Slc39a10 Variant Search Result - Rat Genome Database

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62 records found for search term Slc39a10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8576908	CV111277	single nucleotide variant	NM_001127257.1(SLC39A10):c.2147-4686G>A	Lung cancer [RCV000091800]	uncertain significance	2	195723473	195723473	Human		name
401739723	CV2704664	single nucleotide variant	NM_020342.3(SLC39A10):c.8T>C (p.Val3Ala)	not specified [RCV004313693]	uncertain significance	2	195680050	195680050	Human		name
405709072	CV3329115	single nucleotide variant	NM_020342.3(SLC39A10):c.27T>A (p.Phe9Leu)	not specified [RCV004461503]	uncertain significance	2	195680069	195680069	Human		name
597703222	CV3599947	single nucleotide variant	NM_020342.3(SLC39A10):c.88G>A (p.Asp30Asn)	not specified [RCV004860174]	uncertain significance	2	195680130	195680130	Human		name
156063078	CV2321049	single nucleotide variant	NM_020342.3(SLC39A10):c.208C>T (p.Arg70Cys)	not specified [RCV004172836]	uncertain significance	2	195680250	195680250	Human		name
598243803	CV3914986	single nucleotide variant	NM_020342.3(SLC39A10):c.121C>T (p.Arg41Cys)	not specified [RCV005276761]	uncertain significance	2	195680163	195680163	Human		name
156137426	CV2196257	single nucleotide variant	NM_020342.3(SLC39A10):c.686C>A (p.Pro229Gln)	not specified [RCV004073610]	uncertain significance	2	195680728	195680728	Human		name
156219790	CV2226007	single nucleotide variant	NM_020342.3(SLC39A10):c.664G>A (p.Glu222Lys)	not specified [RCV004105167]	uncertain significance	2	195680706	195680706	Human		name
156125277	CV2237542	single nucleotide variant	NM_020342.3(SLC39A10):c.307G>T (p.Asp103Tyr)	not specified [RCV004106483]	uncertain significance	2	195680349	195680349	Human		name
156054697	CV2326526	single nucleotide variant	NM_020342.3(SLC39A10):c.959C>T (p.Ala320Val)	not specified [RCV004183080]	uncertain significance	2	195681001	195681001	Human		name
329375065	CV2431122	single nucleotide variant	NM_020342.3(SLC39A10):c.865G>A (p.Asp289Asn)	not specified [RCV004250480]	uncertain significance	2	195680907	195680907	Human		name
329388408	CV2437382	single nucleotide variant	NM_020342.3(SLC39A10):c.548G>A (p.Arg183His)	not specified [RCV004256251]	uncertain significance	2	195680590	195680590	Human		name
329389630	CV2445259	single nucleotide variant	NM_020342.3(SLC39A10):c.944A>G (p.His315Arg)	not specified [RCV004263889]	uncertain significance	2	195680986	195680986	Human		name
405709080	CV3329116	single nucleotide variant	NM_020342.3(SLC39A10):c.319G>A (p.Asp107Asn)	not specified [RCV004461504]	uncertain significance	2	195680361	195680361	Human		name
405709086	CV3329117	single nucleotide variant	NM_020342.3(SLC39A10):c.326T>C (p.Val109Ala)	not specified [RCV004461505]	uncertain significance	2	195680368	195680368	Human		name
405709094	CV3329118	single nucleotide variant	NM_020342.3(SLC39A10):c.341T>C (p.Ile114Thr)	not specified [RCV004461506]	uncertain significance	2	195680383	195680383	Human		name
405709101	CV3329119	single nucleotide variant	NM_020342.3(SLC39A10):c.530G>A (p.Arg177His)	not specified [RCV004461507]	uncertain significance	2	195680572	195680572	Human		name
405709113	CV3329121	single nucleotide variant	NM_020342.3(SLC39A10):c.806C>T (p.Pro269Leu)	not specified [RCV004461509]	uncertain significance	2	195680848	195680848	Human		name
407514730	CV3484576	single nucleotide variant	NM_020342.3(SLC39A10):c.521A>G (p.His174Arg)	not specified [RCV004674677]	uncertain significance	2	195680563	195680563	Human		name
407514732	CV3484577	single nucleotide variant	NM_020342.3(SLC39A10):c.475A>G (p.Thr159Ala)	not specified [RCV004674678]	uncertain significance	2	195680517	195680517	Human		name
407514739	CV3484581	single nucleotide variant	NM_020342.3(SLC39A10):c.536G>A (p.Arg179His)	not specified [RCV004674681]	likely benign	2	195680578	195680578	Human		name
597765782	CV3599943	single nucleotide variant	NM_020342.3(SLC39A10):c.862C>T (p.His288Tyr)	not specified [RCV004870494]	uncertain significance	2	195680904	195680904	Human		name
597765786	CV3599944	single nucleotide variant	NM_020342.3(SLC39A10):c.460G>A (p.Asp154Asn)	not specified [RCV004870495]	uncertain significance	2	195680502	195680502	Human		name
597703211	CV3599945	single nucleotide variant	NM_020342.3(SLC39A10):c.772G>C (p.Gly258Arg)	not specified [RCV004860173]	uncertain significance	2	195680814	195680814	Human		name
598237246	CV3914984	single nucleotide variant	NM_020342.3(SLC39A10):c.854G>A (p.Arg285His)	not specified [RCV005275618]	likely benign	2	195680896	195680896	Human		name
598243809	CV3914987	single nucleotide variant	NM_020342.3(SLC39A10):c.535C>T (p.Arg179Cys)	not specified [RCV005276762]	likely benign	2	195680577	195680577	Human		name
598243837	CV3914991	single nucleotide variant	NM_020342.3(SLC39A10):c.698G>T (p.Arg233Met)	not specified [RCV005276766]	uncertain significance	2	195680740	195680740	Human		name
598243843	CV3914992	single nucleotide variant	NM_020342.3(SLC39A10):c.460G>C (p.Asp154His)	not specified [RCV005276767]	uncertain significance	2	195680502	195680502	Human		name
598243862	CV3914995	single nucleotide variant	NM_020342.3(SLC39A10):c.843T>A (p.His281Gln)	not specified [RCV005276770]	uncertain significance	2	195680885	195680885	Human		name
598243870	CV3914996	single nucleotide variant	NM_020342.3(SLC39A10):c.674A>G (p.Asp225Gly)	not specified [RCV005276771]	uncertain significance	2	195680716	195680716	Human		name
8630109	CV85256	single nucleotide variant	NM_001127257.1(SLC39A10):c.162A>G (p.Gln54=)	Malignant melanoma [RCV000065338]	not provided	2	195680204	195680204	Human		name
156198711	CV2312941	single nucleotide variant	NM_020342.3(SLC39A10):c.2023A>T (p.Met675Leu)	not specified [RCV004159452]	uncertain significance	2	195716963	195716963	Human		name
156257827	CV2322095	single nucleotide variant	NM_020342.3(SLC39A10):c.2399A>G (p.Gln800Arg)	not specified [RCV004173837]	uncertain significance	2	195734944	195734944	Human		name
156193173	CV2350483	single nucleotide variant	NM_020342.3(SLC39A10):c.1054A>T (p.Asn352Tyr)	not specified [RCV004204848]	uncertain significance	2	195683744	195683744	Human		name
156346817	CV2353748	single nucleotide variant	NM_020342.3(SLC39A10):c.1873G>A (p.Ala625Thr)	not specified [RCV004201757]	uncertain significance	2	195716813	195716813	Human		name
329363649	CV2446084	single nucleotide variant	NM_020342.3(SLC39A10):c.2266G>A (p.Ala756Thr)	not specified [RCV004270644]	uncertain significance	2	195728278	195728278	Human		name
401772885	CV2698018	single nucleotide variant	NM_020342.3(SLC39A10):c.1813A>G (p.Ile605Val)	not specified [RCV004302822]	uncertain significance	2	195716753	195716753	Human		name
405709022	CV3329108	single nucleotide variant	NM_020342.3(SLC39A10):c.1858G>T (p.Asp620Tyr)	not specified [RCV004461496]	uncertain significance	2	195716798	195716798	Human		name
405709031	CV3329109	single nucleotide variant	NM_020342.3(SLC39A10):c.1891G>A (p.Glu631Lys)	not specified [RCV004461497]	uncertain significance	2	195716831	195716831	Human		name
405709038	CV3329110	single nucleotide variant	NM_020342.3(SLC39A10):c.2182G>A (p.Val728Ile)	not specified [RCV004461498]	uncertain significance	2	195728194	195728194	Human		name
405709045	CV3329111	single nucleotide variant	NM_020342.3(SLC39A10):c.2216C>T (p.Ala739Val)	not specified [RCV004461499]	uncertain significance	2	195728228	195728228	Human		name
405709049	CV3329112	single nucleotide variant	NM_020342.3(SLC39A10):c.2218A>G (p.Met740Val)	not specified [RCV004461500]	uncertain significance	2	195728230	195728230	Human		name
405709055	CV3329113	single nucleotide variant	NM_020342.3(SLC39A10):c.2377C>A (p.His793Asn)	not specified [RCV004461501]	uncertain significance	2	195734922	195734922	Human		name
407514734	CV3484578	single nucleotide variant	NM_020342.3(SLC39A10):c.1733A>T (p.Asn578Ile)	not specified [RCV004674679]	uncertain significance	2	195716673	195716673	Human		name
407451654	CV3484579	single nucleotide variant	NM_020342.3(SLC39A10):c.1351A>G (p.Met451Val)	not specified [RCV004683732]	uncertain significance	2	195706750	195706750	Human		name
407514737	CV3484580	single nucleotide variant	NM_020342.3(SLC39A10):c.1010G>A (p.Cys337Tyr)	not specified [RCV004674680]	uncertain significance	2	195683700	195683700	Human		name
407514742	CV3484583	single nucleotide variant	NM_020342.3(SLC39A10):c.1370T>C (p.Leu457Pro)	not specified [RCV004674683]	uncertain significance	2	195706769	195706769	Human		name
597765790	CV3599946	single nucleotide variant	NM_020342.3(SLC39A10):c.1157A>C (p.Glu386Ala)	not specified [RCV004870496]	uncertain significance	2	195683847	195683847	Human		name
597765793	CV3599948	single nucleotide variant	NM_020342.3(SLC39A10):c.1815A>G (p.Ile605Met)	not specified [RCV004870497]	likely benign	2	195716755	195716755	Human		name
597703234	CV3599949	single nucleotide variant	NM_020342.3(SLC39A10):c.2395G>A (p.Gly799Arg)	not specified [RCV004860175]	uncertain significance	2	195734940	195734940	Human		name
597703243	CV3599950	single nucleotide variant	NM_020342.3(SLC39A10):c.1007A>C (p.Glu336Ala)	not specified [RCV004860176]	uncertain significance	2	195681049	195681049	Human		name
597765797	CV3599951	single nucleotide variant	NM_020342.3(SLC39A10):c.1687C>T (p.Pro563Ser)	not specified [RCV004870498]	uncertain significance	2	195713544	195713544	Human		name
597703254	CV3599952	single nucleotide variant	NM_020342.3(SLC39A10):c.1711G>T (p.Val571Phe)	not specified [RCV004860177]	uncertain significance	2	195716651	195716651	Human		name
598243794	CV3914985	single nucleotide variant	NM_020342.3(SLC39A10):c.1711G>A (p.Val571Ile)	not specified [RCV005276760]	uncertain significance	2	195716651	195716651	Human		name
598243815	CV3914988	single nucleotide variant	NM_020342.3(SLC39A10):c.1448A>C (p.His483Pro)	not specified [RCV005276763]	uncertain significance	2	195708717	195708717	Human		name
598243822	CV3914989	single nucleotide variant	NM_020342.3(SLC39A10):c.1002T>A (p.His334Gln)	not specified [RCV005276764]	likely benign	2	195681044	195681044	Human		name
598243829	CV3914990	single nucleotide variant	NM_020342.3(SLC39A10):c.1267C>G (p.Leu423Val)	not specified [RCV005276765]	uncertain significance	2	195706666	195706666	Human		name
598243855	CV3914994	single nucleotide variant	NM_020342.3(SLC39A10):c.1888G>T (p.Gly630Cys)	not specified [RCV005276769]	uncertain significance	2	195716828	195716828	Human		name
8625238	CV80357	single nucleotide variant	NM_001127257.1(SLC39A10):c.438C>T (p.Ser146=)	Malignant melanoma [RCV000060434]	not provided	2	195680480	195680480	Human		name
8630108	CV85255	single nucleotide variant	NM_001127257.1(SLC39A10):c.91C>T (p.His31Tyr)	Malignant melanoma [RCV000065337]	not provided	2	195680133	195680133	Human		name
8630110	CV85257	single nucleotide variant	NM_001127257.1(SLC39A10):c.1212A>G (p.Ala404=)	Malignant melanoma [RCV000065339]	not provided	2	195683902	195683902	Human		name
8630111	CV85258	single nucleotide variant	NM_001127257.1(SLC39A10):c.1953C>T (p.Ser651=)	Malignant melanoma [RCV000065340]	not provided	2	195716893	195716893	Human		name

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