Arfip1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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25 records found for search term Arfip1

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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

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