Cryl1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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100 records found for search term Cryl1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150502967	CV1241692	single nucleotide variant	NM_015974.3(CRYL1):c.41+65T>G	not provided [RCV001657283]	benign	13	20525689	20525689	Human		name
150481743	CV1222216	single nucleotide variant	NM_015974.3(CRYL1):c.276+13C>T	not provided [RCV001617014]	benign	13	20489357	20489357	Human		name
150502139	CV1224406	single nucleotide variant	NM_015974.3(CRYL1):c.438+49G>T	not provided [RCV001621047]	benign	13	20439544	20439544	Human		name
150495521	CV1225095	single nucleotide variant	NM_015974.3(CRYL1):c.438+47G>T	not provided [RCV001619573]	benign	13	20439546	20439546	Human		name
150516634	CV1227161	single nucleotide variant	NM_015974.3(CRYL1):c.149+24A>G	not provided [RCV001639259]	benign	13	20512419	20512419	Human		name
150503863	CV1257881	single nucleotide variant	NM_015974.3(CRYL1):c.438+45C>T	not provided [RCV001677569]	benign	13	20439548	20439548	Human		name
150468814	CV1267990	single nucleotide variant	NM_015974.3(CRYL1):c.439-40A>G	not provided [RCV001694853]	benign	13	20432336	20432336	Human		name
150460885	CV1275885	single nucleotide variant	NM_015974.3(CRYL1):c.438+62C>T	not provided [RCV001709823]	benign	13	20439531	20439531	Human		name
150331303	CV1172525	single nucleotide variant	NM_015974.3(CRYL1):c.634-872C>A	not provided [RCV001538576]	benign	13	20414259	20414259	Human		name
150455883	CV1220524	single nucleotide variant	NM_015974.3(CRYL1):c.634-137C>T	not provided [RCV001612617]	benign	13	20413524	20413524	Human		name
150482504	CV1223436	single nucleotide variant	NM_015974.3(CRYL1):c.634-202T>C	not provided [RCV001617149]	benign	13	20413589	20413589	Human		name
150482679	CV1223464	single nucleotide variant	NM_015974.3(CRYL1):c.740-224C>T	not provided [RCV001617177]	benign	13	20404965	20404965	Human		name
150508500	CV1229659	single nucleotide variant	NM_015974.3(CRYL1):c.740-148G>T	not provided [RCV001636237]	benign	13	20404889	20404889	Human		name
150435178	CV1233795	duplication	NM_015974.3(CRYL1):c.438+538dup	not provided [RCV001643922]	benign	13	20439050	20439051	Human		name
150459647	CV1236124	single nucleotide variant	NM_015974.3(CRYL1):c.847-123G>A	not provided [RCV001649095]	benign	13	20404365	20404365	Human		name
150478525	CV1238921	single nucleotide variant	NM_015974.3(CRYL1):c.740-147C>T	not provided [RCV001652386]	benign	13	20404888	20404888	Human		name
150470721	CV1248056	single nucleotide variant	NM_015974.3(CRYL1):c.277-102T>G	not provided [RCV001671092]	benign	13	20439856	20439856	Human		name
150436736	CV1249742	single nucleotide variant	NM_015974.3(CRYL1):c.846+159C>T	not provided [RCV001665656]	benign	13	20404476	20404476	Human		name
150459758	CV1252998	single nucleotide variant	NM_015974.3(CRYL1):c.438+426C>T	not provided [RCV001669326]	benign	13	20439167	20439167	Human		name
150486279	CV1262553	single nucleotide variant	NM_015974.3(CRYL1):c.149+209T>C	not provided [RCV001686950]	benign	13	20512234	20512234	Human		name
150476487	CV1263650	single nucleotide variant	NM_015974.3(CRYL1):c.150-195G>A	not provided [RCV001685173]	benign	13	20489691	20489691	Human		name
150491233	CV1267743	single nucleotide variant	NM_015974.3(CRYL1):c.634-868A>C	not provided [RCV001687768]	benign	13	20414255	20414255	Human		name
150456011	CV1269018	single nucleotide variant	NM_015974.3(CRYL1):c.634-870C>A	not provided [RCV001692842]	benign	13	20414257	20414257	Human		name
150447315	CV1270295	single nucleotide variant	NM_015974.3(CRYL1):c.277-202G>A	not provided [RCV001691430]	benign	13	20439956	20439956	Human		name
150464692	CV1276453	single nucleotide variant	NM_015974.3(CRYL1):c.846+110A>G	not provided [RCV001710399]	benign	13	20404525	20404525	Human		name
150509223	CV1284483	single nucleotide variant	NM_015974.3(CRYL1):c.438+312C>T	not provided [RCV001720591]	benign	13	20439281	20439281	Human		name
150339714	CV1167588	single nucleotide variant	NM_015974.3(CRYL1):c.633+8038G>A	not provided [RCV001534499]	benign	13	20424064	20424064	Human		name
150486585	CV1225765	single nucleotide variant	NM_015974.3(CRYL1):c.634-1106T>C	not provided [RCV001617926]	benign	13	20414493	20414493	Human		name
150517509	CV1226959	single nucleotide variant	NM_015974.3(CRYL1):c.276+1231C>T	not provided [RCV001640055]	benign	13	20488139	20488139	Human		name
150430506	CV1230913	single nucleotide variant	NM_015974.3(CRYL1):c.634-5733C>T	not provided [RCV001641462]	benign	13	20419120	20419120	Human		name
150451993	CV1232874	single nucleotide variant	NM_015974.3(CRYL1):c.150-3686C>G	not provided [RCV001647949]	benign	13	20493182	20493182	Human		name
150465392	CV1240232	single nucleotide variant	NM_015974.3(CRYL1):c.633+7804G>C	not provided [RCV001649993]	benign	13	20424298	20424298	Human		name
150460520	CV1253119	single nucleotide variant	NM_015974.3(CRYL1):c.150-3528G>A	not provided [RCV001669448]	benign	13	20493024	20493024	Human		name
150502355	CV1254503	single nucleotide variant	NM_015974.3(CRYL1):c.634-5968T>C	not provided [RCV001677205]	benign	13	20419355	20419355	Human		name
150506977	CV1258102	single nucleotide variant	NM_015974.3(CRYL1):c.150-3576T>C	not provided [RCV001678319]	benign	13	20493072	20493072	Human		name
150486285	CV1262554	single nucleotide variant	NM_015974.3(CRYL1):c.633+3039C>G	not provided [RCV001686951]	benign	13	20429063	20429063	Human		name
150476150	CV1263603	single nucleotide variant	NM_015974.3(CRYL1):c.633+2727T>C	not provided [RCV001685126]	benign	13	20429375	20429375	Human		name
150493607	CV1267181	single nucleotide variant	NM_015974.3(CRYL1):c.276+1156T>C	not provided [RCV001688209]	benign	13	20488214	20488214	Human		name
150470146	CV1268214	single nucleotide variant	NM_015974.3(CRYL1):c.633+7621T>C	not provided [RCV001695078]	benign	13	20424481	20424481	Human		name
150466307	CV1268751	microsatellite	NM_015974.3(CRYL1):c.740-84CT[2]	not provided [RCV001694448]	benign	13	20404820	20404821	Human		name
150464428	CV1276388	single nucleotide variant	NM_015974.3(CRYL1):c.277-9053A>G	not provided [RCV001710333]	benign	13	20448807	20448807	Human		name
150483529	CV1280227	single nucleotide variant	NM_015974.3(CRYL1):c.634-1273C>T	not provided [RCV001715203]	benign	13	20414660	20414660	Human		name
150509211	CV1284480	single nucleotide variant	NM_015974.3(CRYL1):c.150-3772A>C	not provided [RCV001720588]	benign	13	20493268	20493268	Human		name
150509220	CV1284482	single nucleotide variant	NM_015974.3(CRYL1):c.150-3445T>C	not provided [RCV001720590]	benign	13	20492941	20492941	Human		name
150509227	CV1284484	single nucleotide variant	NM_015974.3(CRYL1):c.150-3631A>G	not provided [RCV001720592]	benign	13	20493127	20493127	Human		name
150339031	CV1167589	single nucleotide variant	NM_015974.3(CRYL1):c.276+11013G>A	not provided [RCV001533997]	benign	13	20478357	20478357	Human		name
150330949	CV1172524	microsatellite	NM_015974.3(CRYL1):c.634-841GT[8]	not provided [RCV001538386]	benign	13	20414207	20414212	Human		name
150506065	CV1213685	single nucleotide variant	NM_015974.3(CRYL1):c.276+20662A>G	not provided [RCV001595941]	benign	13	20468708	20468708	Human		name
150484033	CV1222406	single nucleotide variant	NM_015974.3(CRYL1):c.277-23750G>A	not provided [RCV001617409]	benign	13	20463504	20463504	Human		name
150495309	CV1225047	single nucleotide variant	NM_015974.3(CRYL1):c.277-23765T>C	not provided [RCV001619525]	benign	13	20463519	20463519	Human		name
150507674	CV1229148	single nucleotide variant	NM_015974.3(CRYL1):c.276+15773G>A	not provided [RCV001636019]	benign	13	20473597	20473597	Human		name
150471469	CV1259121	microsatellite	NM_015974.3(CRYL1):c.634-841GT[9]	not provided [RCV001684366]	benign	13	20414207	20414210	Human		name
150453106	CV1260474	single nucleotide variant	NM_015974.3(CRYL1):c.276+21003G>A	not provided [RCV001680965]	benign	13	20468367	20468367	Human		name
150484325	CV1263152	single nucleotide variant	NM_015974.3(CRYL1):c.276+10988A>G	not provided [RCV001686552]	benign	13	20478382	20478382	Human		name
150462157	CV1264696	single nucleotide variant	NM_015974.3(CRYL1):c.276+15651G>A	not provided [RCV001682320]	benign	13	20473719	20473719	Human		name
150461656	CV1272910	single nucleotide variant	NM_015974.3(CRYL1):c.276+20613G>A	not provided [RCV001693665]	benign	13	20468757	20468757	Human		name
150479065	CV1273404	single nucleotide variant	NM_015974.3(CRYL1):c.277-24009C>T	not provided [RCV001696607]	benign	13	20463763	20463763	Human		name
150454408	CV1276994	single nucleotide variant	NM_015974.3(CRYL1):c.277-23715G>C	not provided [RCV001708785]	benign	13	20463469	20463469	Human		name
150468551	CV1277746	single nucleotide variant	NM_015974.3(CRYL1):c.277-23961A>G	not provided [RCV001711041]	benign	13	20463715	20463715	Human		name
150485221	CV1280679	deletion	NM_015974.3(CRYL1):c.277-23654del	not provided [RCV001715546]	benign	13	20463408	20463408	Human		name
150438693	CV1221199	microsatellite	NM_015974.3(CRYL1):c.634-841GT[10]	not provided [RCV001609893]	benign	13	20414207	20414208	Human		name
150481502	CV1244113	microsatellite	NM_015974.3(CRYL1):c.634-890CA[12]	not provided [RCV001652958]	benign	13	20414255	20414256	Human		name
150451225	CV1276566	microsatellite	NM_015974.3(CRYL1):c.634-841GT[12]	not provided [RCV001708355]	benign	13	20414206	20414207	Human		name
150335270	CV1164643	microsatellite	NM_015974.3(CRYL1):c.276+6613CA[12]	not provided [RCV001530207]	benign	13	20482739	20482740	Human		name
405275768	CV3199356	single nucleotide variant	NM_015974.3(CRYL1):c.72G>C (p.Leu24=)	CRYL1-related disorder [RCV003916769]	benign	13	20512520	20512520	Human		name , trait , alternate_id
150466021	CV1218119	single nucleotide variant	NM_015974.3(CRYL1):c.261T>C (p.Gly87=)	not provided [RCV001614245]	benign	13	20489385	20489385	Human		name
150481140	CV1279672	single nucleotide variant	NM_015974.3(CRYL1):c.132C>T (p.Asn44=)	not provided [RCV001714787]	benign	13	20512460	20512460	Human		name
405293277	CV3207319	single nucleotide variant	NM_015974.3(CRYL1):c.231T>C (p.Gly77=)	CRYL1-related disorder [RCV003931708]	likely benign	13	20489415	20489415	Human		name , trait , alternate_id
15144418	CV738988	single nucleotide variant	NM_015974.3(CRYL1):c.252A>C (p.Ala84=)	not provided [RCV000900001]	benign	13	20489394	20489394	Human		name
405288960	CV3210025	single nucleotide variant	NM_015974.3(CRYL1):c.795T>A (p.Thr265=)	CRYL1-related disorder [RCV003961498]	likely benign	13	20404686	20404686	Human		name , trait , alternate_id
150465714	CV1268655	insertion	NM_015974.3(CRYL1):c.634-868_634-867insC	not provided [RCV001694351]	benign	13	20414254	20414255	Human		name
405676667	CV3239364	single nucleotide variant	NM_015974.3(CRYL1):c.268C>A (p.His90Asn)	not specified [RCV004370246]	uncertain significance	13	20489378	20489378	Human		name
597800218	CV3657841	single nucleotide variant	NM_015974.3(CRYL1):c.199A>C (p.Ser67Arg)	not specified [RCV004905466]	uncertain significance	13	20489447	20489447	Human		name
597800214	CV3657843	single nucleotide variant	NM_015974.3(CRYL1):c.142A>G (p.Asn48Asp)	not specified [RCV004905468]	uncertain significance	13	20512450	20512450	Human		name
598260516	CV3963091	single nucleotide variant	NM_015974.3(CRYL1):c.133G>A (p.Ala45Thr)	not specified [RCV005324994]	uncertain significance	13	20512459	20512459	Human		name
156384677	CV2231153	single nucleotide variant	NM_015974.3(CRYL1):c.536T>C (p.Ile179Thr)	not specified [RCV004094362]	uncertain significance	13	20432199	20432199	Human		name
155982501	CV2244206	single nucleotide variant	NM_015974.3(CRYL1):c.436C>T (p.Pro146Ser)	not specified [RCV004110698]	uncertain significance	13	20439595	20439595	Human		name
156199329	CV2255983	single nucleotide variant	NM_015974.3(CRYL1):c.946G>C (p.Val316Leu)	not specified [RCV004122429]	uncertain significance	13	20404143	20404143	Human		name
156103337	CV2260498	single nucleotide variant	NM_015974.3(CRYL1):c.757G>A (p.Asp253Asn)	CRYL1-related disorder [RCV003953990]\|not specified [RCV004123286]	likely benign\|uncertain significance	13	20404724	20404724	Human		name , trait , alternate_id
329366953	CV2442001	single nucleotide variant	NM_015974.3(CRYL1):c.470A>G (p.Glu157Gly)	not specified [RCV004262168]	uncertain significance	13	20432265	20432265	Human		name
401893209	CV2755293	single nucleotide variant	NM_015974.3(CRYL1):c.791A>G (p.Gln264Arg)	not specified [RCV004337468]	uncertain significance	13	20404690	20404690	Human		name
401893681	CV2765403	single nucleotide variant	NM_015974.3(CRYL1):c.485C>T (p.Pro162Leu)	not specified [RCV004339903]	uncertain significance	13	20432250	20432250	Human		name
401857860	CV2777799	single nucleotide variant	NM_015974.3(CRYL1):c.338T>C (p.Ile113Thr)	not specified [RCV004345626]	uncertain significance	13	20439693	20439693	Human		name
401898468	CV2787949	single nucleotide variant	NM_015974.3(CRYL1):c.667G>T (p.Val223Phe)	not specified [RCV004358608]	uncertain significance	13	20413354	20413354	Human		name
405294102	CV3203391	single nucleotide variant	NM_015974.3(CRYL1):c.400G>A (p.Gly134Ser)	CRYL1-related disorder [RCV003933938]	benign	13	20439631	20439631	Human		name , trait , alternate_id
405676673	CV3239365	single nucleotide variant	NM_015974.3(CRYL1):c.410A>G (p.His137Arg)	not specified [RCV004370247]	uncertain significance	13	20439621	20439621	Human		name
405676678	CV3239366	single nucleotide variant	NM_015974.3(CRYL1):c.512G>T (p.Arg171Ile)	not specified [RCV004370248]	uncertain significance	13	20432223	20432223	Human		name
405676681	CV3239367	single nucleotide variant	NM_015974.3(CRYL1):c.513A>T (p.Arg171Ser)	not specified [RCV004370249]	uncertain significance	13	20432222	20432222	Human		name
405676688	CV3239368	single nucleotide variant	NM_015974.3(CRYL1):c.652A>G (p.Ser218Gly)	not specified [RCV004370250]	likely benign	13	20413369	20413369	Human		name
405676693	CV3239369	single nucleotide variant	NM_015974.3(CRYL1):c.664C>T (p.Leu222Phe)	not specified [RCV004370251]	uncertain significance	13	20413357	20413357	Human		name
405676699	CV3239370	single nucleotide variant	NM_015974.3(CRYL1):c.691C>T (p.Arg231Trp)	not specified [RCV004370252]	uncertain significance	13	20413330	20413330	Human		name
405676703	CV3239371	single nucleotide variant	NM_015974.3(CRYL1):c.809C>T (p.Pro270Leu)	not specified [RCV004370253]	uncertain significance	13	20404672	20404672	Human		name
407464695	CV3429832	single nucleotide variant	NM_015974.3(CRYL1):c.875C>T (p.Pro292Leu)	not specified [RCV004613519]	uncertain significance	13	20404214	20404214	Human		name
407464701	CV3429834	single nucleotide variant	NM_015974.3(CRYL1):c.743T>C (p.Met248Thr)	not specified [RCV004613521]	uncertain significance	13	20404738	20404738	Human		name
597800219	CV3657840	single nucleotide variant	NM_015974.3(CRYL1):c.554G>A (p.Arg185Gln)	not specified [RCV004905465]	uncertain significance	13	20432181	20432181	Human		name
597800216	CV3657842	single nucleotide variant	NM_015974.3(CRYL1):c.754T>C (p.Cys252Arg)	not specified [RCV004905467]	uncertain significance	13	20404727	20404727	Human		name
597800212	CV3657844	single nucleotide variant	NM_015974.3(CRYL1):c.485C>G (p.Pro162Arg)	not specified [RCV004905469]	uncertain significance	13	20432250	20432250	Human		name
597800210	CV3657845	single nucleotide variant	NM_015974.3(CRYL1):c.921G>A (p.Met307Ile)	not specified [RCV004905470]	uncertain significance	13	20404168	20404168	Human		name
598260523	CV3963092	single nucleotide variant	NM_015974.3(CRYL1):c.446C>T (p.Pro149Leu)	not specified [RCV005324995]	uncertain significance	13	20432289	20432289	Human		name
598260535	CV3963094	single nucleotide variant	NM_015974.3(CRYL1):c.306G>C (p.Lys102Asn)	not specified [RCV005324997]	uncertain significance	13	20439725	20439725	Human		name

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