Tulp2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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58 records found for search term Tulp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156168042	CV2399103	single nucleotide variant	NM_003323.3(TULP2):c.187G>C (p.Glu63Gln)	not specified [RCV004246539]	uncertain significance	19	48896454	48896454	Human		name
401910645	CV2818549	single nucleotide variant	NM_003323.3(TULP2):c.194G>A (p.Arg65His)	not provided [RCV003425314]	uncertain significance	19	48896447	48896447	Human		name
407532380	CV3493051	single nucleotide variant	NM_003323.3(TULP2):c.191A>G (p.Glu64Gly)	not specified [RCV004683024]	uncertain significance	19	48896450	48896450	Human		name
597798152	CV3628666	single nucleotide variant	NM_003323.3(TULP2):c.259C>G (p.Pro87Ala)	not specified [RCV004879107]	uncertain significance	19	48895456	48895456	Human		name
8628367	CV83511	single nucleotide variant	NM_003323.2(TULP2):c.1008C>T (p.Ser336=)	Malignant melanoma [RCV000063592]	not provided	19	48885501	48885501	Human		name
8636924	CV92149	single nucleotide variant	NM_003323.2(TULP2):c.1293G>A (p.Leu431=)	Malignant melanoma [RCV000072247]	not provided	19	48882186	48882186	Human		name
156153454	CV2242084	single nucleotide variant	NM_003323.3(TULP2):c.784C>T (p.Arg262Cys)	not specified [RCV004109309]	uncertain significance	19	48888114	48888114	Human		name
155915035	CV2264853	single nucleotide variant	NM_003323.3(TULP2):c.520C>A (p.Arg174Ser)	not specified [RCV004134608]	likely benign	19	48889626	48889626	Human		name
156191315	CV2289339	single nucleotide variant	NM_003323.3(TULP2):c.965G>A (p.Gly322Glu)	not specified [RCV004152310]	uncertain significance	19	48885544	48885544	Human		name
156014941	CV2301646	single nucleotide variant	NM_003323.3(TULP2):c.797C>T (p.Pro266Leu)	not specified [RCV004162548]	uncertain significance	19	48888101	48888101	Human		name
156084020	CV2369087	single nucleotide variant	NM_003323.3(TULP2):c.841C>T (p.Leu281Phe)	not specified [RCV004208011]	uncertain significance	19	48888057	48888057	Human		name
156134700	CV2379706	single nucleotide variant	NM_003323.3(TULP2):c.550A>C (p.Met184Leu)	not specified [RCV004219826]	uncertain significance	19	48889596	48889596	Human		name
329363141	CV2445889	single nucleotide variant	NM_003323.3(TULP2):c.683C>T (p.Thr228Met)	not specified [RCV004270500]	uncertain significance	19	48888215	48888215	Human		name
401741662	CV2677409	single nucleotide variant	NM_003323.3(TULP2):c.473C>G (p.Pro158Arg)	not specified [RCV004289485]	uncertain significance	19	48895039	48895039	Human		name
401862269	CV2775199	single nucleotide variant	NM_003323.3(TULP2):c.316G>C (p.Glu106Gln)	not specified [RCV004346543]	uncertain significance	19	48895399	48895399	Human		name
405809429	CV3344582	single nucleotide variant	NM_003323.3(TULP2):c.337C>G (p.Arg113Gly)	not specified [RCV004481733]	uncertain significance	19	48895378	48895378	Human		name
405809430	CV3344583	single nucleotide variant	NM_003323.3(TULP2):c.428C>T (p.Ser143Phe)	not specified [RCV004481734]	uncertain significance	19	48895084	48895084	Human		name
405809432	CV3344584	single nucleotide variant	NM_003323.3(TULP2):c.490G>A (p.Gly164Ser)	not specified [RCV004481735]	uncertain significance	19	48895022	48895022	Human		name
405809434	CV3344585	single nucleotide variant	NM_003323.3(TULP2):c.716C>T (p.Ser239Phe)	not specified [RCV004481736]	uncertain significance	19	48888182	48888182	Human		name
405809436	CV3344586	single nucleotide variant	NM_003323.3(TULP2):c.782T>C (p.Ile261Thr)	not specified [RCV004481737]	uncertain significance	19	48888116	48888116	Human		name
405809438	CV3344587	single nucleotide variant	NM_003323.3(TULP2):c.826G>A (p.Val276Met)	not specified [RCV004481738]	uncertain significance	19	48888072	48888072	Human		name
405809713	CV3344588	single nucleotide variant	NM_003323.3(TULP2):c.920T>C (p.Leu307Pro)	not specified [RCV004481739]	uncertain significance	19	48887978	48887978	Human		name
405809442	CV3344589	single nucleotide variant	NM_003323.3(TULP2):c.974G>C (p.Arg325Thr)	not specified [RCV004481740]	uncertain significance	19	48885535	48885535	Human		name
407532381	CV3493052	single nucleotide variant	NM_003323.3(TULP2):c.759G>A (p.Met253Ile)	not specified [RCV004683025]	uncertain significance	19	48888139	48888139	Human		name
407532382	CV3493053	single nucleotide variant	NM_003323.3(TULP2):c.679G>C (p.Gly227Arg)	not specified [RCV004683026]	uncertain significance	19	48888219	48888219	Human		name
597798126	CV3628658	single nucleotide variant	NM_003323.3(TULP2):c.648G>C (p.Leu216Phe)	not specified [RCV004879099]	uncertain significance	19	48888250	48888250	Human		name
597798134	CV3628660	single nucleotide variant	NM_003323.3(TULP2):c.329C>T (p.Pro110Leu)	not specified [RCV004879101]	likely benign	19	48895386	48895386	Human		name
597798140	CV3628662	single nucleotide variant	NM_003323.3(TULP2):c.892G>A (p.Asp298Asn)	not specified [RCV004879103]	uncertain significance	19	48888006	48888006	Human		name
597798146	CV3628664	single nucleotide variant	NM_003323.3(TULP2):c.608G>A (p.Cys203Tyr)	not specified [RCV004879105]	uncertain significance	19	48889538	48889538	Human		name
597798149	CV3628665	single nucleotide variant	NM_003323.3(TULP2):c.899G>A (p.Gly300Asp)	not specified [RCV004879106]	uncertain significance	19	48887999	48887999	Human		name
598231885	CV3936170	single nucleotide variant	NM_003323.3(TULP2):c.407A>C (p.Asp136Ala)	not specified [RCV005295296]	uncertain significance	19	48895105	48895105	Human		name
598255139	CV3936171	single nucleotide variant	NM_003323.3(TULP2):c.950G>A (p.Arg317His)	not specified [RCV005299364]	likely benign	19	48885559	48885559	Human		name
598231891	CV3936173	single nucleotide variant	NM_003323.3(TULP2):c.682A>G (p.Thr228Ala)	not specified [RCV005295297]	uncertain significance	19	48888216	48888216	Human		name
8636925	CV92150	single nucleotide variant	NM_003323.2(TULP2):c.773C>T (p.Ser258Phe)	Malignant melanoma [RCV000072248]	not provided	19	48888125	48888125	Human		name
155923406	CV2215627	single nucleotide variant	NM_003323.3(TULP2):c.1118G>A (p.Arg373Gln)	not specified [RCV004089380]	uncertain significance	19	48883990	48883990	Human		name
155940854	CV2232265	single nucleotide variant	NM_003323.3(TULP2):c.1204C>A (p.Pro402Thr)	not specified [RCV004105048]	uncertain significance	19	48883825	48883825	Human		name
156065029	CV2348710	single nucleotide variant	NM_003323.3(TULP2):c.1552A>C (p.Ser518Arg)	not specified [RCV004201122]	uncertain significance	19	48881022	48881022	Human		name
156075646	CV2350893	single nucleotide variant	NM_003323.3(TULP2):c.1039G>A (p.Asp347Asn)	not specified [RCV004211730]	uncertain significance	19	48885470	48885470	Human		name
156283901	CV2360614	single nucleotide variant	NM_003323.3(TULP2):c.1481G>A (p.Gly494Asp)	not specified [RCV004213416]	uncertain significance	19	48881093	48881093	Human		name
401719047	CV2679398	single nucleotide variant	NM_003323.3(TULP2):c.1141G>A (p.Ala381Thr)	not specified [RCV004285927]	uncertain significance	19	48883967	48883967	Human		name
401766827	CV2680162	single nucleotide variant	NM_003323.3(TULP2):c.1142C>G (p.Ala381Gly)	not specified [RCV004286644]	uncertain significance	19	48883966	48883966	Human		name
401735506	CV2687601	single nucleotide variant	NM_003323.3(TULP2):c.1129A>G (p.Thr377Ala)	not specified [RCV004300822]	uncertain significance	19	48883979	48883979	Human		name
405809423	CV3344579	single nucleotide variant	NM_003323.3(TULP2):c.1000C>T (p.Leu334Phe)	not specified [RCV004481730]	uncertain significance	19	48885509	48885509	Human		name
405809425	CV3344580	single nucleotide variant	NM_003323.3(TULP2):c.1117C>T (p.Arg373Trp)	not specified [RCV004481731]	uncertain significance	19	48883991	48883991	Human		name
405809427	CV3344581	single nucleotide variant	NM_003323.3(TULP2):c.1132A>G (p.Arg378Gly)	not specified [RCV004481732]	uncertain significance	19	48883976	48883976	Human		name
407532376	CV3493047	single nucleotide variant	NM_003323.3(TULP2):c.1031G>A (p.Arg344Gln)	not specified [RCV004683020]	uncertain significance	19	48885478	48885478	Human		name
407532377	CV3493048	single nucleotide variant	NM_003323.3(TULP2):c.1145G>A (p.Arg382Gln)	not specified [RCV004683021]	uncertain significance	19	48883963	48883963	Human		name
407532378	CV3493049	single nucleotide variant	NM_003323.3(TULP2):c.1459G>A (p.Val487Met)	not specified [RCV004683022]	uncertain significance	19	48881115	48881115	Human		name
407532379	CV3493050	single nucleotide variant	NM_003323.3(TULP2):c.1168G>A (p.Val390Met)	not specified [RCV004683023]	uncertain significance	19	48883940	48883940	Human		name
407532383	CV3493054	single nucleotide variant	NM_003323.3(TULP2):c.1165G>C (p.Ala389Pro)	not specified [RCV004683027]	uncertain significance	19	48883943	48883943	Human		name
597798120	CV3628656	single nucleotide variant	NM_003323.3(TULP2):c.1034A>G (p.Asp345Gly)	not specified [RCV004879097]	uncertain significance	19	48885475	48885475	Human		name
597798297	CV3628657	single nucleotide variant	NM_003323.3(TULP2):c.1555T>C (p.Phe519Leu)	not specified [RCV004879098]	uncertain significance	19	48881019	48881019	Human		name
597798130	CV3628659	single nucleotide variant	NM_003323.3(TULP2):c.1505T>C (p.Phe502Ser)	not specified [RCV004879100]	uncertain significance	19	48881069	48881069	Human		name
597798137	CV3628661	single nucleotide variant	NM_003323.3(TULP2):c.1316A>C (p.Lys439Thr)	not specified [RCV004879102]	uncertain significance	19	48882163	48882163	Human		name
597798143	CV3628663	single nucleotide variant	NM_003323.3(TULP2):c.1337A>G (p.His446Arg)	not specified [RCV004879104]	uncertain significance	19	48882142	48882142	Human		name
598255128	CV3936168	single nucleotide variant	NM_003323.3(TULP2):c.1048G>A (p.Val350Met)	not specified [RCV005299362]	uncertain significance	19	48885461	48885461	Human		name
598255133	CV3936169	single nucleotide variant	NM_003323.3(TULP2):c.1186G>A (p.Val396Ile)	not specified [RCV005299363]	likely benign	19	48883843	48883843	Human		name
598255145	CV3936172	single nucleotide variant	NM_003323.3(TULP2):c.1222A>G (p.Ile408Val)	not specified [RCV005299365]	uncertain significance	19	48883807	48883807	Human		name

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