Cdkn2c Variant Search Result - Rat Genome Database

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13 records found for search term Cdkn2c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
14698215	CV623188	single nucleotide variant	NM_078626.3(CDKN2C):c.129+1G>T	not provided [RCV000786793]	not provided	1	50970498	50970498	Human		name
401724189	CV2735684	single nucleotide variant	NM_078626.3(CDKN2C):c.18G>A (p.Gly6=)	not provided [RCV003312127]	uncertain significance	1	50970386	50970386	Human		name
401880598	CV2780269	single nucleotide variant	NM_078626.3(CDKN2C):c.24G>T (p.Glu8Asp)	not specified [RCV004355900]	uncertain significance	1	50970392	50970392	Human		name
405267525	CV3186850	single nucleotide variant	NM_078626.3(CDKN2C):c.189C>T (p.Pro63=)	not provided [RCV003886933]	likely benign	1	50973952	50973952	Human		name
597767176	CV3648704	single nucleotide variant	NM_078626.3(CDKN2C):c.231G>A (p.Ala77=)	not specified [RCV004896282]	likely benign	1	50973994	50973994	Human		name
401927705	CV2812796	single nucleotide variant	NM_078626.3(CDKN2C):c.477C>T (p.Asn159=)	not provided [RCV003406488]	likely benign	1	50974240	50974240	Human		name
597767166	CV3648702	single nucleotide variant	NM_078626.3(CDKN2C):c.49G>C (p.Asp17His)	not specified [RCV004896280]	uncertain significance	1	50970417	50970417	Human		name
405742891	CV3293084	single nucleotide variant	NM_078626.3(CDKN2C):c.117G>T (p.Arg39Ser)	not specified [RCV004431005]	uncertain significance	1	50970485	50970485	Human		name
597767171	CV3648703	single nucleotide variant	NM_078626.3(CDKN2C):c.230C>T (p.Ala77Val)	not specified [RCV004896281]	uncertain significance	1	50973993	50973993	Human		name
15173481	CV788677	single nucleotide variant	NM_078626.3(CDKN2C):c.230C>A (p.Ala77Glu)	Multiple myeloma [RCV000984122]	likely pathogenic	1	50973993	50973993	Human	2	name
155994429	CV2249177	single nucleotide variant	NM_078626.3(CDKN2C):c.408G>C (p.Lys136Asn)	not specified [RCV004118224]	uncertain significance	1	50974171	50974171	Human		name
405742896	CV3293085	single nucleotide variant	NM_078626.3(CDKN2C):c.478G>A (p.Gly160Arg)	not specified [RCV004431006]	likely benign	1	50974241	50974241	Human		name
598193419	CV3940367	single nucleotide variant	NM_078626.3(CDKN2C):c.380C>A (p.Ala127Asp)	not specified [RCV005312977]	uncertain significance	1	50974143	50974143	Human		name