Adam12 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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82 records found for search term Adam12

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8651713	CV128288	single nucleotide variant	NM_003474.5(ADAM12):c.260+50549T>C	Lung cancer [RCV000108775]	uncertain significance	10	126228366	126228366	Human		name
8651714	CV128289	single nucleotide variant	NM_003474.5(ADAM12):c.260+35288A>G	Lung cancer [RCV000108776]	uncertain significance	10	126243627	126243627	Human		name
15168223	CV779456	single nucleotide variant	NM_001288973.2(ADAM12):c.2105-7G>C	not provided [RCV000971570]	benign	10	126039436	126039436	Human		name
8633541	CV88756	single nucleotide variant	NM_003474.5(ADAM12):c.2202G>A (p.Leu734=)	Malignant melanoma [RCV000068851]	not provided	10	126039341	126039341	Human		name
156182596	CV2298623	single nucleotide variant	NM_001288973.2(ADAM12):c.70G>A (p.Ala24Thr)	not specified [RCV004162269]	uncertain significance	10	126388076	126388076	Human		name
329396274	CV2462478	single nucleotide variant	NM_001288973.2(ADAM12):c.49G>T (p.Ala17Ser)	not specified [RCV004276659]	uncertain significance	10	126388097	126388097	Human		name
401720625	CV2673404	single nucleotide variant	NM_001288973.2(ADAM12):c.31G>A (p.Ala11Thr)	not specified [RCV004288380]	uncertain significance	10	126388115	126388115	Human		name
15195336	CV723837	single nucleotide variant	NM_001288973.2(ADAM12):c.357T>C (p.His119=)	not provided [RCV000889475]	benign	10	126135643	126135643	Human		name
156401810	CV2217790	single nucleotide variant	NM_001288973.2(ADAM12):c.265C>T (p.Leu89Phe)	not specified [RCV004083966]	uncertain significance	10	126155301	126155301	Human		name
156208504	CV2304277	single nucleotide variant	NM_001288973.2(ADAM12):c.130A>G (p.Ser44Gly)	not specified [RCV004164400]	uncertain significance	10	126330468	126330468	Human		name
156059806	CV2317008	single nucleotide variant	NM_001288973.2(ADAM12):c.277A>C (p.Ser93Arg)	not specified [RCV004174505]	uncertain significance	10	126155289	126155289	Human		name
329393012	CV2449439	single nucleotide variant	NM_001288973.2(ADAM12):c.115G>A (p.Ala39Thr)	not specified [RCV004266598]	uncertain significance	10	126330483	126330483	Human		name
401903888	CV2809744	single nucleotide variant	NM_001288973.2(ADAM12):c.2607C>T (p.Ala869=)	not provided [RCV003394590]	likely benign	10	126019748	126019748	Human		name
405780457	CV3300623	single nucleotide variant	NM_001288973.2(ADAM12):c.261A>C (p.Glu87Asp)	not specified [RCV004436859]	uncertain significance	10	126155305	126155305	Human		name
598166367	CV3950247	single nucleotide variant	NM_001288973.2(ADAM12):c.278G>C (p.Ser93Thr)	not specified [RCV005307865]	uncertain significance	10	126155288	126155288	Human		name
15134621	CV712224	single nucleotide variant	NM_001288973.2(ADAM12):c.2313C>T (p.Gly771=)	not provided [RCV000965157]	benign	10	126038277	126038277	Human		name
15185826	CV723835	single nucleotide variant	NM_001288973.2(ADAM12):c.2310A>G (p.Lys770=)	not provided [RCV000886804]	benign	10	126038280	126038280	Human		name
15139747	CV737398	single nucleotide variant	NM_001288973.2(ADAM12):c.1545C>T (p.Asp515=)	not provided [RCV000899199]	likely benign	10	126064870	126064870	Human		name
156172832	CV2194297	single nucleotide variant	NM_001288973.2(ADAM12):c.565A>C (p.Asn189His)	not specified [RCV004079414]	uncertain significance	10	126118076	126118076	Human		name
155982129	CV2233150	single nucleotide variant	NM_001288973.2(ADAM12):c.325G>A (p.Ala109Thr)	not specified [RCV004103765]	likely benign	10	126155241	126155241	Human		name
156291249	CV2236409	single nucleotide variant	NM_001288973.2(ADAM12):c.307G>A (p.Gly103Ser)	not specified [RCV004108085]	uncertain significance	10	126155259	126155259	Human		name
156181232	CV2327803	single nucleotide variant	NM_001288973.2(ADAM12):c.854A>C (p.Asp285Ala)	not specified [RCV004179146]	uncertain significance	10	126101129	126101129	Human		name
155977759	CV2338831	single nucleotide variant	NM_001288973.2(ADAM12):c.643C>G (p.Leu215Val)	not specified [RCV004182386]	uncertain significance	10	126109801	126109801	Human		name
155917952	CV2362465	single nucleotide variant	NM_001288973.2(ADAM12):c.854A>G (p.Asp285Gly)	not specified [RCV004213086]	uncertain significance	10	126101129	126101129	Human		name
401887512	CV2773472	single nucleotide variant	NM_001288973.2(ADAM12):c.695A>G (p.Glu232Gly)	not specified [RCV004354105]	uncertain significance	10	126108639	126108639	Human		name
405660670	CV3300630	single nucleotide variant	NM_001288973.2(ADAM12):c.480A>T (p.Arg160Ser)	not specified [RCV004438933]	uncertain significance	10	126118161	126118161	Human		name
405660690	CV3300637	single nucleotide variant	NM_001288973.2(ADAM12):c.556G>A (p.Ala186Thr)	not specified [RCV004438940]	likely benign	10	126118085	126118085	Human		name
405660712	CV3300644	single nucleotide variant	NM_001288973.2(ADAM12):c.617C>A (p.Thr206Asn)	not specified [RCV004438947]	uncertain significance	10	126109827	126109827	Human		name
405660746	CV3300655	single nucleotide variant	NM_001288973.2(ADAM12):c.787G>T (p.Val263Leu)	not specified [RCV004438958]	uncertain significance	10	126101196	126101196	Human		name
405660750	CV3300656	single nucleotide variant	NM_001288973.2(ADAM12):c.796G>A (p.Asp266Asn)	not specified [RCV004438959]	uncertain significance	10	126101187	126101187	Human		name
405660756	CV3300658	single nucleotide variant	NM_001288973.2(ADAM12):c.797A>T (p.Asp266Val)	not specified [RCV004438961]	uncertain significance	10	126101186	126101186	Human		name
407455075	CV3422347	single nucleotide variant	NM_001288973.2(ADAM12):c.598A>G (p.Arg200Gly)	not specified [RCV004610138]	uncertain significance	10	126118043	126118043	Human		name
407455093	CV3422355	single nucleotide variant	NM_001288973.2(ADAM12):c.311C>T (p.Thr104Ile)	not specified [RCV004610146]	uncertain significance	10	126155255	126155255	Human		name
597794514	CV3648084	single nucleotide variant	NM_001288973.2(ADAM12):c.510A>C (p.Lys170Asn)	not specified [RCV004903354]	uncertain significance	10	126118131	126118131	Human		name
598166261	CV3950226	single nucleotide variant	NM_001288973.2(ADAM12):c.952A>G (p.Ile318Val)	not specified [RCV005307848]	uncertain significance	10	126098460	126098460	Human		name
15116687	CV712225	single nucleotide variant	NM_001288973.2(ADAM12):c.500A>G (p.Lys167Arg)	not provided [RCV000962078]	benign	10	126118141	126118141	Human		name
156242807	CV2246286	single nucleotide variant	NM_001288973.2(ADAM12):c.2495C>T (p.Pro832Leu)	not specified [RCV004107733]	uncertain significance	10	126036180	126036180	Human		name
156266718	CV2247239	single nucleotide variant	NM_001288973.2(ADAM12):c.2636C>G (p.Thr879Ser)	not specified [RCV004114752]	likely benign	10	126019719	126019719	Human		name
156179976	CV2288052	single nucleotide variant	NM_001288973.2(ADAM12):c.2248C>T (p.Arg750Cys)	not specified [RCV004147807]	uncertain significance	10	126038342	126038342	Human		name
156183197	CV2294784	single nucleotide variant	NM_001288973.2(ADAM12):c.1336C>T (p.Arg446Cys)	not specified [RCV004162300]	uncertain significance	10	126066794	126066794	Human		name
156283271	CV2334655	single nucleotide variant	NM_001288973.2(ADAM12):c.1852T>C (p.Tyr618His)	not specified [RCV004188640]	uncertain significance	10	126049318	126049318	Human		name
156042086	CV2342197	single nucleotide variant	NM_001288973.2(ADAM12):c.1433C>T (p.Ala478Val)	not specified [RCV004191783]	uncertain significance	10	126064982	126064982	Human		name
156035763	CV2373931	single nucleotide variant	NM_001288973.2(ADAM12):c.1688C>T (p.Ser563Leu)	not specified [RCV004227068]	uncertain significance	10	126049591	126049591	Human		name
155995173	CV2375792	single nucleotide variant	NM_001288973.2(ADAM12):c.2113G>A (p.Gly705Ser)	not specified [RCV004224377]	uncertain significance	10	126039421	126039421	Human		name
155999514	CV2378596	single nucleotide variant	NM_001288973.2(ADAM12):c.2567C>G (p.Pro856Arg)	not specified [RCV004231077]	uncertain significance	10	126019788	126019788	Human		name
156215939	CV2386024	single nucleotide variant	NM_001288973.2(ADAM12):c.2462G>A (p.Arg821Gln)	not specified [RCV004229090]	likely benign	10	126036213	126036213	Human		name
155966637	CV2396096	single nucleotide variant	NM_001288973.2(ADAM12):c.1337G>A (p.Arg446His)	not specified [RCV004237628]	uncertain significance	10	126066793	126066793	Human		name
329392208	CV2441312	single nucleotide variant	NM_001288973.2(ADAM12):c.2407G>A (p.Gly803Ser)	not specified [RCV004257128]	uncertain significance	10	126036268	126036268	Human		name
329365311	CV2444798	single nucleotide variant	NM_001288973.2(ADAM12):c.2215A>G (p.Lys739Glu)	not specified [RCV004259042]	uncertain significance	10	126039319	126039319	Human		name
329356842	CV2460579	single nucleotide variant	NM_001288973.2(ADAM12):c.1996G>C (p.Val666Leu)	not specified [RCV004268856]	uncertain significance	10	126043148	126043148	Human		name
329374627	CV2464209	single nucleotide variant	NM_001288973.2(ADAM12):c.1093A>G (p.Ser365Gly)	not specified [RCV004273885]	uncertain significance	10	126094037	126094037	Human		name
329381332	CV2464639	single nucleotide variant	NM_001288973.2(ADAM12):c.1387C>T (p.His463Tyr)	not specified [RCV004278322]	uncertain significance	10	126066743	126066743	Human		name
401735992	CV2692248	single nucleotide variant	NM_001288973.2(ADAM12):c.2482G>A (p.Val828Ile)	not specified [RCV004303724]	uncertain significance	10	126036193	126036193	Human		name
401744092	CV2696933	single nucleotide variant	NM_001288973.2(ADAM12):c.1430C>T (p.Thr477Ile)	not specified [RCV004292933]	uncertain significance	10	126064985	126064985	Human		name
401774192	CV2702638	single nucleotide variant	NM_001288973.2(ADAM12):c.1654G>A (p.Ala552Thr)	not specified [RCV004318907]	uncertain significance	10	126049625	126049625	Human		name
401873466	CV2761474	single nucleotide variant	NM_001288973.2(ADAM12):c.2187G>T (p.Lys729Asn)	not specified [RCV004334647]	uncertain significance	10	126039347	126039347	Human		name
405780115	CV3300564	single nucleotide variant	NM_001288973.2(ADAM12):c.1559A>G (p.Asn520Ser)	not specified [RCV004436800]	uncertain significance	10	126064856	126064856	Human		name
405780155	CV3300571	single nucleotide variant	NM_001288973.2(ADAM12):c.1843A>G (p.Thr615Ala)	not specified [RCV004436807]	uncertain significance	10	126049327	126049327	Human		name
405780208	CV3300580	single nucleotide variant	NM_001288973.2(ADAM12):c.1858G>A (p.Gly620Ser)	not specified [RCV004436816]	uncertain significance	10	126049312	126049312	Human		name
405780254	CV3300588	single nucleotide variant	NM_001288973.2(ADAM12):c.2078C>G (p.Thr693Arg)	not specified [RCV004436824]	uncertain significance	10	126043066	126043066	Human		name
405780297	CV3300596	single nucleotide variant	NM_001288973.2(ADAM12):c.2167G>A (p.Val723Met)	not specified [RCV004436832]	uncertain significance	10	126039367	126039367	Human		name
405780378	CV3300610	single nucleotide variant	NM_001288973.2(ADAM12):c.2374T>C (p.Cys792Arg)	not specified [RCV004436846]	uncertain significance	10	126036301	126036301	Human		name
405780426	CV3300618	single nucleotide variant	NM_001288973.2(ADAM12):c.2441G>A (p.Arg814Gln)	not specified [RCV004436854]	uncertain significance	10	126036234	126036234	Human		name
407454955	CV3422287	single nucleotide variant	NM_001288973.2(ADAM12):c.2187G>C (p.Lys729Asn)	not specified [RCV004610078]	uncertain significance	10	126039347	126039347	Human		name
407454994	CV3422307	single nucleotide variant	NM_001288973.2(ADAM12):c.1579G>A (p.Glu527Lys)	not specified [RCV004610098]	uncertain significance	10	126064836	126064836	Human		name
407455012	CV3422316	single nucleotide variant	NM_001288973.2(ADAM12):c.1519G>A (p.Asp507Asn)	not specified [RCV004610107]	uncertain significance	10	126064896	126064896	Human		name
407455030	CV3422325	single nucleotide variant	NM_001288973.2(ADAM12):c.1318C>A (p.Pro440Thr)	not specified [RCV004610116]	uncertain significance	10	126071482	126071482	Human		name
407455051	CV3422336	single nucleotide variant	NM_001288973.2(ADAM12):c.2266C>T (p.Arg756Cys)	not specified [RCV004610127]	uncertain significance	10	126038324	126038324	Human		name
597794402	CV3648032	single nucleotide variant	NM_001288973.2(ADAM12):c.2656C>G (p.Leu886Val)	not specified [RCV004903314]	uncertain significance	10	126019699	126019699	Human		name
597794424	CV3648042	single nucleotide variant	NM_001288973.2(ADAM12):c.2707G>A (p.Ala903Thr)	not specified [RCV004903322]	uncertain significance	10	126017293	126017293	Human		name
597761252	CV3648053	single nucleotide variant	NM_001288973.2(ADAM12):c.2705C>G (p.Thr902Ser)	not specified [RCV004894918]	uncertain significance	10	126017295	126017295	Human		name
597794468	CV3648064	single nucleotide variant	NM_001288973.2(ADAM12):c.2258G>A (p.Arg753Gln)	not specified [RCV004903338]	uncertain significance	10	126038332	126038332	Human		name
597761271	CV3648074	single nucleotide variant	NM_001288973.2(ADAM12):c.1375G>A (p.Ala459Thr)	not specified [RCV004894922]	uncertain significance	10	126066755	126066755	Human		name
597761290	CV3648096	single nucleotide variant	NM_001288973.2(ADAM12):c.1987G>A (p.Gly663Ser)	not specified [RCV004894926]	uncertain significance	10	126046063	126046063	Human		name
597794571	CV3648107	single nucleotide variant	NM_001288973.2(ADAM12):c.1433C>G (p.Ala478Gly)	not specified [RCV004903374]	uncertain significance	10	126064982	126064982	Human		name
597794589	CV3648117	single nucleotide variant	NM_001288973.2(ADAM12):c.2464G>T (p.Ala822Ser)	not specified [RCV004903380]	uncertain significance	10	126036211	126036211	Human		name
598166223	CV3950218	single nucleotide variant	NM_001288973.2(ADAM12):c.1438A>G (p.Arg480Gly)	not specified [RCV005307841]	uncertain significance	10	126064977	126064977	Human		name
598166305	CV3950237	single nucleotide variant	NM_001288973.2(ADAM12):c.1384G>A (p.Ala462Thr)	not specified [RCV005307856]	uncertain significance	10	126066746	126066746	Human		name
598166403	CV3950255	single nucleotide variant	NM_001288973.2(ADAM12):c.1194G>C (p.Glu398Asp)	not specified [RCV005307872]	uncertain significance	10	126071606	126071606	Human		name
598226807	CV3950261	single nucleotide variant	NM_001288973.2(ADAM12):c.1744T>C (p.Cys582Arg)	not specified [RCV005318812]	uncertain significance	10	126049426	126049426	Human		name
598166477	CV3950271	single nucleotide variant	NM_001288973.2(ADAM12):c.2341C>T (p.Pro781Ser)	not specified [RCV005307885]	uncertain significance	10	126038249	126038249	Human		name
15160049	CV723836	single nucleotide variant	NM_001288973.2(ADAM12):c.1975A>G (p.Met659Val)	not provided [RCV000881308]	benign	10	126046075	126046075	Human		name

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