Retn Variant Search Result - Rat Genome Database

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27 records found for search term Retn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405271456	CV3219088	single nucleotide variant	NM_020415.4(RETN):c.-9G>T	RETN-related disorder [RCV003971796]	likely benign	19	7669318	7669318	Human		name , trait , alternate_id
8558328	CV19923	single nucleotide variant	NM_020415.4(RETN):c.*62G>A	Diabetes mellitus type 2, susceptibility to [RCV000005160]\|HYPERTENSION, INSULIN RESISTANCE-RELATED, SUSCEPTIBILITY TO [RCV000005161]	risk factor	19	7670411	7670411	Human	4	name
8558328	CV19923	single nucleotide variant	NM_020415.4(RETN):c.*62G>A	Diabetes mellitus type 2, susceptibility to [RCV000005160]\|HYPERTENSION, INSULIN RESISTANCE-RELATED, SUSCEPTIBILITY TO [RCV000005161]	risk factor	19	7670411	7670412	Human	4	name
405694776	CV3315889	single nucleotide variant	NM_020415.4(RETN):c.90G>C (p.Glu30Asp)	not specified [RCV004446028]	uncertain significance	19	7669416	7669416	Human		name
156240269	CV2265481	single nucleotide variant	NM_020415.4(RETN):c.127G>A (p.Ala43Thr)	not specified [RCV004124241]	uncertain significance	19	7669829	7669829	Human		name
407459624	CV3496846	microsatellite	NM_020415.4(RETN):c.12_13del (p.Cys5fs)	Autism [RCV004698661]	uncertain significance	19	7669334	7669335	Human		name
597765376	CV3593506	single nucleotide variant	NM_020415.4(RETN):c.167C>G (p.Ser56Cys)	not specified [RCV004850021]	uncertain significance	19	7669869	7669869	Human		name
597731477	CV3593507	single nucleotide variant	NM_020415.4(RETN):c.278G>A (p.Cys93Tyr)	not specified [RCV004863136]	uncertain significance	19	7670300	7670300	Human		name
156401586	CV2207426	single nucleotide variant	NM_032579.3(RETNLB):c.7C>A (p.Pro3Thr)	not specified [RCV004088122]	uncertain significance	3	108757179	108757179	Human		name
155975230	CV2342646	single nucleotide variant	NM_032579.3(RETNLB):c.7C>T (p.Pro3Ser)	not specified [RCV004196731]	uncertain significance	3	108757179	108757179	Human		name
8625452	CV80575	single nucleotide variant	NM_032579.2(RETNLB):c.75T>C (p.Cys25=)	Malignant melanoma [RCV000060652]	not provided	3	108757111	108757111	Human		name
405694782	CV3315890	single nucleotide variant	NM_032579.3(RETNLB):c.11C>T (p.Ser4Phe)	not specified [RCV004446029]	uncertain significance	3	108757175	108757175	Human		name
156292927	CV2306280	single nucleotide variant	NM_032579.3(RETNLB):c.68C>T (p.Thr23Ile)	not specified [RCV004163001]	uncertain significance	3	108757118	108757118	Human		name
329357243	CV2457607	single nucleotide variant	NM_032579.3(RETNLB):c.38C>T (p.Pro13Leu)	not specified [RCV004269185]	likely benign	3	108757148	108757148	Human		name
405694792	CV3315892	single nucleotide variant	NM_032579.3(RETNLB):c.71A>G (p.Gln24Arg)	not specified [RCV004446031]	uncertain significance	3	108757115	108757115	Human		name
597731486	CV3593510	single nucleotide variant	NM_032579.3(RETNLB):c.88G>T (p.Val30Phe)	not specified [RCV004863137]	uncertain significance	3	108757098	108757098	Human		name
156146598	CV2265143	single nucleotide variant	NM_032579.3(RETNLB):c.189A>T (p.Arg63Ser)	not specified [RCV004126274]	uncertain significance	3	108756527	108756527	Human		name
401889883	CV2763494	single nucleotide variant	NM_032579.3(RETNLB):c.239A>G (p.Tyr80Cys)	not specified [RCV004343022]	uncertain significance	3	108755875	108755875	Human		name
401876804	CV2782996	single nucleotide variant	NM_032579.3(RETNLB):c.178A>C (p.Ser60Arg)	not specified [RCV004361786]	uncertain significance	3	108756538	108756538	Human		name
407459408	CV3465482	single nucleotide variant	NM_032579.3(RETNLB):c.284G>T (p.Cys95Phe)	not specified [RCV004658215]	uncertain significance	3	108755830	108755830	Human		name
407459413	CV3465483	single nucleotide variant	NM_032579.3(RETNLB):c.156G>T (p.Lys52Asn)	not specified [RCV004658216]	uncertain significance	3	108756560	108756560	Human		name
597765384	CV3593509	single nucleotide variant	NM_032579.3(RETNLB):c.251C>T (p.Ser84Leu)	not specified [RCV004850023]	uncertain significance	3	108755863	108755863	Human		name
598215948	CV3905612	single nucleotide variant	NM_032579.3(RETNLB):c.170G>C (p.Ser57Thr)	not specified [RCV005271785]	uncertain significance	3	108756546	108756546	Human		name
598215954	CV3905613	single nucleotide variant	NM_032579.3(RETNLB):c.129G>C (p.Glu43Asp)	not specified [RCV005271786]	uncertain significance	3	108756587	108756587	Human		name
598215961	CV3905614	single nucleotide variant	NM_032579.3(RETNLB):c.123T>A (p.Ser41Arg)	not specified [RCV005271787]	likely benign	3	108757063	108757063	Human		name
405694788	CV3315891	single nucleotide variant	NM_032579.3(RETNLB):c.308C>T (p.Thr103Ile)	not specified [RCV004446030]	uncertain significance	3	108755806	108755806	Human		name
598215971	CV3905615	single nucleotide variant	NM_032579.3(RETNLB):c.302A>T (p.Asp101Val)	not specified [RCV005271788]	uncertain significance	3	108755812	108755812	Human		name

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