	likely benign	11	1245780	1245780	Human		name
12895900	CV389998	single nucleotide variant	NM_002458.3(MUC5B):c.9140C>A (p.Thr3047Asn)	not provided [RCV004705590]\|not specified [RCV000454611]	likely benign	11	1246020	1246020	Human		name
598228618	CV3986695	single nucleotide variant	NM_002458.3(MUC5B):c.9539C>A (p.Thr3180Lys)	not specified [RCV005380904]	uncertain significance	11	1246419	1246419	Human		name
598228626	CV3986696	single nucleotide variant	NM_002458.3(MUC5B):c.9470C>T (p.Thr3157Ile)	not specified [RCV005380905]	uncertain significance	11	1246350	1246350	Human		name
598263712	CV3986703	single nucleotide variant	NM_002458.3(MUC5B):c.9997T>A (p.Trp3333Arg)	not specified [RCV005387540]	likely benign	11	1246877	1246877	Human		name
598228668	CV3986705	single nucleotide variant	NM_002458.3(MUC5B):c.9325C>G (p.Leu3109Val)	not specified [RCV005380910]	uncertain significance	11	1246205	1246205	Human		name
598228685	CV3986707	single nucleotide variant	NM_002458.3(MUC5B):c.8156T>C (p.Leu2719Pro)	not specified [RCV005380912]	uncertain significance	11	1245036	1245036	Human		name
598263718	CV3986714	single nucleotide variant	NM_002458.3(MUC5B):c.9527C>G (p.Pro3176Arg)	not specified [RCV005387542]	uncertain significance	11	1246407	1246407	Human		name
598228737	CV3986715	single nucleotide variant	NM_002458.3(MUC5B):c.4955C>A (p.Thr1652Asn)	not specified [RCV005380918]	uncertain significance	11	1241835	1241835	Human		name
598228784	CV3986724	single nucleotide variant	NM_002458.3(MUC5B):c.3682T>C (p.Tyr1228His)	not specified [RCV005380924]	likely benign	11	1239897	1239897	Human		name
598228809	CV3986728	single nucleotide variant	NM_002458.3(MUC5B):c.5237C>T (p.Ala1746Val)	not specified [RCV005380927]	uncertain significance	11	1242117	1242117	Human		name
598263732	CV3986729	single nucleotide variant	NM_002458.3(MUC5B):c.7703C>T (p.Ser2568Phe)	not specified [RCV005387547]	uncertain significance	11	1244583	1244583	Human		name
598263741	CV3986734	single nucleotide variant	NM_002458.3(MUC5B):c.4617C>G (p.His1539Gln)	not specified [RCV005387550]	uncertain significance	11	1241497	1241497	Human		name
598263744	CV3986735	single nucleotide variant	NM_002458.3(MUC5B):c.9536C>G (p.Ser3179Cys)	not specified [RCV005387551]	uncertain significance	11	1246416	1246416	Human		name
598228849	CV3986738	single nucleotide variant	NM_002458.3(MUC5B):c.4567C>T (p.Leu1523Phe)	not specified [RCV005380932]	uncertain significance	11	1241447	1241447	Human		name
598228882	CV3986742	single nucleotide variant	NM_002458.3(MUC5B):c.7838C>A (p.Thr2613Asn)	not specified [RCV005380936]	uncertain significance	11	1244718	1244718	Human		name
598228900	CV3986744	single nucleotide variant	NM_002458.3(MUC5B):c.4849G>A (p.Glu1617Lys)	not specified [RCV005380938]	uncertain significance	11	1241729	1241729	Human		name
598228933	CV3986748	single nucleotide variant	NM_002458.3(MUC5B):c.6935T>G (p.Met2312Arg)	not specified [RCV005380942]	uncertain significance	11	1243815	1243815	Human		name
598228940	CV3986749	single nucleotide variant	NM_002458.3(MUC5B):c.4254C>G (p.His1418Gln)	not specified [RCV005380943]	uncertain significance	11	1241134	1241134	Human		name
598228956	CV3986751	single nucleotide variant	NM_002458.3(MUC5B):c.7097C>T (p.Pro2366Leu)	not specified [RCV005380945]	uncertain significance	11	1243977	1243977	Human		name
598228971	CV3986753	single nucleotide variant	NM_002458.3(MUC5B):c.8768C>T (p.Pro2923Leu)	not specified [RCV005380947]	uncertain significance	11	1245648	1245648	Human		name
598228978	CV3986754	single nucleotide variant	NM_002458.3(MUC5B):c.7240T>G (p.Cys2414Gly)	not specified [RCV005380948]	uncertain significance	11	1244120	1244120	Human		name
598228994	CV3986756	single nucleotide variant	NM_002458.3(MUC5B):c.5747C>A (p.Thr1916Lys)	not specified [RCV005380950]	uncertain significance	11	1242627	1242627	Human		name
598263747	CV3986757	single nucleotide variant	NM_002458.3(MUC5B):c.6016T>C (p.Ser2006Pro)	not specified [RCV005387552]	uncertain significance	11	1242896	1242896	Human		name
598263758	CV3986761	single nucleotide variant	NM_002458.3(MUC5B):c.6862C>A (p.Pro2288Thr)	not specified [RCV005387556]	likely benign	11	1243742	1243742	Human		name
598229002	CV3986763	single nucleotide variant	NM_002458.3(MUC5B):c.5875C>A (p.Pro1959Thr)	not specified [RCV005380951]	uncertain significance	11	1242755	1242755	Human		name
598229020	CV3986766	single nucleotide variant	NM_002458.3(MUC5B):c.8000C>G (p.Thr2667Arg)	not specified [RCV005380954]	uncertain significance	11	1244880	1244880	Human		name
598229027	CV3986767	single nucleotide variant	NM_002458.3(MUC5B):c.8536A>G (p.Ser2846Gly)	not specified [RCV005380955]	uncertain significance	11	1245416	1245416	Human		name
598229035	CV3986768	single nucleotide variant	NM_002458.3(MUC5B):c.4211G>C (p.Gly1404Ala)	not specified [RCV005380956]	uncertain significance	11	1241091	1241091	Human		name
598229048	CV3986770	single nucleotide variant	NM_002458.3(MUC5B):c.3487G>A (p.Gly1163Ser)	not specified [RCV005380958]	uncertain significance	11	1239470	1239470	Human		name
598229053	CV3986771	single nucleotide variant	NM_002458.3(MUC5B):c.7951T>A (p.Ser2651Thr)	not specified [RCV005380959]	uncertain significance	11	1244831	1244831	Human		name
598229077	CV3986775	single nucleotide variant	NM_002458.3(MUC5B):c.3228C>A (p.Phe1076Leu)	not specified [RCV005380963]	uncertain significance	11	1237095	1237095	Human		name
598263766	CV3986778	single nucleotide variant	NM_002458.3(MUC5B):c.7102G>A (p.Val2368Ile)	not specified [RCV005387559]	uncertain significance	11	1243982	1243982	Human		name
598263769	CV3986779	single nucleotide variant	NM_002458.3(MUC5B):c.9788C>A (p.Ser3263Tyr)	not specified [RCV005387560]	uncertain significance	11	1246668	1246668	Human		name
598229098	CV3986782	single nucleotide variant	NM_002458.3(MUC5B):c.4207C>G (p.Arg1403Gly)	not specified [RCV005380966]	uncertain significance	11	1241087	1241087	Human		name
598229105	CV3986783	single nucleotide variant	NM_002458.3(MUC5B):c.5809A>G (p.Lys1937Glu)	not specified [RCV005380967]	uncertain significance	11	1242689	1242689	Human		name
598229112	CV3986784	single nucleotide variant	NM_002458.3(MUC5B):c.6494C>T (p.Thr2165Ile)	not specified [RCV005380968]	uncertain significance	11	1243374	1243374	Human		name
598263777	CV3986792	single nucleotide variant	NM_002458.3(MUC5B):c.3185C>T (p.Pro1062Leu)	not specified [RCV005387563]	uncertain significance	11	1237052	1237052	Human		name
598229185	CV3986796	single nucleotide variant	NM_002458.3(MUC5B):c.7045G>A (p.Gly2349Arg)	not specified [RCV005380978]	uncertain significance	11	1243925	1243925	Human		name
598263780	CV3986799	single nucleotide variant	NM_002458.3(MUC5B):c.9796A>G (p.Thr3266Ala)	not specified [RCV005387564]	uncertain significance	11	1246676	1246676	Human		name
598263785	CV3986801	single nucleotide variant	NM_002458.3(MUC5B):c.5803C>A (p.Pro1935Thr)	not specified [RCV005387566]	uncertain significance	11	1242683	1242683	Human		name
617152990	CV4020821	single nucleotide variant	NM_002458.3(MUC5B):c.7882C>T (p.Arg2628Cys)	not provided [RCV005428574]	benign	11	1244762	1244762	Human		name
13539006	CV496563	single nucleotide variant	NM_002458.3(MUC5B):c.3926C>T (p.Thr1309Met)	Interstitial lung disease 2 [RCV002476349]\|not specified [RCV000612676]	likely benign	11	1240331	1240331	Human	1	name
8633896	CV89112	single nucleotide variant	NM_002458.3(MUC5B):c.6647C>T (p.Ser2216Leu)	not specified [RCV004318370]	uncertain significance\|not provided	11	1243527	1243527	Human		name
9688488	CV175665	single nucleotide variant	NM_002458.3(MUC5B):c.15542T>C (p.Leu5181Pro)	not provided [RCV004718053]\|not specified [RCV000151046]	benign	11	1254758	1254758	Human		name
9691815	CV175669	single nucleotide variant	NM_002458.3(MUC5B):c.16273G>A (p.Gly5425Arg)	not specified [RCV000151049]	likely benign	11	1257533	1257533	Human		name
9687879	CV175670	single nucleotide variant	NM_002458.3(MUC5B):c.16422G>C (p.Glu5474Asp)	not provided [RCV004718058]\|not specified [RCV000151052]	benign	11	1257682	1257682	Human		name
9687880	CV175671	single nucleotide variant	NM_002458.3(MUC5B):c.16660G>A (p.Asp5554Asn)	MUC5B-related disorder [RCV004758653]\|not provided [RCV004718059]\|not specified [RCV000151053]	benign	11	1259008	1259008	Human	1	name , alternate_id
9688489	CV175806	single nucleotide variant	NM_002458.3(MUC5B):c.15817G>C (p.Ala5273Pro)	not provided [RCV004718054]\|not specified [RCV000151047]	benign	11	1255193	1255193	Human		name
9687878	CV175810	single nucleotide variant	NM_002458.3(MUC5B):c.16306G>A (p.Val5436Met)	not provided [RCV004718057]\|not specified [RCV000151051]	benign	11	1257566	1257566	Human		name
407503809	CV3457915	single nucleotide variant	NM_002458.3(MUC5B):c.10021A>G (p.Thr3341Ala)	not specified [RCV004645593]	uncertain significance	11	1246901	1246901	Human		name
597639676	CV3557744	single nucleotide variant	NM_002458.3(MUC5B):c.15848C>G (p.Thr5283Ser)	not specified [RCV004825187]	likely benign	11	1255224	1255224	Human		name
597639681	CV3557746	single nucleotide variant	NM_002458.3(MUC5B):c.10831C>A (p.Gln3611Lys)	not specified [RCV004825188]	uncertain significance	11	1247711	1247711	Human		name
597639692	CV3557757	single nucleotide variant	NM_002458.3(MUC5B):c.13988C>T (p.Ser4663Phe)	not specified [RCV004825190]	uncertain significance	11	1250868	1250868	Human		name
597639704	CV3557762	single nucleotide variant	NM_002458.3(MUC5B):c.13099A>C (p.Thr4367Pro)	not specified [RCV004825192]	uncertain significance	11	1249979	1249979	Human		name
597639708	CV3557764	single nucleotide variant	NM_002458.3(MUC5B):c.15833G>A (p.Ser5278Asn)	not specified [RCV004825193]	uncertain significance	11	1255209	1255209	Human		name
597643857	CV3557768	single nucleotide variant	NM_002458.3(MUC5B):c.16604C>A (p.Thr5535Asn)	not specified [RCV004825872]	uncertain significance	11	1258952	1258952	Human		name
597639717	CV3557769	single nucleotide variant	NM_002458.3(MUC5B):c.14029C>G (p.Pro4677Ala)	not specified [RCV004825195]	uncertain significance	11	1250909	1250909	Human		name
597643863	CV3557772	single nucleotide variant	NM_002458.3(MUC5B):c.10253T>C (p.Val3418Ala)	not specified [RCV004825873]	uncertain significance	11	1247133	1247133	Human		name
597643892	CV3557777	single nucleotide variant	NM_002458.3(MUC5B):c.17008C>G (p.Gln5670Glu)	not specified [RCV004825878]	uncertain significance	11	1260667	1260667	Human		name
597643903	CV3557779	single nucleotide variant	NM_002458.3(MUC5B):c.13895C>T (p.Thr4632Ile)	not specified [RCV004825880]	uncertain significance	11	1250775	1250775	Human		name
597643910	CV3557780	single nucleotide variant	NM_002458.3(MUC5B):c.10139G>C (p.Ser3380Thr)	not specified [RCV004825881]	uncertain significance	11	1247019	1247019	Human		name
597643916	CV3557782	single nucleotide variant	NM_002458.3(MUC5B):c.12427C>G (p.Pro4143Ala)	not specified [RCV004825882]	uncertain significance	11	1249307	1249307	Human		name
597639741	CV3557784	single nucleotide variant	NM_002458.3(MUC5B):c.15652G>A (p.Glu5218Lys)	not specified [RCV004825199]	uncertain significance	11	1254868	1254868	Human		name
597643928	CV3557785	single nucleotide variant	NM_002458.3(MUC5B):c.13790C>T (p.Thr4597Ile)	not specified [RCV004825884]	uncertain significance	11	1250670	1250670	Human		name
597643938	CV3557787	single nucleotide variant	NM_002458.3(MUC5B):c.11135C>G (p.Pro3712Arg)	not specified [RCV004825886]	uncertain significance	11	1248015	1248015	Human		name
597643943	CV3557788	single nucleotide variant	NM_002458.3(MUC5B):c.10372T>G (p.Ser3458Ala)	not specified [RCV004825887]	uncertain significance	11	1247252	1247252	Human		name
597643956	CV3557791	single nucleotide variant	NM_002458.3(MUC5B):c.11596C>A (p.Pro3866Thr)	not specified [RCV004825889]	uncertain significance	11	1248476	1248476	Human		name
597643963	CV3557793	single nucleotide variant	NM_002458.3(MUC5B):c.15041G>A (p.Arg5014Gln)	not specified [RCV004825890]	uncertain significance	11	1252520	1252520	Human		name
597643995	CV3557798	single nucleotide variant	NM_002458.3(MUC5B):c.14908T>C (p.Tyr4970His)	not specified [RCV004825895]	uncertain significance	11	1252387	1252387	Human		name
597644004	CV3557800	single nucleotide variant	NM_002458.3(MUC5B):c.11770A>C (p.Thr3924Pro)	not specified [RCV004825896]	uncertain significance	11	1248650	1248650	Human		name
597644022	CV3557804	single nucleotide variant	NM_002458.3(MUC5B):c.14216C>G (p.Thr4739Arg)	not specified [RCV004825899]	uncertain significance	11	1251096	1251096	Human		name
597639774	CV3557807	single nucleotide variant	NM_002458.3(MUC5B):c.14101G>T (p.Gly4701Trp)	not specified [RCV004825205]	uncertain significance	11	1250981	1250981	Human		name
597644057	CV3557812	single nucleotide variant	NM_002458.3(MUC5B):c.16279C>T (p.Arg5427Trp)	not specified [RCV004825905]	uncertain significance	11	1257539	1257539	Human		name
597639927	CV3557817	single nucleotide variant	NM_002458.3(MUC5B):c.15148G>A (p.Val5050Met)	not specified [RCV004825207]	uncertain significance	11	1252911	1252911	Human		name
597644093	CV3557820	single nucleotide variant	NM_002458.3(MUC5B):c.14177C>G (p.Ser4726Cys)	not specified [RCV004825911]	uncertain significance	11	1251057	1251057	Human		name
597644103	CV3557822	single nucleotide variant	NM_002458.3(MUC5B):c.13885A>G (p.Thr4629Ala)	not specified [RCV004825913]	uncertain significance	11	1250765	1250765	Human		name
597644145	CV3557829	single nucleotide variant	NM_002458.3(MUC5B):c.15589G>A (p.Val5197Ile)	not specified [RCV004825919]	likely benign	11	1254805	1254805	Human		name
597644165	CV3557833	single nucleotide variant	NM_002458.3(MUC5B):c.11257G>T (p.Val3753Leu)	not specified [RCV004825922]	uncertain significance	11	1248137	1248137	Human		name
597643334	CV3561573	single nucleotide variant	NM_002458.3(MUC5B):c.15760G>A (p.Asp5254Asn)	not specified [RCV004825809]	uncertain significance	11	1255136	1255136	Human		name
597643348	CV3561575	single nucleotide variant	NM_002458.3(MUC5B):c.14891G>A (p.Arg4964Gln)	not specified [RCV004825811]	uncertain significance	11	1252370	1252370	Human		name
597643361	CV3561578	single nucleotide variant	NM_002458.3(MUC5B):c.11468C>A (p.Thr3823Lys)	not specified [RCV004825814]	uncertain significance	11	1248348	1248348	Human		name
597643373	CV3561580	single nucleotide variant	NM_002458.3(MUC5B):c.12275C>G (p.Ala4092Gly)	not specified [RCV004825816]	uncertain significance	11	1249155	1249155	Human		name
597643412	CV3561588	single nucleotide variant	NM_002458.3(MUC5B):c.12014C>T (p.Pro4005Leu)	not specified [RCV004825822]	likely benign	11	1248894	1248894	Human		name
597643419	CV3561592	single nucleotide variant	NM_002458.3(MUC5B):c.15973G>C (p.Glu5325Gln)	not specified [RCV004825823]	uncertain significance	11	1255465	1255465	Human		name
597643425	CV3561594	single nucleotide variant	NM_002458.3(MUC5B):c.13022C>G (p.Thr4341Ser)	not specified [RCV004825824]	uncertain significance	11	1249902	1249902	Human		name
597643437	CV3561596	single nucleotide variant	NM_002458.3(MUC5B):c.12752C>T (p.Thr4251Ile)	not specified [RCV004825826]	uncertain significance	11	1249632	1249632	Human		name
597643462	CV3561600	single nucleotide variant	NM_002458.3(MUC5B):c.14814C>A (p.His4938Gln)	not specified [RCV004825830]	uncertain significance	11	1251694	1251694	Human		name
597643468	CV3561601	single nucleotide variant	NM_002458.3(MUC5B):c.11221G>A (p.Ala3741Thr)	not specified [RCV004825831]	uncertain significance	11	1248101	1248101	Human		name
597639920	CV3561604	single nucleotide variant	NM_002458.3(MUC5B):c.12260C>T (p.Pro4087Leu)	not specified [RCV004825174]	uncertain significance	11	1249140	1249140	Human		name
597643502	CV3561609	single nucleotide variant	NM_002458.3(MUC5B):c.16414C>T (p.Arg5472Trp)	not specified [RCV004825837]	uncertain significance	11	1257674	1257674	Human		name
597643515	CV3561611	single nucleotide variant	NM_002458.3(MUC5B):c.11213C>T (p.Thr3738Met)	not specified [RCV004825839]	uncertain significance	11	1248093	1248093	Human		name
597643521	CV3561612	single nucleotide variant	NM_002458.3(MUC5B):c.10397C>T (p.Thr3466Met)	not specified [RCV004825840]	uncertain significance	11	1247277	1247277	Human		name
597675280	CV3723723	single nucleotide variant	NM_002458.3(MUC5B):c.11465C>A (p.Ala3822Asp)	Interstitial lung disease 2 [RCV005044424]\|not specified [RCV005387347]	uncertain significance	11	1248345	1248345	Human	1	name
598128944	CV3886746	single nucleotide variant	NM_002458.3(MUC5B):c.12020C>T (p.Thr4007Ile)	not provided [RCV005244406]	likely benign	11	1248900	1248900	Human		name
598129017	CV3886820	single nucleotide variant	NM_002458.3(MUC5B):c.14063C>T (p.Thr4688Met)	not provided [RCV005244480]	likely benign	11	1250943	1250943	Human		name
598129590	CV3887007	single nucleotide variant	NM_002458.3(MUC5B):c.12365C>T (p.Thr4122Met)	not provided [RCV005245067]	likely benign	11	1249245	1249245	Human		name
598263702	CV3986698	single nucleotide variant	NM_002458.3(MUC5B):c.14752G>A (p.Val4918Met)	not specified [RCV005387537]	likely benign	11	1251632	1251632	Human		name
598263705	CV3986699	single nucleotide variant	NM_002458.3(MUC5B):c.14286G>T (p.Trp4762Cys)	not specified [RCV005387538]	uncertain significance	11	1251166	1251166	Human		name
598263708	CV3986701	single nucleotide variant	NM_002458.3(MUC5B):c.11312C>A (p.Ser3771Tyr)	not specified [RCV005387539]	uncertain significance	11	1248192	1248192	Human		name
598228652	CV3986702	single nucleotide variant	NM_002458.3(MUC5B):c.12437G>A (p.Gly4146Glu)	not specified [RCV005380908]	uncertain significance	11	1249317	1249317	Human		name
598228660	CV3986704	single nucleotide variant	NM_002458.3(MUC5B):c.12524G>A (p.Arg4175His)	not specified [RCV005380909]	uncertain significance	11	1249404	1249404	Human		name
598228693	CV3986708	single nucleotide variant	NM_002458.3(MUC5B):c.10373C>T (p.Ser3458Phe)	not specified [RCV005380913]	uncertain significance	11	1247253	1247253	Human		name
598228712	CV3986710	single nucleotide variant	NM_002458.3(MUC5B):c.15436G>A (p.Val5146Ile)	not specified [RCV005380915]	likely benign	11	1254310	1254310	Human		name
598263715	CV3986712	single nucleotide variant	NM_002458.3(MUC5B):c.16033A>G (p.Ser5345Gly)	not specified [RCV005387541]	uncertain significance	11	1255525	1255525	Human		name
598228744	CV3986716	single nucleotide variant	NM_002458.3(MUC5B):c.12803C>T (p.Thr4268Ile)	not specified [RCV005380919]	uncertain significance	11	1249683	1249683	Human		name
598263721	CV3986717	single nucleotide variant	NM_002458.3(MUC5B):c.15403G>A (p.Ala5135Thr)	not specified [RCV005387543]	uncertain significance	11	1254277	1254277	Human		name
598228750	CV3986718	single nucleotide variant	NM_002458.3(MUC5B):c.14678C>G (p.Thr4893Arg)	not specified [RCV005380920]	uncertain significance	11	1251558	1251558	Human		name
598263724	CV3986719	single nucleotide variant	NM_002458.3(MUC5B):c.13157C>T (p.Pro4386Leu)	not specified [RCV005387544]	uncertain significance	11	1250037	1250037	Human		name
598263725	CV3986721	single nucleotide variant	NM_002458.3(MUC5B):c.11326G>T (p.Ala3776Ser)	not specified [RCV005387545]	uncertain significance	11	1248206	1248206	Human		name
598228766	CV3986722	single nucleotide variant	NM_002458.3(MUC5B):c.11482C>G (p.Pro3828Ala)	not specified [RCV005380922]	uncertain significance	11	1248362	1248362	Human		name
598228776	CV3986723	single nucleotide variant	NM_002458.3(MUC5B):c.11678C>G (p.Thr3893Arg)	not specified [RCV005380923]	uncertain significance	11	1248558	1248558	Human		name
598228791	CV3986725	single nucleotide variant	NM_002458.3(MUC5B):c.11224T>G (p.Ser3742Ala)	not specified [RCV005380925]	uncertain significance	11	1248104	1248104	Human		name
598263728	CV3986726	single nucleotide variant	NM_002458.3(MUC5B):c.16964A>G (p.Glu5655Gly)	not specified [RCV005387546]	uncertain significance	11	1260391	1260391	Human		name
598263738	CV3986731	single nucleotide variant	NM_002458.3(MUC5B):c.11030C>T (p.Thr3677Ile)	not specified [RCV005387549]	uncertain significance	11	1247910	1247910	Human		name
598228818	CV3986732	single nucleotide variant	NM_002458.3(MUC5B):c.11249C>A (p.Thr3750Asn)	not specified [RCV005380928]	uncertain significance	11	1248129	1248129	Human		name
598228827	CV3986733	single nucleotide variant	NM_002458.3(MUC5B):c.10130C>G (p.Pro3377Arg)	not specified [RCV005380929]	uncertain significance	11	1247010	1247010	Human		name
598228833	CV3986736	single nucleotide variant	NM_002458.3(MUC5B):c.10007C>G (p.Thr3336Arg)	not specified [RCV005380930]	uncertain significance	11	1246887	1246887	Human		name
598228857	CV3986739	single nucleotide variant	NM_002458.3(MUC5B):c.16942G>A (p.Gly5648Ser)	not specified [RCV005380933]	uncertain significance	11	1260369	1260369	Human		name
598228866	CV3986740	single nucleotide variant	NM_002458.3(MUC5B):c.15952G>A (p.Asp5318Asn)	not specified [RCV005380934]	uncertain significance	11	1255444	1255444	Human		name
598228892	CV3986743	single nucleotide variant	NM_002458.3(MUC5B):c.12850A>C (p.Ser4284Arg)	not specified [RCV005380937]	uncertain significance	11	1249730	1249730	Human		name
598228917	CV3986746	single nucleotide variant	NM_002458.3(MUC5B):c.13625C>T (p.Thr4542Ile)	not specified [RCV005380940]	uncertain significance	11	1250505	1250505	Human		name
598228925	CV3986747	single nucleotide variant	NM_002458.3(MUC5B):c.11201C>T (p.Pro3734Leu)	not specified [RCV005380941]	uncertain significance	11	1248081	1248081	Human		name
598228948	CV3986750	single nucleotide variant	NM_002458.3(MUC5B):c.11422C>T (p.Arg3808Cys)	not specified [RCV005380944]	uncertain significance	11	1248302	1248302	Human		name
598228987	CV3986755	single nucleotide variant	NM_002458.3(MUC5B):c.10876C>T (p.Pro3626Ser)	not specified [RCV005380949]	likely benign	11	1247756	1247756	Human		name
598263749	CV3986758	single nucleotide variant	NM_002458.3(MUC5B):c.10381C>G (p.Pro3461Ala)	not specified [RCV005387553]	uncertain significance	11	1247261	1247261	Human		name
598263755	CV3986760	single nucleotide variant	NM_002458.3(MUC5B):c.16325T>C (p.Val5442Ala)	not specified [RCV005387555]	uncertain significance	11	1257585	1257585	Human		name
598263761	CV3986762	single nucleotide variant	NM_002458.3(MUC5B):c.16396G>A (p.Val5466Ile)	not specified [RCV005387557]	uncertain significance	11	1257656	1257656	Human		name
598229008	CV3986764	single nucleotide variant	NM_002458.3(MUC5B):c.13736C>A (p.Ala4579Asp)	not specified [RCV005380952]	uncertain significance	11	1250616	1250616	Human		name
598229014	CV3986765	single nucleotide variant	NM_002458.3(MUC5B):c.13937C>T (p.Thr4646Ile)	not specified [RCV005380953]	uncertain significance	11	1250817	1250817	Human		name
598229042	CV3986769	single nucleotide variant	NM_002458.3(MUC5B):c.14447C>T (p.Thr4816Ile)	not specified [RCV005380957]	uncertain significance	11	1251327	1251327	Human		name
598229060	CV3986772	single nucleotide variant	NM_002458.3(MUC5B):c.14543T>C (p.Leu4848Pro)	not specified [RCV005380960]	uncertain significance	11	1251423	1251423	Human		name
598229070	CV3986774	single nucleotide variant	NM_002458.3(MUC5B):c.13904C>G (p.Ser4635Cys)	not specified [RCV005380962]	uncertain significance	11	1250784	1250784	Human		name
598263764	CV3986776	single nucleotide variant	NM_002458.3(MUC5B):c.14585G>A (p.Gly4862Asp)	not specified [RCV005387558]	uncertain significance	11	1251465	1251465	Human		name
598229083	CV3986777	single nucleotide variant	NM_002458.3(MUC5B):c.12445G>A (p.Gly4149Ser)	not specified [RCV005380964]	uncertain significance	11	1249325	1249325	Human		name
598229128	CV3986786	single nucleotide variant	NM_002458.3(MUC5B):c.11861T>C (p.Ile3954Thr)	not specified [RCV005380970]	uncertain significance	11	1248741	1248741	Human		name
598263774	CV3986787	single nucleotide variant	NM_002458.3(MUC5B):c.12235C>T (p.Pro4079Ser)	not specified [RCV005387562]	uncertain significance	11	1249115	1249115	Human		name
598229135	CV3986788	single nucleotide variant	NM_002458.3(MUC5B):c.16025G>C (p.Gly5342Ala)	not specified [RCV005380971]	uncertain significance	11	1255517	1255517	Human		name
598229143	CV3986789	single nucleotide variant	NM_002458.3(MUC5B):c.11755C>A (p.Leu3919Met)	not specified [RCV005380972]	uncertain significance	11	1248635	1248635	Human		name
598229148	CV3986790	single nucleotide variant	NM_002458.3(MUC5B):c.11017A>G (p.Ser3673Gly)	not specified [RCV005380973]	uncertain significance	11	1247897	1247897	Human		name
598229156	CV3986791	single nucleotide variant	NM_002458.3(MUC5B):c.13105A>G (p.Lys4369Glu)	not specified [RCV005380974]	uncertain significance	11	1249985	1249985	Human		name
598229163	CV3986793	single nucleotide variant	NM_002458.3(MUC5B):c.11234A>C (p.Gln3745Pro)	not specified [RCV005380975]	likely benign	11	1248114	1248114	Human		name
598229178	CV3986795	single nucleotide variant	NM_002458.3(MUC5B):c.11123C>A (p.Ser3708Tyr)	not specified [RCV005380977]	uncertain significance	11	1248003	1248003	Human		name
598229198	CV3986798	single nucleotide variant	NM_002458.3(MUC5B):c.17228C>T (p.Pro5743Leu)	not specified [RCV005380980]	uncertain significance	11	1261547	1261547	Human		name
598263783	CV3986800	single nucleotide variant	NM_002458.3(MUC5B):c.16183C>T (p.Pro5395Ser)	not specified [RCV005387565]	uncertain significance	11	1256717	1256717	Human		name
598263788	CV3986802	single nucleotide variant	NM_002458.3(MUC5B):c.15842C>T (p.Thr5281Ile)	not specified [RCV005387567]	uncertain significance	11	1255218	1255218	Human		name
401909939	CV2806625	single nucleotide variant	NM_002458.3(MUC5B):c.14683C>T (p.Pro4895Ser)	MUC5B-related disorder [RCV004758935]\|not provided [RCV003424722]	benign\|likely benign	11	1251563	1251563	Human	1	alternate_id
408367704	CV3512014	single nucleotide variant	NM_002458.3(MUC5B):c.14690C>T (p.Ser4897Leu)	MUC5B-related disorder [RCV004759115]	benign	11	1251570	1251570	Human		trait , alternate_id

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