Cd274 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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9 records found for search term Cd274

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150504765	CV1240819	single nucleotide variant	NM_014143.4(CD274):c.*93G>A	not provided [RCV001657662]	benign	9	5467955	5467955	Human		name
150468064	CV1240984	single nucleotide variant	NM_014143.4(CD274):c.*2635A>G	not provided [RCV001650442]	benign	9	5470497	5470497	Human		name
15184814	CV711993	single nucleotide variant	NM_014143.4(CD274):c.198A>G (p.Gln66=)	not provided [RCV000975204]	benign	9	5457224	5457224	Human		name
15098339	CV751742	single nucleotide variant	NM_014143.4(CD274):c.363C>A (p.Ala121=)	not provided [RCV000914224]	benign	9	5457389	5457389	Human		name
155916537	CV2197468	single nucleotide variant	NM_014143.4(CD274):c.548A>C (p.Asn183Thr)	not specified [RCV004081201]	uncertain significance	9	5462987	5462987	Human		name
156344955	CV2294319	single nucleotide variant	NM_014143.4(CD274):c.829A>G (p.Thr277Ala)	not specified [RCV004151444]	uncertain significance	9	5466808	5466808	Human		name
401924295	CV2828743	single nucleotide variant	NM_014143.4(CD274):c.437C>G (p.Pro146Arg)	not provided [RCV003435700]	likely benign	9	5462876	5462876	Human		name
405759421	CV3299679	single nucleotide variant	NM_014143.4(CD274):c.649G>A (p.Glu217Lys)	not specified [RCV004433368]	uncertain significance	9	5463088	5463088	Human		name
407498024	CV3424926	single nucleotide variant	NM_014143.4(CD274):c.436C>A (p.Pro146Thr)	not specified [RCV004606515]	uncertain significance	9	5462875	5462875	Human		name