Ccnjl Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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49 records found for search term Ccnjl

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401732022	CV2712262	single nucleotide variant	NM_001308173.3(CCNJL):c.11A>C (p.Glu4Ala)	not specified [RCV004313760]	uncertain significance	5	160311913	160311913	Human		name
405263549	CV3185172	single nucleotide variant	NM_001308173.3(CCNJL):c.189C>G (p.Ala63=)	not provided [RCV003885736]	benign	5	160280616	160280616	Human		name
156399224	CV2204991	single nucleotide variant	NM_001308173.3(CCNJL):c.133A>T (p.Ile45Phe)	not specified [RCV004077610]	uncertain significance	5	160280672	160280672	Human		name
155919777	CV2254926	single nucleotide variant	NM_001308173.3(CCNJL):c.226G>A (p.Val76Ile)	Inborn genetic diseases [RCV002772831]	likely benign	5	160280579	160280579	Human	1	name
156180909	CV2374800	single nucleotide variant	NM_001308173.3(CCNJL):c.178C>T (p.Arg60Trp)	not specified [RCV004225401]	uncertain significance	5	160280627	160280627	Human		name
405742047	CV3303160	single nucleotide variant	NM_001308173.3(CCNJL):c.253G>A (p.Val85Met)	not specified [RCV004430781]	uncertain significance	5	160280552	160280552	Human		name
405742041	CV3303161	single nucleotide variant	NM_001308173.3(CCNJL):c.296G>A (p.Arg99Gln)	not specified [RCV004430782]	uncertain significance	5	160259756	160259756	Human		name
156399047	CV2194953	single nucleotide variant	NM_001308173.3(CCNJL):c.523C>T (p.Arg175Cys)	not specified [RCV004075476]	uncertain significance	5	160259529	160259529	Human		name
156092867	CV2256705	single nucleotide variant	NM_001308173.3(CCNJL):c.872C>T (p.Pro291Leu)	not specified [RCV004118878]	uncertain significance	5	160253670	160253670	Human		name
156265819	CV2312266	single nucleotide variant	NM_001308173.3(CCNJL):c.875C>T (p.Ala292Val)	not specified [RCV004166979]	uncertain significance	5	160253667	160253667	Human		name
156360847	CV2329681	single nucleotide variant	NM_001308173.3(CCNJL):c.793T>G (p.Leu265Val)	not specified [RCV004180792]	uncertain significance	5	160253749	160253749	Human		name
155989077	CV2355220	single nucleotide variant	NM_001308173.3(CCNJL):c.820A>C (p.Thr274Pro)	not specified [RCV004198595]	uncertain significance	5	160253722	160253722	Human		name
155999369	CV2373408	single nucleotide variant	NM_001308173.3(CCNJL):c.611C>G (p.Ser204Cys)	not specified [RCV004220109]	uncertain significance	5	160255681	160255681	Human		name
156252793	CV2390082	single nucleotide variant	NM_001308173.3(CCNJL):c.715C>G (p.Leu239Val)	not specified [RCV004238684]	uncertain significance	5	160255577	160255577	Human		name
156248547	CV2393977	single nucleotide variant	NM_001308173.3(CCNJL):c.928C>T (p.Arg310Trp)	not specified [RCV004236203]	uncertain significance	5	160253614	160253614	Human		name
329398403	CV2464530	single nucleotide variant	NM_001308173.3(CCNJL):c.967T>C (p.Ser323Pro)	not specified [RCV004278228]	uncertain significance	5	160253575	160253575	Human		name
401727228	CV2684523	single nucleotide variant	NM_001308173.3(CCNJL):c.890A>G (p.Gln297Arg)	not specified [RCV004291592]	uncertain significance	5	160253652	160253652	Human		name
401899047	CV2785978	single nucleotide variant	NM_001308173.3(CCNJL):c.857C>A (p.Pro286Gln)	not specified [RCV004359817]	uncertain significance	5	160253685	160253685	Human		name
401918112	CV2825503	single nucleotide variant	NM_001308173.3(CCNJL):c.307G>A (p.Val103Ile)	not provided [RCV003429959]	benign	5	160259745	160259745	Human		name
405741532	CV3292688	single nucleotide variant	NM_001308173.3(CCNJL):c.865G>A (p.Gly289Ser)	not specified [RCV004430777]	likely benign	5	160253677	160253677	Human		name
405742066	CV3292689	single nucleotide variant	NM_001308173.3(CCNJL):c.871C>G (p.Pro291Ala)	not specified [RCV004430778]	uncertain significance	5	160253671	160253671	Human		name
405742061	CV3303158	single nucleotide variant	NM_001308173.3(CCNJL):c.904G>A (p.Val302Met)	not specified [RCV004430779]	uncertain significance	5	160253638	160253638	Human		name
405742034	CV3303162	single nucleotide variant	NM_001308173.3(CCNJL):c.377A>T (p.Glu126Val)	not specified [RCV004430783]	uncertain significance	5	160259675	160259675	Human		name
405742028	CV3303163	single nucleotide variant	NM_001308173.3(CCNJL):c.437C>T (p.Thr146Met)	not specified [RCV004430784]	uncertain significance	5	160259615	160259615	Human		name
405742022	CV3303164	single nucleotide variant	NM_001308173.3(CCNJL):c.442G>A (p.Ala148Thr)	not specified [RCV004430785]	uncertain significance	5	160259610	160259610	Human		name
405742017	CV3303165	single nucleotide variant	NM_001308173.3(CCNJL):c.486G>C (p.Lys162Asn)	not specified [RCV004430786]	uncertain significance	5	160259566	160259566	Human		name
405742010	CV3303166	single nucleotide variant	NM_001308173.3(CCNJL):c.697A>C (p.Ser233Arg)	not specified [RCV004430787]	uncertain significance	5	160255595	160255595	Human		name
405742001	CV3303167	single nucleotide variant	NM_001308173.3(CCNJL):c.799A>G (p.Met267Val)	not specified [RCV004430788]	uncertain significance	5	160253743	160253743	Human		name
407491997	CV3428652	single nucleotide variant	NM_001308173.3(CCNJL):c.301G>C (p.Asp101His)	not specified [RCV004604848]	uncertain significance	5	160259751	160259751	Human		name
407492000	CV3428653	single nucleotide variant	NM_001308173.3(CCNJL):c.689G>A (p.Arg230Lys)	not specified [RCV004604849]	uncertain significance	5	160255603	160255603	Human		name
407492003	CV3428654	single nucleotide variant	NM_001308173.3(CCNJL):c.875C>G (p.Ala292Gly)	not specified [RCV004604850]	uncertain significance	5	160253667	160253667	Human		name
597766125	CV3638227	single nucleotide variant	NM_001308173.3(CCNJL):c.931G>A (p.Asp311Asn)	not specified [RCV004896075]	uncertain significance	5	160253611	160253611	Human		name
597766126	CV3638228	single nucleotide variant	NM_001308173.3(CCNJL):c.965T>C (p.Leu322Pro)	not specified [RCV004896076]	uncertain significance	5	160253577	160253577	Human		name
597762182	CV3638229	single nucleotide variant	NM_001308173.3(CCNJL):c.757G>A (p.Val253Ile)	not specified [RCV004895098]	uncertain significance	5	160253785	160253785	Human		name
598205285	CV3939812	single nucleotide variant	NM_001308173.3(CCNJL):c.722C>G (p.Thr241Arg)	not specified [RCV005314929]	uncertain significance	5	160255570	160255570	Human		name
598205294	CV3939813	single nucleotide variant	NM_001308173.3(CCNJL):c.808G>T (p.Gly270Cys)	not specified [RCV005314930]	uncertain significance	5	160253734	160253734	Human		name
598205308	CV3939815	single nucleotide variant	NM_001308173.3(CCNJL):c.929G>A (p.Arg310Gln)	not specified [RCV005314932]	uncertain significance	5	160253613	160253613	Human		name
598205315	CV3939816	single nucleotide variant	NM_001308173.3(CCNJL):c.571G>T (p.Val191Phe)	not specified [RCV005314933]	uncertain significance	5	160259481	160259481	Human		name
598205325	CV3939817	single nucleotide variant	NM_001308173.3(CCNJL):c.524G>T (p.Arg175Leu)	not specified [RCV005314934]	uncertain significance	5	160259528	160259528	Human		name
598228382	CV3939818	single nucleotide variant	NM_001308173.3(CCNJL):c.968C>T (p.Ser323Leu)	not specified [RCV005319075]	uncertain significance	5	160253574	160253574	Human		name
598205334	CV3939819	single nucleotide variant	NM_001308173.3(CCNJL):c.619G>T (p.Ala207Ser)	not specified [RCV005314935]	uncertain significance	5	160255673	160255673	Human		name
598205342	CV3939820	single nucleotide variant	NM_001308173.3(CCNJL):c.851C>T (p.Ala284Val)	not specified [RCV005314936]	uncertain significance	5	160253691	160253691	Human		name
155931476	CV2221040	single nucleotide variant	NM_001308173.3(CCNJL):c.1148G>C (p.Gly383Ala)	not specified [RCV004092718]	uncertain significance	5	160253394	160253394	Human		name
155979097	CV2247188	single nucleotide variant	NM_001308173.3(CCNJL):c.1051C>T (p.Leu351Phe)	not specified [RCV004114709]	uncertain significance	5	160253491	160253491	Human		name
155991745	CV2355519	single nucleotide variant	NM_001308173.3(CCNJL):c.1148G>T (p.Gly383Val)	not specified [RCV004205369]	uncertain significance	5	160253394	160253394	Human		name
401751942	CV2723064	single nucleotide variant	NM_001308173.3(CCNJL):c.1100C>A (p.Thr367Asn)	not specified [RCV004327544]	uncertain significance	5	160253442	160253442	Human		name
405742054	CV3303159	single nucleotide variant	NM_001308173.3(CCNJL):c.1138T>C (p.Phe380Leu)	not specified [RCV004430780]	uncertain significance	5	160253404	160253404	Human		name
407492007	CV3428655	single nucleotide variant	NM_001308173.3(CCNJL):c.1160G>A (p.Arg387Lys)	not specified [RCV004604851]	uncertain significance	5	160253382	160253382	Human		name
598205300	CV3939814	single nucleotide variant	NM_001308173.3(CCNJL):c.1067C>T (p.Ala356Val)	not specified [RCV005314931]	uncertain significance	5	160253475	160253475	Human		name

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