Snx25 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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59 records found for search term Snx25

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401923620	CV2820295	single nucleotide variant	NM_001378034.2(SNX25):c.2760C>T (p.Thr920=)	not provided [RCV003435218]	likely benign	4	185362032	185362032	Human		name
597745515	CV3607312	single nucleotide variant	NM_001378034.2(SNX25):c.1092G>A (p.Arg364=)	not specified [RCV004865683]	likely benign	4	185288012	185288012	Human		name
156363203	CV2330593	single nucleotide variant	NM_001378034.2(SNX25):c.841C>G (p.Pro281Ala)	not specified [RCV004183190]	uncertain significance	4	185264547	185264547	Human		name
156291450	CV2342900	single nucleotide variant	NM_001378034.2(SNX25):c.871C>T (p.Arg291Cys)	not specified [RCV004189933]	uncertain significance	4	185264577	185264577	Human		name
401759799	CV2707152	single nucleotide variant	NM_001378034.2(SNX25):c.645T>A (p.Ser215Arg)	not specified [RCV004315516]	uncertain significance	4	185258978	185258978	Human		name
407504012	CV3484828	single nucleotide variant	NM_001378034.2(SNX25):c.974C>T (p.Ala325Val)	not specified [RCV004670407]	uncertain significance	4	185267038	185267038	Human		name
597741126	CV3607315	single nucleotide variant	NM_001378034.2(SNX25):c.899C>T (p.Thr300Ile)	not specified [RCV004864798]	uncertain significance	4	185264605	185264605	Human		name
597755435	CV3607323	single nucleotide variant	NM_001378034.2(SNX25):c.955A>T (p.Met319Leu)	not specified [RCV004868171]	uncertain significance	4	185267019	185267019	Human		name
598172059	CV3911729	single nucleotide variant	NM_001378034.2(SNX25):c.799T>C (p.Phe267Leu)	not specified [RCV005284960]	uncertain significance	4	185264505	185264505	Human		name
598172075	CV3911733	single nucleotide variant	NM_001378034.2(SNX25):c.655G>A (p.Val219Met)	not specified [RCV005284963]	uncertain significance	4	185258988	185258988	Human		name
598172087	CV3911735	single nucleotide variant	NM_001378034.2(SNX25):c.689C>T (p.Thr230Ile)	not specified [RCV005284965]	uncertain significance	4	185259022	185259022	Human		name
153301272	CV1689120	single nucleotide variant	NM_001378034.2(SNX25):c.1396G>T (p.Gly466Ter)	SNX25-related autism spectrum disorder [RCV002266848]	uncertain significance	4	185320784	185320784	Human		name , trait
155975072	CV2211236	single nucleotide variant	NM_001378034.2(SNX25):c.2389G>A (p.Val797Met)	not specified [RCV004090177]	uncertain significance	4	185351532	185351532	Human		name
155975125	CV2235823	single nucleotide variant	NM_001378034.2(SNX25):c.2897C>G (p.Ala966Gly)	not specified [RCV004111943]	uncertain significance	4	185362674	185362674	Human		name
155916273	CV2239694	single nucleotide variant	NM_001378034.2(SNX25):c.1052T>G (p.Ile351Ser)	not specified [RCV004108239]	uncertain significance	4	185267116	185267116	Human		name
155921784	CV2240578	single nucleotide variant	NM_001378034.2(SNX25):c.1093T>C (p.Tyr365His)	not specified [RCV004119227]	uncertain significance	4	185288013	185288013	Human		name
156300934	CV2248897	single nucleotide variant	NM_001378034.2(SNX25):c.2737A>C (p.Asn913His)	not specified [RCV004115906]	likely benign	4	185362009	185362009	Human		name
156200549	CV2256085	single nucleotide variant	NM_001378034.2(SNX25):c.2135C>G (p.Thr712Arg)	not specified [RCV004116376]	uncertain significance	4	185342064	185342064	Human		name
156015509	CV2298876	single nucleotide variant	NM_001378034.2(SNX25):c.2113G>A (p.Gly705Arg)	not specified [RCV004156418]	uncertain significance	4	185342042	185342042	Human		name
155956886	CV2304085	single nucleotide variant	NM_001378034.2(SNX25):c.2620G>C (p.Val874Leu)	not specified [RCV004170128]	uncertain significance	4	185357706	185357706	Human		name
156132952	CV2350219	single nucleotide variant	NM_001378034.2(SNX25):c.1538T>C (p.Ile513Thr)	not specified [RCV004200129]	uncertain significance	4	185323589	185323589	Human		name
156107542	CV2355334	single nucleotide variant	NM_001378034.2(SNX25):c.1048C>T (p.Leu350Phe)	not specified [RCV004203182]	uncertain significance	4	185267112	185267112	Human		name
155930224	CV2366627	single nucleotide variant	NM_001378034.2(SNX25):c.1417G>C (p.Asp473His)	not specified [RCV004210640]	uncertain significance	4	185320805	185320805	Human		name
155994868	CV2379601	single nucleotide variant	NM_001378034.2(SNX25):c.1780G>A (p.Val594Met)	not specified [RCV004217300]	uncertain significance	4	185332625	185332625	Human		name
329392789	CV2468935	single nucleotide variant	NM_001378034.2(SNX25):c.2044G>A (p.Glu682Lys)	not specified [RCV004274203]	uncertain significance	4	185339508	185339508	Human		name
401761617	CV2726839	single nucleotide variant	NM_001378034.2(SNX25):c.2834A>C (p.Asp945Ala)	not specified [RCV004323143]	uncertain significance	4	185362611	185362611	Human		name
401886068	CV2771054	single nucleotide variant	NM_001378034.2(SNX25):c.2958T>G (p.Ile986Met)	not specified [RCV004346063]	uncertain significance	4	185363408	185363408	Human		name
401865270	CV2791586	single nucleotide variant	NM_001378034.2(SNX25):c.1385G>A (p.Arg462Gln)	not specified [RCV004358955]	uncertain significance	4	185320773	185320773	Human		name
405733153	CV3322642	single nucleotide variant	NM_001378034.2(SNX25):c.1525G>A (p.Glu509Lys)	not specified [RCV004464604]	uncertain significance	4	185323576	185323576	Human		name
405733160	CV3322643	single nucleotide variant	NM_001378034.2(SNX25):c.1805A>G (p.Asn602Ser)	not specified [RCV004464605]	uncertain significance	4	185332650	185332650	Human		name
405733172	CV3322644	single nucleotide variant	NM_001378034.2(SNX25):c.1951G>A (p.Glu651Lys)	not specified [RCV004464606]	uncertain significance	4	185339415	185339415	Human		name
405733181	CV3322645	single nucleotide variant	NM_001378034.2(SNX25):c.1960C>T (p.Arg654Cys)	not specified [RCV004464607]	uncertain significance	4	185339424	185339424	Human		name
405733190	CV3322646	single nucleotide variant	NM_001378034.2(SNX25):c.2224C>G (p.Leu742Val)	not specified [RCV004464608]	uncertain significance	4	185346573	185346573	Human		name
405733199	CV3322647	single nucleotide variant	NM_001378034.2(SNX25):c.2444G>A (p.Arg815His)	not specified [RCV004464609]	uncertain significance	4	185351587	185351587	Human		name
405733205	CV3322648	single nucleotide variant	NM_001378034.2(SNX25):c.2551A>G (p.Met851Val)	not specified [RCV004464610]	uncertain significance	4	185353569	185353569	Human		name
405733215	CV3322649	single nucleotide variant	NM_001378034.2(SNX25):c.2557A>T (p.Ile853Phe)	not specified [RCV004464611]	uncertain significance	4	185353575	185353575	Human		name
405733222	CV3322650	single nucleotide variant	NM_001378034.2(SNX25):c.2626G>C (p.Val876Leu)	not specified [RCV004464612]	uncertain significance	4	185357712	185357712	Human		name
405733230	CV3322651	single nucleotide variant	NM_001378034.2(SNX25):c.2737A>G (p.Asn913Asp)	not specified [RCV004464613]	uncertain significance	4	185362009	185362009	Human		name
405733237	CV3322652	single nucleotide variant	NM_001378034.2(SNX25):c.2890T>C (p.Phe964Leu)	not specified [RCV004464614]	uncertain significance	4	185362667	185362667	Human		name
405733251	CV3322654	single nucleotide variant	NM_001378034.2(SNX25):c.1046A>G (p.Lys349Arg)	not specified [RCV004464616]	uncertain significance	4	185267110	185267110	Human		name
407504017	CV3484829	single nucleotide variant	NM_001378034.2(SNX25):c.2830C>T (p.Pro944Ser)	not specified [RCV004670408]	uncertain significance	4	185362102	185362102	Human		name
597741121	CV3607311	single nucleotide variant	NM_001378034.2(SNX25):c.1649G>A (p.Arg550Lys)	not specified [RCV004864797]	uncertain significance	4	185323700	185323700	Human		name
597745520	CV3607313	single nucleotide variant	NM_001378034.2(SNX25):c.2029T>A (p.Ser677Thr)	not specified [RCV004865684]	uncertain significance	4	185339493	185339493	Human		name
597745525	CV3607314	single nucleotide variant	NM_001378034.2(SNX25):c.1909A>G (p.Lys637Glu)	not specified [RCV004865685]	uncertain significance	4	185332754	185332754	Human		name
597741131	CV3607316	single nucleotide variant	NM_001378034.2(SNX25):c.2209G>T (p.Val737Phe)	not specified [RCV004864799]	uncertain significance	4	185346558	185346558	Human		name
597745530	CV3607317	single nucleotide variant	NM_001378034.2(SNX25):c.1894G>A (p.Ala632Thr)	not specified [RCV004865686]	uncertain significance	4	185332739	185332739	Human		name
597745536	CV3607318	single nucleotide variant	NM_001378034.2(SNX25):c.2249T>C (p.Ile750Thr)	not specified [RCV004865687]	uncertain significance	4	185346598	185346598	Human		name
597741135	CV3607319	single nucleotide variant	NM_001378034.2(SNX25):c.1718C>A (p.Ala573Asp)	not specified [RCV004864800]	uncertain significance	4	185323769	185323769	Human		name
597745541	CV3607320	single nucleotide variant	NM_001378034.2(SNX25):c.1994A>G (p.Asp665Gly)	not specified [RCV004865688]	uncertain significance	4	185339458	185339458	Human		name
597755617	CV3607321	single nucleotide variant	NM_001378034.2(SNX25):c.1699A>C (p.Lys567Gln)	not specified [RCV004868169]	uncertain significance	4	185323750	185323750	Human		name
597755521	CV3607322	single nucleotide variant	NM_001378034.2(SNX25):c.1643A>C (p.Lys548Thr)	not specified [RCV004868170]	uncertain significance	4	185323694	185323694	Human		name
597755431	CV3607324	single nucleotide variant	NM_001378034.2(SNX25):c.1795A>T (p.Asn599Tyr)	not specified [RCV004868172]	uncertain significance	4	185332640	185332640	Human		name
598238488	CV3911730	single nucleotide variant	NM_001378034.2(SNX25):c.1373A>G (p.Asn458Ser)	not specified [RCV005275841]	uncertain significance	4	185320761	185320761	Human		name
598172065	CV3911731	single nucleotide variant	NM_001378034.2(SNX25):c.1898C>G (p.Pro633Arg)	not specified [RCV005284961]	uncertain significance	4	185332743	185332743	Human		name
598172070	CV3911732	single nucleotide variant	NM_001378034.2(SNX25):c.2273C>T (p.Ser758Leu)	not specified [RCV005284962]	uncertain significance	4	185346622	185346622	Human		name
598172080	CV3911734	single nucleotide variant	NM_001378034.2(SNX25):c.1737C>A (p.Asn579Lys)	not specified [RCV005284964]	uncertain significance	4	185323788	185323788	Human		name
598172092	CV3911736	single nucleotide variant	NM_001378034.2(SNX25):c.1411A>G (p.Arg471Gly)	not specified [RCV005284966]	uncertain significance	4	185320799	185320799	Human		name
598172097	CV3911737	single nucleotide variant	NM_001378034.2(SNX25):c.1297C>A (p.Gln433Lys)	not specified [RCV005284967]	uncertain significance	4	185310769	185310769	Human		name
598172103	CV3911738	single nucleotide variant	NM_001378034.2(SNX25):c.1964C>T (p.Thr655Ile)	not specified [RCV005284968]	uncertain significance	4	185339428	185339428	Human		name

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