Mmp15 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

95 records found for search term Mmp15

Refine Term:

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message