Cdr2l Variant Search Result - Rat Genome Database

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51 records found for search term Cdr2l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156095632	CV2253049	single nucleotide variant	NM_014603.3(CDR2L):c.13G>T (p.Ala5Ser)	not specified [RCV004120840]	uncertain significance	17	74988056	74988056	Human		name
156379597	CV2217919	single nucleotide variant	NM_014603.3(CDR2L):c.52T>C (p.Trp18Arg)	not specified [RCV004086377]	uncertain significance	17	74988095	74988095	Human		name
597767345	CV3648747	single nucleotide variant	NM_014603.3(CDR2L):c.58G>A (p.Asp20Asn)	not specified [RCV004896315]	uncertain significance	17	74988101	74988101	Human		name
155908095	CV2302354	single nucleotide variant	NM_014603.3(CDR2L):c.221G>A (p.Arg74Gln)	not specified [RCV004161108]	uncertain significance	17	75001369	75001369	Human		name
401870253	CV2792321	single nucleotide variant	NM_014603.3(CDR2L):c.143C>T (p.Ser48Phe)	not specified [RCV004361500]	uncertain significance	17	74999567	74999567	Human		name
405743321	CV3293124	single nucleotide variant	NM_014603.3(CDR2L):c.140G>T (p.Gly47Val)	not specified [RCV004431045]	uncertain significance	17	74999564	74999564	Human		name
597767361	CV3648750	single nucleotide variant	NM_014603.3(CDR2L):c.241G>T (p.Ala81Ser)	not specified [RCV004896318]	uncertain significance	17	75001389	75001389	Human		name
598240729	CV3940399	single nucleotide variant	NM_014603.3(CDR2L):c.226G>A (p.Val76Met)	not specified [RCV005321430]	uncertain significance	17	75001374	75001374	Human		name
156185441	CV2222614	single nucleotide variant	NM_014603.3(CDR2L):c.301C>A (p.Leu101Met)	not specified [RCV004099441]	uncertain significance	17	75001449	75001449	Human		name
156311791	CV2256768	single nucleotide variant	NM_014603.3(CDR2L):c.452G>A (p.Arg151His)	not specified [RCV004120995]	uncertain significance	17	75002174	75002174	Human		name
155980026	CV2263609	single nucleotide variant	NM_014603.3(CDR2L):c.771G>A (p.Met257Ile)	not specified [RCV004135614]	uncertain significance	17	75003447	75003447	Human		name
155979100	CV2266595	single nucleotide variant	NM_014603.3(CDR2L):c.541C>G (p.Leu181Val)	not specified [RCV004131144]	uncertain significance	17	75003217	75003217	Human		name
155957395	CV2304151	single nucleotide variant	NM_014603.3(CDR2L):c.664G>A (p.Ala222Thr)	not specified [RCV004170185]	uncertain significance	17	75003340	75003340	Human		name
329380541	CV2466677	single nucleotide variant	NM_014603.3(CDR2L):c.437G>A (p.Arg146Gln)	not specified [RCV004276187]	uncertain significance	17	75002159	75002159	Human		name
401735279	CV2687539	single nucleotide variant	NM_014603.3(CDR2L):c.940C>T (p.Arg314Cys)	not specified [RCV004300769]	uncertain significance	17	75003616	75003616	Human		name
401893996	CV2770204	single nucleotide variant	NM_014603.3(CDR2L):c.997C>T (p.Arg333Trp)	not specified [RCV004356095]	uncertain significance	17	75003673	75003673	Human		name
401895609	CV2774530	single nucleotide variant	NM_014603.3(CDR2L):c.467A>T (p.His156Leu)	not specified [RCV004350017]	uncertain significance	17	75002189	75002189	Human		name
401895258	CV2786297	single nucleotide variant	NM_014603.3(CDR2L):c.457C>T (p.Arg153Cys)	not specified [RCV004361912]	uncertain significance	17	75002179	75002179	Human		name
405743328	CV3293125	single nucleotide variant	NM_014603.3(CDR2L):c.436C>T (p.Arg146Trp)	not specified [RCV004431046]	uncertain significance	17	75002158	75002158	Human		name
405743342	CV3303598	single nucleotide variant	NM_014603.3(CDR2L):c.821C>A (p.Ala274Asp)	not specified [RCV004431048]	uncertain significance	17	75003497	75003497	Human		name
407460648	CV3418681	single nucleotide variant	NM_014603.3(CDR2L):c.505C>T (p.Arg169Trp)	not specified [RCV004612382]	uncertain significance	17	75002227	75002227	Human		name
407460661	CV3418684	single nucleotide variant	NM_014603.3(CDR2L):c.527T>A (p.Leu176Gln)	not specified [RCV004612385]	uncertain significance	17	75003203	75003203	Human		name
407460665	CV3418685	single nucleotide variant	NM_014603.3(CDR2L):c.602C>A (p.Ala201Glu)	not specified [RCV004612386]	uncertain significance	17	75003278	75003278	Human		name
597767305	CV3648739	single nucleotide variant	NM_014603.3(CDR2L):c.451C>T (p.Arg151Cys)	not specified [RCV004896307]	uncertain significance	17	75002173	75002173	Human		name
597767310	CV3648740	single nucleotide variant	NM_014603.3(CDR2L):c.338A>T (p.His113Leu)	not specified [RCV004896308]	uncertain significance	17	75001486	75001486	Human		name
597767325	CV3648743	single nucleotide variant	NM_014603.3(CDR2L):c.544G>A (p.Glu182Lys)	not specified [RCV004896311]	uncertain significance	17	75003220	75003220	Human		name
597767330	CV3648744	single nucleotide variant	NM_014603.3(CDR2L):c.362G>A (p.Arg121His)	not specified [RCV004896312]	uncertain significance	17	75002084	75002084	Human		name
597767335	CV3648745	single nucleotide variant	NM_014603.3(CDR2L):c.592C>G (p.Leu198Val)	not specified [RCV004896313]	uncertain significance	17	75003268	75003268	Human		name
597767366	CV3648751	single nucleotide variant	NM_014603.3(CDR2L):c.343C>A (p.Leu115Met)	not specified [RCV004896319]	uncertain significance	17	75002065	75002065	Human		name
597767371	CV3648752	single nucleotide variant	NM_014603.3(CDR2L):c.928G>T (p.Gly310Cys)	not specified [RCV004896320]	uncertain significance	17	75003604	75003604	Human		name
597767382	CV3648754	single nucleotide variant	NM_014603.3(CDR2L):c.929G>A (p.Gly310Asp)	not specified [RCV004896322]	uncertain significance	17	75003605	75003605	Human		name
597767387	CV3648755	single nucleotide variant	NM_014603.3(CDR2L):c.632A>C (p.Gln211Pro)	not specified [RCV004896323]	uncertain significance	17	75003308	75003308	Human		name
598193524	CV3940396	single nucleotide variant	NM_014603.3(CDR2L):c.505C>G (p.Arg169Gly)	not specified [RCV005312999]	uncertain significance	17	75002227	75002227	Human		name
598193530	CV3940397	single nucleotide variant	NM_014603.3(CDR2L):c.524G>A (p.Arg175His)	not specified [RCV005313000]	uncertain significance	17	75003200	75003200	Human		name
598193538	CV3940400	single nucleotide variant	NM_014603.3(CDR2L):c.710T>C (p.Met237Thr)	not specified [RCV005313002]	uncertain significance	17	75003386	75003386	Human		name
598240734	CV3940401	single nucleotide variant	NM_014603.3(CDR2L):c.369G>C (p.Gln123His)	not specified [RCV005321431]	uncertain significance	17	75002091	75002091	Human		name
598193542	CV3940402	single nucleotide variant	NM_014603.3(CDR2L):c.731T>A (p.Val244Glu)	not specified [RCV005313003]	uncertain significance	17	75003407	75003407	Human		name
598240740	CV3940404	single nucleotide variant	NM_014603.3(CDR2L):c.668T>A (p.Val223Glu)	not specified [RCV005321432]	uncertain significance	17	75003344	75003344	Human		name
156167494	CV2201013	single nucleotide variant	NM_014603.3(CDR2L):c.1282C>T (p.Arg428Trp)	not specified [RCV004074778]	uncertain significance	17	75003958	75003958	Human		name
156261123	CV2314692	single nucleotide variant	NM_014603.3(CDR2L):c.1161G>C (p.Gln387His)	not specified [RCV004170842]	uncertain significance	17	75003837	75003837	Human		name
155932128	CV2399960	single nucleotide variant	NM_014603.3(CDR2L):c.1124G>A (p.Arg375Gln)	not specified [RCV004246890]	uncertain significance	17	75003800	75003800	Human		name
401762788	CV2720074	single nucleotide variant	NM_014603.3(CDR2L):c.1364A>G (p.Asn455Ser)	not specified [RCV004323645]	uncertain significance	17	75004040	75004040	Human		name
405743301	CV3293121	single nucleotide variant	NM_014603.3(CDR2L):c.1002C>G (p.His334Gln)	not specified [RCV004431042]	uncertain significance	17	75003678	75003678	Human		name
405743307	CV3293122	single nucleotide variant	NM_014603.3(CDR2L):c.1220G>A (p.Gly407Asp)	not specified [RCV004431043]	uncertain significance	17	75003896	75003896	Human		name
407460653	CV3418682	single nucleotide variant	NM_014603.3(CDR2L):c.1205G>A (p.Arg402His)	not specified [RCV004612383]	uncertain significance	17	75003881	75003881	Human		name
597767314	CV3648741	single nucleotide variant	NM_014603.3(CDR2L):c.1138G>A (p.Gly380Arg)	not specified [RCV004896309]	uncertain significance	17	75003814	75003814	Human		name
597767319	CV3648742	single nucleotide variant	NM_014603.3(CDR2L):c.1046G>T (p.Gly349Val)	not specified [RCV004896310]	uncertain significance	17	75003722	75003722	Human		name
597767350	CV3648748	single nucleotide variant	NM_014603.3(CDR2L):c.1141G>A (p.Val381Met)	not specified [RCV004896316]	uncertain significance	17	75003817	75003817	Human		name
597767355	CV3648749	single nucleotide variant	NM_014603.3(CDR2L):c.1215G>T (p.Glu405Asp)	not specified [RCV004896317]	uncertain significance	17	75003891	75003891	Human		name
597767376	CV3648753	single nucleotide variant	NM_014603.3(CDR2L):c.1210G>A (p.Gly404Ser)	not specified [RCV004896321]	uncertain significance	17	75003886	75003886	Human		name
598193534	CV3940398	single nucleotide variant	NM_014603.3(CDR2L):c.1283G>T (p.Arg428Leu)	not specified [RCV005313001]	uncertain significance	17	75003959	75003959	Human		name

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