Rlim Variant Search Result - Rat Genome Database

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131 records found for search term Rlim

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
152154582	CV1667936	single nucleotide variant	NM_016120.4(RLIM):c.*1380C>T	not provided [RCV002221829]	uncertain significance	X	74590060	74590060	Human		name
401928918	CV2829322	single nucleotide variant	NM_016120.4(RLIM):c.169+6C>T	not provided [RCV003439658]	likely benign	X	74595803	74595803	Human		name
596943815	CV3544394	single nucleotide variant	NM_016120.4(RLIM):c.170-19C>T	not specified [RCV004800874]	likely benign	X	74594408	74594408	Human		name
408380561	CV3520781	microsatellite	NM_183353.2(RLIM):c.257_259del	not provided [RCV004761614]	uncertain significance	X	74593056	74593058	Human		name
13462797	CV439348	deletion	NM_016120.4(RLIM):c.-23-12_-23-11del	not provided [RCV000514839]	likely benign	X	74596011	74596012	Human		name
15163034	CV717865	single nucleotide variant	NM_016120.4(RLIM):c.66G>A (p.Gln22=)	not provided [RCV000970395]	benign	X	74595912	74595912	Human		name
598176752	CV4008181	single nucleotide variant	NM_016120.4(RLIM):c.17C>T (p.Ser6Phe)	Intellectual disability, X-linked 61 [RCV005393697]	likely benign	X	74595961	74595961	Human	1	name
15154815	CV717864	single nucleotide variant	NM_016120.4(RLIM):c.240A>C (p.Ser80=)	not provided [RCV000968807]	benign	X	74594319	74594319	Human		name
150548971	CV1294001	single nucleotide variant	NM_016120.4(RLIM):c.83G>A (p.Arg28Gln)	not provided [RCV001764841]	uncertain significance	X	74595895	74595895	Human		name
9687165	CV171693	deletion	NM_016120.4(RLIM):c.260del (p.Asp87fs)	Prostate cancer [RCV000149384]	uncertain significance	X	74593055	74593055	Human	2	name
329848851	CV2523600	single nucleotide variant	NM_016120.4(RLIM):c.74G>T (p.Arg25Leu)	Intellectual disability, X-linked 61 [RCV003225614]	uncertain significance	X	74595904	74595904	Human	1	name
405273936	CV3194907	single nucleotide variant	NM_016120.4(RLIM):c.85G>C (p.Glu29Gln)	RLIM-related disorder [RCV003902149]	uncertain significance	X	74595893	74595893	Human		name , trait , alternate_id
408391857	CV3523472	single nucleotide variant	NM_016120.4(RLIM):c.69G>A (p.Met23Ile)	not provided [RCV004770846]	uncertain significance	X	74595909	74595909	Human		name
617150390	CV4019028	single nucleotide variant	NM_016120.4(RLIM):c.82C>G (p.Arg28Gly)	not provided [RCV005423436]	uncertain significance	X	74595896	74595896	Human		name
13518446	CV492707	single nucleotide variant	NM_016120.4(RLIM):c.777G>A (p.Thr259=)	not provided [RCV000884376]\|not specified [RCV000597432]	benign\|likely benign	X	74592538	74592538	Human		name
127243516	CV1086838	single nucleotide variant	NM_016120.4(RLIM):c.1389C>A (p.Ser463=)	not provided [RCV001393536]	likely benign	X	74591926	74591926	Human		name
127294870	CV1150942	single nucleotide variant	NM_016120.4(RLIM):c.1413A>T (p.Ser471=)	Inborn genetic diseases [RCV005271330]\|not provided [RCV001497095]	likely benign	X	74591902	74591902	Human	1	name
150429458	CV1189250	single nucleotide variant	NM_016120.4(RLIM):c.230C>T (p.Pro77Leu)	RLIM-related syndromic intellectual disability [RCV001563635]\|not provided [RCV003312009]	uncertain significance	X	74594329	74594329	Human	1	name , trait
155945369	CV1935588	single nucleotide variant	NM_016120.4(RLIM):c.274G>C (p.Val92Leu)	not provided [RCV002511336]	likely benign\|uncertain significance	X	74593041	74593041	Human		name
329351103	CV2477932	single nucleotide variant	NM_016120.4(RLIM):c.191T>G (p.Leu64Trp)	not provided [RCV003224045]	uncertain significance	X	74594368	74594368	Human		name
401796439	CV2740625	single nucleotide variant	NM_016120.4(RLIM):c.226C>A (p.Pro76Thr)	not provided [RCV003321295]	uncertain significance	X	74594333	74594333	Human		name
401830113	CV2744098	single nucleotide variant	NM_016120.4(RLIM):c.1455T>C (p.Ser485=)	not provided [RCV003327243]	likely benign	X	74591860	74591860	Human		name
401928912	CV2829320	single nucleotide variant	NM_016120.4(RLIM):c.1431T>G (p.Pro477=)	not provided [RCV003439656]	likely benign	X	74591884	74591884	Human		name
401928915	CV2829321	single nucleotide variant	NM_016120.4(RLIM):c.292A>C (p.Ile98Leu)	Inborn genetic diseases [RCV004364653]\|not provided [RCV003439657]	likely benign	X	74593023	74593023	Human	1	name
407456700	CV3415956	single nucleotide variant	NM_016120.4(RLIM):c.1194A>G (p.Thr398=)	not provided [RCV004598833]	likely benign	X	74592121	74592121	Human		name
408389339	CV3529340	single nucleotide variant	NM_016120.4(RLIM):c.290C>G (p.Ser97Cys)	not provided [RCV004774162]	uncertain significance	X	74593025	74593025	Human		name
596945078	CV3543705	single nucleotide variant	NM_016120.4(RLIM):c.147T>G (p.Asp49Glu)	not provided [RCV004801827]	uncertain significance	X	74595831	74595831	Human		name
598127420	CV3888181	single nucleotide variant	NM_016120.4(RLIM):c.1359T>C (p.Ser453=)	not provided [RCV005242867]	likely benign	X	74591956	74591956	Human		name
598176451	CV3891145	single nucleotide variant	NM_016120.4(RLIM):c.257G>A (p.Gly86Glu)	not provided [RCV005251998]	uncertain significance	X	74593058	74593058	Human		name
13446227	CV438454	single nucleotide variant	NM_016120.4(RLIM):c.141G>A (p.Met47Ile)	not provided [RCV000513445]	uncertain significance	X	74595837	74595837	Human		name
13706472	CV537575	single nucleotide variant	NM_016120.4(RLIM):c.223C>G (p.Pro75Ala)	Intellectual disability, X-linked 61 [RCV004723043]\|not provided [RCV000659166]	likely benign\|uncertain significance	X	74594336	74594336	Human	1	name
15185901	CV706314	single nucleotide variant	NM_016120.4(RLIM):c.1395G>C (p.Ser465=)	not provided [RCV000953121]	likely benign	X	74591920	74591920	Human		name
15170355	CV706315	single nucleotide variant	NM_016120.4(RLIM):c.1395G>A (p.Ser465=)	not provided [RCV000949635]	benign	X	74591920	74591920	Human		name
15201356	CV758652	single nucleotide variant	NM_016120.4(RLIM):c.1515A>C (p.Ser505=)	not provided [RCV000913114]	likely benign	X	74591800	74591800	Human		name
41408262	CV980821	single nucleotide variant	NM_016120.4(RLIM):c.131A>G (p.Tyr44Cys)	Intellectual disability, X-linked 61 [RCV003333147]\|not provided [RCV001281645]	likely pathogenic\|uncertain significance	X	74595847	74595847	Human	1	name
126726670	CV1019066	single nucleotide variant	NM_016120.4(RLIM):c.736A>G (p.Ile246Val)	Inborn genetic diseases [RCV004035729]\|Intellectual disability, X-linked 61 [RCV001332108]	uncertain significance	X	74592579	74592579	Human	2	name
127230272	CV1087120	single nucleotide variant	NM_016120.4(RLIM):c.366G>C (p.Trp122Cys)	See cases [RCV001420213]	likely pathogenic	X	74592949	74592949	Human		name
150338601	CV1174406	single nucleotide variant	NM_016120.4(RLIM):c.992G>A (p.Gly331Glu)	Intellectual disability, X-linked 61 [RCV001542628]	likely pathogenic	X	74592323	74592323	Human	1	name
150426075	CV1185857	single nucleotide variant	NM_016120.4(RLIM):c.656G>A (p.Arg219Gln)	not provided [RCV001558875]	uncertain significance	X	74592659	74592659	Human		name
150419541	CV1199541	single nucleotide variant	NM_016120.4(RLIM):c.388C>A (p.Pro130Thr)	not provided [RCV001577224]	uncertain significance	X	74592927	74592927	Human		name
150530899	CV1299170	single nucleotide variant	NM_016120.4(RLIM):c.496G>A (p.Glu166Lys)	not provided [RCV001756863]	uncertain significance	X	74592819	74592819	Human		name
150527937	CV1300950	single nucleotide variant	NM_016120.4(RLIM):c.433C>T (p.Arg145Cys)	not provided [RCV001754810]	uncertain significance	X	74592882	74592882	Human		name
152034039	CV1669088	single nucleotide variant	NM_016120.4(RLIM):c.796C>T (p.Arg266Trp)	not provided [RCV002223432]	uncertain significance	X	74592519	74592519	Human		name
153001445	CV1680008	single nucleotide variant	NM_016120.4(RLIM):c.443G>T (p.Gly148Val)	not provided [RCV002251687]	uncertain significance	X	74592872	74592872	Human		name
156148065	CV2197003	single nucleotide variant	NM_016120.4(RLIM):c.587C>T (p.Thr196Ile)	Inborn genetic diseases [RCV002641698]	likely benign	X	74592728	74592728	Human	1	name
156143889	CV2268826	single nucleotide variant	NM_016120.4(RLIM):c.703A>G (p.Met235Val)	Inborn genetic diseases [RCV002826370]	uncertain significance	X	74592612	74592612	Human	1	name
156451026	CV2402403	single nucleotide variant	NM_016120.4(RLIM):c.379C>T (p.Arg127Trp)	not provided [RCV003123202]	uncertain significance	X	74592936	74592936	Human		name
243051490	CV2404087	single nucleotide variant	NM_016120.4(RLIM):c.583T>C (p.Ser195Pro)	not provided [RCV003128942]	uncertain significance	X	74592732	74592732	Human		name
243060185	CV2413754	single nucleotide variant	NM_016120.4(RLIM):c.507A>C (p.Glu169Asp)	Intellectual disability, X-linked 61 [RCV003135774]	uncertain significance	X	74592808	74592808	Human	1	name
243060211	CV2413756	single nucleotide variant	NM_016120.4(RLIM):c.826T>C (p.Ser276Pro)	Intellectual disability, X-linked 61 [RCV003135776]	uncertain significance	X	74592489	74592489	Human	1	name
243053709	CV2418252	single nucleotide variant	NM_016120.4(RLIM):c.493G>A (p.Gly165Arg)	not provided [RCV003154321]	uncertain significance	X	74592822	74592822	Human		name
401755974	CV2686194	single nucleotide variant	NM_016120.4(RLIM):c.539G>T (p.Arg180Leu)	Inborn genetic diseases [RCV003255446]	uncertain significance	X	74592776	74592776	Human	1	name
401751580	CV2727054	single nucleotide variant	NM_016120.4(RLIM):c.925T>C (p.Ser309Pro)	Inborn genetic diseases [RCV003295544]	uncertain significance	X	74592390	74592390	Human	1	name
401917331	CV2829802	single nucleotide variant	NM_016120.4(RLIM):c.670A>G (p.Arg224Gly)	not provided [RCV003443846]	uncertain significance	X	74592645	74592645	Human		name
404985889	CV2852377	single nucleotide variant	NM_016120.4(RLIM):c.485G>A (p.Arg162His)	Inborn genetic diseases [RCV005273708]\|not specified [RCV003489613]	uncertain significance	X	74592830	74592830	Human	1	name
405753159	CV3316212	single nucleotide variant	NM_016120.4(RLIM):c.512A>G (p.Asn171Ser)	Inborn genetic diseases [RCV004454097]	uncertain significance	X	74592803	74592803	Human	1	name
405753164	CV3316213	single nucleotide variant	NM_016120.4(RLIM):c.586A>G (p.Thr196Ala)	Inborn genetic diseases [RCV004454098]	uncertain significance	X	74592729	74592729	Human	1	name
407426850	CV3411650	single nucleotide variant	NM_016120.4(RLIM):c.704T>G (p.Met235Arg)	not provided [RCV004590828]	uncertain significance	X	74592611	74592611	Human		name
408367084	CV3512943	single nucleotide variant	NM_016120.4(RLIM):c.497A>G (p.Glu166Gly)	RLIM-related disorder [RCV004757814]	uncertain significance	X	74592818	74592818	Human		name , trait , alternate_id
408390864	CV3521053	single nucleotide variant	NM_016120.4(RLIM):c.956T>C (p.Ile319Thr)	not provided [RCV004762875]	uncertain significance	X	74592359	74592359	Human		name
408381995	CV3526668	single nucleotide variant	NM_016120.4(RLIM):c.655C>T (p.Arg219Trp)	not provided [RCV004771981]	uncertain significance	X	74592660	74592660	Human		name
596926291	CV3530759	single nucleotide variant	NM_016120.4(RLIM):c.728A>G (p.His243Arg)	not provided [RCV004778344]	uncertain significance	X	74592587	74592587	Human		name
596948270	CV3549352	single nucleotide variant	NM_016120.4(RLIM):c.938G>C (p.Gly313Ala)	not provided [RCV004812172]	uncertain significance	X	74592377	74592377	Human		name
616935351	CV4015988	single nucleotide variant	NM_016120.4(RLIM):c.785G>A (p.Ser262Asn)	not provided [RCV005414852]	uncertain significance	X	74592530	74592530	Human		name
617149668	CV4017619	single nucleotide variant	NM_016120.4(RLIM):c.339A>C (p.Arg113Ser)	not provided [RCV005417277]	uncertain significance	X	74592976	74592976	Human		name
14691267	CV622004	single nucleotide variant	NM_016120.4(RLIM):c.659G>A (p.Arg220Lys)	not provided [RCV000782041]	likely pathogenic	X	74592656	74592656	Human		name
15112468	CV729702	single nucleotide variant	NM_016120.4(RLIM):c.533A>C (p.Asn178Thr)	not provided [RCV000894475]	benign	X	74592782	74592782	Human		name
150555159	CV1295978	single nucleotide variant	NM_016120.4(RLIM):c.1094G>A (p.Arg365His)	not provided [RCV001772487]	uncertain significance	X	74592221	74592221	Human		name
150555163	CV1295982	single nucleotide variant	NM_016120.4(RLIM):c.1000C>T (p.Arg334Trp)	not provided [RCV001772491]	uncertain significance	X	74592315	74592315	Human		name
150556218	CV1296765	single nucleotide variant	NM_016120.4(RLIM):c.1430C>T (p.Pro477Leu)	not provided [RCV001774055]	uncertain significance	X	74591885	74591885	Human		name
151235052	CV1318311	single nucleotide variant	NM_016120.4(RLIM):c.1403G>A (p.Ser468Asn)	not provided [RCV001794634]	uncertain significance	X	74591912	74591912	Human		name
151348776	CV1324215	single nucleotide variant	NM_016120.4(RLIM):c.1490A>G (p.Asn497Ser)	Intellectual disability, X-linked 61 [RCV001808131]	uncertain significance	X	74591825	74591825	Human	1	name
10042961	CV166020	single nucleotide variant	NM_016120.4(RLIM):c.1067A>G (p.Tyr356Cys)	Global developmental delay [RCV001526527]\|Intellectual disability, X-linked 61 [RCV000207499]\|Non-syndromic X-linked intellectual disability [RCV000170337]	pathogenic\|likely pathogenic\|uncertain significance	X	74592248	74592248	Human	4	name
155641974	CV1706113	single nucleotide variant	NM_016120.4(RLIM):c.1468T>A (p.Ser490Thr)	not provided [RCV002286975]	uncertain significance	X	74591847	74591847	Human		name
155642916	CV1707562	single nucleotide variant	NM_016120.4(RLIM):c.1311G>A (p.Met437Ile)	Intellectual disability, X-linked 61 [RCV002289023]	uncertain significance	X	74592004	74592004	Human	1	name
155797321	CV1859284	single nucleotide variant	NM_016120.4(RLIM):c.1283C>T (p.Pro428Leu)	not provided [RCV002464912]	uncertain significance	X	74592032	74592032	Human		name
155797647	CV1860415	single nucleotide variant	NM_016120.4(RLIM):c.1743C>G (p.Asn581Lys)	not provided [RCV002467057]	uncertain significance	X	74591572	74591572	Human		name
156051400	CV1867714	single nucleotide variant	NM_016120.4(RLIM):c.1011T>G (p.Asp337Glu)	not provided [RCV002510187]	uncertain significance	X	74592304	74592304	Human		name
156237013	CV2193531	single nucleotide variant	NM_016120.4(RLIM):c.1271G>A (p.Ser424Asn)	Inborn genetic diseases [RCV002645326]	uncertain significance	X	74592044	74592044	Human	1	name
155960987	CV2204416	single nucleotide variant	NM_016120.4(RLIM):c.1321G>C (p.Glu441Gln)	Inborn genetic diseases [RCV002686612]	uncertain significance	X	74591994	74591994	Human	1	name
156064008	CV2317664	single nucleotide variant	NM_016120.4(RLIM):c.1172A>G (p.Asn391Ser)	Inborn genetic diseases [RCV002925225]	uncertain significance	X	74592143	74592143	Human	1	name
156242751	CV2347025	single nucleotide variant	NM_016120.4(RLIM):c.1691A>G (p.Asn564Ser)	Inborn genetic diseases [RCV002987485]	uncertain significance	X	74591624	74591624	Human	1	name
155909834	CV2360045	single nucleotide variant	NM_016120.4(RLIM):c.1343G>A (p.Gly448Asp)	Inborn genetic diseases [RCV002991088]\|not provided [RCV003435951]	likely benign	X	74591972	74591972	Human	1	name
156163729	CV2389609	single nucleotide variant	NM_016120.4(RLIM):c.1864A>G (p.Ser622Gly)	Inborn genetic diseases [RCV002764884]	uncertain significance	X	74591451	74591451	Human	1	name
156434904	CV2403184	single nucleotide variant	NM_016120.4(RLIM):c.1057A>G (p.Thr353Ala)	not provided [RCV003127140]	uncertain significance	X	74592258	74592258	Human		name
243052276	CV2417810	single nucleotide variant	NM_016120.4(RLIM):c.1115G>A (p.Arg372Gln)	Inborn genetic diseases [RCV005273640]\|Intellectual disability, X-linked 61 [RCV003152874]	uncertain significance	X	74592200	74592200	Human	2	name
11531273	CV247498	single nucleotide variant	NM_016120.4(RLIM):c.1760C>G (p.Pro587Arg)	Intellectual disability, X-linked 61 [RCV000239584]	pathogenic	X	74591555	74591555	Human	1	name
11531239	CV247499	single nucleotide variant	NM_016120.4(RLIM):c.1159C>T (p.Arg387Cys)	Inborn genetic diseases [RCV002518541]\|Intellectual disability, X-linked 61 [RCV000239497]\|Non-syndromic X-linked intellectual disability [RCV004017569]\|not provided [RCV002292497]	pathogenic\|likely pathogenic	X	74592156	74592156	Human	3	name
11531256	CV247500	single nucleotide variant	NM_016120.4(RLIM):c.1795C>T (p.Arg599Cys)	Intellectual disability, X-linked 61 [RCV000239547]	pathogenic	X	74591520	74591520	Human	1	name
329350346	CV2477331	single nucleotide variant	NM_016120.4(RLIM):c.1384A>G (p.Ser462Gly)	not provided [RCV003221656]	uncertain significance	X	74591931	74591931	Human		name
329848532	CV2523275	single nucleotide variant	NM_016120.4(RLIM):c.1454G>T (p.Ser485Ile)	not provided [RCV003225289]	uncertain significance	X	74591861	74591861	Human		name
329954803	CV2670735	single nucleotide variant	NM_016120.4(RLIM):c.1250G>A (p.Ser417Asn)	not provided [RCV003236003]	uncertain significance	X	74592065	74592065	Human		name
401830580	CV2748236	single nucleotide variant	NM_016120.4(RLIM):c.1334G>C (p.Gly445Ala)	not provided [RCV003329844]	uncertain significance	X	74591981	74591981	Human		name
401855072	CV2752745	single nucleotide variant	NM_016120.4(RLIM):c.1358G>A (p.Ser453Asn)	Intellectual disability, X-linked 61 [RCV003337799]	uncertain significance	X	74591957	74591957	Human	1	name
401914501	CV2830722	single nucleotide variant	NM_016120.4(RLIM):c.1508C>T (p.Ser503Leu)	Intellectual disability, X-linked 61 [RCV004594700]\|not provided [RCV003442460]	uncertain significance	X	74591807	74591807	Human	1	name
402480744	CV2910993	single nucleotide variant	NM_016120.4(RLIM):c.1273G>A (p.Asp425Asn)	not provided [RCV003572049]	uncertain significance	X	74592042	74592042	Human		name
404982657	CV2979441	single nucleotide variant	NM_016120.4(RLIM):c.1121G>A (p.Gly374Asp)	not provided [RCV003691463]	uncertain significance	X	74592194	74592194	Human		name
405753149	CV3316210	single nucleotide variant	NM_016120.4(RLIM):c.1436C>G (p.Ser479Cys)	Inborn genetic diseases [RCV004454095]	uncertain significance	X	74591879	74591879	Human	1	name
405753155	CV3316211	single nucleotide variant	NM_016120.4(RLIM):c.1520G>A (p.Gly507Asp)	Inborn genetic diseases [RCV004454096]	uncertain significance	X	74591795	74591795	Human	1	name
407475753	CV3483375	single nucleotide variant	NM_016120.4(RLIM):c.1357A>G (p.Ser453Gly)	Inborn genetic diseases [RCV004663307]	likely benign	X	74591958	74591958	Human	1	name
407475756	CV3483376	single nucleotide variant	NM_016120.4(RLIM):c.1328G>A (p.Arg443Gln)	Inborn genetic diseases [RCV004663308]	uncertain significance	X	74591987	74591987	Human	1	name
408369961	CV3502922	single nucleotide variant	NM_016120.4(RLIM):c.1571G>T (p.Gly524Val)	not provided [RCV004724043]	uncertain significance	X	74591744	74591744	Human		name
408394317	CV3521933	single nucleotide variant	NM_016120.4(RLIM):c.1529G>A (p.Arg510Gln)	Intellectual disability, X-linked 61 [RCV004764732]	uncertain significance	X	74591786	74591786	Human	1	name
408381986	CV3526665	single nucleotide variant	NM_016120.4(RLIM):c.1406C>G (p.Ser469Cys)	not provided [RCV004771978]	uncertain significance	X	74591909	74591909	Human		name
408385755	CV3528665	single nucleotide variant	NM_016120.4(RLIM):c.1743C>A (p.Asn581Lys)	not provided [RCV004772498]	uncertain significance	X	74591572	74591572	Human		name
596922549	CV3529979	single nucleotide variant	NM_016120.4(RLIM):c.1113G>T (p.Glu371Asp)	not provided [RCV004776578]	uncertain significance	X	74592202	74592202	Human		name
596923432	CV3530417	single nucleotide variant	NM_016120.4(RLIM):c.1795C>A (p.Arg599Ser)	not provided [RCV004777016]	uncertain significance	X	74591520	74591520	Human		name
596926140	CV3530709	single nucleotide variant	NM_016120.4(RLIM):c.1650A>C (p.Lys550Asn)	not provided [RCV004778294]	uncertain significance	X	74591665	74591665	Human		name
597718634	CV3593762	single nucleotide variant	NM_016120.4(RLIM):c.1066T>G (p.Tyr356Asp)	Inborn genetic diseases [RCV004960164]	uncertain significance	X	74592249	74592249	Human	1	name
598219162	CV3891762	single nucleotide variant	NM_016120.4(RLIM):c.1045A>G (p.Thr349Ala)	Intellectual disability, X-linked 61 [RCV005252605]	uncertain significance	X	74592270	74592270	Human	1	name
616936198	CV4016237	single nucleotide variant	NM_016120.4(RLIM):c.1343G>T (p.Gly448Val)	not provided [RCV005415103]	uncertain significance	X	74591972	74591972	Human		name
617152092	CV4018285	single nucleotide variant	NM_016120.4(RLIM):c.1260G>A (p.Met420Ile)	not specified [RCV005418545]	uncertain significance	X	74592055	74592055	Human		name
617150894	CV4019250	single nucleotide variant	NM_016120.4(RLIM):c.1685G>A (p.Gly562Asp)	not provided [RCV005423658]	uncertain significance	X	74591630	74591630	Human		name
12912743	CV422517	single nucleotide variant	NM_016120.4(RLIM):c.1571G>A (p.Gly524Asp)	not provided [RCV000492961]	uncertain significance	X	74591744	74591744	Human		name
13216728	CV430917	single nucleotide variant	NM_016120.4(RLIM):c.1373G>A (p.Ser458Asn)	not specified [RCV000504032]	uncertain significance	X	74591942	74591942	Human		name
13486570	CV446768	single nucleotide variant	NM_016120.4(RLIM):c.1865G>A (p.Ser622Asn)	not provided [RCV000522953]	uncertain significance	X	74591450	74591450	Human		name
13802073	CV576292	single nucleotide variant	NM_016120.4(RLIM):c.1792G>A (p.Asp598Asn)	Intellectual disability, X-linked 61 [RCV000709994]\|not provided [RCV001585663]	pathogenic\|likely pathogenic	X	74591523	74591523	Human	1	name
13802074	CV576293	single nucleotide variant	NM_016120.4(RLIM):c.1093C>T (p.Arg365Cys)	Intellectual disability, X-linked 61 [RCV000709995]\|not provided [RCV001726316]	pathogenic\|likely pathogenic	X	74592222	74592222	Human	1	name
13802075	CV576294	single nucleotide variant	NM_016120.4(RLIM):c.1831C>T (p.Arg611Cys)	Intellectual disability, X-linked 61 [RCV000709996]\|not provided [RCV003148841]	pathogenic\|likely pathogenic	X	74591484	74591484	Human	1	name
13831472	CV590027	single nucleotide variant	NM_016120.4(RLIM):c.1729T>C (p.Tyr577His)	Intellectual disability, X-linked 61 [RCV000735274]	likely pathogenic	X	74591586	74591586	Human	1	name
14697936	CV623369	single nucleotide variant	NM_016120.4(RLIM):c.1364C>A (p.Ser455Tyr)	Intellectual disability, X-linked 61 [RCV000786999]	uncertain significance	X	74591951	74591951	Human	1	name
14725872	CV656802	single nucleotide variant	NM_016120.4(RLIM):c.1079G>A (p.Arg360Gln)	not provided [RCV000833628]	likely benign	X	74592236	74592236	Human		name
15185897	CV706313	single nucleotide variant	NM_016120.4(RLIM):c.1411T>C (p.Ser471Pro)	not provided [RCV000953120]	benign	X	74591904	74591904	Human		name
126728621	CV967246	single nucleotide variant	NM_016120.4(RLIM):c.1262A>G (p.Tyr421Cys)	Intellectual disability, X-linked 61 [RCV001293455]	likely pathogenic	X	74592053	74592053	Human	1	name
153002392	CV1685511	indel	NM_016120.4(RLIM):c.1611_1614delinsG (p.Asn538del)	not provided [RCV002259498]	uncertain significance	X	74591701	74591704	Human		name
150531056	CV1299268	deletion	NM_016120.4(RLIM):c.1413_1424del (p.Ser473_Ser476del)	not provided [RCV001756961]	uncertain significance	X	74591891	74591902	Human		name
243060186	CV2413755	deletion	NM_016120.4(RLIM):c.1401_1412del (p.Ser473_Ser476del)	Intellectual disability, X-linked 61 [RCV003135775]	uncertain significance	X	74591903	74591914	Human	1	name
405260070	CV3186543	deletion	NM_016120.4(RLIM):c.1429_1440del (p.Pro477_Ser480del)	not provided [RCV003884302]	likely benign	X	74591875	74591886	Human		name
38468007	CV921027	microsatellite	NM_016120.4(RLIM):c.1401CAGTTC[3] (p.Ser475_Ser476dup)	not provided [RCV001200508]	likely benign	X	74591902	74591903	Human		name
155264962	CV1704512	duplication	NM_016120.4(RLIM):c.1377_1382dup (p.Ser476_Pro477insSerSer)	not provided [RCV002284728]	uncertain significance	X	74591932	74591933	Human		name
596946020	CV3548177	microsatellite	NM_016120.4(RLIM):c.1383CAGTTC[3] (p.Ser476_Pro477insSerSer)	not provided [RCV004809508]	likely benign	X	74591920	74591921	Human		name

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