Slc22a14 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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65 records found for search term Slc22a14

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15196019	CV777253	single nucleotide variant	NM_001320033.2(SLC22A14):c.621-8A>C	not provided [RCV000956082]	benign	3	38307558	38307558	Human		name
407508988	CV3473842	single nucleotide variant	NM_001320033.2(SLC22A14):c.25G>C (p.Glu9Gln)	not specified [RCV004672221]	uncertain significance	3	38306051	38306051	Human		name
401926313	CV2827260	single nucleotide variant	NM_001320033.2(SLC22A14):c.489C>T (p.Asp163=)	not provided [RCV003437759]	likely benign	3	38306515	38306515	Human		name
401922186	CV2827261	single nucleotide variant	NM_001320033.2(SLC22A14):c.822G>A (p.Leu274=)	not provided [RCV003433518]	likely benign	3	38309000	38309000	Human		name
598269470	CV3921849	single nucleotide variant	NM_001320033.2(SLC22A14):c.89A>G (p.His30Arg)	not specified [RCV005281966]	uncertain significance	3	38306115	38306115	Human		name
15144609	CV708817	single nucleotide variant	NM_001320033.2(SLC22A14):c.772T>C (p.Leu258=)	not provided [RCV000966860]	benign	3	38307717	38307717	Human		name
8630787	CV85942	single nucleotide variant	NM_004803.3(SLC22A14):c.1661C>T (p.Ser554Phe)	Malignant melanoma [RCV000066026]	not provided	3	38316452	38316452	Human		name
329398553	CV2471605	single nucleotide variant	NM_001320033.2(SLC22A14):c.118A>G (p.Arg40Gly)	not specified [RCV004286902]	uncertain significance	3	38306144	38306144	Human		name
405712910	CV3325199	single nucleotide variant	NM_001320033.2(SLC22A14):c.199C>A (p.Gln67Lys)	not specified [RCV004448746]	uncertain significance	3	38306225	38306225	Human		name
405712919	CV3325200	single nucleotide variant	NM_001320033.2(SLC22A14):c.214C>T (p.Leu72Phe)	not specified [RCV004448747]	uncertain significance	3	38306240	38306240	Human		name
597677755	CV3596477	single nucleotide variant	NM_001320033.2(SLC22A14):c.238T>C (p.Ser80Pro)	not specified [RCV004857101]	uncertain significance	3	38306264	38306264	Human		name
597677821	CV3596483	single nucleotide variant	NM_001320033.2(SLC22A14):c.1533G>A (p.Arg511=)	not specified [RCV004857107]	likely benign	3	38316324	38316324	Human		name
597677831	CV3596484	single nucleotide variant	NM_001320033.2(SLC22A14):c.131T>A (p.Val44Asp)	not specified [RCV004857108]	likely benign	3	38306157	38306157	Human		name
617149891	CV4021285	single nucleotide variant	NM_001320033.2(SLC22A14):c.1239C>T (p.His413=)	not provided [RCV005425254]	likely benign	3	38313802	38313802	Human		name
156239215	CV2217205	single nucleotide variant	NM_001320033.2(SLC22A14):c.608T>C (p.Leu203Pro)	not specified [RCV004087660]	uncertain significance	3	38307345	38307345	Human		name
156140630	CV2280842	single nucleotide variant	NM_001320033.2(SLC22A14):c.655C>G (p.Leu219Val)	not specified [RCV004145098]	uncertain significance	3	38307600	38307600	Human		name
156018850	CV2301685	single nucleotide variant	NM_001320033.2(SLC22A14):c.341A>G (p.Glu114Gly)	not specified [RCV004156509]	uncertain significance	3	38306367	38306367	Human		name
155959249	CV2313888	single nucleotide variant	NM_001320033.2(SLC22A14):c.428C>T (p.Ser143Phe)	not specified [RCV004164200]	uncertain significance	3	38306454	38306454	Human		name
156161093	CV2323417	single nucleotide variant	NM_001320033.2(SLC22A14):c.331T>C (p.Ser111Pro)	not specified [RCV004171810]	uncertain significance	3	38306357	38306357	Human		name
156177631	CV2327213	single nucleotide variant	NM_001320033.2(SLC22A14):c.677T>C (p.Phe226Ser)	not specified [RCV004174673]	uncertain significance	3	38307622	38307622	Human		name
329389214	CV2448800	single nucleotide variant	NM_001320033.2(SLC22A14):c.872A>G (p.Tyr291Cys)	not specified [RCV004261493]	uncertain significance	3	38309050	38309050	Human		name
401775668	CV2710663	single nucleotide variant	NM_001320033.2(SLC22A14):c.776C>G (p.Ala259Gly)	not specified [RCV004319570]	uncertain significance	3	38308954	38308954	Human		name
401874534	CV2774020	single nucleotide variant	NM_001320033.2(SLC22A14):c.992A>G (p.Lys331Arg)	not specified [RCV004358426]	uncertain significance	3	38313046	38313046	Human		name
405712926	CV3325201	single nucleotide variant	NM_001320033.2(SLC22A14):c.629G>A (p.Arg210His)	not specified [RCV004448748]	uncertain significance	3	38307574	38307574	Human		name
405712934	CV3325202	single nucleotide variant	NM_001320033.2(SLC22A14):c.673G>A (p.Gly225Ser)	not specified [RCV004448749]	uncertain significance	3	38307618	38307618	Human		name
405712942	CV3325203	single nucleotide variant	NM_001320033.2(SLC22A14):c.817A>T (p.Ile273Phe)	not specified [RCV004448750]	uncertain significance	3	38308995	38308995	Human		name
405712949	CV3325204	single nucleotide variant	NM_001320033.2(SLC22A14):c.821T>C (p.Leu274Pro)	not specified [RCV004448751]	uncertain significance	3	38308999	38308999	Human		name
405712955	CV3325205	single nucleotide variant	NM_001320033.2(SLC22A14):c.962C>T (p.Pro321Leu)	not specified [RCV004448752]	uncertain significance	3	38313016	38313016	Human		name
407508978	CV3473838	single nucleotide variant	NM_001320033.2(SLC22A14):c.983G>A (p.Gly328Glu)	not specified [RCV004672218]	uncertain significance	3	38313037	38313037	Human		name
407508981	CV3473839	single nucleotide variant	NM_001320033.2(SLC22A14):c.666C>G (p.Ile222Met)	not specified [RCV004672219]	uncertain significance	3	38307611	38307611	Human		name
407519548	CV3473841	single nucleotide variant	NM_001320033.2(SLC22A14):c.449A>G (p.Asn150Ser)	not specified [RCV004676573]	uncertain significance	3	38306475	38306475	Human		name
597677735	CV3596475	single nucleotide variant	NM_001320033.2(SLC22A14):c.512A>G (p.Asn171Ser)	not specified [RCV004857099]	uncertain significance	3	38306538	38306538	Human		name
597677744	CV3596476	single nucleotide variant	NM_001320033.2(SLC22A14):c.428C>A (p.Ser143Tyr)	not specified [RCV004857100]	uncertain significance	3	38306454	38306454	Human		name
597677766	CV3596478	single nucleotide variant	NM_001320033.2(SLC22A14):c.556G>A (p.Ala186Thr)	not specified [RCV004857102]	uncertain significance	3	38307293	38307293	Human		name
597677786	CV3596480	single nucleotide variant	NM_001320033.2(SLC22A14):c.935C>A (p.Ser312Tyr)	not specified [RCV004857104]	uncertain significance	3	38309113	38309113	Human		name
597677798	CV3596481	single nucleotide variant	NM_001320033.2(SLC22A14):c.399G>A (p.Met133Ile)	not specified [RCV004857105]	uncertain significance	3	38306425	38306425	Human		name
597677810	CV3596482	single nucleotide variant	NM_001320033.2(SLC22A14):c.691A>G (p.Met231Val)	not specified [RCV004857106]	likely benign	3	38307636	38307636	Human		name
598269475	CV3921850	single nucleotide variant	NM_001320033.2(SLC22A14):c.853T>G (p.Leu285Val)	not specified [RCV005281967]	uncertain significance	3	38309031	38309031	Human		name
15144603	CV708816	single nucleotide variant	NM_001320033.2(SLC22A14):c.323C>A (p.Pro108His)	not provided [RCV000966859]	benign	3	38306349	38306349	Human		name
150331546	CV1171111	single nucleotide variant	NM_001320033.2(SLC22A14):c.1535C>T (p.Ala512Val)	not provided [RCV001538675]	benign	3	38316326	38316326	Human		name
156219134	CV2254016	single nucleotide variant	NM_001320033.2(SLC22A14):c.1284C>G (p.Ile428Met)	not specified [RCV004129472]	uncertain significance	3	38313847	38313847	Human		name
156314414	CV2257155	single nucleotide variant	NM_001320033.2(SLC22A14):c.1567G>A (p.Val523Met)	not specified [RCV004123111]	uncertain significance	3	38316358	38316358	Human		name
155906967	CV2279588	single nucleotide variant	NM_001320033.2(SLC22A14):c.1746G>T (p.Lys582Asn)	not specified [RCV004142089]	uncertain significance	3	38318210	38318210	Human		name
156049302	CV2319297	single nucleotide variant	NM_001320033.2(SLC22A14):c.1250G>C (p.Ser417Thr)	not specified [RCV004180123]	uncertain significance	3	38313813	38313813	Human		name
329389593	CV2445221	single nucleotide variant	NM_001320033.2(SLC22A14):c.1408C>T (p.Arg470Cys)	not specified [RCV004263855]	likely benign	3	38315587	38315587	Human		name
329373822	CV2452558	single nucleotide variant	NM_001320033.2(SLC22A14):c.1731A>G (p.Ile577Met)	not specified [RCV004273144]	likely benign	3	38316522	38316522	Human		name
329362948	CV2464855	single nucleotide variant	NM_001320033.2(SLC22A14):c.1094G>A (p.Arg365Gln)	not specified [RCV004284800]	likely benign	3	38313416	38313416	Human		name
401863320	CV2775891	single nucleotide variant	NM_001320033.2(SLC22A14):c.1780G>A (p.Val594Ile)	not specified [RCV004344922]	uncertain significance	3	38318244	38318244	Human		name
405712863	CV3325192	single nucleotide variant	NM_001320033.2(SLC22A14):c.1184A>C (p.Tyr395Ser)	not specified [RCV004448739]	uncertain significance	3	38313747	38313747	Human		name
405712873	CV3325193	single nucleotide variant	NM_001320033.2(SLC22A14):c.1225G>A (p.Val409Ile)	not specified [RCV004448740]	likely benign	3	38313788	38313788	Human		name
405712878	CV3325194	single nucleotide variant	NM_001320033.2(SLC22A14):c.1447G>A (p.Val483Met)	not specified [RCV004448741]	uncertain significance	3	38315626	38315626	Human		name
405712883	CV3325195	single nucleotide variant	NM_001320033.2(SLC22A14):c.1486A>G (p.Thr496Ala)	not specified [RCV004448742]	uncertain significance	3	38315665	38315665	Human		name
405712889	CV3325196	single nucleotide variant	NM_001320033.2(SLC22A14):c.1615C>T (p.Leu539Phe)	not specified [RCV004448743]	likely benign	3	38316406	38316406	Human		name
405712895	CV3325197	single nucleotide variant	NM_001320033.2(SLC22A14):c.1651G>A (p.Val551Met)	not specified [RCV004448744]	uncertain significance	3	38316442	38316442	Human		name
405712900	CV3325198	single nucleotide variant	NM_001320033.2(SLC22A14):c.1678C>T (p.Pro560Ser)	not specified [RCV004448745]	uncertain significance	3	38316469	38316469	Human		name
407519547	CV3473835	single nucleotide variant	NM_001320033.2(SLC22A14):c.1717C>A (p.His573Asn)	not specified [RCV004676572]	uncertain significance	3	38316508	38316508	Human		name
407508971	CV3473836	single nucleotide variant	NM_001320033.2(SLC22A14):c.1570G>A (p.Ala524Thr)	not specified [RCV004672216]	likely benign	3	38316361	38316361	Human		name
407508975	CV3473837	single nucleotide variant	NM_001320033.2(SLC22A14):c.1021G>A (p.Ala341Thr)	not specified [RCV004672217]	uncertain significance	3	38313075	38313075	Human		name
598269427	CV3921841	single nucleotide variant	NM_001320033.2(SLC22A14):c.1261G>T (p.Val421Leu)	not specified [RCV005281959]	uncertain significance	3	38313824	38313824	Human		name
598269433	CV3921842	single nucleotide variant	NM_001320033.2(SLC22A14):c.1349G>C (p.Trp450Ser)	not specified [RCV005281960]	uncertain significance	3	38313912	38313912	Human		name
598269439	CV3921843	single nucleotide variant	NM_001320033.2(SLC22A14):c.1100C>G (p.Ser367Cys)	not specified [RCV005281961]	uncertain significance	3	38313422	38313422	Human		name
598269445	CV3921844	single nucleotide variant	NM_001320033.2(SLC22A14):c.1109A>G (p.Asp370Gly)	not specified [RCV005281962]	uncertain significance	3	38313431	38313431	Human		name
598269458	CV3921847	single nucleotide variant	NM_001320033.2(SLC22A14):c.1295A>C (p.Gln432Pro)	not specified [RCV005281964]	uncertain significance	3	38313858	38313858	Human		name
598269464	CV3921848	single nucleotide variant	NM_001320033.2(SLC22A14):c.1222A>G (p.Ser408Gly)	not specified [RCV005281965]	uncertain significance	3	38313785	38313785	Human		name
15150721	CV708818	single nucleotide variant	NM_001320033.2(SLC22A14):c.1505C>T (p.Thr502Ile)	not provided [RCV000967999]	benign	3	38315684	38315684	Human		name

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