Tmem132d Variant Search Result - Rat Genome Database

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160 records found for search term Tmem132d

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405280863	CV3190595	single nucleotide variant	NM_133448.3(TMEM132D):c.1443+6T>C	TMEM132D-related disorder [RCV003907033]	likely benign	12	129209514	129209514	Human		name , trait , alternate_id
8653698	CV130273	single nucleotide variant	NM_133448.2(TMEM132D):c.1116-101G>C	Lung cancer [RCV000110760]	uncertain significance	12	129337918	129337918	Human		name
8653704	CV130279	single nucleotide variant	NM_133448.2(TMEM132D):c.80-92022G>C	Lung cancer [RCV000110766]	uncertain significance	12	129792720	129792720	Human		name
8653700	CV130275	single nucleotide variant	NM_133448.2(TMEM132D):c.969-63071T>G	Lung cancer [RCV000110762]	uncertain significance	12	129594276	129594276	Human		name
8653701	CV130276	single nucleotide variant	NM_133448.2(TMEM132D):c.968+62579T>A	Lung cancer [RCV000110763]	uncertain significance	12	129637231	129637231	Human		name
8653702	CV130277	single nucleotide variant	NM_133448.2(TMEM132D):c.968+54040C>A	Lung cancer [RCV000110764]	uncertain significance	12	129645770	129645770	Human		name
8653703	CV130278	single nucleotide variant	NM_133448.2(TMEM132D):c.968+46839C>T	Lung cancer [RCV000110765]	uncertain significance	12	129652971	129652971	Human		name
153000026	CV1683580	single nucleotide variant	NM_133448.3(TMEM132D):c.969-61346A>G	Vascular endothelial growth factor (VEGF) inhibitor response [RCV002254035]	association	12	129592551	129592551	Human		name
8653690	CV130265	single nucleotide variant	NM_133448.2(TMEM132D):c.1444-38061C>G	Lung cancer [RCV000110752]	uncertain significance	12	129122763	129122763	Human		name
8653691	CV130266	single nucleotide variant	NM_133448.2(TMEM132D):c.1443+53442T>C	Lung cancer [RCV000110753]	uncertain significance	12	129156078	129156078	Human		name
8653692	CV130267	single nucleotide variant	NM_133448.2(TMEM132D):c.1443+16277C>G	Lung cancer [RCV000110754]	uncertain significance	12	129193243	129193243	Human		name
8653694	CV130269	single nucleotide variant	NM_133448.2(TMEM132D):c.1300-36991A>T	Lung cancer [RCV000110756]	uncertain significance	12	129246654	129246654	Human		name
8653695	CV130270	single nucleotide variant	NM_133448.2(TMEM132D):c.1299+52246T>C	Lung cancer [RCV000110757]	uncertain significance	12	129285388	129285388	Human		name
8653696	CV130271	single nucleotide variant	NM_133448.2(TMEM132D):c.1299+26782C>A	Lung cancer [RCV000110758]	uncertain significance	12	129310852	129310852	Human		name
8653697	CV130272	single nucleotide variant	NM_133448.2(TMEM132D):c.1299+20006C>G	Lung cancer [RCV000110759]	uncertain significance	12	129317628	129317628	Human		name
8653699	CV130274	single nucleotide variant	NM_133448.2(TMEM132D):c.1115+60219A>G	Lung cancer [RCV000110761]	uncertain significance	12	129470840	129470840	Human		name
156054056	CV2243041	single nucleotide variant	NM_133448.3(TMEM132D):c.44C>T (p.Pro15Leu)	not specified [RCV004109960]	uncertain significance	12	129903296	129903296	Human		name
156367766	CV2266874	single nucleotide variant	NM_133448.3(TMEM132D):c.97A>T (p.Ile33Phe)	not specified [RCV004131541]	uncertain significance	12	129700681	129700681	Human		name
156175465	CV2327151	single nucleotide variant	NM_133448.3(TMEM132D):c.43C>G (p.Pro15Ala)	not specified [RCV004178715]	uncertain significance	12	129903297	129903297	Human		name
405277182	CV3198782	single nucleotide variant	NM_133448.3(TMEM132D):c.390A>G (p.Lys130=)	TMEM132D-related disorder [RCV003904105]	likely benign	12	129700388	129700388	Human		name , trait , alternate_id
405274805	CV3204474	single nucleotide variant	NM_133448.3(TMEM132D):c.334C>T (p.Leu112=)	TMEM132D-related disorder [RCV003951909]	likely benign	12	129700444	129700444	Human		name , trait , alternate_id
405291806	CV3206114	single nucleotide variant	NM_133448.3(TMEM132D):c.894C>T (p.Thr298=)	TMEM132D-related disorder [RCV003964188]	likely benign	12	129699884	129699884	Human		name , trait , alternate_id
405274565	CV3208907	single nucleotide variant	NM_133448.3(TMEM132D):c.618C>A (p.Pro206=)	TMEM132D-related disorder [RCV003951694]	likely benign	12	129700160	129700160	Human		name , trait , alternate_id
405278949	CV3212723	single nucleotide variant	NM_133448.3(TMEM132D):c.999C>T (p.Ile333=)	TMEM132D-related disorder [RCV003954746]	likely benign	12	129531175	129531175	Human		name , trait , alternate_id
405279458	CV3217461	single nucleotide variant	NM_133448.3(TMEM132D):c.396C>T (p.His132=)	TMEM132D-related disorder [RCV003976870]	likely benign	12	129700382	129700382	Human		name , trait , alternate_id
405266187	CV3221073	single nucleotide variant	NM_133448.3(TMEM132D):c.519C>T (p.Phe173=)	TMEM132D-related disorder [RCV003969198]	likely benign	12	129700259	129700259	Human		name , trait , alternate_id
15181148	CV713435	single nucleotide variant	NM_133448.3(TMEM132D):c.354A>G (p.Gly118=)	not provided [RCV000974322]	benign	12	129700424	129700424	Human		name
15142713	CV738545	single nucleotide variant	NM_133448.3(TMEM132D):c.729C>T (p.Asp243=)	not provided [RCV000899719]	benign	12	129700049	129700049	Human		name
8689415	CV97503	single nucleotide variant	NM_133448.3(TMEM132D):c.315G>T (p.Val105=)	not provided [RCV000122582]	uncertain significance	12	129700463	129700463	Human		name
156188067	CV2292514	single nucleotide variant	NM_133448.3(TMEM132D):c.233G>T (p.Arg78Leu)	not specified [RCV004150292]	uncertain significance	12	129700545	129700545	Human		name
405288489	CV3197425	single nucleotide variant	NM_133448.3(TMEM132D):c.2163G>A (p.Thr721=)	TMEM132D-related disorder [RCV003982521]	benign	12	129075012	129075012	Human		name , trait , alternate_id
405279764	CV3200110	single nucleotide variant	NM_133448.3(TMEM132D):c.1506G>A (p.Val502=)	TMEM132D-related disorder [RCV003977055]	likely benign	12	129084640	129084640	Human		name , trait , alternate_id
405291931	CV3207729	single nucleotide variant	NM_133448.3(TMEM132D):c.1353G>A (p.Pro451=)	TMEM132D-related disorder [RCV003929422]	likely benign	12	129209610	129209610	Human		name , trait , alternate_id
405289701	CV3213225	single nucleotide variant	NM_133448.3(TMEM132D):c.1656C>T (p.Ala552=)	TMEM132D-related disorder [RCV003961933]	likely benign	12	129082026	129082026	Human		name , trait , alternate_id
405279473	CV3217465	single nucleotide variant	NM_133448.3(TMEM132D):c.1047G>A (p.Thr349=)	TMEM132D-related disorder [RCV003976873]	likely benign	12	129531127	129531127	Human		name , trait , alternate_id
405279696	CV3217595	single nucleotide variant	NM_133448.3(TMEM132D):c.2385T>C (p.Val795=)	TMEM132D-related disorder [RCV003976974]	likely benign	12	129074790	129074790	Human		name , trait , alternate_id
405271093	CV3218892	single nucleotide variant	NM_133448.3(TMEM132D):c.1584C>T (p.Ile528=)	TMEM132D-related disorder [RCV003971638]	likely benign	12	129084562	129084562	Human		name , trait , alternate_id
405266107	CV3221045	single nucleotide variant	NM_133448.3(TMEM132D):c.1599C>T (p.Thr533=)	TMEM132D-related disorder [RCV003969177]	likely benign	12	129084547	129084547	Human		name , trait , alternate_id
598212753	CV3917337	single nucleotide variant	NM_133448.3(TMEM132D):c.157A>G (p.Ile53Val)	not specified [RCV005292199]	uncertain significance	12	129700621	129700621	Human		name
15157267	CV713434	single nucleotide variant	NM_133448.3(TMEM132D):c.1302G>A (p.Glu434=)	not provided [RCV000969277]	benign	12	129209661	129209661	Human		name
15111850	CV713436	single nucleotide variant	NM_133448.3(TMEM132D):c.269T>A (p.Leu90Gln)	TMEM132D-related disorder [RCV003916042]\|not provided [RCV000961187]	benign	12	129700509	129700509	Human		name , trait , alternate_id
15188123	CV724985	single nucleotide variant	NM_133448.3(TMEM132D):c.1434C>T (p.Asp478=)	not provided [RCV000887442]	likely benign	12	129209529	129209529	Human		name
156145976	CV2196845	single nucleotide variant	NM_133448.3(TMEM132D):c.542G>A (p.Gly181Asp)	not specified [RCV004069854]	uncertain significance	12	129700236	129700236	Human		name
156299161	CV2244706	single nucleotide variant	NM_133448.3(TMEM132D):c.722G>A (p.Arg241Lys)	not specified [RCV004102707]	likely benign	12	129700056	129700056	Human		name
156080048	CV2259304	single nucleotide variant	NM_133448.3(TMEM132D):c.662G>A (p.Gly221Glu)	not specified [RCV004122318]	uncertain significance	12	129700116	129700116	Human		name
156078316	CV2281726	single nucleotide variant	NM_133448.3(TMEM132D):c.790T>A (p.Leu264Met)	not specified [RCV004147872]	uncertain significance	12	129699988	129699988	Human		name
156007861	CV2288402	single nucleotide variant	NM_133448.3(TMEM132D):c.485G>A (p.Gly162Glu)	not specified [RCV004151953]	uncertain significance	12	129700293	129700293	Human		name
155931185	CV2297258	single nucleotide variant	NM_133448.3(TMEM132D):c.491A>G (p.Lys164Arg)	not specified [RCV004151135]	likely benign	12	129700287	129700287	Human		name
156155951	CV2314341	single nucleotide variant	NM_133448.3(TMEM132D):c.792G>T (p.Leu264Phe)	not specified [RCV004166684]	uncertain significance	12	129699986	129699986	Human		name
156045364	CV2319012	single nucleotide variant	NM_133448.3(TMEM132D):c.497C>T (p.Pro166Leu)	not specified [RCV004178101]	uncertain significance	12	129700281	129700281	Human		name
156255641	CV2397677	single nucleotide variant	NM_133448.3(TMEM132D):c.772G>A (p.Asp258Asn)	not specified [RCV004237124]	uncertain significance	12	129700006	129700006	Human		name
401720576	CV2701975	single nucleotide variant	NM_133448.3(TMEM132D):c.345C>A (p.Asn115Lys)	not specified [RCV004320572]	uncertain significance	12	129700433	129700433	Human		name
401731607	CV2712068	single nucleotide variant	NM_133448.3(TMEM132D):c.781G>A (p.Gly261Arg)	not specified [RCV004311806]	uncertain significance	12	129699997	129699997	Human		name
401899819	CV2758867	single nucleotide variant	NM_133448.3(TMEM132D):c.613C>A (p.Pro205Thr)	not specified [RCV004339956]	uncertain significance	12	129700165	129700165	Human		name
401872782	CV2776220	single nucleotide variant	NM_133448.3(TMEM132D):c.962C>A (p.Thr321Lys)	not specified [RCV004353590]	uncertain significance	12	129699816	129699816	Human		name
405277343	CV3195434	single nucleotide variant	NM_133448.3(TMEM132D):c.484G>A (p.Gly162Arg)	TMEM132D-related disorder [RCV003904219]	likely benign	12	129700294	129700294	Human		name , trait , alternate_id
405285775	CV3209705	single nucleotide variant	NM_133448.3(TMEM132D):c.3258A>G (p.Lys1086=)	TMEM132D-related disorder [RCV003959272]	likely benign	12	129073917	129073917	Human		name , trait , alternate_id
405266710	CV3211867	single nucleotide variant	NM_133448.3(TMEM132D):c.3003A>G (p.Lys1001=)	TMEM132D-related disorder [RCV003947146]	likely benign	12	129074172	129074172	Human		name , trait , alternate_id
405286830	CV3213789	single nucleotide variant	NM_133448.3(TMEM132D):c.3171C>T (p.Asp1057=)	TMEM132D-related disorder [RCV003924188]	benign	12	129074004	129074004	Human		name , trait , alternate_id
405794132	CV3339716	single nucleotide variant	NM_133448.3(TMEM132D):c.309G>C (p.Glu103Asp)	not specified [RCV004475127]	uncertain significance	12	129700469	129700469	Human		name
405794141	CV3339719	single nucleotide variant	NM_133448.3(TMEM132D):c.910G>A (p.Val304Met)	not specified [RCV004475130]	uncertain significance	12	129699868	129699868	Human		name
407453260	CV3486364	single nucleotide variant	NM_133448.3(TMEM132D):c.671T>C (p.Val224Ala)	not specified [RCV004684466]	uncertain significance	12	129700107	129700107	Human		name
407453262	CV3486365	single nucleotide variant	NM_133448.3(TMEM132D):c.544A>C (p.Ser182Arg)	not specified [RCV004684467]	uncertain significance	12	129700234	129700234	Human		name
408384604	CV3504398	single nucleotide variant	NM_133448.3(TMEM132D):c.529C>T (p.Arg177Ter)	TMEM132D-related disorder [RCV004731948]	uncertain significance	12	129700249	129700249	Human		name , trait , alternate_id
597785781	CV3616780	single nucleotide variant	NM_133448.3(TMEM132D):c.551G>A (p.Arg184Gln)	not specified [RCV004875169]	uncertain significance	12	129700227	129700227	Human		name
597785789	CV3616782	single nucleotide variant	NM_133448.3(TMEM132D):c.701G>A (p.Gly234Asp)	not specified [RCV004875171]	likely benign	12	129700077	129700077	Human		name
597785793	CV3616784	single nucleotide variant	NM_133448.3(TMEM132D):c.463G>T (p.Asp155Tyr)	not specified [RCV004875172]	uncertain significance	12	129700315	129700315	Human		name
598212762	CV3917338	single nucleotide variant	NM_133448.3(TMEM132D):c.471C>G (p.Asp157Glu)	not specified [RCV005292200]	uncertain significance	12	129700307	129700307	Human		name
598212779	CV3917343	single nucleotide variant	NM_133448.3(TMEM132D):c.700G>A (p.Gly234Ser)	not specified [RCV005292203]	uncertain significance	12	129700078	129700078	Human		name
598212795	CV3917346	single nucleotide variant	NM_133448.3(TMEM132D):c.874A>G (p.Ile292Val)	not specified [RCV005292205]	likely benign	12	129699904	129699904	Human		name
598212823	CV3917350	single nucleotide variant	NM_133448.3(TMEM132D):c.890A>C (p.Lys297Thr)	not specified [RCV005292209]	uncertain significance	12	129699888	129699888	Human		name
598212849	CV3917353	single nucleotide variant	NM_133448.3(TMEM132D):c.980A>G (p.Lys327Arg)	not specified [RCV005292212]	uncertain significance	12	129531194	129531194	Human		name
15185452	CV702223	single nucleotide variant	NM_133448.3(TMEM132D):c.3183C>T (p.Thr1061=)	not provided [RCV000952988]	benign	12	129073992	129073992	Human		name
15106128	CV753201	single nucleotide variant	NM_133448.3(TMEM132D):c.3255C>T (p.Cys1085=)	not provided [RCV000915684]	likely benign	12	129073920	129073920	Human		name
156236486	CV2210533	single nucleotide variant	NM_133448.3(TMEM132D):c.2660G>A (p.Ser887Asn)	not specified [RCV004089661]	uncertain significance	12	129074515	129074515	Human		name
155935521	CV2225621	single nucleotide variant	NM_133448.3(TMEM132D):c.1046C>A (p.Thr349Lys)	not specified [RCV004100992]	uncertain significance	12	129531128	129531128	Human		name
155945798	CV2238033	single nucleotide variant	NM_133448.3(TMEM132D):c.1285G>T (p.Val429Leu)	not specified [RCV004111061]	uncertain significance	12	129337648	129337648	Human		name
156046723	CV2244705	single nucleotide variant	NM_133448.3(TMEM132D):c.1567C>T (p.Arg523Trp)	not specified [RCV004102706]	uncertain significance	12	129084579	129084579	Human		name
156048250	CV2245060	single nucleotide variant	NM_133448.3(TMEM132D):c.1504G>A (p.Val502Met)	not specified [RCV004104779]	uncertain significance	12	129084642	129084642	Human		name
156252296	CV2268384	single nucleotide variant	NM_133448.3(TMEM132D):c.2092G>A (p.Glu698Lys)	not specified [RCV004138658]	uncertain significance	12	129078557	129078557	Human		name
156259648	CV2274132	single nucleotide variant	NM_133448.3(TMEM132D):c.2323G>A (p.Glu775Lys)	not specified [RCV004134771]	uncertain significance	12	129074852	129074852	Human		name
155940320	CV2294060	single nucleotide variant	NM_133448.3(TMEM132D):c.1729G>C (p.Val577Leu)	not specified [RCV004149443]	uncertain significance	12	129081953	129081953	Human		name
156183733	CV2295683	single nucleotide variant	NM_133448.3(TMEM132D):c.1450G>C (p.Asp484His)	not specified [RCV004149836]	uncertain significance	12	129084696	129084696	Human		name
155999997	CV2296261	single nucleotide variant	NM_133448.3(TMEM132D):c.1102G>A (p.Gly368Ser)	not specified [RCV004154165]	uncertain significance	12	129531072	129531072	Human		name
156208452	CV2298124	single nucleotide variant	NM_133448.3(TMEM132D):c.1120G>A (p.Asp374Asn)	not specified [RCV004159790]	uncertain significance	12	129337813	129337813	Human		name
156192482	CV2301893	single nucleotide variant	NM_133448.3(TMEM132D):c.1628T>C (p.Val543Ala)	not specified [RCV004156682]	uncertain significance	12	129084518	129084518	Human		name
156280541	CV2338398	single nucleotide variant	NM_133448.3(TMEM132D):c.2477G>A (p.Arg826Lys)	not specified [RCV004186445]	uncertain significance	12	129074698	129074698	Human		name
156125721	CV2350225	single nucleotide variant	NM_133448.3(TMEM132D):c.1775G>A (p.Gly592Glu)	not specified [RCV004200135]	uncertain significance	12	129081907	129081907	Human		name
156050434	CV2367507	single nucleotide variant	NM_133448.3(TMEM132D):c.2489C>T (p.Pro830Leu)	not specified [RCV004211443]	uncertain significance	12	129074686	129074686	Human		name
156070614	CV2381327	single nucleotide variant	NM_133448.3(TMEM132D):c.2675T>A (p.Val892Glu)	not specified [RCV004227386]	uncertain significance	12	129074500	129074500	Human		name
155928739	CV2388970	single nucleotide variant	NM_133448.3(TMEM132D):c.1381G>A (p.Gly461Ser)	not specified [RCV004241969]	uncertain significance	12	129209582	129209582	Human		name
156046912	CV2390897	single nucleotide variant	NM_133448.3(TMEM132D):c.1720C>T (p.His574Tyr)	not specified [RCV004234912]	uncertain significance	12	129081962	129081962	Human		name
329365475	CV2444905	single nucleotide variant	NM_133448.3(TMEM132D):c.1879G>A (p.Gly627Arg)	not specified [RCV004259141]	uncertain significance	12	129081803	129081803	Human		name
329355485	CV2445500	single nucleotide variant	NM_133448.3(TMEM132D):c.1007G>A (p.Arg336Gln)	not specified [RCV004257558]	uncertain significance	12	129531167	129531167	Human		name
329391007	CV2447614	single nucleotide variant	NM_133448.3(TMEM132D):c.1174G>A (p.Asp392Asn)	not specified [RCV004258418]	uncertain significance	12	129337759	129337759	Human		name
329353556	CV2466881	single nucleotide variant	NM_133448.3(TMEM132D):c.1630C>T (p.Pro544Ser)	not specified [RCV004282652]	uncertain significance	12	129084516	129084516	Human		name
329353558	CV2466882	single nucleotide variant	NM_133448.3(TMEM132D):c.1672G>A (p.Glu558Lys)	not specified [RCV004282653]	uncertain significance	12	129082010	129082010	Human		name
401738166	CV2676152	single nucleotide variant	NM_133448.3(TMEM132D):c.1523A>C (p.Tyr508Ser)	not specified [RCV004284373]	uncertain significance	12	129084623	129084623	Human		name
401739054	CV2676427	single nucleotide variant	NM_133448.3(TMEM132D):c.1400T>C (p.Leu467Pro)	not specified [RCV004286447]	uncertain significance	12	129209563	129209563	Human		name
401779735	CV2676670	single nucleotide variant	NM_133448.3(TMEM132D):c.1042C>T (p.Arg348Cys)	not specified [RCV004290852]	uncertain significance	12	129531132	129531132	Human		name
401732432	CV2708828	single nucleotide variant	NM_133448.3(TMEM132D):c.2462A>G (p.Asn821Ser)	not specified [RCV004307778]	uncertain significance	12	129074713	129074713	Human		name
401730983	CV2711601	single nucleotide variant	NM_133448.3(TMEM132D):c.2610C>G (p.Ser870Arg)	not specified [RCV004306906]	uncertain significance	12	129074565	129074565	Human		name
401876666	CV2754427	single nucleotide variant	NM_133448.3(TMEM132D):c.1841T>C (p.Met614Thr)	not specified [RCV004336641]	uncertain significance	12	129081841	129081841	Human		name
401876729	CV2754459	single nucleotide variant	NM_133448.3(TMEM132D):c.1465G>A (p.Val489Ile)	not specified [RCV004336671]	uncertain significance	12	129084681	129084681	Human		name
401883396	CV2757907	single nucleotide variant	NM_133448.3(TMEM132D):c.1435G>A (p.Val479Met)	not specified [RCV004337044]	uncertain significance	12	129209528	129209528	Human		name
401880901	CV2763176	single nucleotide variant	NM_133448.3(TMEM132D):c.2753T>C (p.Ile918Thr)	not specified [RCV004336216]	uncertain significance	12	129074422	129074422	Human		name
401943467	CV2840054	single nucleotide variant	NM_133448.3(TMEM132D):c.1099G>C (p.Ala367Pro)	TMEM132D-related disorder [RCV003954220]\|not provided [RCV003456841]	likely benign	12	129531075	129531075	Human		name , trait , alternate_id
405284529	CV3196892	single nucleotide variant	NM_133448.3(TMEM132D):c.2299G>A (p.Val767Ile)	TMEM132D-related disorder [RCV003979751]	benign	12	129074876	129074876	Human	1	name , trait , alternate_id
405284768	CV3196961	single nucleotide variant	NM_133448.3(TMEM132D):c.2634G>T (p.Leu878Phe)	TMEM132D-related disorder [RCV003979805]	benign	12	129074541	129074541	Human		name , trait , alternate_id
405275037	CV3199917	single nucleotide variant	NM_133448.3(TMEM132D):c.2657C>A (p.Thr886Asn)	TMEM132D-related disorder [RCV003973945]	benign	12	129074518	129074518	Human		name , trait , alternate_id
405794069	CV3339696	single nucleotide variant	NM_133448.3(TMEM132D):c.1124G>A (p.Gly375Asp)	not specified [RCV004475107]	uncertain significance	12	129337809	129337809	Human		name
405794075	CV3339698	single nucleotide variant	NM_133448.3(TMEM132D):c.1166A>G (p.Glu389Gly)	not specified [RCV004475109]	uncertain significance	12	129337767	129337767	Human		name
405794078	CV3339699	single nucleotide variant	NM_133448.3(TMEM132D):c.1190A>C (p.Gln397Pro)	not specified [RCV004475110]	uncertain significance	12	129337743	129337743	Human		name
405794081	CV3339700	single nucleotide variant	NM_133448.3(TMEM132D):c.1224G>C (p.Glu408Asp)	not specified [RCV004475111]	likely benign	12	129337709	129337709	Human		name
405794084	CV3339701	single nucleotide variant	NM_133448.3(TMEM132D):c.1229C>T (p.Thr410Met)	not specified [RCV004475112]	uncertain significance	12	129337704	129337704	Human		name
405794087	CV3339702	single nucleotide variant	NM_133448.3(TMEM132D):c.1277T>C (p.Ile426Thr)	not specified [RCV004475113]	uncertain significance	12	129337656	129337656	Human		name
405794090	CV3339703	single nucleotide variant	NM_133448.3(TMEM132D):c.1331C>T (p.Thr444Met)	not specified [RCV004475114]	uncertain significance	12	129209632	129209632	Human		name
405794096	CV3339705	single nucleotide variant	NM_133448.3(TMEM132D):c.1568G>A (p.Arg523Gln)	not specified [RCV004475116]	uncertain significance	12	129084578	129084578	Human		name
405794104	CV3339707	single nucleotide variant	NM_133448.3(TMEM132D):c.1676A>C (p.Glu559Ala)	not specified [RCV004475118]	uncertain significance	12	129082006	129082006	Human		name
405794107	CV3339708	single nucleotide variant	NM_133448.3(TMEM132D):c.1765G>A (p.Gly589Ser)	not specified [RCV004475119]	uncertain significance	12	129081917	129081917	Human		name
405794110	CV3339709	single nucleotide variant	NM_133448.3(TMEM132D):c.1979A>G (p.Asp660Gly)	not specified [RCV004475120]	uncertain significance	12	129078670	129078670	Human		name
405794116	CV3339711	single nucleotide variant	NM_133448.3(TMEM132D):c.2419A>G (p.Ser807Gly)	not specified [RCV004475122]	uncertain significance	12	129074756	129074756	Human		name
405794119	CV3339712	single nucleotide variant	NM_133448.3(TMEM132D):c.2545C>T (p.Leu849Phe)	not specified [RCV004475123]	uncertain significance	12	129074630	129074630	Human		name
405794122	CV3339713	single nucleotide variant	NM_133448.3(TMEM132D):c.2638A>T (p.Thr880Ser)	not specified [RCV004475124]	uncertain significance	12	129074537	129074537	Human		name
405794128	CV3339715	single nucleotide variant	NM_133448.3(TMEM132D):c.2959C>G (p.Gln987Glu)	not specified [RCV004475126]	uncertain significance	12	129074216	129074216	Human		name
407453258	CV3486363	single nucleotide variant	NM_133448.3(TMEM132D):c.1141A>G (p.Met381Val)	not specified [RCV004684465]	uncertain significance	12	129337792	129337792	Human		name
407453264	CV3486366	single nucleotide variant	NM_133448.3(TMEM132D):c.2540T>C (p.Met847Thr)	not specified [RCV004684468]	uncertain significance	12	129074635	129074635	Human		name
597785786	CV3616781	single nucleotide variant	NM_133448.3(TMEM132D):c.1417A>G (p.Arg473Gly)	not specified [RCV004875170]	uncertain significance	12	129209546	129209546	Human		name
597795440	CV3616783	single nucleotide variant	NM_133448.3(TMEM132D):c.2909G>A (p.Arg970Gln)	not specified [RCV004878135]	uncertain significance	12	129074266	129074266	Human		name
597795327	CV3616785	single nucleotide variant	NM_133448.3(TMEM132D):c.1348G>A (p.Val450Ile)	not specified [RCV004878136]	uncertain significance	12	129209615	129209615	Human		name
597795229	CV3616786	single nucleotide variant	NM_133448.3(TMEM132D):c.1271A>G (p.Asp424Gly)	not specified [RCV004878137]	uncertain significance	12	129337662	129337662	Human		name
597785801	CV3616788	single nucleotide variant	NM_133448.3(TMEM132D):c.1150G>T (p.Asp384Tyr)	not specified [RCV004875174]	uncertain significance	12	129337783	129337783	Human		name
597785804	CV3616789	single nucleotide variant	NM_133448.3(TMEM132D):c.1588G>T (p.Val530Phe)	not specified [RCV004875175]	uncertain significance	12	129084558	129084558	Human		name
597785808	CV3616790	single nucleotide variant	NM_133448.3(TMEM132D):c.2675T>G (p.Val892Gly)	not specified [RCV004875176]	uncertain significance	12	129074500	129074500	Human		name
597785812	CV3616791	single nucleotide variant	NM_133448.3(TMEM132D):c.2597A>G (p.Lys866Arg)	not specified [RCV004875177]	uncertain significance	12	129074578	129074578	Human		name
597752559	CV3616793	single nucleotide variant	NM_133448.3(TMEM132D):c.1123G>A (p.Gly375Ser)	not specified [RCV004867177]	uncertain significance	12	129337810	129337810	Human		name
598212769	CV3917339	single nucleotide variant	NM_133448.3(TMEM132D):c.1396C>A (p.Leu466Met)	not specified [RCV005292201]	uncertain significance	12	129209567	129209567	Human		name
598178171	CV3917341	single nucleotide variant	NM_133448.3(TMEM132D):c.2179G>A (p.Asp727Asn)	not specified [RCV005285937]	uncertain significance	12	129074996	129074996	Human		name
598178178	CV3917342	single nucleotide variant	NM_133448.3(TMEM132D):c.1594G>A (p.Asp532Asn)	not specified [RCV005285938]	uncertain significance	12	129084552	129084552	Human		name
598178185	CV3917344	single nucleotide variant	NM_133448.3(TMEM132D):c.2392G>A (p.Gly798Ser)	not specified [RCV005285939]	uncertain significance	12	129074783	129074783	Human		name
598212787	CV3917345	single nucleotide variant	NM_133448.3(TMEM132D):c.1669G>A (p.Glu557Lys)	not specified [RCV005292204]	uncertain significance	12	129082013	129082013	Human		name
598212802	CV3917347	single nucleotide variant	NM_133448.3(TMEM132D):c.1742C>T (p.Thr581Met)	not specified [RCV005292206]	uncertain significance	12	129081940	129081940	Human		name
598212816	CV3917349	single nucleotide variant	NM_133448.3(TMEM132D):c.2731A>G (p.Lys911Glu)	not specified [RCV005292208]	uncertain significance	12	129074444	129074444	Human		name
598212831	CV3917351	single nucleotide variant	NM_133448.3(TMEM132D):c.1781T>C (p.Leu594Pro)	not specified [RCV005292210]	uncertain significance	12	129081901	129081901	Human		name
598212842	CV3917352	single nucleotide variant	NM_133448.3(TMEM132D):c.1690A>T (p.Arg564Trp)	not specified [RCV005292211]	uncertain significance	12	129081992	129081992	Human		name
15102803	CV702224	single nucleotide variant	NM_133448.3(TMEM132D):c.2492C>T (p.Ser831Leu)	not provided [RCV000959355]	benign	12	129074683	129074683	Human		name
15189791	CV702225	single nucleotide variant	NM_133448.3(TMEM132D):c.1661A>G (p.Asp554Gly)	not provided [RCV000954284]	likely benign	12	129082021	129082021	Human		name
8627223	CV82367	single nucleotide variant	NM_133448.2(TMEM132D):c.1346C>T (p.Ala449Val)	Malignant melanoma [RCV000062446]	not provided	12	129209617	129209617	Human		name
155919315	CV2254845	single nucleotide variant	NM_133448.3(TMEM132D):c.3226G>T (p.Val1076Phe)	not specified [RCV004115306]	uncertain significance	12	129073949	129073949	Human		name
156065174	CV2316321	single nucleotide variant	NM_133448.3(TMEM132D):c.3287A>G (p.His1096Arg)	not specified [RCV004174337]	likely benign	12	129073888	129073888	Human		name
155968062	CV2339267	single nucleotide variant	NM_133448.3(TMEM132D):c.3274A>G (p.Met1092Val)	not specified [RCV004191507]	uncertain significance	12	129073901	129073901	Human		name
156304110	CV2341408	single nucleotide variant	NM_133448.3(TMEM132D):c.3154G>A (p.Ala1052Thr)	not specified [RCV004188807]	likely benign	12	129074021	129074021	Human		name
329362721	CV2439153	single nucleotide variant	NM_133448.3(TMEM132D):c.3208G>A (p.Glu1070Lys)	not specified [RCV004266434]	uncertain significance	12	129073967	129073967	Human		name
329402587	CV2451097	single nucleotide variant	NM_133448.3(TMEM132D):c.3115A>G (p.Thr1039Ala)	not specified [RCV004270038]	uncertain significance	12	129074060	129074060	Human		name
401774505	CV2713512	single nucleotide variant	NM_133448.3(TMEM132D):c.3196G>A (p.Val1066Met)	not specified [RCV004319112]	uncertain significance	12	129073979	129073979	Human		name
401882740	CV2788570	single nucleotide variant	NM_133448.3(TMEM132D):c.3217A>G (p.Ile1073Val)	not specified [RCV004361068]	uncertain significance	12	129073958	129073958	Human		name
407453266	CV3486368	single nucleotide variant	NM_133448.3(TMEM132D):c.3288T>G (p.His1096Gln)	not specified [RCV004684470]	uncertain significance	12	129073887	129073887	Human		name
597795210	CV3616792	single nucleotide variant	NM_133448.3(TMEM132D):c.3172G>A (p.Glu1058Lys)	not specified [RCV004878138]	uncertain significance	12	129074003	129074003	Human		name
598212809	CV3917348	single nucleotide variant	NM_133448.3(TMEM132D):c.3206G>A (p.Ser1069Asn)	not specified [RCV005292207]	uncertain significance	12	129073969	129073969	Human		name
14979092	CV678070	single nucleotide variant	NM_133448.3(TMEM132D):c.3247G>A (p.Gly1083Arg)	not provided [RCV000851314]	uncertain significance	12	129073928	129073928	Human		name

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