Crmp1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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76 records found for search term Crmp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15171882	CV730297	single nucleotide variant	NM_001014809.3(CRMP1):c.964-8T>C	not provided [RCV000883734]	benign	4	5843169	5843169	Human		name
15150882	CV779044	single nucleotide variant	NM_001014809.3(CRMP1):c.820+8A>G	not provided [RCV000968028]	benign	4	5856135	5856135	Human		name
405867534	CV2842259	single nucleotide variant	NM_001014809.3(CRMP1):c.99C>T (p.Gly33=)	EBV-positive nodal T- and NK-cell lymphoma [RCV004560208]	likely benign	4	5892871	5892871	Human		name
598259530	CV3941850	single nucleotide variant	NM_001014809.3(CRMP1):c.24G>T (p.Trp8Cys)	not specified [RCV005324802]	uncertain significance	4	5892946	5892946	Human		name
155951204	CV2267964	single nucleotide variant	NM_001014809.3(CRMP1):c.97G>T (p.Gly33Cys)	not specified [RCV004136245]	uncertain significance	4	5892873	5892873	Human		name
156288482	CV2332878	single nucleotide variant	NM_001014809.3(CRMP1):c.80C>A (p.Thr27Asn)	not specified [RCV004192139]	uncertain significance	4	5892890	5892890	Human		name
405664880	CV3238996	single nucleotide variant	NM_001014809.3(CRMP1):c.80C>T (p.Thr27Ile)	not specified [RCV004367428]	uncertain significance	4	5892890	5892890	Human		name
15133840	CV749021	single nucleotide variant	NM_001014809.3(CRMP1):c.699T>G (p.Ser233=)	not provided [RCV000920584]	benign	4	5856264	5856264	Human		name
15195363	CV764597	single nucleotide variant	NM_001014809.3(CRMP1):c.315G>T (p.Arg105=)	not provided [RCV000933917]	likely benign	4	5892655	5892655	Human		name
156046615	CV2216098	single nucleotide variant	NM_001014809.3(CRMP1):c.218T>G (p.Val73Gly)	not specified [RCV004097112]	uncertain significance	4	5892752	5892752	Human		name
156112095	CV2228386	single nucleotide variant	NM_001014809.3(CRMP1):c.178T>G (p.Ser60Ala)	not specified [RCV004098366]	uncertain significance	4	5892792	5892792	Human		name
401759354	CV2708614	single nucleotide variant	NM_001014809.3(CRMP1):c.122G>A (p.Gly41Asp)	not specified [RCV004307600]	uncertain significance	4	5892848	5892848	Human		name
401888695	CV2754714	single nucleotide variant	NM_001014809.3(CRMP1):c.199G>T (p.Ala67Ser)	not specified [RCV004339382]	uncertain significance	4	5892771	5892771	Human		name
401895263	CV2786302	single nucleotide variant	NM_001014809.3(CRMP1):c.263T>G (p.Val88Gly)	not specified [RCV004361917]	uncertain significance	4	5892707	5892707	Human		name
401927875	CV2822378	single nucleotide variant	NM_001014809.3(CRMP1):c.1368G>A (p.Ala456=)	not provided [RCV003439227]	likely benign	4	5836849	5836849	Human		name
405664864	CV3238993	single nucleotide variant	NM_001014809.3(CRMP1):c.259G>A (p.Asp87Asn)	not specified [RCV004367425]	uncertain significance	4	5892711	5892711	Human		name
597799494	CV3657574	single nucleotide variant	NM_001014809.3(CRMP1):c.215C>G (p.Ala72Gly)	not specified [RCV004905233]	uncertain significance	4	5892755	5892755	Human		name
597799848	CV3657577	single nucleotide variant	NM_001014809.3(CRMP1):c.109G>A (p.Ala37Thr)	not specified [RCV004905236]	uncertain significance	4	5892861	5892861	Human		name
597799846	CV3657578	single nucleotide variant	NM_001014809.3(CRMP1):c.236G>A (p.Gly79Glu)	not specified [RCV004905237]	uncertain significance	4	5892734	5892734	Human		name
598259518	CV3941848	single nucleotide variant	NM_001014809.3(CRMP1):c.295C>T (p.Pro99Ser)	not specified [RCV005324800]	uncertain significance	4	5892675	5892675	Human		name
598259524	CV3941849	single nucleotide variant	NM_001014809.3(CRMP1):c.150C>G (p.Phe50Leu)	not specified [RCV005324801]	uncertain significance	4	5892820	5892820	Human		name
15150877	CV709404	single nucleotide variant	NM_001014809.3(CRMP1):c.1572C>A (p.Val524=)	not provided [RCV000968027]	benign	4	5835966	5835966	Human		name
15165514	CV709405	single nucleotide variant	NM_001014809.3(CRMP1):c.1071G>A (p.Ala357=)	not provided [RCV000970966]	benign	4	5841390	5841390	Human		name
15176147	CV721032	single nucleotide variant	NM_001014809.3(CRMP1):c.1821G>C (p.Gly607=)	not provided [RCV000884521]	benign	4	5825642	5825642	Human		name
15181782	CV734685	single nucleotide variant	NM_001014809.3(CRMP1):c.1398C>G (p.Pro466=)	not provided [RCV000907663]	benign	4	5836819	5836819	Human		name
15167620	CV749020	single nucleotide variant	NM_001014809.3(CRMP1):c.1584C>T (p.Pro528=)	not provided [RCV000927125]	likely benign	4	5835954	5835954	Human		name
15122720	CV782023	single nucleotide variant	NM_001014809.3(CRMP1):c.1065C>G (p.Thr355=)	not provided [RCV000979697]	benign	4	5841396	5841396	Human		name
156133241	CV2195941	single nucleotide variant	NM_001014809.3(CRMP1):c.778G>A (p.Asp260Asn)	not specified [RCV004072197]	uncertain significance	4	5856185	5856185	Human		name
156238140	CV2224262	single nucleotide variant	NM_001014809.3(CRMP1):c.922G>A (p.Val308Met)	not specified [RCV004096087]	uncertain significance	4	5849433	5849433	Human		name
155934717	CV2225382	single nucleotide variant	NM_001014809.3(CRMP1):c.421G>T (p.Asp141Tyr)	not specified [RCV004100795]	uncertain significance	4	5866717	5866717	Human		name
156056029	CV2243248	single nucleotide variant	NM_001014809.3(CRMP1):c.368G>A (p.Arg123Gln)	not specified [RCV004110134]	uncertain significance	4	5892602	5892602	Human		name
156084591	CV2299078	single nucleotide variant	NM_001014809.3(CRMP1):c.361C>G (p.Leu121Val)	not specified [RCV004158590]	uncertain significance	4	5892609	5892609	Human		name
155930016	CV2366477	single nucleotide variant	NM_001014809.3(CRMP1):c.901T>C (p.Phe301Leu)	not specified [RCV004208454]	uncertain significance	4	5849454	5849454	Human		name
156347596	CV2375505	single nucleotide variant	NM_001014809.3(CRMP1):c.987G>A (p.Met329Ile)	not specified [RCV004226016]	uncertain significance	4	5843138	5843138	Human		name
329377285	CV2462518	single nucleotide variant	NM_001014809.3(CRMP1):c.451C>G (p.Leu151Val)	not specified [RCV004276689]	uncertain significance	4	5866687	5866687	Human		name
401866093	CV2775411	single nucleotide variant	NM_001014809.3(CRMP1):c.595G>T (p.Ala199Ser)	not specified [RCV004348809]	uncertain significance	4	5861086	5861086	Human		name
401892415	CV2781910	single nucleotide variant	NM_001014809.3(CRMP1):c.521C>T (p.Ala174Val)	not specified [RCV004357153]	uncertain significance	4	5861160	5861160	Human		name
405664870	CV3238994	single nucleotide variant	NM_001014809.3(CRMP1):c.529C>T (p.Arg177Trp)	not specified [RCV004367426]	uncertain significance	4	5861152	5861152	Human		name
405664874	CV3238995	single nucleotide variant	NM_001014809.3(CRMP1):c.703G>A (p.Glu235Lys)	not specified [RCV004367427]	uncertain significance	4	5856260	5856260	Human		name
407464111	CV3429682	single nucleotide variant	NM_001014809.3(CRMP1):c.887A>G (p.Tyr296Cys)	not specified [RCV004613369]	uncertain significance	4	5849468	5849468	Human		name
407459072	CV3496698	deletion	NM_001014809.3(CRMP1):c.1755del (p.Lys586fs)	See cases [RCV004698409]	likely pathogenic	4	5828537	5828537	Human		name
597799482	CV3657568	single nucleotide variant	NM_001014809.3(CRMP1):c.445G>A (p.Val149Ile)	not specified [RCV004905227]	uncertain significance	4	5866693	5866693	Human		name
597799484	CV3657569	single nucleotide variant	NM_001014809.3(CRMP1):c.823G>A (p.Val275Ile)	not specified [RCV004905228]	uncertain significance	4	5851467	5851467	Human		name
597799492	CV3657573	single nucleotide variant	NM_001014809.3(CRMP1):c.995C>T (p.Thr332Met)	not specified [RCV004905232]	uncertain significance	4	5843130	5843130	Human		name
597799852	CV3657575	single nucleotide variant	NM_001014809.3(CRMP1):c.708G>C (p.Lys236Asn)	not specified [RCV004905234]	uncertain significance	4	5856255	5856255	Human		name
597799850	CV3657576	single nucleotide variant	NM_001014809.3(CRMP1):c.893C>T (p.Ala298Val)	not specified [RCV004905235]	uncertain significance	4	5849462	5849462	Human		name
597713074	CV3733000	single nucleotide variant	NM_001014809.3(CRMP1):c.626C>T (p.Ala209Val)	CRMP1-related neurodevelopmental disorder [RCV005052189]	uncertain significance	4	5861055	5861055	Human		name , trait
15116623	CV709406	single nucleotide variant	NM_001014809.3(CRMP1):c.781G>C (p.Gly261Arg)	not provided [RCV000962067]	benign	4	5856182	5856182	Human		name
156027768	CV2195583	single nucleotide variant	NM_001014809.3(CRMP1):c.1786G>A (p.Val596Ile)	not specified [RCV004082794]	uncertain significance	4	5828506	5828506	Human		name
155963540	CV2282751	single nucleotide variant	NM_001014809.3(CRMP1):c.1118G>C (p.Ser373Thr)	not specified [RCV004141609]	uncertain significance	4	5841343	5841343	Human		name
156150084	CV2307455	single nucleotide variant	NM_001014809.3(CRMP1):c.1978A>C (p.Ile660Leu)	not specified [RCV004166119]	uncertain significance	4	5821843	5821843	Human		name
156040697	CV2310826	single nucleotide variant	NM_001014809.3(CRMP1):c.1400A>C (p.Glu467Ala)	not specified [RCV004163874]	uncertain significance	4	5836817	5836817	Human		name
155960011	CV2390620	single nucleotide variant	NM_001014809.3(CRMP1):c.1177A>C (p.Ile393Leu)	not specified [RCV004239143]	uncertain significance	4	5839655	5839655	Human		name
156002535	CV2396591	single nucleotide variant	NM_001014809.3(CRMP1):c.1741C>T (p.Arg581Cys)	not specified [RCV004240420]	uncertain significance	4	5828551	5828551	Human		name
329392931	CV2449386	single nucleotide variant	NM_001014809.3(CRMP1):c.1933A>G (p.Ile645Val)	not specified [RCV004266546]	uncertain significance	4	5825530	5825530	Human		name
401756243	CV2687049	single nucleotide variant	NM_001014809.3(CRMP1):c.1126G>A (p.Asp376Asn)	not specified [RCV004304371]	uncertain significance	4	5841335	5841335	Human		name
401776227	CV2692641	single nucleotide variant	NM_001014809.3(CRMP1):c.1079T>C (p.Ile360Thr)	not specified [RCV004312369]	uncertain significance	4	5841382	5841382	Human		name
401757239	CV2692883	single nucleotide variant	NM_001014809.3(CRMP1):c.1099A>G (p.Thr367Ala)	not specified [RCV004306414]	uncertain significance	4	5841362	5841362	Human		name
401777999	CV2718419	single nucleotide variant	NM_001014809.3(CRMP1):c.1857G>T (p.Glu619Asp)	not specified [RCV004318239]	uncertain significance	4	5825606	5825606	Human		name
405664831	CV3238986	single nucleotide variant	NM_001014809.3(CRMP1):c.1150A>G (p.Lys384Glu)	not specified [RCV004367418]	uncertain significance	4	5841311	5841311	Human		name
405664835	CV3238987	single nucleotide variant	NM_001014809.3(CRMP1):c.1382A>C (p.Asn461Thr)	not specified [RCV004367419]	uncertain significance	4	5836835	5836835	Human		name
405664840	CV3238988	single nucleotide variant	NM_001014809.3(CRMP1):c.1409A>T (p.Asn470Ile)	not specified [RCV004367420]	uncertain significance	4	5836808	5836808	Human		name
405664845	CV3238989	single nucleotide variant	NM_001014809.3(CRMP1):c.1772A>T (p.His591Leu)	not specified [RCV004367421]	uncertain significance	4	5828520	5828520	Human		name
405664851	CV3238990	single nucleotide variant	NM_001014809.3(CRMP1):c.1773C>A (p.His591Gln)	not specified [RCV004367422]	uncertain significance	4	5828519	5828519	Human		name
405664855	CV3238991	single nucleotide variant	NM_001014809.3(CRMP1):c.1972G>T (p.Ala658Ser)	not specified [RCV004367423]	uncertain significance	4	5821849	5821849	Human		name
405664860	CV3238992	single nucleotide variant	NM_001014809.3(CRMP1):c.1982A>G (p.Asp661Gly)	not specified [RCV004367424]	uncertain significance	4	5821839	5821839	Human		name
407464107	CV3429681	single nucleotide variant	NM_001014809.3(CRMP1):c.1735A>G (p.Met579Val)	not specified [RCV004613368]	uncertain significance	4	5828557	5828557	Human		name
407464115	CV3429683	single nucleotide variant	NM_001014809.3(CRMP1):c.1781A>G (p.Gln594Arg)	not specified [RCV004613370]	uncertain significance	4	5828511	5828511	Human		name
407464120	CV3429684	single nucleotide variant	NM_001014809.3(CRMP1):c.1336G>A (p.Gly446Ser)	not specified [RCV004613371]	uncertain significance	4	5836881	5836881	Human		name
597799486	CV3657570	single nucleotide variant	NM_001014809.3(CRMP1):c.1024C>T (p.Pro342Ser)	not specified [RCV004905229]	uncertain significance	4	5843101	5843101	Human		name
597799488	CV3657571	single nucleotide variant	NM_001014809.3(CRMP1):c.2039C>G (p.Ser680Cys)	not specified [RCV004905230]	uncertain significance	4	5821782	5821782	Human		name
598259490	CV3941844	single nucleotide variant	NM_001014809.3(CRMP1):c.1987A>G (p.Asn663Asp)	not specified [RCV005324796]	uncertain significance	4	5821834	5821834	Human		name
598259497	CV3941845	single nucleotide variant	NM_001014809.3(CRMP1):c.1759G>A (p.Ala587Thr)	not specified [RCV005324797]	uncertain significance	4	5828533	5828533	Human		name
598259510	CV3941847	single nucleotide variant	NM_001014809.3(CRMP1):c.1750C>T (p.Pro584Ser)	not specified [RCV005324799]	uncertain significance	4	5828542	5828542	Human		name
598259536	CV3941851	single nucleotide variant	NM_001014809.3(CRMP1):c.1918C>T (p.His640Tyr)	not specified [RCV005324803]	uncertain significance	4	5825545	5825545	Human		name
155644953	CV1708884	deletion	NM_001014809.3(CRMP1):c.214_236del (p.Ala72fs)	not provided [RCV002291481]	uncertain significance	4	5892734	5892756	Human		name

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