Arfip1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

25 records found for search term Arfip1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156232202	CV2245144	single nucleotide variant	NM_001025595.3(ARFIP1):c.98T>G (p.Leu33Trp)	not specified [RCV004106929]	uncertain significance	4	152863610	152863610	Human		name
156297569	CV2297695	single nucleotide variant	NM_001025595.3(ARFIP1):c.49A>G (p.Ser17Gly)	not specified [RCV004155376]	uncertain significance	4	152829682	152829682	Human		name
156042950	CV2311013	single nucleotide variant	NM_001025595.3(ARFIP1):c.74G>A (p.Arg25His)	not specified [RCV004164034]	likely benign	4	152829707	152829707	Human		name
405674484	CV3286345	single nucleotide variant	NM_001025595.3(ARFIP1):c.53A>G (p.Asn18Ser)	not specified [RCV004420325]	uncertain significance	4	152829686	152829686	Human		name
156365158	CV2193139	single nucleotide variant	NM_001025595.3(ARFIP1):c.182T>C (p.Ile61Thr)	not specified [RCV004071139]	uncertain significance	4	152863694	152863694	Human		name
156091849	CV2216688	single nucleotide variant	NM_001025595.3(ARFIP1):c.161A>G (p.Asp54Gly)	not specified [RCV004083141]	uncertain significance	4	152863673	152863673	Human		name
405674469	CV3286341	single nucleotide variant	NM_001025595.3(ARFIP1):c.215C>T (p.Pro72Leu)	not specified [RCV004420321]	uncertain significance	4	152870765	152870765	Human		name
8631049	CV86205	single nucleotide variant	NM_001025595.2(ARFIP1):c.208C>T (p.Pro70Ser)	Malignant melanoma [RCV000066296]	not provided	4	152870758	152870758	Human		name
156061168	CV2280351	single nucleotide variant	NM_001025595.3(ARFIP1):c.446G>A (p.Arg149His)	not specified [RCV004140542]	uncertain significance	4	152880997	152880997	Human		name
156036725	CV2283088	single nucleotide variant	NM_001025595.3(ARFIP1):c.734T>C (p.Leu245Ser)	not specified [RCV004143699]	uncertain significance	4	152882823	152882823	Human		name
401742274	CV2718731	single nucleotide variant	NM_001025595.3(ARFIP1):c.365T>C (p.Met122Thr)	not specified [RCV004328487]	uncertain significance	4	152872518	152872518	Human		name
405674472	CV3286342	single nucleotide variant	NM_001025595.3(ARFIP1):c.449G>C (p.Gly150Ala)	not specified [RCV004420322]	uncertain significance	4	152881000	152881000	Human		name
405674481	CV3286344	single nucleotide variant	NM_001025595.3(ARFIP1):c.491T>C (p.Ile164Thr)	not specified [RCV004420324]	uncertain significance	4	152881042	152881042	Human		name
405674486	CV3286346	single nucleotide variant	NM_001025595.3(ARFIP1):c.930T>A (p.Asp310Glu)	not specified [RCV004420326]	uncertain significance	4	152888271	152888271	Human		name
407513665	CV3461311	single nucleotide variant	NM_001025595.3(ARFIP1):c.721A>G (p.Ser241Gly)	not specified [RCV004648905]	uncertain significance	4	152882810	152882810	Human		name
407466212	CV3461322	single nucleotide variant	NM_001025595.3(ARFIP1):c.569T>C (p.Val190Ala)	not specified [RCV004660414]	uncertain significance	4	152881120	152881120	Human		name
407466235	CV3461333	single nucleotide variant	NM_001025595.3(ARFIP1):c.794T>C (p.Ile265Thr)	not specified [RCV004660420]	uncertain significance	4	152888135	152888135	Human		name
597682982	CV3573099	single nucleotide variant	NM_001025595.3(ARFIP1):c.703A>G (p.Ile235Val)	not specified [RCV004837636]	uncertain significance	4	152882792	152882792	Human		name
597683126	CV3573116	single nucleotide variant	NM_001025595.3(ARFIP1):c.364A>G (p.Met122Val)	not specified [RCV004837652]	uncertain significance	4	152872517	152872517	Human		name
598272475	CV4006605	single nucleotide variant	NM_001025595.3(ARFIP1):c.528A>T (p.Leu176Phe)	not specified [RCV005389386]	uncertain significance	4	152881079	152881079	Human		name
156068779	CV2320494	single nucleotide variant	NM_001025595.3(ARFIP1):c.1001A>G (p.His334Arg)	not specified [RCV004172128]	uncertain significance	4	152910098	152910098	Human		name
401876149	CV2789311	single nucleotide variant	NM_001025595.3(ARFIP1):c.1050G>T (p.Gln350His)	not specified [RCV004365334]	uncertain significance	4	152910147	152910147	Human		name
405674453	CV3286338	single nucleotide variant	NM_001025595.3(ARFIP1):c.1011T>G (p.Ile337Met)	not specified [RCV004420318]	uncertain significance	4	152910108	152910108	Human		name
405674457	CV3286339	single nucleotide variant	NM_001025595.3(ARFIP1):c.1015G>T (p.Ala339Ser)	not specified [RCV004420319]	uncertain significance	4	152910112	152910112	Human		name
405674464	CV3286340	single nucleotide variant	NM_001025595.3(ARFIP1):c.1099C>A (p.Pro367Thr)	not specified [RCV004420320]	uncertain significance	4	152910196	152910196	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