Mmp15 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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95 records found for search term Mmp15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15112017	CV779895	single nucleotide variant	NM_002428.4(MMP15):c.1165-9C>T	not provided [RCV000961220]	benign	16	58042222	58042222	Human		name
401911699	CV2807983	indel	NM_002428.4(MMP15):c.910_910+3delinsA	not provided [RCV003426721]	uncertain significance	16	58040698	58040701	Human		name
597642216	CV3553929	single nucleotide variant	NM_002428.4(MMP15):c.7A>G (p.Ser3Gly)	not specified [RCV004825592]	uncertain significance	16	58026357	58026357	Human		name
405755047	CV3316484	single nucleotide variant	NM_002428.4(MMP15):c.25G>A (p.Gly9Arg)	not specified [RCV004454369]	uncertain significance	16	58026375	58026375	Human		name
155984591	CV2241136	single nucleotide variant	NM_002428.4(MMP15):c.41C>G (p.Thr14Arg)	not specified [RCV004104167]	uncertain significance	16	58026391	58026391	Human		name
156058015	CV2383329	single nucleotide variant	NM_002428.4(MMP15):c.47G>C (p.Ser16Thr)	not specified [RCV004222370]	uncertain significance	16	58026397	58026397	Human		name
401753912	CV2685100	single nucleotide variant	NM_002428.4(MMP15):c.32C>G (p.Pro11Arg)	not specified [RCV004289672]	uncertain significance	16	58026382	58026382	Human		name
597642181	CV3553922	single nucleotide variant	NM_002428.4(MMP15):c.97C>T (p.Leu33Phe)	not specified [RCV004825586]	uncertain significance	16	58026447	58026447	Human		name
598167227	CV3989621	single nucleotide variant	NM_002428.4(MMP15):c.441C>T (p.Ser147=)	not specified [RCV005369483]	likely benign	16	58039875	58039875	Human		name
15101669	CV726716	single nucleotide variant	NM_002428.4(MMP15):c.960G>A (p.Thr320=)	not provided [RCV000892325]	benign	16	58041666	58041666	Human		name
15165374	CV755297	single nucleotide variant	NM_002428.4(MMP15):c.534C>T (p.Val178=)	not provided [RCV000926608]	likely benign	16	58039968	58039968	Human		name
156332807	CV2270375	single nucleotide variant	NM_002428.4(MMP15):c.140A>C (p.Glu47Ala)	not specified [RCV004135572]	uncertain significance	16	58026490	58026490	Human		name
156327663	CV2332134	single nucleotide variant	NM_002428.4(MMP15):c.172C>T (p.Arg58Trp)	not specified [RCV004189173]	uncertain significance	16	58037481	58037481	Human		name
401766483	CV2725573	single nucleotide variant	NM_002428.4(MMP15):c.217A>C (p.Met73Leu)	not specified [RCV004321966]	uncertain significance	16	58037526	58037526	Human		name
405752799	CV3316158	single nucleotide variant	NM_002428.4(MMP15):c.173G>A (p.Arg58Gln)	not specified [RCV004454043]	uncertain significance	16	58037482	58037482	Human		name
405754679	CV3316431	single nucleotide variant	NM_002428.4(MMP15):c.203G>A (p.Arg68His)	not specified [RCV004454316]	uncertain significance	16	58037512	58037512	Human		name
407487563	CV3457524	single nucleotide variant	NM_002428.4(MMP15):c.156T>A (p.His52Gln)	not specified [RCV004641093]	uncertain significance	16	58026506	58026506	Human		name
597636815	CV3553921	single nucleotide variant	NM_002428.4(MMP15):c.295G>A (p.Asp99Asn)	not specified [RCV004824606]	uncertain significance	16	58037604	58037604	Human		name
597642210	CV3553927	single nucleotide variant	NM_002428.4(MMP15):c.272G>A (p.Gly91Glu)	not specified [RCV004825591]	uncertain significance	16	58037581	58037581	Human		name
598167220	CV3989619	single nucleotide variant	NM_002428.4(MMP15):c.202C>A (p.Arg68Ser)	not specified [RCV005369481]	uncertain significance	16	58037511	58037511	Human		name
598167223	CV3989620	single nucleotide variant	NM_002428.4(MMP15):c.144C>G (p.Asp48Glu)	not specified [RCV005369482]	uncertain significance	16	58026494	58026494	Human		name
598200060	CV3989623	single nucleotide variant	NM_002428.4(MMP15):c.220C>T (p.Arg74Cys)	not specified [RCV005375794]	uncertain significance	16	58037529	58037529	Human		name
156207238	CV2250023	single nucleotide variant	NM_002428.4(MMP15):c.995C>T (p.Pro332Leu)	not specified [RCV004122985]	uncertain significance	16	58041701	58041701	Human		name
155965715	CV2261831	single nucleotide variant	NM_002428.4(MMP15):c.989G>A (p.Arg330Gln)	not specified [RCV004126102]	uncertain significance	16	58041695	58041695	Human		name
156206778	CV2297993	single nucleotide variant	NM_002428.4(MMP15):c.352G>A (p.Gly118Arg)	not specified [RCV004157909]	uncertain significance	16	58038306	58038306	Human		name
156173573	CV2333728	single nucleotide variant	NM_002428.4(MMP15):c.562C>T (p.Arg188Trp)	not specified [RCV004181241]	uncertain significance	16	58039996	58039996	Human		name
156055796	CV2370948	single nucleotide variant	NM_002428.4(MMP15):c.298G>A (p.Glu100Lys)	not specified [RCV004218675]	uncertain significance	16	58037607	58037607	Human		name
156076757	CV2375058	single nucleotide variant	NM_002428.4(MMP15):c.377G>A (p.Arg126Gln)	not specified [RCV004230106]	uncertain significance	16	58038331	58038331	Human		name
155954403	CV2379206	single nucleotide variant	NM_002428.4(MMP15):c.877G>A (p.Glu293Lys)	not specified [RCV004235991]	uncertain significance	16	58040665	58040665	Human		name
156066500	CV2381014	single nucleotide variant	NM_002428.4(MMP15):c.997C>T (p.Arg333Trp)	not specified [RCV004225053]	uncertain significance	16	58041703	58041703	Human		name
401768826	CV2686385	single nucleotide variant	NM_002428.4(MMP15):c.994C>T (p.Pro332Ser)	not specified [RCV004297456]	uncertain significance	16	58041700	58041700	Human		name
401733934	CV2697907	single nucleotide variant	NM_002428.4(MMP15):c.455C>T (p.Thr152Met)	not specified [RCV004300615]	uncertain significance	16	58039889	58039889	Human		name
401733985	CV2713288	single nucleotide variant	NM_002428.4(MMP15):c.563G>A (p.Arg188Gln)	not specified [RCV004316810]	uncertain significance	16	58039997	58039997	Human		name
401770551	CV2715222	single nucleotide variant	NM_002428.4(MMP15):c.857T>C (p.Val286Ala)	not specified [RCV004324573]	uncertain significance	16	58040645	58040645	Human		name
401767212	CV2728721	single nucleotide variant	NM_002428.4(MMP15):c.505C>T (p.Arg169Cys)	not specified [RCV004331649]	uncertain significance	16	58039939	58039939	Human		name
405699194	CV3309532	single nucleotide variant	NM_002428.4(MMP15):c.667T>G (p.Tyr223Asp)	not specified [RCV004446800]	uncertain significance	16	58040101	58040101	Human		name
405699442	CV3309574	single nucleotide variant	NM_002428.4(MMP15):c.747T>A (p.His249Gln)	not specified [RCV004446842]	uncertain significance	16	58040181	58040181	Human		name
405717635	CV3309665	single nucleotide variant	NM_002428.4(MMP15):c.988C>T (p.Arg330Trp)	not specified [RCV004449413]	uncertain significance	16	58041694	58041694	Human		name
405697133	CV3313038	single nucleotide variant	NM_002428.4(MMP15):c.328C>A (p.Arg110Ser)	not specified [RCV004446414]	uncertain significance	16	58038282	58038282	Human		name
405697522	CV3313128	single nucleotide variant	NM_002428.4(MMP15):c.359G>A (p.Arg120Gln)	not specified [RCV004446504]	uncertain significance	16	58038313	58038313	Human		name
405698600	CV3313291	single nucleotide variant	NM_002428.4(MMP15):c.494G>A (p.Arg165His)	not specified [RCV004446667]	uncertain significance	16	58039928	58039928	Human		name
405699624	CV3313394	single nucleotide variant	NM_002428.4(MMP15):c.577A>G (p.Lys193Glu)	not specified [RCV004446770]	uncertain significance	16	58040011	58040011	Human		name
407487567	CV3457525	single nucleotide variant	NM_002428.4(MMP15):c.323G>A (p.Arg108Gln)	not specified [RCV004641094]	uncertain significance	16	58038277	58038277	Human		name
407487572	CV3457526	single nucleotide variant	NM_002428.4(MMP15):c.383G>A (p.Arg128His)	not specified [RCV004641095]	uncertain significance	16	58038337	58038337	Human		name
407487588	CV3457529	single nucleotide variant	NM_002428.4(MMP15):c.496A>G (p.Arg166Gly)	not specified [RCV004641098]	uncertain significance	16	58039930	58039930	Human		name
596944528	CV3543172	deletion	NM_002428.4(MMP15):c.1058del (p.Pro353fs)	Developmental disorder [RCV004799044]	pathogenic	16	58041759	58041759	Human	1	name
597636810	CV3553916	single nucleotide variant	NM_002428.4(MMP15):c.889C>T (p.Arg297Cys)	not specified [RCV004824605]	uncertain significance	16	58040677	58040677	Human		name
597642158	CV3553917	single nucleotide variant	NM_002428.4(MMP15):c.991C>T (p.Pro331Ser)	not specified [RCV004825582]	uncertain significance	16	58041697	58041697	Human		name
597642162	CV3553918	single nucleotide variant	NM_002428.4(MMP15):c.574C>G (p.Gln192Glu)	not specified [RCV004825583]	uncertain significance	16	58040008	58040008	Human		name
597642170	CV3553919	single nucleotide variant	NM_002428.4(MMP15):c.959C>T (p.Thr320Met)	not specified [RCV004825584]	uncertain significance	16	58041665	58041665	Human		name
597642188	CV3553923	single nucleotide variant	NM_002428.4(MMP15):c.376C>T (p.Arg126Trp)	not specified [RCV004825587]	uncertain significance	16	58038330	58038330	Human		name
597642203	CV3553926	single nucleotide variant	NM_002428.4(MMP15):c.629C>G (p.Ser210Trp)	not specified [RCV004825590]	uncertain significance	16	58040063	58040063	Human		name
598200053	CV3989617	single nucleotide variant	NM_002428.4(MMP15):c.869A>G (p.Lys290Arg)	not specified [RCV005375793]	uncertain significance	16	58040657	58040657	Human		name
598167213	CV3989618	single nucleotide variant	NM_002428.4(MMP15):c.371A>G (p.Asn124Ser)	not specified [RCV005369480]	uncertain significance	16	58038325	58038325	Human		name
156329205	CV2213784	single nucleotide variant	NM_002428.4(MMP15):c.1961C>G (p.Ala654Gly)	not specified [RCV004089847]	uncertain significance	16	58045397	58045397	Human		name
155941220	CV2232507	single nucleotide variant	NM_002428.4(MMP15):c.1961C>T (p.Ala654Val)	not specified [RCV004099112]	uncertain significance	16	58045397	58045397	Human		name
155988202	CV2234185	single nucleotide variant	NM_002428.4(MMP15):c.1661G>C (p.Arg554Pro)	not specified [RCV004106270]	uncertain significance	16	58045097	58045097	Human		name
156155742	CV2238267	single nucleotide variant	NM_002428.4(MMP15):c.1379G>A (p.Gly460Asp)	not specified [RCV004113350]	uncertain significance	16	58043285	58043285	Human		name
156121942	CV2240985	single nucleotide variant	NM_002428.4(MMP15):c.1186C>T (p.Arg396Trp)	not specified [RCV004102256]	uncertain significance	16	58042252	58042252	Human		name
156215630	CV2257593	single nucleotide variant	NM_002428.4(MMP15):c.1331C>T (p.Ala444Val)	not specified [RCV004127423]	uncertain significance	16	58043237	58043237	Human		name
155928899	CV2281309	single nucleotide variant	NM_002428.4(MMP15):c.1144G>T (p.Gly382Trp)	not specified [RCV004147540]	uncertain significance	16	58041850	58041850	Human		name
156284984	CV2291949	single nucleotide variant	NM_002428.4(MMP15):c.1594A>G (p.Thr532Ala)	not specified [RCV004158461]	uncertain significance	16	58045030	58045030	Human		name
156069247	CV2295724	single nucleotide variant	NM_002428.4(MMP15):c.1181G>A (p.Arg394Gln)	not specified [RCV004149870]	uncertain significance	16	58042247	58042247	Human		name
156363363	CV2329843	single nucleotide variant	NM_002428.4(MMP15):c.1052G>T (p.Gly351Val)	not specified [RCV004183304]	uncertain significance	16	58041758	58041758	Human		name
156334918	CV2333454	single nucleotide variant	NM_002428.4(MMP15):c.1036C>T (p.Arg346Trp)	not specified [RCV004190155]	uncertain significance	16	58041742	58041742	Human		name
156285648	CV2334864	single nucleotide variant	NM_002428.4(MMP15):c.1628G>A (p.Arg543Gln)	not specified [RCV004181972]	uncertain significance	16	58045064	58045064	Human		name
155975883	CV2342714	single nucleotide variant	NM_002428.4(MMP15):c.1376T>C (p.Leu459Pro)	not specified [RCV004196791]	uncertain significance	16	58043282	58043282	Human		name
155930093	CV2354091	single nucleotide variant	NM_002428.4(MMP15):c.1070G>A (p.Arg357Gln)	not specified [RCV004206530]	uncertain significance	16	58041776	58041776	Human		name
156392733	CV2386639	single nucleotide variant	NM_002428.4(MMP15):c.1337T>A (p.Leu446Gln)	not specified [RCV004230981]	uncertain significance	16	58043243	58043243	Human		name
329388580	CV2447672	single nucleotide variant	NM_002428.4(MMP15):c.1889T>A (p.Leu630Gln)	not specified [RCV004258469]	uncertain significance	16	58045325	58045325	Human		name
329388143	CV2468589	single nucleotide variant	NM_002428.4(MMP15):c.1037G>A (p.Arg346Gln)	not provided [RCV004696396]\|not specified [RCV004278152]	uncertain significance	16	58041743	58041743	Human		name
401751442	CV2672454	single nucleotide variant	NM_002428.4(MMP15):c.1081C>T (p.Arg361Trp)	not specified [RCV004285708]	uncertain significance	16	58041787	58041787	Human		name
401741629	CV2697591	single nucleotide variant	NM_002428.4(MMP15):c.1288T>G (p.Phe430Val)	not specified [RCV004298343]	uncertain significance	16	58042354	58042354	Human		name
401764463	CV2727953	single nucleotide variant	NM_002428.4(MMP15):c.1943A>G (p.Gln648Arg)	not specified [RCV004324124]	uncertain significance	16	58045379	58045379	Human		name
401862720	CV2758861	single nucleotide variant	NM_002428.4(MMP15):c.1087G>A (p.Asp363Asn)	not specified [RCV004339951]	uncertain significance	16	58041793	58041793	Human		name
401888459	CV2761425	single nucleotide variant	NM_002428.4(MMP15):c.1690G>A (p.Glu564Lys)	not specified [RCV004334604]	uncertain significance	16	58045126	58045126	Human		name
401894877	CV2781989	single nucleotide variant	NM_002428.4(MMP15):c.1463G>A (p.Arg488His)	not specified [RCV004359005]	uncertain significance	16	58043520	58043520	Human		name
401871285	CV2783467	single nucleotide variant	NM_002428.4(MMP15):c.1802T>C (p.Phe601Ser)	not specified [RCV004365809]	likely benign	16	58045238	58045238	Human		name
401863993	CV2784883	single nucleotide variant	NM_002428.4(MMP15):c.1082G>A (p.Arg361Gln)	not specified [RCV004352662]	uncertain significance	16	58041788	58041788	Human		name
401898933	CV2792133	single nucleotide variant	NM_002428.4(MMP15):c.1807G>T (p.Ala603Ser)	not specified [RCV004361351]	uncertain significance	16	58045243	58045243	Human		name
405734407	CV3309439	single nucleotide variant	NM_002428.4(MMP15):c.1094A>G (p.Tyr365Cys)	not specified [RCV004451445]	uncertain significance	16	58041800	58041800	Human		name
405734680	CV3309471	single nucleotide variant	NM_002428.4(MMP15):c.1111G>A (p.Asp371Asn)	not specified [RCV004451477]	uncertain significance	16	58041817	58041817	Human		name
405753462	CV3316257	single nucleotide variant	NM_002428.4(MMP15):c.1857G>T (p.Glu619Asp)	not specified [RCV004454142]	uncertain significance	16	58045293	58045293	Human		name
405753717	CV3316294	single nucleotide variant	NM_002428.4(MMP15):c.1876G>A (p.Val626Met)	not specified [RCV004454179]	likely benign	16	58045312	58045312	Human		name
405751974	CV3319927	single nucleotide variant	NM_002428.4(MMP15):c.1703G>A (p.Arg568Gln)	not specified [RCV004453922]	uncertain significance	16	58045139	58045139	Human		name
407487577	CV3457527	single nucleotide variant	NM_002428.4(MMP15):c.1394G>A (p.Arg465His)	not specified [RCV004641096]	uncertain significance	16	58043300	58043300	Human		name
407487581	CV3457528	single nucleotide variant	NM_002428.4(MMP15):c.1727C>G (p.Pro576Arg)	not specified [RCV004641097]	uncertain significance	16	58045163	58045163	Human		name
407487594	CV3457530	single nucleotide variant	NM_002428.4(MMP15):c.1080G>C (p.Glu360Asp)	not specified [RCV004641099]	uncertain significance	16	58041786	58041786	Human		name
597642176	CV3553920	single nucleotide variant	NM_002428.4(MMP15):c.1358C>T (p.Pro453Leu)	not specified [RCV004825585]	uncertain significance	16	58043264	58043264	Human		name
597642193	CV3553924	single nucleotide variant	NM_002428.4(MMP15):c.1723C>A (p.Pro575Thr)	not specified [RCV004825588]	uncertain significance	16	58045159	58045159	Human		name
597642198	CV3553925	single nucleotide variant	NM_002428.4(MMP15):c.1768G>A (p.Ala590Thr)	not specified [RCV004825589]	uncertain significance	16	58045204	58045204	Human		name
597642222	CV3553930	single nucleotide variant	NM_002428.4(MMP15):c.1211A>G (p.Tyr404Cys)	not specified [RCV004825593]	uncertain significance	16	58042277	58042277	Human		name
598200045	CV3989615	single nucleotide variant	NM_002428.4(MMP15):c.1249G>A (p.Gly417Ser)	not specified [RCV005375792]	likely benign	16	58042315	58042315	Human		name
598167233	CV3989622	single nucleotide variant	NM_002428.4(MMP15):c.1981T>C (p.Cys661Arg)	not specified [RCV005369484]	uncertain significance	16	58045417	58045417	Human		name
598200066	CV3989624	single nucleotide variant	NM_002428.4(MMP15):c.1444C>A (p.Gln482Lys)	not specified [RCV005375795]	uncertain significance	16	58043350	58043350	Human		name

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