Apobec3f Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

37 records found for search term Apobec3f

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405662507	CV3289847	single nucleotide variant	NM_145298.5(APOBEC3F):c.196G>C	not specified [RCV004417792]	uncertain significance	22	39044965	39044965	Human		name
156396608	CV2322472	single nucleotide variant	NM_145298.6(APOBEC3F):c.7C>A (p.Pro3Thr)	not specified [RCV004180593]	uncertain significance	22	39040967	39040967	Human		name
155921029	CV2350601	single nucleotide variant	NM_145298.6(APOBEC3F):c.85C>G (p.Arg29Gly)	not specified [RCV004204946]	uncertain significance	22	39043004	39043004	Human		name
598246078	CV3999210	single nucleotide variant	NM_145298.6(APOBEC3F):c.86G>A (p.Arg29His)	not specified [RCV005383995]	uncertain significance	22	39043005	39043005	Human		name
15121324	CV717449	single nucleotide variant	NM_145298.6(APOBEC3F):c.573G>A (p.Pro191=)	not provided [RCV000962874]	benign	22	39049431	39049431	Human		name
15199754	CV773555	single nucleotide variant	NM_145298.6(APOBEC3F):c.787C>T (p.Leu263=)	not provided [RCV000935191]	likely benign	22	39052137	39052137	Human		name
155979197	CV2222821	single nucleotide variant	NM_145298.6(APOBEC3F):c.280A>G (p.Thr94Ala)	not specified [RCV004101654]	uncertain significance	22	39045049	39045049	Human		name
407480762	CV3464020	single nucleotide variant	NM_145298.6(APOBEC3F):c.175T>C (p.Tyr59His)	not specified [RCV004664460]	uncertain significance	22	39044944	39044944	Human		name
156365516	CV2193217	single nucleotide variant	NM_145298.6(APOBEC3F):c.525C>A (p.Asp175Glu)	not specified [RCV004071207]	uncertain significance	22	39045501	39045501	Human		name
155968004	CV2261947	single nucleotide variant	NM_145298.6(APOBEC3F):c.622C>T (p.Arg208Cys)	not specified [RCV004126444]	uncertain significance	22	39049480	39049480	Human		name
156285906	CV2289113	single nucleotide variant	NM_145298.6(APOBEC3F):c.298G>A (p.Val100Met)	not specified [RCV004150049]	uncertain significance	22	39045067	39045067	Human		name
156259680	CV2304985	single nucleotide variant	NM_145298.6(APOBEC3F):c.383G>A (p.Arg128Lys)	not specified [RCV004168880]	uncertain significance	22	39045152	39045152	Human		name
156054499	CV2320466	single nucleotide variant	NM_145298.6(APOBEC3F):c.444C>A (p.Asp148Glu)	not specified [RCV004172104]	uncertain significance	22	39045213	39045213	Human		name
156279688	CV2325320	single nucleotide variant	NM_145298.6(APOBEC3F):c.695C>G (p.Ser232Cys)	not specified [RCV004177706]	uncertain significance	22	39049553	39049553	Human		name
156335059	CV2333475	single nucleotide variant	NM_145298.6(APOBEC3F):c.791C>G (p.Ser264Cys)	not specified [RCV004190173]	uncertain significance	22	39052141	39052141	Human		name
155968510	CV2337851	single nucleotide variant	NM_145298.6(APOBEC3F):c.955C>T (p.Arg319Cys)	not specified [RCV004183861]	uncertain significance	22	39052305	39052305	Human		name
329376971	CV2456770	single nucleotide variant	NM_145298.6(APOBEC3F):c.883A>G (p.Ser295Gly)	not specified [RCV004270746]	uncertain significance	22	39052233	39052233	Human		name
401749688	CV2694713	single nucleotide variant	NM_145298.6(APOBEC3F):c.695C>T (p.Ser232Phe)	not specified [RCV004298803]	uncertain significance	22	39049553	39049553	Human		name
401749694	CV2694715	single nucleotide variant	NM_145298.6(APOBEC3F):c.697T>C (p.Trp233Arg)	not specified [RCV004298805]	uncertain significance	22	39049555	39049555	Human		name
401741848	CV2697642	single nucleotide variant	NM_145298.6(APOBEC3F):c.688C>G (p.Pro230Ala)	not specified [RCV004300387]	uncertain significance	22	39049546	39049546	Human		name
405662512	CV3289848	single nucleotide variant	NM_145298.6(APOBEC3F):c.545G>A (p.Arg182His)	not specified [RCV004417793]	uncertain significance	22	39045521	39045521	Human		name
405662518	CV3289850	single nucleotide variant	NM_145298.6(APOBEC3F):c.995G>C (p.Gly332Ala)	not specified [RCV004417795]	uncertain significance	22	39052345	39052345	Human		name
407480756	CV3464019	single nucleotide variant	NM_145298.6(APOBEC3F):c.536T>C (p.Phe179Ser)	not specified [RCV004664459]	uncertain significance	22	39045512	39045512	Human		name
407524481	CV3464024	single nucleotide variant	NM_145298.6(APOBEC3F):c.430G>C (p.Val144Leu)	not specified [RCV004653673]	uncertain significance	22	39045199	39045199	Human		name
597675075	CV3572028	single nucleotide variant	NM_145298.6(APOBEC3F):c.392G>A (p.Arg131Gln)	not specified [RCV004836761]	likely benign	22	39045161	39045161	Human		name
597675176	CV3572039	single nucleotide variant	NM_145298.6(APOBEC3F):c.413G>C (p.Ser138Thr)	not specified [RCV004836770]	uncertain significance	22	39045182	39045182	Human		name
597675278	CV3572049	single nucleotide variant	NM_145298.6(APOBEC3F):c.428G>A (p.Arg143His)	not specified [RCV004836780]	uncertain significance	22	39045197	39045197	Human		name
597675344	CV3572058	single nucleotide variant	NM_145298.6(APOBEC3F):c.463T>G (p.Cys155Gly)	not specified [RCV004836786]	uncertain significance	22	39045439	39045439	Human		name
597675426	CV3572067	single nucleotide variant	NM_145298.6(APOBEC3F):c.635G>T (p.Gly212Val)	not specified [RCV004836794]	uncertain significance	22	39049493	39049493	Human		name
598195101	CV3999202	single nucleotide variant	NM_145298.6(APOBEC3F):c.332C>A (p.Pro111His)	not specified [RCV005397484]	uncertain significance	22	39045101	39045101	Human		name
598246134	CV3999221	single nucleotide variant	NM_145298.6(APOBEC3F):c.584T>C (p.Met195Thr)	not specified [RCV005384003]	likely benign	22	39049442	39049442	Human		name
598246199	CV3999231	single nucleotide variant	NM_145298.6(APOBEC3F):c.923A>G (p.Tyr308Cys)	not specified [RCV005384012]	uncertain significance	22	39052273	39052273	Human		name
15123305	CV717450	single nucleotide variant	NM_145298.6(APOBEC3F):c.920A>G (p.Tyr307Cys)	not provided [RCV000963215]	benign	22	39052270	39052270	Human		name
15177876	CV742908	single nucleotide variant	NM_145298.6(APOBEC3F):c.453A>C (p.Glu151Asp)	not provided [RCV000906749]	likely benign	22	39045429	39045429	Human		name
405662505	CV3289846	single nucleotide variant	NM_145298.6(APOBEC3F):c.1045G>A (p.Glu349Lys)	not specified [RCV004417791]	uncertain significance	22	39052618	39052618	Human		name
15191481	CV705943	single nucleotide variant	NM_145298.6(APOBEC3F):c.1037A>G (p.Asn346Ser)	not provided [RCV000954789]	benign\|likely benign	22	39052610	39052610	Human		name
15129022	CV717451	single nucleotide variant	NM_145298.6(APOBEC3F):c.1117G>A (p.Glu373Lys)	not provided [RCV000964188]	likely benign	22	39052690	39052690	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message