Api5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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15 records found for search term Api5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401863099	CV2779190	single nucleotide variant	NM_001142930.2(API5):c.274G>A (p.Gly92Arg)	not specified [RCV004349096]	uncertain significance	11	43320863	43320863	Human		name
405662105	CV3289710	single nucleotide variant	NM_001142930.2(API5):c.1512G>A (p.Arg504=)	not specified [RCV004417653]	likely benign	11	43342447	43342447	Human		name
155995359	CV2375811	single nucleotide variant	NM_001142930.2(API5):c.803C>G (p.Pro268Arg)	not specified [RCV004224394]	uncertain significance	11	43326559	43326559	Human		name
329393679	CV2449789	single nucleotide variant	NM_001142930.2(API5):c.587A>G (p.Lys196Arg)	not specified [RCV004267108]	uncertain significance	11	43323473	43323473	Human		name
401883752	CV2785755	single nucleotide variant	NM_001142930.2(API5):c.760C>G (p.His254Asp)	not specified [RCV004365008]	uncertain significance	11	43326516	43326516	Human		name
407530699	CV3463541	single nucleotide variant	NM_001142930.2(API5):c.824C>T (p.Thr275Ile)	not specified [RCV004657194]	uncertain significance	11	43326580	43326580	Human		name
597696049	CV3574764	single nucleotide variant	NM_001142930.2(API5):c.727C>T (p.Arg243Trp)	not specified [RCV004839188]	uncertain significance	11	43323613	43323613	Human		name
597696333	CV3574776	single nucleotide variant	NM_001142930.2(API5):c.952A>G (p.Met318Val)	not specified [RCV004839198]	uncertain significance	11	43328718	43328718	Human		name
598242354	CV4005282	single nucleotide variant	NM_001142930.2(API5):c.512T>C (p.Val171Ala)	not specified [RCV005383415]	uncertain significance	11	43322105	43322105	Human		name
156361217	CV2269193	single nucleotide variant	NM_001142930.2(API5):c.1204G>A (p.Ala402Thr)	not specified [RCV004130353]	uncertain significance	11	43330041	43330041	Human		name
405662099	CV3289708	single nucleotide variant	NM_001142930.2(API5):c.1108C>G (p.Leu370Val)	not specified [RCV004417651]	uncertain significance	11	43328874	43328874	Human		name
405662102	CV3289709	single nucleotide variant	NM_001142930.2(API5):c.1388G>A (p.Gly463Asp)	not specified [RCV004417652]	uncertain significance	11	43335890	43335890	Human		name
597696016	CV3574760	single nucleotide variant	NM_001142930.2(API5):c.1372G>A (p.Glu458Lys)	not specified [RCV004839184]	uncertain significance	11	43335874	43335874	Human		name
597696106	CV3574770	single nucleotide variant	NM_001142930.2(API5):c.1379C>A (p.Thr460Lys)	not specified [RCV004839194]	uncertain significance	11	43335881	43335881	Human		name
598242391	CV4005291	single nucleotide variant	NM_001142930.2(API5):c.1406C>G (p.Ser469Cys)	not specified [RCV005383422]	uncertain significance	11	43335908	43335908	Human		name