C1d Variant Search Result - Rat Genome Database

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8 records found for search term C1d

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15156662	CV708335	single nucleotide variant	NM_173177.3(C1D):c.12A>G (p.Glu4=)	not provided [RCV000969156]	benign	2	68047299	68047299	Human		name
156366189	CV2272253	single nucleotide variant	NM_173177.3(C1D):c.203G>T (p.Trp68Leu)	not specified [RCV004126925]	uncertain significance	2	68046346	68046346	Human		name
405732060	CV3294930	single nucleotide variant	NM_173177.3(C1D):c.105G>C (p.Met35Ile)	not specified [RCV004429475]	uncertain significance	2	68047206	68047206	Human		name
598187576	CV3950000	single nucleotide variant	NM_173177.3(C1D):c.196A>G (p.Met66Val)	not specified [RCV005312051]	uncertain significance	2	68046353	68046353	Human		name
156326959	CV2219730	single nucleotide variant	NM_173177.3(C1D):c.398T>G (p.Val133Gly)	not specified [RCV004095431]	uncertain significance	2	68042917	68042917	Human		name
405732067	CV3294931	single nucleotide variant	NM_173177.3(C1D):c.349T>C (p.Phe117Leu)	not specified [RCV004429476]	uncertain significance	2	68042966	68042966	Human		name
405732074	CV3294932	single nucleotide variant	NM_173177.3(C1D):c.364C>T (p.Leu122Phe)	not specified [RCV004429477]	uncertain significance	2	68042951	68042951	Human		name
407490258	CV3418082	single nucleotide variant	NM_173177.3(C1D):c.356A>G (p.Lys119Arg)	not specified [RCV004604382]	uncertain significance	2	68042959	68042959	Human		name