Fyn Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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32 records found for search term Fyn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15157888	CV777593	single nucleotide variant	NM_002037.5(FYN):c.1273+8C>T	not provided [RCV000946967]	benign	6	111694367	111694367	Human		name
15170824	CV777650	single nucleotide variant	NM_002037.5(FYN):c.1119+8C>A	not provided [RCV000949721]	benign	6	111694620	111694620	Human		name
8644858	CV104265	single nucleotide variant	NM_002037.5(FYN):c.862+530G>A	not provided [RCV000084663]	not provided	6	111699574	111699574	Human		name
15170819	CV777514	single nucleotide variant	NM_002037.5(FYN):c.1120-10G>A	not provided [RCV000949720]	benign	6	111694538	111694538	Human		name
8581470	CV115909	single nucleotide variant	NM_002037.5(FYN):c.-81-19491A>T	Lung cancer [RCV000096432]	uncertain significance	6	111800126	111800126	Human		name
155959711	CV2285308	single nucleotide variant	NM_002037.5(FYN):c.24T>A (p.Asp8Glu)	not specified [RCV004139188]	uncertain significance	6	111720028	111720028	Human		name
407485450	CV3439452	single nucleotide variant	NM_002037.5(FYN):c.162C>T (p.His54=)	not specified [RCV004618921]	likely benign	6	111719890	111719890	Human		name
15155372	CV721676	single nucleotide variant	NM_002037.5(FYN):c.126C>T (p.Phe42=)	not provided [RCV000880404]	benign	6	111719926	111719926	Human		name
8644856	CV104263	single nucleotide variant	NM_002037.5(FYN):c.984G>A (p.Gln328=)	not provided [RCV000084661]	not provided	6	111696335	111696335	Human		name
8644859	CV104266	single nucleotide variant	NM_002037.5(FYN):c.573T>C (p.Asp191=)	not provided [RCV000084664]	not provided	6	111703009	111703009	Human		name
15185122	CV721675	single nucleotide variant	NM_002037.5(FYN):c.969C>T (p.His323=)	not provided [RCV000886610]	benign	6	111696350	111696350	Human		name
8644855	CV104262	single nucleotide variant	NM_002037.5(FYN):c.1347G>A (p.Val449=)	not provided [RCV000084660]	not provided	6	111674557	111674557	Human		name
156183977	CV2198553	single nucleotide variant	NM_002037.5(FYN):c.163G>A (p.Ala55Thr)	not specified [RCV004075579]	uncertain significance	6	111719889	111719889	Human		name
156063414	CV2199916	single nucleotide variant	NM_002037.5(FYN):c.187G>A (p.Val63Ile)	not specified [RCV004074096]	uncertain significance	6	111719865	111719865	Human		name
156256888	CV2322025	single nucleotide variant	NM_002037.5(FYN):c.274G>A (p.Asp92Asn)	not specified [RCV004173777]	uncertain significance	6	111714417	111714417	Human		name
405867576	CV2842333	single nucleotide variant	NM_002037.5(FYN):c.286C>G (p.Arg96Gly)	EBV-positive nodal T- and NK-cell lymphoma [RCV004560282]	pathogenic	6	111714405	111714405	Human		name
405867577	CV2842334	single nucleotide variant	NM_002037.5(FYN):c.286C>T (p.Arg96Trp)	EBV-positive nodal T- and NK-cell lymphoma [RCV004560283]	pathogenic	6	111714405	111714405	Human		name
405867578	CV2842335	single nucleotide variant	NM_002037.5(FYN):c.289A>G (p.Thr97Ala)	EBV-positive nodal T- and NK-cell lymphoma [RCV004560284]	pathogenic	6	111714402	111714402	Human		name
405730632	CV3257777	single nucleotide variant	NM_002037.5(FYN):c.184A>G (p.Thr62Ala)	not specified [RCV004389950]	uncertain significance	6	111719868	111719868	Human		name
407485445	CV3439451	single nucleotide variant	NM_002037.5(FYN):c.271T>C (p.Tyr91His)	not specified [RCV004618920]	uncertain significance	6	111714420	111714420	Human		name
40903964	CV918106	single nucleotide variant	NM_002037.5(FYN):c.206C>G (p.Ser69Cys)	Premature ovarian failure [RCV001270202]	uncertain significance	6	111719846	111719846	Human	2	name
8644857	CV104264	single nucleotide variant	NM_002037.5(FYN):c.944C>G (p.Ala315Gly)	not provided [RCV000084662]	not provided	6	111696375	111696375	Human		name
8644860	CV104267	single nucleotide variant	NM_002037.5(FYN):c.333A>G (p.Ile111Met)	not provided [RCV000084665]	not provided	6	111714358	111714358	Human		name
156388272	CV2231754	single nucleotide variant	NM_002037.5(FYN):c.919T>G (p.Ser307Ala)	not specified [RCV004098570]	uncertain significance	6	111696400	111696400	Human		name
156040717	CV2384379	single nucleotide variant	NM_002037.5(FYN):c.367C>T (p.Arg123Cys)	not specified [RCV004229802]	uncertain significance	6	111707998	111707998	Human		name
401734567	CV2690619	single nucleotide variant	NM_002037.5(FYN):c.699G>C (p.Glu233Asp)	not specified [RCV004304706]	uncertain significance	6	111700267	111700267	Human		name
401777944	CV2718395	single nucleotide variant	NM_002037.5(FYN):c.814C>G (p.Gln272Glu)	not specified [RCV004318221]	uncertain significance	6	111700152	111700152	Human		name
597742943	CV3676908	single nucleotide variant	NM_002037.5(FYN):c.920C>A (p.Ser307Tyr)	not specified [RCV004921966]	uncertain significance	6	111696399	111696399	Human		name
156034510	CV2256717	single nucleotide variant	NM_002037.5(FYN):c.1204C>T (p.Leu402Phe)	not specified [RCV004118889]	uncertain significance	6	111694444	111694444	Human		name
329387933	CV2468490	single nucleotide variant	NM_002037.5(FYN):c.1103T>C (p.Val368Ala)	not specified [RCV004278072]	uncertain significance	6	111694644	111694644	Human		name
405730622	CV3257776	single nucleotide variant	NM_002037.5(FYN):c.1552A>G (p.Ser518Gly)	not specified [RCV004389949]	likely benign	6	111661801	111661801	Human		name
15169143	CV710128	single nucleotide variant	NM_002037.5(FYN):c.1518C>G (p.Asp506Glu)	not provided [RCV000971753]	benign	6	111661835	111661835	Human		name

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