Apcdd1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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197 records found for search term Apcdd1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150461757	CV1214552	single nucleotide variant	NM_153000.5(APCDD1):c.*56G>T	not provided [RCV001613545]	benign	18	10488094	10488094	Human		name
150470218	CV1219204	single nucleotide variant	NM_153000.5(APCDD1):c.-19C>G	not provided [RCV001614956]	benign	18	10454963	10454963	Human		name
150489757	CV1279226	single nucleotide variant	NM_153000.5(APCDD1):c.*29C>T	not provided [RCV001716354]	benign	18	10488067	10488067	Human		name
150505520	CV1213548	single nucleotide variant	NM_153000.5(APCDD1):c.58+97C>T	not provided [RCV001595804]	benign	18	10455136	10455136	Human		name
150447932	CV1261889	single nucleotide variant	NM_153000.5(APCDD1):c.58+41A>G	not provided [RCV001680274]	benign	18	10455080	10455080	Human		name
150477963	CV1272129	single nucleotide variant	NM_153000.5(APCDD1):c.59-13C>T	not provided [RCV001696415]	benign	18	10468456	10468456	Human	2	name
150477963	CV1272129	single nucleotide variant	NM_153000.5(APCDD1):c.59-13C>T	not provided [RCV001696415]	benign	18	10468456	10468457	Human	2	name
156342104	CV2175949	single nucleotide variant	NM_153000.5(APCDD1):c.243-5C>T	not provided [RCV003030340]	likely benign	18	10471525	10471525	Human		name
15153162	CV780147	single nucleotide variant	NM_153000.5(APCDD1):c.243-6G>A	not provided [RCV000968494]	benign	18	10471524	10471524	Human		name
150509723	CV1229974	single nucleotide variant	NM_153000.5(APCDD1):c.59-139A>G	not provided [RCV001636554]	benign	18	10468330	10468330	Human		name
150492120	CV1238115	single nucleotide variant	NM_153000.5(APCDD1):c.775-90G>A	not provided [RCV001654961]	benign	18	10485372	10485372	Human		name
150448826	CV1253605	single nucleotide variant	NM_153000.5(APCDD1):c.775-96T>C	not provided [RCV001667533]	benign	18	10485366	10485366	Human		name
150459608	CV1264042	single nucleotide variant	NM_153000.5(APCDD1):c.59-151A>G	not provided [RCV001681957]	benign	18	10468318	10468318	Human		name
155957128	CV2040208	single nucleotide variant	NM_153000.5(APCDD1):c.774+16G>A	not provided [RCV002776075]	benign	18	10472077	10472077	Human		name
150440324	CV1220144	single nucleotide variant	NM_153000.5(APCDD1):c.775-102T>C	not provided [RCV001610127]	benign	18	10485360	10485360	Human		name
150507121	CV1242381	single nucleotide variant	NM_153000.5(APCDD1):c.243-243A>C	not provided [RCV001658736]	benign	18	10471287	10471287	Human		name
150469369	CV1249083	single nucleotide variant	NM_153000.5(APCDD1):c.775-209A>G	not provided [RCV001670845]	benign	18	10485253	10485253	Human		name
150506476	CV1257350	single nucleotide variant	NM_153000.5(APCDD1):c.1096+76G>A	not provided [RCV001678189]	benign	18	10485859	10485859	Human		name
150470717	CV1269906	single nucleotide variant	NM_153000.5(APCDD1):c.1097-144T>C	not provided [RCV001695193]	benign	18	10487446	10487446	Human		name
150437350	CV1286531	single nucleotide variant	NM_153000.5(APCDD1):c.1097-234A>G	not provided [RCV001724610]	benign	18	10487356	10487356	Human		name
597908187	CV3738992	single nucleotide variant	NM_153000.5(APCDD1):c.4T>C (p.Ser2Pro)	not provided [RCV005073227]	uncertain significance	18	10454985	10454985	Human		name
8596035	CV18200	single nucleotide variant	NM_153000.5(APCDD1):c.26T>G (p.Leu9Arg)	Hypotrichosis 1 [RCV000003311]	pathogenic	18	10455007	10455007	Human	1	name
156374184	CV1917342	single nucleotide variant	NM_153000.5(APCDD1):c.22C>G (p.Leu8Val)	Hypotrichosis 1 [RCV005356292]\|not provided [RCV002603444]	uncertain significance	18	10455003	10455003	Human	1	name
156089418	CV2092790	single nucleotide variant	NM_153000.5(APCDD1):c.189A>C (p.Ala63=)	APCDD1-related disorder [RCV003973533]\|not provided [RCV002926621]	benign\|likely benign	18	10468599	10468599	Human	1	name , trait , alternate_id
156314294	CV2196623	single nucleotide variant	NM_153000.5(APCDD1):c.10C>T (p.Pro4Ser)	not specified [RCV004073891]	uncertain significance	18	10454991	10454991	Human		name
405274008	CV3194902	single nucleotide variant	NM_153000.5(APCDD1):c.228C>T (p.His76=)	APCDD1-related disorder [RCV003902144]	likely benign	18	10468638	10468638	Human		name , trait , alternate_id
597915016	CV3740676	single nucleotide variant	NM_153000.5(APCDD1):c.150A>G (p.Ser50=)	not provided [RCV005074013]	likely benign	18	10468560	10468560	Human		name
150449952	CV1215179	single nucleotide variant	NM_153000.5(APCDD1):c.489C>G (p.Leu163=)	not provided [RCV001611769]	benign	18	10471776	10471776	Human		name
150475074	CV1271141	single nucleotide variant	NM_153000.5(APCDD1):c.480C>T (p.Ala160=)	not provided [RCV001695964]	benign	18	10471767	10471767	Human		name
156245330	CV2105593	single nucleotide variant	NM_153000.5(APCDD1):c.750C>T (p.Tyr250=)	not provided [RCV002933349]	benign	18	10472037	10472037	Human		name
401878983	CV2754912	single nucleotide variant	NM_153000.5(APCDD1):c.79C>T (p.Leu27Phe)	not specified [RCV004341384]	uncertain significance	18	10468489	10468489	Human		name
405205748	CV2854896	single nucleotide variant	NM_153000.5(APCDD1):c.510A>G (p.Thr170=)	not provided [RCV003551842]	likely benign	18	10471797	10471797	Human		name
405253499	CV3178231	single nucleotide variant	NM_153000.5(APCDD1):c.531C>T (p.Asp177=)	not provided [RCV003871012]	likely benign	18	10471818	10471818	Human		name
597695165	CV3578478	single nucleotide variant	NM_153000.5(APCDD1):c.70G>A (p.Gly24Ser)	not specified [RCV004839100]	uncertain significance	18	10468480	10468480	Human		name
597969162	CV3761355	single nucleotide variant	NM_153000.5(APCDD1):c.780C>T (p.His260=)	not provided [RCV005083742]	likely benign	18	10485467	10485467	Human		name
15187414	CV727629	single nucleotide variant	NM_153000.5(APCDD1):c.819A>G (p.Ser273=)	not provided [RCV000887248]	benign	18	10485506	10485506	Human		name
150506071	CV1226255	single nucleotide variant	NM_153000.5(APCDD1):c.1509C>T (p.Cys503=)	not provided [RCV001635623]	benign	18	10488002	10488002	Human		name
150488812	CV1284101	single nucleotide variant	NM_153000.5(APCDD1):c.1428C>T (p.Leu476=)	not provided [RCV001716165]	benign	18	10487921	10487921	Human		name
156446126	CV1951212	single nucleotide variant	NM_153000.5(APCDD1):c.1176C>T (p.Ala392=)	not provided [RCV003117090]	likely benign	18	10487669	10487669	Human		name
156145996	CV2122829	single nucleotide variant	NM_153000.5(APCDD1):c.1230C>T (p.Cys410=)	not provided [RCV002954399]	likely benign	18	10487723	10487723	Human		name
156375797	CV2124103	single nucleotide variant	NM_153000.5(APCDD1):c.1335C>T (p.Asp445=)	not provided [RCV002942704]	likely benign	18	10487828	10487828	Human		name
156064767	CV2229036	single nucleotide variant	NM_153000.5(APCDD1):c.195C>G (p.Ile65Met)	not specified [RCV004098819]	uncertain significance	18	10468605	10468605	Human		name
405017963	CV2856045	single nucleotide variant	NM_153000.5(APCDD1):c.1050C>T (p.Gly350=)	not provided [RCV003577312]	benign	18	10485737	10485737	Human		name
402477455	CV2914177	single nucleotide variant	NM_153000.5(APCDD1):c.1500A>C (p.Ala500=)	not provided [RCV003571586]	benign	18	10487993	10487993	Human		name
405197979	CV2972999	single nucleotide variant	NM_153000.5(APCDD1):c.242G>A (p.Gly81Asp)	not provided [RCV003677879]	uncertain significance	18	10468652	10468652	Human		name
405237045	CV3076603	single nucleotide variant	NM_153000.5(APCDD1):c.1410G>A (p.Ser470=)	not provided [RCV003735991]	likely benign	18	10487903	10487903	Human		name
404999474	CV3173083	single nucleotide variant	NM_153000.5(APCDD1):c.1026C>T (p.Tyr342=)	not provided [RCV003882366]	likely benign	18	10485713	10485713	Human		name
407511596	CV3463331	single nucleotide variant	NM_153000.5(APCDD1):c.170A>T (p.Lys57Ile)	not specified [RCV004648100]	uncertain significance	18	10468580	10468580	Human		name
597947799	CV3852348	single nucleotide variant	NM_153000.5(APCDD1):c.1329C>A (p.Pro443=)	not provided [RCV005189425]	likely benign	18	10487822	10487822	Human		name
15186744	CV704532	single nucleotide variant	NM_153000.5(APCDD1):c.1294C>A (p.Arg432=)	not provided [RCV000953376]	benign	18	10487787	10487787	Human		name
15103673	CV785835	single nucleotide variant	NM_153000.5(APCDD1):c.1221C>T (p.Thr407=)	not provided [RCV000976063]	likely benign	18	10487714	10487714	Human		name
150464552	CV1276419	single nucleotide variant	NM_153000.5(APCDD1):c.448G>A (p.Val150Ile)	not provided [RCV001710364]	benign	18	10471735	10471735	Human		name
156323121	CV1870862	single nucleotide variant	NM_153000.5(APCDD1):c.877G>A (p.Gly293Arg)	Hypotrichosis 1 [RCV005356262]\|not provided [RCV003063210]\|not specified [RCV004070454]	uncertain significance	18	10485564	10485564	Human	1	name
155922650	CV2099387	single nucleotide variant	NM_153000.5(APCDD1):c.863C>T (p.Thr288Ile)	not provided [RCV002903425]	uncertain significance	18	10485550	10485550	Human		name
155997177	CV2105705	single nucleotide variant	NM_153000.5(APCDD1):c.865A>G (p.Ile289Val)	not provided [RCV002947614]	benign\|likely benign	18	10485552	10485552	Human		name
156377810	CV2207555	single nucleotide variant	NM_153000.5(APCDD1):c.793A>G (p.Ile265Val)	not specified [RCV004090347]	uncertain significance	18	10485480	10485480	Human		name
156123011	CV2349985	single nucleotide variant	NM_153000.5(APCDD1):c.526G>A (p.Ala176Thr)	not provided [RCV005099005]\|not specified [RCV004199913]	uncertain significance	18	10471813	10471813	Human		name
156200940	CV2350951	single nucleotide variant	NM_153000.5(APCDD1):c.815G>A (p.Arg272Gln)	not specified [RCV004211782]	uncertain significance	18	10485502	10485502	Human		name
156169906	CV2354826	single nucleotide variant	NM_153000.5(APCDD1):c.532G>A (p.Gly178Arg)	not specified [RCV004191324]	uncertain significance	18	10471819	10471819	Human		name
156154815	CV2359652	single nucleotide variant	NM_153000.5(APCDD1):c.505C>T (p.Arg169Cys)	not specified [RCV004210479]	uncertain significance	18	10471792	10471792	Human		name
329377100	CV2435809	single nucleotide variant	NM_153000.5(APCDD1):c.583G>A (p.Gly195Ser)	not specified [RCV004253431]	uncertain significance	18	10471870	10471870	Human		name
329355123	CV2449249	single nucleotide variant	NM_153000.5(APCDD1):c.422C>T (p.Thr141Met)	not provided [RCV005101276]\|not specified [RCV004257387]	uncertain significance	18	10471709	10471709	Human		name
401757102	CV2678234	single nucleotide variant	NM_153000.5(APCDD1):c.515C>T (p.Pro172Leu)	not specified [RCV004289828]	uncertain significance	18	10471802	10471802	Human		name
401774413	CV2691727	single nucleotide variant	NM_153000.5(APCDD1):c.718A>G (p.Thr240Ala)	not specified [RCV004299184]	uncertain significance	18	10472005	10472005	Human		name
401775232	CV2692305	single nucleotide variant	NM_153000.5(APCDD1):c.754C>G (p.Pro252Ala)	not provided [RCV003575062]\|not specified [RCV004310296]	uncertain significance	18	10472041	10472041	Human		name
401861514	CV2756323	single nucleotide variant	NM_153000.5(APCDD1):c.802C>G (p.Arg268Gly)	not specified [RCV004342869]	uncertain significance	18	10485489	10485489	Human		name
401890559	CV2768305	single nucleotide variant	NM_153000.5(APCDD1):c.341G>A (p.Arg114Gln)	not specified [RCV004350289]	uncertain significance	18	10471628	10471628	Human		name
401887742	CV2770402	single nucleotide variant	NM_153000.5(APCDD1):c.688C>G (p.Leu230Val)	not specified [RCV004358048]	uncertain significance	18	10471975	10471975	Human		name
405183888	CV3057866	single nucleotide variant	NM_153000.5(APCDD1):c.481G>A (p.Glu161Lys)	not provided [RCV003729070]	uncertain significance	18	10471768	10471768	Human		name
405164553	CV3059446	single nucleotide variant	NM_153000.5(APCDD1):c.739C>T (p.Pro247Ser)	not provided [RCV003727338]	uncertain significance	18	10472026	10472026	Human		name
404996914	CV3123827	single nucleotide variant	NM_153000.5(APCDD1):c.506G>A (p.Arg169His)	not provided [RCV003827734]\|not specified [RCV004654349]	uncertain significance	18	10471793	10471793	Human		name
405661956	CV3289659	single nucleotide variant	NM_153000.5(APCDD1):c.385C>T (p.Arg129Cys)	not specified [RCV004417602]	uncertain significance	18	10471672	10471672	Human		name
405661959	CV3289660	single nucleotide variant	NM_153000.5(APCDD1):c.392G>A (p.Arg131His)	not specified [RCV004417603]	uncertain significance	18	10471679	10471679	Human		name
405661961	CV3289661	single nucleotide variant	NM_153000.5(APCDD1):c.499G>A (p.Val167Met)	not specified [RCV004417604]	uncertain significance	18	10471786	10471786	Human		name
405661964	CV3289662	single nucleotide variant	NM_153000.5(APCDD1):c.574G>C (p.Glu192Gln)	not specified [RCV004417605]	uncertain significance	18	10471861	10471861	Human		name
405661967	CV3289663	single nucleotide variant	NM_153000.5(APCDD1):c.674A>C (p.His225Pro)	not provided [RCV005104553]\|not specified [RCV004417606]	uncertain significance	18	10471961	10471961	Human		name
405661968	CV3289664	single nucleotide variant	NM_153000.5(APCDD1):c.709A>G (p.Thr237Ala)	not specified [RCV004417607]	uncertain significance	18	10471996	10471996	Human		name
405661970	CV3289665	single nucleotide variant	NM_153000.5(APCDD1):c.812A>G (p.Tyr271Cys)	not specified [RCV004417608]	uncertain significance	18	10485499	10485499	Human		name
405661974	CV3289666	single nucleotide variant	NM_153000.5(APCDD1):c.907C>T (p.Arg303Cys)	not specified [RCV004417609]	uncertain significance	18	10485594	10485594	Human		name
405661977	CV3289667	single nucleotide variant	NM_153000.5(APCDD1):c.913G>A (p.Glu305Lys)	not specified [RCV004417610]	uncertain significance	18	10485600	10485600	Human		name
405661980	CV3289668	single nucleotide variant	NM_153000.5(APCDD1):c.941T>C (p.Ile314Thr)	not specified [RCV004417611]	uncertain significance	18	10485628	10485628	Human		name
407511616	CV3463342	single nucleotide variant	NM_153000.5(APCDD1):c.432C>G (p.Asp144Glu)	not specified [RCV004648106]	uncertain significance	18	10471719	10471719	Human		name
407511643	CV3463353	single nucleotide variant	NM_153000.5(APCDD1):c.743C>T (p.Ser248Phe)	not specified [RCV004648113]	uncertain significance	18	10472030	10472030	Human		name
407511672	CV3463363	single nucleotide variant	NM_153000.5(APCDD1):c.736C>T (p.Arg246Trp)	not specified [RCV004648121]	uncertain significance	18	10472023	10472023	Human		name
597695366	CV3574601	single nucleotide variant	NM_153000.5(APCDD1):c.748T>C (p.Tyr250His)	not specified [RCV004839118]	uncertain significance	18	10472035	10472035	Human		name
597696155	CV3578456	single nucleotide variant	NM_153000.5(APCDD1):c.572G>A (p.Arg191Gln)	not specified [RCV004839084]	uncertain significance	18	10471859	10471859	Human		name
597695110	CV3578468	single nucleotide variant	NM_153000.5(APCDD1):c.439C>G (p.Leu147Val)	not specified [RCV004839095]	uncertain significance	18	10471726	10471726	Human		name
597657175	CV3578489	single nucleotide variant	NM_153000.5(APCDD1):c.959A>C (p.Asn320Thr)	not specified [RCV004827589]	uncertain significance	18	10485646	10485646	Human		name
597831051	CV3743762	single nucleotide variant	NM_153000.5(APCDD1):c.638G>A (p.Arg213Gln)	not provided [RCV005062579]	uncertain significance	18	10471925	10471925	Human		name
597952401	CV3843765	single nucleotide variant	NM_153000.5(APCDD1):c.896G>A (p.Arg299His)	not provided [RCV005190627]	uncertain significance	18	10485583	10485583	Human		name
598240825	CV3995595	single nucleotide variant	NM_153000.5(APCDD1):c.868G>A (p.Gly290Ser)	not specified [RCV005383164]	uncertain significance	18	10485555	10485555	Human		name
151866980	CV1422478	single nucleotide variant	NM_153000.5(APCDD1):c.1103A>T (p.His368Leu)	not provided [RCV001884658]	uncertain significance	18	10487596	10487596	Human		name
156377167	CV1896255	single nucleotide variant	NM_153000.5(APCDD1):c.1262A>T (p.Glu421Val)	not provided [RCV003092970]\|not specified [RCV004073235]	uncertain significance	18	10487755	10487755	Human		name
155902309	CV2010251	single nucleotide variant	NM_153000.5(APCDD1):c.1337G>A (p.Gly446Glu)	not provided [RCV002726257]	uncertain significance	18	10487830	10487830	Human		name
156293247	CV2111518	single nucleotide variant	NM_153000.5(APCDD1):c.1051G>A (p.Val351Ile)	not provided [RCV002922241]	benign	18	10485738	10485738	Human		name
155952500	CV2123601	single nucleotide variant	NM_153000.5(APCDD1):c.1046G>A (p.Arg349His)	APCDD1-related disorder [RCV003943671]\|not provided [RCV002971942]	benign	18	10485733	10485733	Human	1	name , trait , alternate_id
156221122	CV2124368	single nucleotide variant	NM_153000.5(APCDD1):c.1460G>A (p.Arg487Gln)	not provided [RCV002958145]	benign	18	10487953	10487953	Human		name
155906431	CV2130802	single nucleotide variant	NM_153000.5(APCDD1):c.1332C>A (p.Ser444Arg)	not provided [RCV002967739]	likely benign	18	10487825	10487825	Human		name
156330221	CV2226961	single nucleotide variant	NM_153000.5(APCDD1):c.1030C>T (p.Arg344Trp)	not provided [RCV005099578]\|not specified [RCV004097357]	uncertain significance	18	10485717	10485717	Human		name
156288825	CV2229811	single nucleotide variant	NM_153000.5(APCDD1):c.1037G>A (p.Arg346His)	not specified [RCV004105384]	uncertain significance	18	10485724	10485724	Human		name
156131419	CV2235237	single nucleotide variant	NM_153000.5(APCDD1):c.1477A>G (p.Thr493Ala)	not specified [RCV004107285]	likely benign	18	10487970	10487970	Human		name
156047885	CV2244960	single nucleotide variant	NM_153000.5(APCDD1):c.1195G>A (p.Gly399Ser)	not specified [RCV004104699]	uncertain significance	18	10487688	10487688	Human		name
156134701	CV2260187	single nucleotide variant	NM_153000.5(APCDD1):c.1027G>A (p.Ala343Thr)	not provided [RCV005099684]\|not specified [RCV004120964]	uncertain significance	18	10485714	10485714	Human		name
156325338	CV2335240	single nucleotide variant	NM_153000.5(APCDD1):c.1484C>G (p.Ser495Cys)	not specified [RCV004186810]	uncertain significance	18	10487977	10487977	Human		name
156066685	CV2340919	single nucleotide variant	NM_153000.5(APCDD1):c.1127C>T (p.Ala376Val)	not specified [RCV004181414]	uncertain significance	18	10487620	10487620	Human		name
156156291	CV2359827	single nucleotide variant	NM_153000.5(APCDD1):c.1295G>A (p.Arg432Gln)	Hypotrichosis 1 [RCV005356334]\|not specified [RCV004212682]	uncertain significance	18	10487788	10487788	Human	1	name
401754529	CV2682205	single nucleotide variant	NM_153000.5(APCDD1):c.1287G>C (p.Gln429His)	not specified [RCV004297169]	uncertain significance	18	10487780	10487780	Human		name
401878596	CV2754707	single nucleotide variant	NM_153000.5(APCDD1):c.1177G>A (p.Glu393Lys)	not provided [RCV003777508]\|not specified [RCV004339375]	uncertain significance	18	10487670	10487670	Human		name
405119709	CV2891647	single nucleotide variant	NM_153000.5(APCDD1):c.1259C>T (p.Thr420Met)	not provided [RCV003558956]	likely benign	18	10487752	10487752	Human		name
405116272	CV2951573	single nucleotide variant	NM_153000.5(APCDD1):c.1196G>C (p.Gly399Ala)	not provided [RCV003670906]	uncertain significance	18	10487689	10487689	Human		name
405078353	CV3050154	single nucleotide variant	NM_153000.5(APCDD1):c.1058C>T (p.Ser353Leu)	not provided [RCV003716941]	likely benign	18	10485745	10485745	Human		name
405661945	CV3289655	single nucleotide variant	NM_153000.5(APCDD1):c.1150G>A (p.Val384Ile)	not specified [RCV004417598]	uncertain significance	18	10487643	10487643	Human		name
405661948	CV3289656	single nucleotide variant	NM_153000.5(APCDD1):c.1291G>A (p.Ala431Thr)	not specified [RCV004417599]	uncertain significance	18	10487784	10487784	Human		name
405661951	CV3289657	single nucleotide variant	NM_153000.5(APCDD1):c.1301G>A (p.Arg434His)	not specified [RCV004417600]	uncertain significance	18	10487794	10487794	Human		name
405661954	CV3289658	single nucleotide variant	NM_153000.5(APCDD1):c.1412C>T (p.Pro471Leu)	not specified [RCV004417601]	uncertain significance	18	10487905	10487905	Human		name
407530504	CV3467241	single nucleotide variant	NM_153000.5(APCDD1):c.1048G>A (p.Gly350Ser)	not specified [RCV004657088]	uncertain significance	18	10485735	10485735	Human		name
407511578	CV3467261	single nucleotide variant	NM_153000.5(APCDD1):c.1381A>G (p.Met461Val)	not specified [RCV004648095]	uncertain significance	18	10487874	10487874	Human		name
597657231	CV3574612	single nucleotide variant	NM_153000.5(APCDD1):c.1459C>T (p.Arg487Trp)	not specified [RCV004827597]	uncertain significance	18	10487952	10487952	Human		name
597657122	CV3578414	single nucleotide variant	NM_153000.5(APCDD1):c.1243A>G (p.Ile415Val)	not specified [RCV004827582]	uncertain significance	18	10487736	10487736	Human		name
597696262	CV3578434	single nucleotide variant	NM_153000.5(APCDD1):c.1360A>G (p.Lys454Glu)	not specified [RCV004839070]	uncertain significance	18	10487853	10487853	Human		name
597657153	CV3578445	single nucleotide variant	NM_153000.5(APCDD1):c.1097T>C (p.Val366Ala)	not specified [RCV004827586]	uncertain significance	18	10487590	10487590	Human		name
598244703	CV3895849	single nucleotide variant	NM_153000.5(APCDD1):c.1336G>A (p.Gly446Arg)	Hypotrichosis 1 [RCV005365707]	uncertain significance	18	10487829	10487829	Human	1	name
598182711	CV3995587	single nucleotide variant	NM_153000.5(APCDD1):c.1538G>A (p.Arg513His)	not specified [RCV005395185]	uncertain significance	18	10488031	10488031	Human		name
598240873	CV4004996	single nucleotide variant	NM_153000.5(APCDD1):c.1451T>C (p.Leu484Pro)	not specified [RCV005383171]	uncertain significance	18	10487944	10487944	Human		name
405262375	CV3212912	microsatellite	NM_153000.5(APCDD1):c.574GAG[1] (p.Glu193del)	APCDD1-related disorder [RCV003944762]	likely benign	18	10471861	10471863	Human		name , trait , alternate_id
8586568	CV121172	single nucleotide variant	NM_153360.2(APCDD1L):c.189-700C>A	Lung cancer [RCV000101692]	uncertain significance	20	58468358	58468358	Human		name
8586569	CV121173	single nucleotide variant	NR_034147.1(APCDD1L-AS1):n.944-30533A>G	Lung cancer [RCV000101693]	uncertain significance	20	58588207	58588207	Human		name
156036408	CV2303707	single nucleotide variant	NM_153360.3(APCDD1L):c.7G>T (p.Ala3Ser)	not specified [RCV004161775]	uncertain significance	20	58514701	58514701	Human		name
155991925	CV2255748	single nucleotide variant	NM_153360.3(APCDD1L):c.92T>C (p.Leu31Pro)	not specified [RCV004120134]	uncertain significance	20	58470705	58470705	Human		name
156364202	CV2341865	single nucleotide variant	NM_153360.3(APCDD1L):c.95G>A (p.Arg32His)	not specified [RCV004184815]	likely benign	20	58470702	58470702	Human		name
156068793	CV2356934	single nucleotide variant	NM_153360.3(APCDD1L):c.79G>A (p.Gly27Arg)	not specified [RCV004204305]	uncertain significance	20	58470718	58470718	Human		name
155989283	CV2371921	single nucleotide variant	NM_153360.3(APCDD1L):c.37G>T (p.Val13Leu)	not specified [RCV004221606]	uncertain significance	20	58514671	58514671	Human		name
156302732	CV2311968	single nucleotide variant	NM_153360.3(APCDD1L):c.164T>C (p.Leu55Pro)	not specified [RCV004170785]	uncertain significance	20	58470633	58470633	Human		name
156049249	CV2336506	single nucleotide variant	NM_153360.3(APCDD1L):c.160C>T (p.Arg54Cys)	not specified [RCV004194714]	uncertain significance	20	58470637	58470637	Human		name
401728770	CV2673041	single nucleotide variant	NM_153360.3(APCDD1L):c.125C>A (p.Pro42Gln)	not specified [RCV004284033]	uncertain significance	20	58470672	58470672	Human		name
401890291	CV2755692	single nucleotide variant	NM_153360.3(APCDD1L):c.127G>T (p.Asp43Tyr)	not specified [RCV004342076]	uncertain significance	20	58470670	58470670	Human		name
401866395	CV2786282	single nucleotide variant	NM_153360.3(APCDD1L):c.200G>T (p.Arg67Leu)	not specified [RCV004361595]	uncertain significance	20	58467647	58467647	Human		name
405661992	CV3289672	single nucleotide variant	NM_153360.3(APCDD1L):c.244A>T (p.Ser82Cys)	not specified [RCV004417615]	uncertain significance	20	58467603	58467603	Human		name
405661995	CV3289673	single nucleotide variant	NM_153360.3(APCDD1L):c.247C>T (p.Arg83Trp)	not specified [RCV004417616]	uncertain significance	20	58467600	58467600	Human		name
405661998	CV3289674	single nucleotide variant	NM_153360.3(APCDD1L):c.256C>G (p.Arg86Gly)	not specified [RCV004417617]	uncertain significance	20	58467591	58467591	Human		name
407530595	CV3463412	single nucleotide variant	NM_153360.3(APCDD1L):c.223C>T (p.Arg75Cys)	not specified [RCV004657133]	uncertain significance	20	58467624	58467624	Human		name
407511764	CV3463415	single nucleotide variant	NM_153360.3(APCDD1L):c.178A>G (p.Ile60Val)	not specified [RCV004648152]	uncertain significance	20	58470619	58470619	Human		name
407530602	CV3463431	single nucleotide variant	NM_153360.3(APCDD1L):c.267G>T (p.Gln89His)	not specified [RCV004657137]	uncertain significance	20	58467580	58467580	Human		name
597695492	CV3574619	single nucleotide variant	NM_153360.3(APCDD1L):c.118C>T (p.Pro40Ser)	not specified [RCV004839130]	uncertain significance	20	58470679	58470679	Human		name
597657238	CV3574621	single nucleotide variant	NM_153360.3(APCDD1L):c.274T>C (p.Tyr92His)	not specified [RCV004827598]	uncertain significance	20	58467573	58467573	Human		name
597695524	CV3574624	single nucleotide variant	NM_153360.3(APCDD1L):c.199C>A (p.Arg67Ser)	not specified [RCV004839133]	uncertain significance	20	58467648	58467648	Human		name
597657250	CV3574628	single nucleotide variant	NM_153360.3(APCDD1L):c.266A>C (p.Gln89Pro)	not specified [RCV004827600]	uncertain significance	20	58467581	58467581	Human		name
598240982	CV4005017	single nucleotide variant	NM_153360.3(APCDD1L):c.161G>A (p.Arg54His)	not specified [RCV005383188]	uncertain significance	20	58470636	58470636	Human		name
598241136	CV4005043	single nucleotide variant	NM_153360.3(APCDD1L):c.185C>T (p.Thr62Ile)	not specified [RCV005383211]	uncertain significance	20	58470612	58470612	Human		name
598241256	CV4005064	single nucleotide variant	NM_153360.3(APCDD1L):c.167A>G (p.Asn56Ser)	not specified [RCV005383229]	likely benign	20	58470630	58470630	Human		name
598241335	CV4005085	single nucleotide variant	NM_153360.3(APCDD1L):c.109T>C (p.Cys37Arg)	not specified [RCV005383242]	uncertain significance	20	58470688	58470688	Human		name
8637396	CV92622	single nucleotide variant	NM_153360.2(APCDD1L):c.1173G>A (p.Arg391=)	Malignant melanoma [RCV000072720]	not provided	20	58461123	58461123	Human		name
156324883	CV2195054	single nucleotide variant	NM_153360.3(APCDD1L):c.422C>T (p.Ala141Val)	not specified [RCV004077971]	uncertain significance	20	58467425	58467425	Human		name
156279970	CV2206336	single nucleotide variant	NM_153360.3(APCDD1L):c.887T>C (p.Leu296Pro)	not specified [RCV004078673]	uncertain significance	20	58461409	58461409	Human		name
156087241	CV2241307	single nucleotide variant	NM_153360.3(APCDD1L):c.787G>T (p.Asp263Tyr)	not specified [RCV004102450]	uncertain significance	20	58461509	58461509	Human		name
156065056	CV2272468	single nucleotide variant	NM_153360.3(APCDD1L):c.736G>T (p.Ala246Ser)	not specified [RCV004133386]	uncertain significance	20	58467111	58467111	Human		name
156274109	CV2279684	single nucleotide variant	NM_153360.3(APCDD1L):c.745C>T (p.His249Tyr)	not specified [RCV004144307]	uncertain significance	20	58461551	58461551	Human		name
156239702	CV2285988	single nucleotide variant	NM_153360.3(APCDD1L):c.323G>T (p.Gly108Val)	not specified [RCV004143900]	uncertain significance	20	58467524	58467524	Human		name
156179561	CV2324266	single nucleotide variant	NM_153360.3(APCDD1L):c.476C>A (p.Ala159Glu)	not specified [RCV004176999]	uncertain significance	20	58467371	58467371	Human		name
156003687	CV2357482	single nucleotide variant	NM_153360.3(APCDD1L):c.722G>A (p.Arg241His)	not specified [RCV004202769]	likely benign	20	58467125	58467125	Human		name
156147697	CV2394431	single nucleotide variant	NM_153360.3(APCDD1L):c.805G>A (p.Val269Met)	not specified [RCV004240799]	uncertain significance	20	58461491	58461491	Human		name
401891186	CV2769127	single nucleotide variant	NM_153360.3(APCDD1L):c.491C>T (p.Pro164Leu)	not specified [RCV004348975]	uncertain significance	20	58467356	58467356	Human		name
405662001	CV3289675	single nucleotide variant	NM_153360.3(APCDD1L):c.307T>C (p.Ser103Pro)	not specified [RCV004417618]	uncertain significance	20	58467540	58467540	Human		name
405662008	CV3289677	single nucleotide variant	NM_153360.3(APCDD1L):c.416G>A (p.Arg139His)	not specified [RCV004417620]	uncertain significance	20	58467431	58467431	Human		name
405662010	CV3289678	single nucleotide variant	NM_153360.3(APCDD1L):c.416G>C (p.Arg139Pro)	not specified [RCV004417621]	uncertain significance	20	58467431	58467431	Human		name
405662013	CV3289679	single nucleotide variant	NM_153360.3(APCDD1L):c.434T>G (p.Val145Gly)	not specified [RCV004417622]	uncertain significance	20	58467413	58467413	Human		name
405662016	CV3289680	single nucleotide variant	NM_153360.3(APCDD1L):c.748G>A (p.Val250Met)	not specified [RCV004417623]	uncertain significance	20	58461548	58461548	Human		name
405662019	CV3289681	single nucleotide variant	NM_153360.3(APCDD1L):c.748G>T (p.Val250Leu)	not specified [RCV004417624]	uncertain significance	20	58461548	58461548	Human		name
405662021	CV3289682	single nucleotide variant	NM_153360.3(APCDD1L):c.782G>A (p.Arg261His)	not specified [RCV004417625]	uncertain significance	20	58461514	58461514	Human		name
405662024	CV3289683	single nucleotide variant	NM_153360.3(APCDD1L):c.872T>C (p.Val291Ala)	not specified [RCV004417626]	uncertain significance	20	58461424	58461424	Human		name
407511703	CV3463384	single nucleotide variant	NM_153360.3(APCDD1L):c.352G>A (p.Val118Ile)	not specified [RCV004648130]	uncertain significance	20	58467495	58467495	Human		name
407511725	CV3463394	single nucleotide variant	NM_153360.3(APCDD1L):c.997G>A (p.Ala333Thr)	not specified [RCV004648137]	uncertain significance	20	58461299	58461299	Human		name
597695504	CV3574620	single nucleotide variant	NM_153360.3(APCDD1L):c.970C>T (p.Arg324Trp)	not specified [RCV004839131]	uncertain significance	20	58461326	58461326	Human		name
597657244	CV3574627	single nucleotide variant	NM_153360.3(APCDD1L):c.308C>T (p.Ser103Leu)	not specified [RCV004827599]	uncertain significance	20	58467539	58467539	Human		name
598240933	CV4005008	single nucleotide variant	NM_153360.3(APCDD1L):c.925C>T (p.Arg309Cys)	not specified [RCV005383181]	uncertain significance	20	58461371	58461371	Human		name
598241025	CV4005025	single nucleotide variant	NM_153360.3(APCDD1L):c.704G>C (p.Arg235Pro)	not specified [RCV005383194]	uncertain significance	20	58467143	58467143	Human		name
598241205	CV4005054	single nucleotide variant	NM_153360.3(APCDD1L):c.892C>T (p.Leu298Phe)	not specified [RCV005383221]	uncertain significance	20	58461404	58461404	Human		name
598241394	CV4005094	single nucleotide variant	NM_153360.3(APCDD1L):c.496C>T (p.Arg166Trp)	not specified [RCV005383251]	uncertain significance	20	58467351	58467351	Human		name
156239181	CV2193696	single nucleotide variant	NM_153360.3(APCDD1L):c.1381G>A (p.Asp461Asn)	not specified [RCV004074290]	uncertain significance	20	58460915	58460915	Human		name
156132703	CV2195897	single nucleotide variant	NM_153360.3(APCDD1L):c.1234G>A (p.Glu412Lys)	not specified [RCV004072160]	uncertain significance	20	58461062	58461062	Human		name
156140602	CV2199867	single nucleotide variant	NM_153360.3(APCDD1L):c.1319C>T (p.Thr440Ile)	not specified [RCV004074059]	uncertain significance	20	58460977	58460977	Human		name
156073787	CV2240775	single nucleotide variant	NM_153360.3(APCDD1L):c.1039G>A (p.Gly347Ser)	not specified [RCV004119383]	uncertain significance	20	58461257	58461257	Human		name
156076993	CV2331848	single nucleotide variant	NM_153360.3(APCDD1L):c.1285G>A (p.Gly429Arg)	not specified [RCV004186506]	uncertain significance	20	58461011	58461011	Human		name
156383306	CV2361493	single nucleotide variant	NM_153360.3(APCDD1L):c.1019C>T (p.Thr340Met)	not specified [RCV004221131]	uncertain significance	20	58461277	58461277	Human		name
329384653	CV2435161	single nucleotide variant	NM_153360.3(APCDD1L):c.1283T>C (p.Ile428Thr)	not specified [RCV004252800]	uncertain significance	20	58461013	58461013	Human		name
401727754	CV2678431	single nucleotide variant	NM_153360.3(APCDD1L):c.1141G>C (p.Gly381Arg)	not specified [RCV004292454]	uncertain significance	20	58461155	58461155	Human		name
401730099	CV2683948	single nucleotide variant	NM_153360.3(APCDD1L):c.1202C>T (p.Pro401Leu)	not specified [RCV004286499]	uncertain significance	20	58461094	58461094	Human		name
401735083	CV2706657	single nucleotide variant	NM_153360.3(APCDD1L):c.1204C>G (p.Leu402Val)	not specified [RCV004319234]	uncertain significance	20	58461092	58461092	Human		name
401732998	CV2712936	single nucleotide variant	NM_153360.3(APCDD1L):c.1147G>A (p.Gly383Arg)	not specified [RCV004314648]	uncertain significance	20	58461149	58461149	Human		name
401891038	CV2768939	single nucleotide variant	NM_153360.3(APCDD1L):c.1262T>C (p.Leu421Pro)	not specified [RCV004347037]	uncertain significance	20	58461034	58461034	Human		name
405661985	CV3289670	single nucleotide variant	NM_153360.3(APCDD1L):c.1351C>A (p.Pro451Thr)	not specified [RCV004417613]	uncertain significance	20	58460945	58460945	Human		name
405661989	CV3289671	single nucleotide variant	NM_153360.3(APCDD1L):c.1492C>T (p.Leu498Phe)	not specified [RCV004417614]	uncertain significance	20	58460804	58460804	Human		name
407511745	CV3463403	single nucleotide variant	NM_153360.3(APCDD1L):c.1283T>A (p.Ile428Asn)	not specified [RCV004648144]	uncertain significance	20	58461013	58461013	Human		name
407511778	CV3463421	single nucleotide variant	NM_153360.3(APCDD1L):c.1292G>A (p.Arg431Lys)	not specified [RCV004648157]	uncertain significance	20	58461004	58461004	Human		name
597695515	CV3574623	single nucleotide variant	NM_153360.3(APCDD1L):c.1247T>C (p.Met416Thr)	not specified [RCV004839132]	uncertain significance	20	58461049	58461049	Human		name
598241280	CV4005074	single nucleotide variant	NM_153360.3(APCDD1L):c.1032G>C (p.Arg344Ser)	not specified [RCV005383233]	uncertain significance	20	58461264	58461264	Human		name
8637397	CV92623	single nucleotide variant	NM_153360.2(APCDD1L):c.1172G>A (p.Arg391Gln)	Malignant melanoma [RCV000072721]	not provided	20	58461124	58461124	Human		name

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