Fbf1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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21 records found for search term Fbf1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156138666	CV2236721	single nucleotide variant	NM_001319193.2(FBF1):c.238A>G (p.Ile80Val)	not specified [RCV004110676]	likely benign	17	75930038	75930038	Human		name
156153722	CV2242148	single nucleotide variant	NM_001319193.2(FBF1):c.286G>C (p.Asp96His)	not specified [RCV004109362]	uncertain significance	17	75928187	75928187	Human		name
401935880	CV2808394	single nucleotide variant	NM_001319193.2(FBF1):c.2358G>A (p.Gly786=)	not provided [RCV003413343]	likely benign	17	75917959	75917959	Human		name
156223192	CV2232929	single nucleotide variant	NM_001319193.2(FBF1):c.338G>T (p.Ser113Ile)	not specified [RCV004103310]	uncertain significance	17	75928135	75928135	Human		name
156061378	CV2239984	single nucleotide variant	NM_001319193.2(FBF1):c.887G>C (p.Gly296Ala)	not specified [RCV004110776]	uncertain significance	17	75925428	75925428	Human		name
156398740	CV2194760	single nucleotide variant	NM_001319193.2(FBF1):c.1852C>T (p.Arg618Trp)	not specified [RCV004075309]	uncertain significance	17	75920086	75920086	Human		name
156230256	CV2199558	single nucleotide variant	NM_001319193.2(FBF1):c.1937G>T (p.Arg646Leu)	not specified [RCV004072309]	uncertain significance	17	75919869	75919869	Human		name
156373351	CV2201079	single nucleotide variant	NM_001319193.2(FBF1):c.1669G>A (p.Val557Ile)	not specified [RCV004075202]	likely benign	17	75921249	75921249	Human		name
156401465	CV2207247	single nucleotide variant	NM_001319193.2(FBF1):c.2368C>T (p.Arg790Cys)	not specified [RCV004087972]	uncertain significance	17	75917949	75917949	Human		name
156080446	CV2226627	single nucleotide variant	NM_001319193.2(FBF1):c.1699C>T (p.Arg567Trp)	not specified [RCV004101874]	uncertain significance	17	75920405	75920405	Human		name
156335042	CV2228337	single nucleotide variant	NM_001319193.2(FBF1):c.1094A>C (p.Glu365Ala)	not specified [RCV004098328]	uncertain significance	17	75923516	75923516	Human		name
156283104	CV2230876	single nucleotide variant	NM_001319193.2(FBF1):c.1475G>A (p.Ser492Asn)	not specified [RCV004092354]	uncertain significance	17	75921996	75921996	Human		name
156283825	CV2231065	single nucleotide variant	NM_001319193.2(FBF1):c.2924A>G (p.Lys975Arg)	not specified [RCV004094296]	uncertain significance	17	75914189	75914189	Human		name
156195095	CV2251809	single nucleotide variant	NM_001319193.2(FBF1):c.1511G>C (p.Arg504Thr)	not specified [RCV004119799]	uncertain significance	17	75921960	75921960	Human		name
156336095	CV2360667	single nucleotide variant	NM_001319193.2(FBF1):c.1388A>G (p.His463Arg)	not specified [RCV004213463]	uncertain significance	17	75923222	75923222	Human		name
156142365	CV2383771	single nucleotide variant	NM_001319193.2(FBF1):c.1114G>C (p.Ala372Pro)	not specified [RCV004231649]	likely benign	17	75923496	75923496	Human		name
156142381	CV2383772	single nucleotide variant	NM_001319193.2(FBF1):c.1247G>A (p.Gly416Glu)	not specified [RCV004231650]	uncertain significance	17	75923363	75923363	Human		name
155908425	CV2387319	single nucleotide variant	NM_001319193.2(FBF1):c.1795C>T (p.His599Tyr)	not specified [RCV004238407]	uncertain significance	17	75920309	75920309	Human		name
156200748	CV2392432	single nucleotide variant	NM_001319193.2(FBF1):c.1394C>T (p.Ala465Val)	not specified [RCV004244012]	likely benign	17	75923216	75923216	Human		name
405777044	CV3249981	single nucleotide variant	NM_001319193.2(FBF1):c.2298C>G (p.His766Gln)	not specified [RCV004386137]	uncertain significance	17	75918019	75918019	Human		name
156084422	CV2205585	single nucleotide variant	NM_001319193.2(FBF1):c.3275G>A (p.Arg1092His)	not specified [RCV004082508]	uncertain significance	17	75912280	75912280	Human		name

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