Col14a1 Variant Search Result - Rat Genome Database

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275 records found for search term Col14a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150510462	CV1211703	single nucleotide variant	NM_021110.4(COL14A1):c.712+81C>T	not provided [RCV001597598]	benign	8	120198011	120198011	Human		name
150511764	CV1212830	single nucleotide variant	NM_021110.4(COL14A1):c.89-169G>T	not provided [RCV001598062]	benign	8	120157961	120157961	Human		name
150468611	CV1218938	single nucleotide variant	NM_021110.4(COL14A1):c.2480-9T>C	not provided [RCV001614690]	benign	8	120247604	120247604	Human		name
150449876	CV1232606	single nucleotide variant	NM_021110.4(COL14A1):c.3647-3C>T	not provided [RCV001647680]	benign	8	120280708	120280708	Human	1	name
150449876	CV1232606	single nucleotide variant	NM_021110.4(COL14A1):c.3647-3C>T	not provided [RCV001647680]	benign	8	120280708	120280709	Human	1	name
150431051	CV1235318	single nucleotide variant	NM_021110.4(COL14A1):c.713-72G>A	not provided [RCV001641688]	benign	8	120199330	120199330	Human		name
150511961	CV1242843	single nucleotide variant	NM_021110.4(COL14A1):c.349+29C>G	not provided [RCV001661197]	benign	8	120162598	120162598	Human		name
150471499	CV1248237	single nucleotide variant	NM_021110.4(COL14A1):c.877+42C>T	not provided [RCV001671275]	benign	8	120199608	120199608	Human		name
150468812	CV1257106	single nucleotide variant	NM_021110.4(COL14A1):c.437-30A>C	not provided [RCV001670752]	benign	8	120196761	120196761	Human		name
15103122	CV730535	single nucleotide variant	NM_021110.4(COL14A1):c.5312-6C>T	not provided [RCV000892612]	benign	8	120371146	120371146	Human		name
15129801	CV744283	single nucleotide variant	NM_021110.4(COL14A1):c.1737+9C>T	not provided [RCV000897502]	likely benign	8	120216499	120216499	Human		name
150500703	CV1213208	single nucleotide variant	NM_021110.4(COL14A1):c.436+178G>A	not provided [RCV001594620]	benign	8	120168425	120168425	Human		name
150505153	CV1213459	single nucleotide variant	NM_021110.4(COL14A1):c.-37-178C>T	not provided [RCV001595715]	benign	8	120147628	120147628	Human		name
150467333	CV1218452	single nucleotide variant	NM_021110.4(COL14A1):c.3481+95G>A	not provided [RCV001614489]	benign	8	120278673	120278673	Human		name
150478903	CV1218867	single nucleotide variant	NM_021110.4(COL14A1):c.4314+35A>T	not provided [RCV001616495]	benign	8	120297623	120297623	Human		name
150453103	CV1219793	deletion	NM_021110.4(COL14A1):c.206-103del	not provided [RCV001612174]	benign	8	120162323	120162323	Human		name
150488032	CV1225998	single nucleotide variant	NM_021110.4(COL14A1):c.205+318G>A	not provided [RCV001618159]	benign	8	120158564	120158564	Human		name
150514411	CV1228206	single nucleotide variant	NM_021110.4(COL14A1):c.3646+69G>A	not provided [RCV001638484]	benign	8	120280168	120280168	Human		name
150443955	CV1232945	single nucleotide variant	NM_021110.4(COL14A1):c.2752+71T>C	not provided [RCV001645617]	benign	8	120250837	120250837	Human		name
150431002	CV1243551	single nucleotide variant	NM_021110.4(COL14A1):c.3968-54C>A	not provided [RCV001663170]	benign	8	120285807	120285807	Human		name
150431434	CV1243694	single nucleotide variant	NM_021110.4(COL14A1):c.4237-71A>T	not provided [RCV001663314]	benign	8	120297440	120297440	Human		name
150434091	CV1243865	single nucleotide variant	NM_021110.4(COL14A1):c.4713+28A>G	not provided [RCV001665071]	benign	8	120332222	120332222	Human		name
150494084	CV1257688	single nucleotide variant	NM_021110.4(COL14A1):c.4821+93A>T	not provided [RCV001675361]	benign	8	120341453	120341453	Human		name
150503396	CV1257787	single nucleotide variant	NM_021110.4(COL14A1):c.436+181C>T	not provided [RCV001677475]	benign	8	120168428	120168428	Human		name
150481193	CV1258872	single nucleotide variant	NM_021110.4(COL14A1):c.3967+28A>G	not provided [RCV001686002]	benign	8	120283806	120283806	Human		name
150471836	CV1259194	single nucleotide variant	NM_021110.4(COL14A1):c.3824+33G>A	not provided [RCV001684439]	benign	8	120281092	120281092	Human		name
150454471	CV1260673	single nucleotide variant	NM_021110.4(COL14A1):c.4552-99C>T	not provided [RCV001681166]	benign	8	120315434	120315434	Human		name
150439243	CV1264943	single nucleotide variant	NM_021110.4(COL14A1):c.2603-81A>G	not provided [RCV001678936]	benign	8	120250536	120250536	Human		name
8649923	CV126497	single nucleotide variant	NM_021110.2(COL14A1):c.349+269A>T	Lung cancer [RCV000106984]	uncertain significance	8	120162838	120162838	Human		name
150438768	CV1266672	single nucleotide variant	NM_021110.4(COL14A1):c.1192-76G>A	not provided [RCV001690107]	benign	8	120208156	120208156	Human		name
150489556	CV1268920	single nucleotide variant	NM_021110.4(COL14A1):c.3824+78A>G	not provided [RCV001687484]	benign	8	120281137	120281137	Human		name
150467765	CV1269286	single nucleotide variant	NM_021110.4(COL14A1):c.2869+22C>T	not provided [RCV001694694]	benign	8	120255378	120255378	Human		name
150484968	CV1273871	single nucleotide variant	NM_021110.4(COL14A1):c.592+206C>T	not provided [RCV001698615]	benign	8	120197152	120197152	Human		name
150485362	CV1273883	single nucleotide variant	NM_021110.4(COL14A1):c.2602+46T>G	not provided [RCV001698706]	benign	8	120247781	120247781	Human		name
150471257	CV1280939	single nucleotide variant	NM_021110.4(COL14A1):c.4821+52A>G	not provided [RCV001713150]	benign	8	120341412	120341412	Human		name
150512201	CV1284888	single nucleotide variant	NM_021110.4(COL14A1):c.4714-59T>G	not provided [RCV001721757]	benign	8	120332605	120332605	Human		name
15162329	CV744391	single nucleotide variant	NM_021110.4(COL14A1):c.2603-10T>C	not provided [RCV000903530]	likely benign	8	120250607	120250607	Human		name
150333514	CV1171809	single nucleotide variant	NM_021110.4(COL14A1):c.2869+134A>G	not provided [RCV001539534]	benign	8	120255490	120255490	Human		name
150445454	CV1215496	single nucleotide variant	NM_021110.4(COL14A1):c.1865-320T>A	not provided [RCV001611089]	benign	8	120226307	120226307	Human		name
150461188	CV1215775	single nucleotide variant	NM_021110.4(COL14A1):c.4821+283G>C	not provided [RCV001613477]	benign	8	120341643	120341643	Human		name
150469793	CV1219133	single nucleotide variant	NM_021110.4(COL14A1):c.2869+141A>G	not provided [RCV001614885]	benign	8	120255497	120255497	Human		name
150497334	CV1219389	single nucleotide variant	NM_021110.4(COL14A1):c.4822-290T>C	not provided [RCV001620058]	benign	8	120342090	120342090	Human		name
150482079	CV1222279	single nucleotide variant	NM_021110.4(COL14A1):c.4660-294T>C	not provided [RCV001617077]	benign	8	120331847	120331847	Human		name
150497930	CV1224051	single nucleotide variant	NM_021110.4(COL14A1):c.3214-305A>T	not provided [RCV001620163]	benign	8	120277806	120277806	Human		name
150500582	CV1224818	single nucleotide variant	NM_021110.4(COL14A1):c.1322-124C>G	not provided [RCV001620650]	benign	8	120209632	120209632	Human		name
150493579	CV1225692	single nucleotide variant	NM_021110.4(COL14A1):c.3337+100T>A	not provided [RCV001619208]	benign	8	120278334	120278334	Human		name
150516606	CV1227146	single nucleotide variant	NM_021110.4(COL14A1):c.4888+166G>A	not provided [RCV001639244]	benign	8	120342612	120342612	Human		name
150461045	CV1234727	single nucleotide variant	NM_021110.4(COL14A1):c.4786-148G>A	not provided [RCV001649309]	benign	8	120341177	120341177	Human		name
150496644	CV1236875	single nucleotide variant	NM_021110.4(COL14A1):c.2752+127C>T	not provided [RCV001655939]	benign	8	120250893	120250893	Human		name
150464255	CV1237755	single nucleotide variant	NM_021110.4(COL14A1):c.3967+148G>A	not provided [RCV001649762]	benign	8	120283926	120283926	Human		name
150494109	CV1238802	duplication	NM_021110.4(COL14A1):c.2480-173dup	not provided [RCV001655346]	benign	8	120247429	120247430	Human		name
150483224	CV1245075	single nucleotide variant	NM_021110.4(COL14A1):c.2138-303G>A	not provided [RCV001653252]	benign	8	120228407	120228407	Human		name
150484145	CV1245237	single nucleotide variant	NM_021110.4(COL14A1):c.2138-137G>A	not provided [RCV001653414]	benign	8	120228573	120228573	Human		name
150484473	CV1250031	single nucleotide variant	NM_021110.4(COL14A1):c.4551+161G>T	not provided [RCV001673644]	benign	8	120314188	120314188	Human		name
150484654	CV1250069	single nucleotide variant	NM_021110.4(COL14A1):c.2752+120A>C	not provided [RCV001673682]	benign	8	120250886	120250886	Human		name
150446738	CV1250709	single nucleotide variant	NM_021110.4(COL14A1):c.1191+264A>T	not provided [RCV001667214]	benign	8	120207358	120207358	Human		name
150474187	CV1252528	single nucleotide variant	NM_021110.4(COL14A1):c.2349+209C>T	not provided [RCV001671731]	benign	8	120231827	120231827	Human		name
150465811	CV1255095	single nucleotide variant	NM_021110.4(COL14A1):c.2349+232G>T	not provided [RCV001670268]	benign	8	120231850	120231850	Human		name
150503873	CV1257883	single nucleotide variant	NM_021110.4(COL14A1):c.5156-232G>C	not provided [RCV001677571]	benign	8	120369098	120369098	Human		name
150458385	CV1259037	single nucleotide variant	NM_021110.4(COL14A1):c.1040-215T>C	not provided [RCV001681756]	benign	8	120206728	120206728	Human		name
150452254	CV1260370	single nucleotide variant	NM_021110.4(COL14A1):c.3647-145G>C	not provided [RCV001680860]	benign	8	120280566	120280566	Human		name
150484580	CV1263210	single nucleotide variant	NM_021110.4(COL14A1):c.4551+207A>G	not provided [RCV001686610]	benign	8	120314234	120314234	Human	4	name
150484580	CV1263210	single nucleotide variant	NM_021110.4(COL14A1):c.4551+207A>G	not provided [RCV001686610]	benign	8	120314234	120314235	Human	4	name
150476262	CV1263619	single nucleotide variant	NM_021110.4(COL14A1):c.2870-256A>C	not provided [RCV001685142]	benign	8	120262612	120262612	Human		name
8649924	CV126498	single nucleotide variant	NM_021110.2(COL14A1):c.4888+975G>A	Lung cancer [RCV000106985]	uncertain significance	8	120343421	120343421	Human		name
150495220	CV1266191	single nucleotide variant	NM_021110.4(COL14A1):c.4714-153G>A	not provided [RCV001688513]	benign	8	120332511	120332511	Human		name
150493556	CV1267170	single nucleotide variant	NM_021110.4(COL14A1):c.3017-285A>G	not provided [RCV001688198]	benign	8	120266542	120266542	Human		name
150491259	CV1267747	single nucleotide variant	NM_021110.4(COL14A1):c.4822-114G>A	not provided [RCV001687772]	benign	8	120342266	120342266	Human		name
150466609	CV1268802	single nucleotide variant	NM_021110.4(COL14A1):c.4077+167T>C	not provided [RCV001694499]	benign	8	120286137	120286137	Human		name
150456642	CV1269104	single nucleotide variant	NM_021110.4(COL14A1):c.4314+275C>T	not provided [RCV001692928]	benign	8	120297863	120297863	Human		name
150447268	CV1270288	single nucleotide variant	NM_021110.4(COL14A1):c.4888+277G>A	not provided [RCV001691423]	benign	8	120342723	120342723	Human		name
150497797	CV1271401	single nucleotide variant	NM_021110.4(COL14A1):c.3214-244T>C	not provided [RCV001689091]	benign	8	120277867	120277867	Human		name
150496758	CV1271609	single nucleotide variant	NM_021110.4(COL14A1):c.4822-113G>A	not provided [RCV001688910]	benign	8	120342267	120342267	Human		name
150445889	CV1271784	single nucleotide variant	NM_021110.4(COL14A1):c.1737+294T>G	not provided [RCV001691198]	benign	8	120216784	120216784	Human		name
150449258	CV1275648	single nucleotide variant	NM_021110.4(COL14A1):c.3825-131T>C	not provided [RCV001708103]	benign	8	120283505	120283505	Human	2	name
150449258	CV1275648	single nucleotide variant	NM_021110.4(COL14A1):c.3825-131T>C	not provided [RCV001708103]	benign	8	120283505	120283506	Human	2	name
150451275	CV1276573	deletion	NM_021110.4(COL14A1):c.1865-320del	not provided [RCV001708362]	benign	8	120226305	120226305	Human		name
150462110	CV1276039	deletion	NM_021110.4(COL14A1):c.3686-4_3686-3del	not provided [RCV001709978]	benign	8	120280904	120280905	Human		name
15179030	CV722823	single nucleotide variant	NM_021110.4(COL14A1):c.16C>T (p.Arg6Cys)	not provided [RCV000885198]	likely benign	8	120147858	120147858	Human		name
15153741	CV750894	single nucleotide variant	NM_021110.4(COL14A1):c.147A>G (p.Ser49=)	not provided [RCV000924116]	benign	8	120158188	120158188	Human		name
150513455	CV1229015	single nucleotide variant	NM_021110.4(COL14A1):c.921T>C (p.Ser307=)	not provided [RCV001637857]	benign	8	120203752	120203752	Human		name
150511419	CV1229458	single nucleotide variant	NM_021110.4(COL14A1):c.612T>C (p.Gly204=)	not provided [RCV001637387]	benign	8	120197830	120197830	Human		name
156191280	CV2255236	single nucleotide variant	NM_021110.4(COL14A1):c.59T>C (p.Val20Ala)	not specified [RCV004117631]	likely benign	8	120147901	120147901	Human		name
407451109	CV3426036	single nucleotide variant	NM_021110.4(COL14A1):c.67T>A (p.Cys23Ser)	not specified [RCV004607939]	uncertain significance	8	120147909	120147909	Human		name
15127494	CV711260	single nucleotide variant	NM_021110.4(COL14A1):c.834A>G (p.Pro278=)	not provided [RCV000963913]	benign\|likely benign	8	120199523	120199523	Human		name
15134185	CV711261	single nucleotide variant	NM_021110.4(COL14A1):c.904C>T (p.Leu302=)	not provided [RCV000965083]	benign	8	120203735	120203735	Human		name
15106569	CV722824	single nucleotide variant	NM_021110.4(COL14A1):c.342A>G (p.Gln114=)	not provided [RCV000893308]	benign	8	120162562	120162562	Human		name
15117775	CV750895	single nucleotide variant	NM_021110.4(COL14A1):c.570G>A (p.Val190=)	not provided [RCV000917856]	likely benign	8	120196924	120196924	Human		name
8632817	CV88032	single nucleotide variant	NM_021110.2(COL14A1):c.540C>T (p.Phe180=)	Malignant melanoma [RCV000068124]	not provided	8	120196894	120196894	Human		name
8632819	CV88034	single nucleotide variant	NM_021110.2(COL14A1):c.960C>T (p.Phe320=)	Malignant melanoma [RCV000068126]	not provided	8	120203791	120203791	Human		name
150447072	CV1250767	single nucleotide variant	NM_021110.4(COL14A1):c.2382T>C (p.Leu794=)	not provided [RCV001667272]	benign	8	120243911	120243911	Human		name
150442830	CV1287789	single nucleotide variant	NM_021110.4(COL14A1):c.2490G>A (p.Ser830=)	not provided [RCV001725510]	benign	8	120247623	120247623	Human		name
401733835	CV2687848	single nucleotide variant	NM_021110.4(COL14A1):c.152A>G (p.Lys51Arg)	not specified [RCV004303156]	uncertain significance	8	120158193	120158193	Human		name
401875558	CV2789088	single nucleotide variant	NM_021110.4(COL14A1):c.121A>G (p.Ile41Val)	not specified [RCV004363378]	uncertain significance	8	120158162	120158162	Human		name
401924185	CV2821269	single nucleotide variant	NM_021110.4(COL14A1):c.1621C>T (p.Leu541=)	not provided [RCV003435616]	likely benign	8	120216374	120216374	Human		name
405686782	CV3306991	single nucleotide variant	NM_021110.4(COL14A1):c.104G>A (p.Arg35Lys)	not specified [RCV004444541]	uncertain significance	8	120158145	120158145	Human		name
598216829	CV3952242	single nucleotide variant	NM_021110.4(COL14A1):c.279G>T (p.Gln93His)	not specified [RCV005316980]	uncertain significance	8	120162499	120162499	Human		name
15189444	CV700376	single nucleotide variant	NM_021110.4(COL14A1):c.2061G>A (p.Thr687=)	not provided [RCV000954177]	benign	8	120227276	120227276	Human		name
15183847	CV700378	single nucleotide variant	NM_021110.4(COL14A1):c.2550C>T (p.Asp850=)	not provided [RCV000952560]	benign	8	120247683	120247683	Human		name
15127130	CV736414	single nucleotide variant	NM_021110.4(COL14A1):c.275A>G (p.Asp92Gly)	not provided [RCV000897053]	benign	8	120162495	120162495	Human		name
15150039	CV750896	single nucleotide variant	NM_021110.4(COL14A1):c.1581G>A (p.Thr527=)	not provided [RCV000923399]	benign\|likely benign	8	120212561	120212561	Human		name
15200280	CV750897	single nucleotide variant	NM_021110.4(COL14A1):c.2724C>T (p.Ser908=)	not provided [RCV000912800]	likely benign	8	120250738	120250738	Human		name
15193056	CV766528	single nucleotide variant	NM_021110.4(COL14A1):c.1188C>T (p.Asp396=)	not provided [RCV000933259]	likely benign	8	120207091	120207091	Human		name
150503618	CV1241841	duplication	NM_021110.4(COL14A1):c.2480-174_2480-173dup	not provided [RCV001657433]	benign	8	120247429	120247430	Human		name
150506553	CV1257369	deletion	NM_021110.4(COL14A1):c.2350-195_2350-189del	not provided [RCV001678209]	benign	8	120243684	120243690	Human		name
150458612	CV1278797	deletion	NM_021110.4(COL14A1):c.4552-143_4552-140del	not provided [RCV001709414]	benign	8	120315370	120315373	Human		name
156266827	CV2198777	single nucleotide variant	NM_021110.4(COL14A1):c.374A>T (p.Asp125Val)	not specified [RCV004077824]	uncertain significance	8	120168185	120168185	Human		name
156083560	CV2298998	single nucleotide variant	NM_021110.4(COL14A1):c.524G>C (p.Arg175Thr)	not specified [RCV004158522]	uncertain significance	8	120196878	120196878	Human		name
155977470	CV2321144	single nucleotide variant	NM_021110.4(COL14A1):c.701A>G (p.Asn234Ser)	not specified [RCV004175272]	uncertain significance	8	120197919	120197919	Human		name
156153994	CV2328594	single nucleotide variant	NM_021110.4(COL14A1):c.319G>A (p.Glu107Lys)	not specified [RCV004177852]	uncertain significance	8	120162539	120162539	Human		name
155981393	CV2337035	single nucleotide variant	NM_021110.4(COL14A1):c.946A>G (p.Asn316Asp)	not specified [RCV004192802]	uncertain significance	8	120203777	120203777	Human		name
401909298	CV2828479	single nucleotide variant	NM_021110.4(COL14A1):c.3588C>T (p.Asp1196=)	not provided [RCV003423985]	likely benign	8	120280041	120280041	Human		name
401909300	CV2828480	single nucleotide variant	NM_021110.4(COL14A1):c.4686G>A (p.Ser1562=)	not provided [RCV003423986]	likely benign	8	120332167	120332167	Human		name
405686851	CV3307004	single nucleotide variant	NM_021110.4(COL14A1):c.308A>G (p.Asn103Ser)	not specified [RCV004444554]	uncertain significance	8	120162528	120162528	Human		name
405686935	CV3307020	single nucleotide variant	NM_021110.4(COL14A1):c.565G>A (p.Asp189Asn)	not specified [RCV004444570]	likely benign	8	120196919	120196919	Human		name
405852909	CV3393337	single nucleotide variant	NM_021110.4(COL14A1):c.3630C>T (p.Cys1210=)	not provided [RCV004546067]	likely benign	8	120280083	120280083	Human		name
405853085	CV3393516	single nucleotide variant	NM_021110.4(COL14A1):c.5022A>T (p.Pro1674=)	not provided [RCV004546246]	likely benign	8	120345508	120345508	Human		name
407451097	CV3426032	single nucleotide variant	NM_021110.4(COL14A1):c.350T>C (p.Ile117Thr)	not specified [RCV004607935]	uncertain significance	8	120168161	120168161	Human		name
597772696	CV3660660	single nucleotide variant	NM_021110.4(COL14A1):c.623T>C (p.Ile208Thr)	not specified [RCV004897402]	uncertain significance	8	120197841	120197841	Human		name
597772723	CV3660666	single nucleotide variant	NM_021110.4(COL14A1):c.859G>A (p.Val287Ile)	not specified [RCV004897408]	uncertain significance	8	120199548	120199548	Human		name
12844793	CV369328	single nucleotide variant	NM_021110.4(COL14A1):c.676C>T (p.Arg226Ter)	not provided [RCV000438618]	uncertain significance	8	120197894	120197894	Human		name
598216687	CV3952220	single nucleotide variant	NM_021110.4(COL14A1):c.814C>G (p.Gln272Glu)	not specified [RCV005316960]	uncertain significance	8	120199503	120199503	Human		name
598216771	CV3952234	single nucleotide variant	NM_021110.4(COL14A1):c.796A>G (p.Ile266Val)	not specified [RCV005316972]	uncertain significance	8	120199485	120199485	Human		name
598216813	CV3952240	single nucleotide variant	NM_021110.4(COL14A1):c.584C>T (p.Thr195Ile)	not specified [RCV005316978]	uncertain significance	8	120196938	120196938	Human		name
15183843	CV700374	single nucleotide variant	NM_021110.4(COL14A1):c.448G>C (p.Val150Leu)	not provided [RCV000952559]	benign	8	120196802	120196802	Human		name
15158745	CV700381	single nucleotide variant	NM_021110.4(COL14A1):c.4824T>C (p.Gly1608=)	not provided [RCV000947131]	benign	8	120342382	120342382	Human		name
15138378	CV711264	single nucleotide variant	NM_021110.4(COL14A1):c.3171C>T (p.Ser1057=)	not provided [RCV000965781]	benign	8	120270132	120270132	Human		name
15177444	CV711266	single nucleotide variant	NM_021110.4(COL14A1):c.4809A>G (p.Glu1603=)	not provided [RCV000973427]	benign	8	120341348	120341348	Human		name
15160311	CV722826	single nucleotide variant	NM_021110.4(COL14A1):c.3525G>A (p.Ser1175=)	not provided [RCV000881358]	benign	8	120279978	120279978	Human		name
15154676	CV722827	single nucleotide variant	NM_021110.4(COL14A1):c.4486C>T (p.Leu1496=)	not provided [RCV000880265]	likely benign	8	120313962	120313962	Human		name
15167856	CV736416	single nucleotide variant	NM_021110.4(COL14A1):c.4518A>G (p.Gln1506=)	not provided [RCV000904735]	benign	8	120313994	120313994	Human		name
15171109	CV736417	single nucleotide variant	NM_021110.4(COL14A1):c.4668G>A (p.Pro1556=)	not provided [RCV000905400]	benign	8	120332149	120332149	Human		name
15160151	CV750898	single nucleotide variant	NM_021110.4(COL14A1):c.4128G>A (p.Lys1376=)	not provided [RCV000925426]	likely benign	8	120289658	120289658	Human		name
15150269	CV750899	single nucleotide variant	NM_021110.4(COL14A1):c.4860G>A (p.Ala1620=)	not provided [RCV000923442]	benign	8	120342418	120342418	Human		name
8632818	CV88033	single nucleotide variant	NM_021110.2(COL14A1):c.922G>A (p.Glu308Lys)	Malignant melanoma [RCV000068125]	not provided	8	120203753	120203753	Human		name
8632823	CV88038	single nucleotide variant	NM_021110.2(COL14A1):c.3738G>A (p.Val1246=)	Malignant melanoma [RCV000068130]	not provided	8	120280973	120280973	Human		name
8632825	CV88040	single nucleotide variant	NM_021110.2(COL14A1):c.4050G>A (p.Arg1350=)	Malignant melanoma [RCV000068132]	not provided	8	120285943	120285943	Human		name
150335173	CV1171808	single nucleotide variant	NM_021110.4(COL14A1):c.1687A>C (p.Asn563His)	not provided [RCV001540440]	benign	8	120216440	120216440	Human		name
150493969	CV1238774	insertion	NM_021110.4(COL14A1):c.4659+147_4659+148insT	not provided [RCV001655318]	benign	8	120316144	120316145	Human		name
155963100	CV2197750	single nucleotide variant	NM_021110.4(COL14A1):c.2555C>T (p.Pro852Leu)	not specified [RCV004074950]	uncertain significance	8	120247688	120247688	Human		name
155922823	CV2219174	single nucleotide variant	NM_021110.4(COL14A1):c.1188C>A (p.Asp396Glu)	not specified [RCV004087328]	likely benign	8	120207091	120207091	Human		name
155990262	CV2255471	single nucleotide variant	NM_021110.4(COL14A1):c.2749A>C (p.Thr917Pro)	not specified [RCV004118126]	uncertain significance	8	120250763	120250763	Human		name
156294602	CV2302970	single nucleotide variant	NM_021110.4(COL14A1):c.1985A>G (p.Tyr662Cys)	not specified [RCV004156771]	uncertain significance	8	120226747	120226747	Human		name
156347675	CV2375529	single nucleotide variant	NM_021110.4(COL14A1):c.2679G>T (p.Met893Ile)	not specified [RCV004226034]	uncertain significance	8	120250693	120250693	Human		name
155905473	CV2393070	single nucleotide variant	NM_021110.4(COL14A1):c.1453G>C (p.Gly485Arg)	not specified [RCV004226558]	uncertain significance	8	120209887	120209887	Human		name
329380944	CV2464404	single nucleotide variant	NM_021110.4(COL14A1):c.1043C>T (p.Ser348Leu)	not specified [RCV004276338]	uncertain significance	8	120206946	120206946	Human		name
329381921	CV2467421	single nucleotide variant	NM_021110.4(COL14A1):c.2373C>A (p.Asn791Lys)	not specified [RCV004287038]	uncertain significance	8	120243902	120243902	Human		name
401732557	CV2675119	single nucleotide variant	NM_021110.4(COL14A1):c.1960C>G (p.His654Asp)	not specified [RCV004289899]	uncertain significance	8	120226722	120226722	Human		name
401745010	CV2681170	single nucleotide variant	NM_021110.4(COL14A1):c.2083G>A (p.Ala695Thr)	not specified [RCV004289313]	uncertain significance	8	120227298	120227298	Human		name
401773479	CV2698228	single nucleotide variant	NM_021110.4(COL14A1):c.2405C>T (p.Thr802Ile)	not specified [RCV004304791]	uncertain significance	8	120243934	120243934	Human		name
401758059	CV2704150	single nucleotide variant	NM_021110.4(COL14A1):c.2060C>T (p.Thr687Met)	not provided [RCV004696447]\|not specified [RCV004311166]	uncertain significance	8	120227275	120227275	Human		name
401721369	CV2709932	single nucleotide variant	NM_021110.4(COL14A1):c.2880G>C (p.Lys960Asn)	not specified [RCV004315006]	uncertain significance	8	120262878	120262878	Human		name
401750583	CV2715691	single nucleotide variant	NM_021110.4(COL14A1):c.2636C>T (p.Ala879Val)	not specified [RCV004327060]	uncertain significance	8	120250650	120250650	Human		name
401779780	CV2732016	single nucleotide variant	NM_021110.4(COL14A1):c.1022A>G (p.Gln341Arg)	not specified [RCV004333249]	uncertain significance	8	120203853	120203853	Human		name
401881645	CV2767816	single nucleotide variant	NM_021110.4(COL14A1):c.2561C>T (p.Ser854Phe)	not specified [RCV004345935]	uncertain significance	8	120247694	120247694	Human		name
401895935	CV2779357	single nucleotide variant	NM_021110.4(COL14A1):c.2006T>C (p.Val669Ala)	not specified [RCV004351011]	uncertain significance	8	120227221	120227221	Human		name
405694522	CV3226486	single nucleotide variant	NM_021110.4(COL14A1):c.1239G>A (p.Met413Ile)	not provided [RCV003992879]	likely benign	8	120208279	120208279	Human		name
405686788	CV3306992	single nucleotide variant	NM_021110.4(COL14A1):c.1064C>A (p.Pro355Gln)	not specified [RCV004444542]	uncertain significance	8	120206967	120206967	Human		name
405686791	CV3306993	single nucleotide variant	NM_021110.4(COL14A1):c.1316C>G (p.Thr439Ser)	not specified [RCV004444543]	uncertain significance	8	120208356	120208356	Human		name
405686796	CV3306994	single nucleotide variant	NM_021110.4(COL14A1):c.1390G>A (p.Asp464Asn)	not specified [RCV004444544]	likely benign	8	120209824	120209824	Human		name
405686801	CV3306995	single nucleotide variant	NM_021110.4(COL14A1):c.1568G>A (p.Ser523Asn)	not specified [RCV004444545]	uncertain significance	8	120212548	120212548	Human		name
405686806	CV3306996	single nucleotide variant	NM_021110.4(COL14A1):c.1780A>T (p.Thr594Ser)	not specified [RCV004444546]	uncertain significance	8	120225130	120225130	Human		name
405686813	CV3306997	single nucleotide variant	NM_021110.4(COL14A1):c.2309T>A (p.Met770Lys)	not specified [RCV004444547]	uncertain significance	8	120231578	120231578	Human		name
405686820	CV3306998	single nucleotide variant	NM_021110.4(COL14A1):c.2438C>T (p.Thr813Met)	not specified [RCV004444548]	uncertain significance	8	120243967	120243967	Human		name
405686825	CV3306999	single nucleotide variant	NM_021110.4(COL14A1):c.2501A>G (p.Asn834Ser)	not specified [RCV004444549]	uncertain significance	8	120247634	120247634	Human		name
405686832	CV3307000	single nucleotide variant	NM_021110.4(COL14A1):c.2705C>T (p.Ser902Phe)	not specified [RCV004444550]	uncertain significance	8	120250719	120250719	Human		name
405686836	CV3307001	single nucleotide variant	NM_021110.4(COL14A1):c.2848G>T (p.Val950Phe)	not specified [RCV004444551]	uncertain significance	8	120255335	120255335	Human		name
405686847	CV3307003	single nucleotide variant	NM_021110.4(COL14A1):c.2867A>G (p.Gln956Arg)	not specified [RCV004444553]	uncertain significance	8	120255354	120255354	Human		name
407425227	CV3409402	single nucleotide variant	NM_021110.4(COL14A1):c.2855T>C (p.Ile952Thr)	not provided [RCV004585333]	likely benign	8	120255342	120255342	Human		name
407451077	CV3426025	single nucleotide variant	NM_021110.4(COL14A1):c.1303C>T (p.Arg435Trp)	not specified [RCV004607928]	uncertain significance	8	120208343	120208343	Human		name
407451085	CV3426028	single nucleotide variant	NM_021110.4(COL14A1):c.2683T>C (p.Tyr895His)	not specified [RCV004607931]	uncertain significance	8	120250697	120250697	Human		name
407451091	CV3426030	single nucleotide variant	NM_021110.4(COL14A1):c.1747G>A (p.Asp583Asn)	not specified [RCV004607933]	uncertain significance	8	120225097	120225097	Human		name
407451100	CV3426033	single nucleotide variant	NM_021110.4(COL14A1):c.2987G>A (p.Gly996Glu)	not specified [RCV004607936]	uncertain significance	8	120262985	120262985	Human		name
407451103	CV3426034	single nucleotide variant	NM_021110.4(COL14A1):c.1430C>G (p.Ala477Gly)	not specified [RCV004607937]	uncertain significance	8	120209864	120209864	Human		name
597772690	CV3660659	single nucleotide variant	NM_021110.4(COL14A1):c.2464G>A (p.Ala822Thr)	not specified [RCV004897401]	uncertain significance	8	120243993	120243993	Human		name
597772704	CV3660662	single nucleotide variant	NM_021110.4(COL14A1):c.2422G>A (p.Val808Met)	not specified [RCV004897404]	uncertain significance	8	120243951	120243951	Human		name
597772715	CV3660664	single nucleotide variant	NM_021110.4(COL14A1):c.2104G>A (p.Glu702Lys)	not specified [RCV004897406]	uncertain significance	8	120227319	120227319	Human		name
597772730	CV3660667	single nucleotide variant	NM_021110.4(COL14A1):c.1189G>A (p.Glu397Lys)	not specified [RCV004897409]	uncertain significance	8	120207092	120207092	Human		name
597772734	CV3660668	single nucleotide variant	NM_021110.4(COL14A1):c.2228T>C (p.Val743Ala)	not specified [RCV004897410]	uncertain significance	8	120231497	120231497	Human		name
597772738	CV3660669	single nucleotide variant	NM_021110.4(COL14A1):c.2153C>T (p.Thr718Ile)	not specified [RCV004897411]	uncertain significance	8	120228725	120228725	Human		name
597772752	CV3660672	single nucleotide variant	NM_021110.4(COL14A1):c.2428C>A (p.Pro810Thr)	not specified [RCV004897414]	uncertain significance	8	120243957	120243957	Human		name
597772767	CV3660675	single nucleotide variant	NM_021110.4(COL14A1):c.1379G>A (p.Arg460Gln)	not specified [RCV004897417]	uncertain significance	8	120209813	120209813	Human		name
598216657	CV3952216	single nucleotide variant	NM_021110.4(COL14A1):c.1007C>G (p.Ser336Cys)	not specified [RCV005316956]	uncertain significance	8	120203838	120203838	Human		name
598216694	CV3952221	single nucleotide variant	NM_021110.4(COL14A1):c.1580C>T (p.Thr527Met)	not specified [RCV005316961]	uncertain significance	8	120212560	120212560	Human		name
598216708	CV3952223	single nucleotide variant	NM_021110.4(COL14A1):c.2372A>G (p.Asn791Ser)	not specified [RCV005316963]	uncertain significance	8	120243901	120243901	Human		name
598264758	CV3952224	single nucleotide variant	NM_021110.4(COL14A1):c.2311A>G (p.Thr771Ala)	not specified [RCV005326196]	uncertain significance	8	120231580	120231580	Human		name
598216717	CV3952225	single nucleotide variant	NM_021110.4(COL14A1):c.2210G>T (p.Gly737Val)	not specified [RCV005316964]	uncertain significance	8	120231479	120231479	Human		name
598216730	CV3952227	single nucleotide variant	NM_021110.4(COL14A1):c.2912G>A (p.Arg971Lys)	not specified [RCV005316966]	uncertain significance	8	120262910	120262910	Human		name
598216745	CV3952229	single nucleotide variant	NM_021110.4(COL14A1):c.1898A>G (p.Asp633Gly)	not specified [RCV005316968]	uncertain significance	8	120226660	120226660	Human		name
598216786	CV3952236	single nucleotide variant	NM_021110.4(COL14A1):c.1987G>A (p.Gly663Arg)	not specified [RCV005316974]	uncertain significance	8	120226749	120226749	Human		name
15158739	CV700375	single nucleotide variant	NM_021110.4(COL14A1):c.1880A>C (p.Gln627Pro)	not provided [RCV000947130]	benign	8	120226642	120226642	Human		name
15185283	CV700377	single nucleotide variant	NM_021110.4(COL14A1):c.2230G>A (p.Gly744Ser)	not provided [RCV000952934]	benign	8	120231499	120231499	Human		name
15193527	CV700379	single nucleotide variant	NM_021110.4(COL14A1):c.2764G>A (p.Val922Ile)	not provided [RCV000955396]	likely benign	8	120255251	120255251	Human		name
15141837	CV711262	single nucleotide variant	NM_021110.4(COL14A1):c.1373G>A (p.Ser458Asn)	not provided [RCV000966372]	likely benign	8	120209807	120209807	Human		name
15175770	CV711263	single nucleotide variant	NM_021110.4(COL14A1):c.2530C>T (p.Arg844Trp)	not provided [RCV000973028]	likely benign	8	120247663	120247663	Human		name
15179035	CV722825	single nucleotide variant	NM_021110.4(COL14A1):c.2564C>T (p.Pro855Leu)	not provided [RCV000885199]	benign	8	120247697	120247697	Human		name
15165721	CV736415	single nucleotide variant	NM_021110.4(COL14A1):c.1562A>C (p.Glu521Ala)	not provided [RCV000904285]	likely benign	8	120212542	120212542	Human		name
8632820	CV88035	single nucleotide variant	NM_021110.2(COL14A1):c.1018G>A (p.Glu340Lys)	Malignant melanoma [RCV000068127]	not provided	8	120203849	120203849	Human		name
156368660	CV2193750	single nucleotide variant	NM_021110.4(COL14A1):c.3070G>A (p.Glu1024Lys)	not specified [RCV004074513]	uncertain significance	8	120266880	120266880	Human		name
156377536	CV2217043	single nucleotide variant	NM_021110.4(COL14A1):c.3377C>A (p.Ala1126Glu)	not specified [RCV004085727]	uncertain significance	8	120278474	120278474	Human		name
156387215	CV2221444	single nucleotide variant	NM_021110.4(COL14A1):c.3772G>A (p.Val1258Met)	not specified [RCV004096733]	uncertain significance	8	120281007	120281007	Human		name
155944050	CV2241864	single nucleotide variant	NM_021110.4(COL14A1):c.5056C>A (p.Pro1686Thr)	not specified [RCV004106786]	uncertain significance	8	120345542	120345542	Human		name
156294333	CV2243675	single nucleotide variant	NM_021110.4(COL14A1):c.4895T>C (p.Met1632Thr)	not specified [RCV004114384]	uncertain significance	8	120345381	120345381	Human		name
155994515	CV2253700	single nucleotide variant	NM_021110.4(COL14A1):c.4112T>C (p.Val1371Ala)	not specified [RCV004127156]	uncertain significance	8	120289642	120289642	Human		name
156303162	CV2258791	single nucleotide variant	NM_021110.4(COL14A1):c.3220A>T (p.Met1074Leu)	not specified [RCV004118018]	uncertain significance	8	120278117	120278117	Human		name
155975624	CV2270093	single nucleotide variant	NM_021110.4(COL14A1):c.4532T>C (p.Leu1511Pro)	not specified [RCV004129056]	uncertain significance	8	120314008	120314008	Human		name
156014538	CV2272151	single nucleotide variant	NM_021110.4(COL14A1):c.4799C>A (p.Ala1600Glu)	not specified [RCV004124928]	uncertain significance	8	120341338	120341338	Human		name
155917505	CV2278792	single nucleotide variant	NM_021110.4(COL14A1):c.3306C>A (p.His1102Gln)	not specified [RCV004134969]	uncertain significance	8	120278203	120278203	Human		name
155904080	CV2282356	single nucleotide variant	NM_021110.4(COL14A1):c.5010A>C (p.Glu1670Asp)	not specified [RCV004133178]	uncertain significance	8	120345496	120345496	Human		name
155993542	CV2286308	single nucleotide variant	NM_021110.4(COL14A1):c.3151A>T (p.Ile1051Phe)	not specified [RCV004146259]	uncertain significance	8	120270112	120270112	Human		name
156149023	CV2292879	single nucleotide variant	NM_021110.4(COL14A1):c.4343C>G (p.Pro1448Arg)	not specified [RCV004148383]	uncertain significance	8	120300760	120300760	Human		name
156168419	CV2299416	single nucleotide variant	NM_021110.4(COL14A1):c.3067A>G (p.Lys1023Glu)	not specified [RCV004154500]	uncertain significance	8	120266877	120266877	Human		name
156104388	CV2310959	single nucleotide variant	NM_021110.4(COL14A1):c.5141C>A (p.Pro1714His)	not specified [RCV004163992]	uncertain significance	8	120367234	120367234	Human		name
156175734	CV2327047	single nucleotide variant	NM_021110.4(COL14A1):c.3283A>G (p.Thr1095Ala)	not specified [RCV004178635]	uncertain significance	8	120278180	120278180	Human		name
156344354	CV2349525	single nucleotide variant	NM_021110.4(COL14A1):c.3341A>G (p.Lys1114Arg)	not specified [RCV004201489]	uncertain significance	8	120278438	120278438	Human		name
156002124	CV2353610	single nucleotide variant	NM_021110.4(COL14A1):c.3479A>G (p.Asp1160Gly)	not specified [RCV004199587]	uncertain significance	8	120278576	120278576	Human		name
156219190	CV2393564	single nucleotide variant	NM_021110.4(COL14A1):c.3188A>G (p.Asn1063Ser)	not specified [RCV004231381]	uncertain significance	8	120270149	120270149	Human		name
329382437	CV2448969	single nucleotide variant	NM_021110.4(COL14A1):c.3275C>T (p.Thr1092Ile)	not specified [RCV004264053]	uncertain significance	8	120278172	120278172	Human		name
329382528	CV2449077	single nucleotide variant	NM_021110.4(COL14A1):c.5173C>T (p.Arg1725Trp)	not specified [RCV004264143]	uncertain significance	8	120369347	120369347	Human		name
329379944	CV2452850	single nucleotide variant	NM_021110.4(COL14A1):c.3154A>G (p.Ile1052Val)	not specified [RCV004277501]	uncertain significance	8	120270115	120270115	Human		name
329372156	CV2455071	single nucleotide variant	NM_021110.4(COL14A1):c.4945A>G (p.Ile1649Val)	not specified [RCV004272320]	likely benign	8	120345431	120345431	Human		name
401727390	CV2684626	single nucleotide variant	NM_021110.4(COL14A1):c.4472G>A (p.Arg1491Gln)	not specified [RCV004293728]	uncertain significance	8	120313948	120313948	Human		name
401725103	CV2697276	single nucleotide variant	NM_021110.4(COL14A1):c.3083C>T (p.Ala1028Val)	not specified [RCV004304038]	uncertain significance	8	120270044	120270044	Human		name
401855879	CV2757589	single nucleotide variant	NM_021110.4(COL14A1):c.4444C>T (p.Pro1482Ser)	not specified [RCV004340957]	uncertain significance	8	120310051	120310051	Human		name
401889748	CV2758430	single nucleotide variant	NM_021110.4(COL14A1):c.4316G>A (p.Arg1439Lys)	not specified [RCV004335084]	uncertain significance	8	120300733	120300733	Human		name
401856035	CV2764283	single nucleotide variant	NM_021110.4(COL14A1):c.4013A>T (p.Asp1338Val)	not specified [RCV004336815]	uncertain significance	8	120285906	120285906	Human		name
401879910	CV2788553	single nucleotide variant	NM_021110.4(COL14A1):c.3192G>T (p.Lys1064Asn)	not specified [RCV004361055]	uncertain significance	8	120270153	120270153	Human		name
401870261	CV2792323	single nucleotide variant	NM_021110.4(COL14A1):c.3532G>A (p.Val1178Ile)	not specified [RCV004361501]	uncertain significance	8	120279985	120279985	Human		name
405686862	CV3307006	single nucleotide variant	NM_021110.4(COL14A1):c.3352T>C (p.Tyr1118His)	not specified [RCV004444556]	likely benign	8	120278449	120278449	Human		name
405686868	CV3307007	single nucleotide variant	NM_021110.4(COL14A1):c.3361G>A (p.Asp1121Asn)	not specified [RCV004444557]	uncertain significance	8	120278458	120278458	Human		name
405686873	CV3307008	single nucleotide variant	NM_021110.4(COL14A1):c.3430G>A (p.Gly1144Arg)	not specified [RCV004444558]	uncertain significance	8	120278527	120278527	Human		name
405686882	CV3307010	single nucleotide variant	NM_021110.4(COL14A1):c.3524C>T (p.Ser1175Leu)	not specified [RCV004444560]	uncertain significance	8	120279977	120279977	Human		name
405686887	CV3307011	single nucleotide variant	NM_021110.4(COL14A1):c.3635C>T (p.Thr1212Ile)	not specified [RCV004444561]	uncertain significance	8	120280088	120280088	Human		name
405686892	CV3307012	single nucleotide variant	NM_021110.4(COL14A1):c.3823A>G (p.Arg1275Gly)	not specified [RCV004444562]	uncertain significance	8	120281058	120281058	Human		name
405686896	CV3307013	single nucleotide variant	NM_021110.4(COL14A1):c.3910G>T (p.Ala1304Ser)	not specified [RCV004444563]	uncertain significance	8	120283721	120283721	Human		name
405686907	CV3307015	single nucleotide variant	NM_021110.4(COL14A1):c.4370A>G (p.Asn1457Ser)	not specified [RCV004444565]	likely benign	8	120300787	120300787	Human		name
405686913	CV3307016	single nucleotide variant	NM_021110.4(COL14A1):c.4481T>C (p.Ile1494Thr)	not specified [RCV004444566]	likely benign	8	120313957	120313957	Human		name
405686918	CV3307017	single nucleotide variant	NM_021110.4(COL14A1):c.4600C>T (p.Pro1534Ser)	not specified [RCV004444567]	uncertain significance	8	120315581	120315581	Human		name
405686924	CV3307018	single nucleotide variant	NM_021110.4(COL14A1):c.5317C>A (p.His1773Asn)	not specified [RCV004444568]	uncertain significance	8	120371157	120371157	Human		name
405686930	CV3307019	single nucleotide variant	NM_021110.4(COL14A1):c.5339C>T (p.Thr1780Ile)	not specified [RCV004444569]	uncertain significance	8	120371179	120371179	Human		name
407451079	CV3426026	single nucleotide variant	NM_021110.4(COL14A1):c.4100C>G (p.Thr1367Ser)	not specified [RCV004607929]	uncertain significance	8	120289630	120289630	Human		name
407451083	CV3426027	single nucleotide variant	NM_021110.4(COL14A1):c.3199A>G (p.Thr1067Ala)	not specified [RCV004607930]	likely benign	8	120270160	120270160	Human		name
407451089	CV3426029	single nucleotide variant	NM_021110.4(COL14A1):c.3377C>T (p.Ala1126Val)	not specified [RCV004607932]	uncertain significance	8	120278474	120278474	Human		name
407451095	CV3426031	single nucleotide variant	NM_021110.4(COL14A1):c.3227A>G (p.Gln1076Arg)	not specified [RCV004607934]	uncertain significance	8	120278124	120278124	Human		name
407451105	CV3426035	single nucleotide variant	NM_021110.4(COL14A1):c.3442G>A (p.Asp1148Asn)	not specified [RCV004607938]	uncertain significance	8	120278539	120278539	Human		name
597772687	CV3660658	single nucleotide variant	NM_021110.4(COL14A1):c.5365A>G (p.Met1789Val)	not specified [RCV004897400]	uncertain significance	8	120371205	120371205	Human		name
597772701	CV3660661	single nucleotide variant	NM_021110.4(COL14A1):c.4391C>T (p.Ala1464Val)	not specified [RCV004897403]	uncertain significance	8	120300808	120300808	Human		name
597772709	CV3660663	single nucleotide variant	NM_021110.4(COL14A1):c.5339C>A (p.Thr1780Asn)	not specified [RCV004897405]	uncertain significance	8	120371179	120371179	Human		name
597772744	CV3660670	single nucleotide variant	NM_021110.4(COL14A1):c.3724G>T (p.Asp1242Tyr)	not specified [RCV004897412]	uncertain significance	8	120280959	120280959	Human		name
597772748	CV3660671	single nucleotide variant	NM_021110.4(COL14A1):c.4213G>C (p.Gly1405Arg)	not specified [RCV004897413]	uncertain significance	8	120289743	120289743	Human		name
597772757	CV3660673	single nucleotide variant	NM_021110.4(COL14A1):c.3751A>G (p.Met1251Val)	not specified [RCV004897415]	uncertain significance	8	120280986	120280986	Human		name
597772763	CV3660674	single nucleotide variant	NM_021110.4(COL14A1):c.3563A>G (p.His1188Arg)	not specified [RCV004897416]	uncertain significance	8	120280016	120280016	Human		name
597772778	CV3660677	single nucleotide variant	NM_021110.4(COL14A1):c.5267C>T (p.Pro1756Leu)	not specified [RCV004897419]	uncertain significance	8	120369441	120369441	Human		name
597772782	CV3660678	single nucleotide variant	NM_021110.4(COL14A1):c.4375G>A (p.Val1459Met)	not specified [RCV004897420]	uncertain significance	8	120300792	120300792	Human		name
598216672	CV3952218	single nucleotide variant	NM_021110.4(COL14A1):c.5053G>C (p.Val1685Leu)	not specified [RCV005316958]	uncertain significance	8	120345539	120345539	Human		name
598216680	CV3952219	single nucleotide variant	NM_021110.4(COL14A1):c.4569A>C (p.Lys1523Asn)	not specified [RCV005316959]	uncertain significance	8	120315550	120315550	Human		name
598216701	CV3952222	single nucleotide variant	NM_021110.4(COL14A1):c.5383G>A (p.Gly1795Arg)	not specified [RCV005316962]	uncertain significance	8	120371223	120371223	Human		name
598216723	CV3952226	single nucleotide variant	NM_021110.4(COL14A1):c.3554G>C (p.Ser1185Thr)	not specified [RCV005316965]	uncertain significance	8	120280007	120280007	Human		name
598216752	CV3952230	single nucleotide variant	NM_021110.4(COL14A1):c.3146A>G (p.Asn1049Ser)	not specified [RCV005316969]	uncertain significance	8	120270107	120270107	Human		name
598216758	CV3952231	single nucleotide variant	NM_021110.4(COL14A1):c.4861C>T (p.Arg1621Cys)	not specified [RCV005316970]	uncertain significance	8	120342419	120342419	Human		name
598216764	CV3952232	single nucleotide variant	NM_021110.4(COL14A1):c.5158C>A (p.Pro1720Thr)	not specified [RCV005316971]	uncertain significance	8	120369332	120369332	Human		name
598264763	CV3952233	single nucleotide variant	NM_021110.4(COL14A1):c.3220A>G (p.Met1074Val)	not specified [RCV005326197]	uncertain significance	8	120278117	120278117	Human		name
598216778	CV3952235	single nucleotide variant	NM_021110.4(COL14A1):c.4484G>A (p.Gly1495Asp)	not specified [RCV005316973]	uncertain significance	8	120313960	120313960	Human		name
598216793	CV3952237	single nucleotide variant	NM_021110.4(COL14A1):c.3098T>C (p.Leu1033Pro)	not specified [RCV005316975]	uncertain significance	8	120270059	120270059	Human		name
598216801	CV3952238	single nucleotide variant	NM_021110.4(COL14A1):c.3363T>A (p.Asp1121Glu)	not specified [RCV005316976]	uncertain significance	8	120278460	120278460	Human		name
598216821	CV3952241	single nucleotide variant	NM_021110.4(COL14A1):c.3753G>A (p.Met1251Ile)	not specified [RCV005316979]	uncertain significance	8	120280988	120280988	Human		name
598216837	CV3952243	single nucleotide variant	NM_021110.4(COL14A1):c.4049G>A (p.Arg1350Lys)	not specified [RCV005316981]	uncertain significance	8	120285942	120285942	Human		name
8604375	CV48398	single nucleotide variant	NM_021110.4(COL14A1):c.4505C>T (p.Pro1502Leu)	Variant of unknown significance [RCV000033021]	uncertain significance	8	120313981	120313981	Human		name
15189447	CV700380	single nucleotide variant	NM_021110.4(COL14A1):c.3565G>A (p.Val1189Ile)	not provided [RCV000954178]	benign	8	120280018	120280018	Human		name
15111692	CV711265	single nucleotide variant	NM_021110.4(COL14A1):c.3407A>G (p.Lys1136Arg)	not provided [RCV000961156]	benign	8	120278504	120278504	Human		name
8632821	CV88036	single nucleotide variant	NM_021110.2(COL14A1):c.3311C>T (p.Ser1104Leu)	Malignant melanoma [RCV000068128]	not provided	8	120278208	120278208	Human		name
8632822	CV88037	single nucleotide variant	NM_021110.2(COL14A1):c.3434G>A (p.Arg1145Lys)	Malignant melanoma [RCV000068129]	not provided	8	120278531	120278531	Human		name
8632824	CV88039	single nucleotide variant	NM_021110.2(COL14A1):c.4033G>A (p.Glu1345Lys)	Malignant melanoma [RCV000068131]	not provided	8	120285926	120285926	Human		name
8632826	CV88041	single nucleotide variant	NM_021110.2(COL14A1):c.4688G>A (p.Gly1563Glu)	Malignant melanoma [RCV000068133]	not provided	8	120332169	120332169	Human		name
8632827	CV88042	single nucleotide variant	NM_021110.2(COL14A1):c.4750G>A (p.Gly1584Arg)	Malignant melanoma [RCV000068134]	not provided	8	120332700	120332700	Human		name

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