Ficd Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

55 records found for search term Ficd

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
616938127	CV4015779	variation	FICD, ARG374HIS	Spastic paraplegia 92, autosomal recessive [RCV005414311]	pathogenic				Human		name
155945935	CV2301424	single nucleotide variant	NM_007076.3(FICD):c.14C>T (p.Pro5Leu)	not specified [RCV004162359]	uncertain significance	12	108516986	108516986	Human		name
616938128	CV4015780	deletion	FICD, 2-BP DEL, 1109GG (rs1191700402)	Spastic paraplegia 92, autosomal recessive [RCV005414312]	pathogenic				Human	1	name
405779273	CV3250638	single nucleotide variant	NM_007076.3(FICD):c.66C>G (p.Ser22Arg)	not specified [RCV004386511]	uncertain significance	12	108517038	108517038	Human		name
405779279	CV3250639	single nucleotide variant	NM_007076.3(FICD):c.68G>A (p.Arg23His)	not specified [RCV004386512]	uncertain significance	12	108517040	108517040	Human		name
405779284	CV3250640	single nucleotide variant	NM_007076.3(FICD):c.83C>T (p.Thr28Met)	not specified [RCV004386513]	likely benign	12	108517055	108517055	Human		name
597753235	CV3669567	single nucleotide variant	NM_007076.3(FICD):c.67C>T (p.Arg23Cys)	not specified [RCV004924085]	uncertain significance	12	108517039	108517039	Human		name
155907363	CV2302199	single nucleotide variant	NM_007076.3(FICD):c.106T>G (p.Ser36Ala)	not specified [RCV004159199]	uncertain significance	12	108517078	108517078	Human		name
329356525	CV2460384	single nucleotide variant	NM_007076.3(FICD):c.188G>A (p.Ser63Asn)	not specified [RCV004268699]	uncertain significance	12	108517160	108517160	Human		name
598200076	CV3955774	single nucleotide variant	NM_007076.3(FICD):c.265G>A (p.Ala89Thr)	not specified [RCV005336599]	uncertain significance	12	108517237	108517237	Human		name
598200089	CV3955776	single nucleotide variant	NM_007076.3(FICD):c.169G>A (p.Gly57Ser)	not specified [RCV005336601]	uncertain significance	12	108517141	108517141	Human		name
15139115	CV713309	single nucleotide variant	NM_007076.3(FICD):c.1152G>A (p.Ala384=)	not provided [RCV000965910]	benign	12	108519250	108519250	Human		name
155916674	CV2197548	single nucleotide variant	NM_007076.3(FICD):c.839C>G (p.Ser280Trp)	not specified [RCV004081269]	uncertain significance	12	108518937	108518937	Human		name
156026902	CV2199222	single nucleotide variant	NM_007076.3(FICD):c.571G>A (p.Asp191Asn)	not specified [RCV004082585]	uncertain significance	12	108518669	108518669	Human		name
156141448	CV2199932	single nucleotide variant	NM_007076.3(FICD):c.839C>T (p.Ser280Leu)	not specified [RCV004074108]	uncertain significance	12	108518937	108518937	Human		name
156177426	CV2220408	single nucleotide variant	NM_007076.3(FICD):c.746C>A (p.Thr249Asn)	not specified [RCV004095813]	uncertain significance	12	108518844	108518844	Human		name
156026722	CV2242383	single nucleotide variant	NM_007076.3(FICD):c.901G>A (p.Val301Met)	not specified [RCV004111385]	uncertain significance	12	108518999	108518999	Human		name
156163364	CV2305494	single nucleotide variant	NM_007076.3(FICD):c.449C>G (p.Ser150Trp)	not specified [RCV004165205]	uncertain significance	12	108518547	108518547	Human		name
156041232	CV2310874	single nucleotide variant	NM_007076.3(FICD):c.418G>A (p.Val140Met)	not specified [RCV004163915]	uncertain significance	12	108518516	108518516	Human		name
156348234	CV2312686	single nucleotide variant	NM_007076.3(FICD):c.668A>G (p.Tyr223Cys)	not specified [RCV004169415]	uncertain significance	12	108518766	108518766	Human		name
156363014	CV2330482	single nucleotide variant	NM_007076.3(FICD):c.754G>A (p.Ala252Thr)	not specified [RCV004181049]	uncertain significance	12	108518852	108518852	Human		name
155979374	CV2340043	single nucleotide variant	NM_007076.3(FICD):c.929G>A (p.Arg310Gln)	not specified [RCV004192289]	uncertain significance	12	108519027	108519027	Human		name
329375512	CV2440968	single nucleotide variant	NM_007076.3(FICD):c.865G>A (p.Asp289Asn)	not specified [RCV004261350]	uncertain significance	12	108518963	108518963	Human		name
401780047	CV2676794	single nucleotide variant	NM_007076.3(FICD):c.760C>A (p.Pro254Thr)	not specified [RCV004290964]	uncertain significance	12	108518858	108518858	Human		name
401771152	CV2679095	single nucleotide variant	NM_007076.3(FICD):c.424G>A (p.Ala142Thr)	not specified [RCV004295088]	uncertain significance	12	108518522	108518522	Human		name
401740273	CV2684314	single nucleotide variant	NM_007076.3(FICD):c.319A>G (p.Arg107Gly)	not specified [RCV004288966]	uncertain significance	12	108518417	108518417	Human		name
401723834	CV2684883	single nucleotide variant	NM_007076.3(FICD):c.449C>T (p.Ser150Leu)	not specified [RCV004296388]	uncertain significance	12	108518547	108518547	Human		name
401780644	CV2685590	single nucleotide variant	NM_007076.3(FICD):c.425C>T (p.Ala142Val)	not specified [RCV004294601]	uncertain significance	12	108518523	108518523	Human		name
401736554	CV2689372	single nucleotide variant	NM_007076.3(FICD):c.430A>G (p.Thr144Ala)	not specified [RCV004306192]	uncertain significance	12	108518528	108518528	Human		name
401753594	CV2722521	single nucleotide variant	NM_007076.3(FICD):c.680T>C (p.Ile227Thr)	not specified [RCV004322906]	uncertain significance	12	108518778	108518778	Human		name
401892318	CV2777418	single nucleotide variant	NM_007076.3(FICD):c.857C>T (p.Thr286Ile)	not specified [RCV004356201]	uncertain significance	12	108518955	108518955	Human		name
405779263	CV3250636	single nucleotide variant	NM_007076.3(FICD):c.476C>T (p.Ala159Val)	not specified [RCV004386509]	uncertain significance	12	108518574	108518574	Human		name
405779267	CV3250637	single nucleotide variant	NM_007076.3(FICD):c.514T>C (p.Tyr172His)	not specified [RCV004386510]	uncertain significance	12	108518612	108518612	Human		name
405779288	CV3250641	single nucleotide variant	NM_007076.3(FICD):c.841C>T (p.Arg281Cys)	not specified [RCV004386514]	uncertain significance	12	108518939	108518939	Human		name
407502627	CV3435862	single nucleotide variant	NM_007076.3(FICD):c.344A>T (p.Glu115Val)	not specified [RCV004623506]	uncertain significance	12	108518442	108518442	Human		name
407502630	CV3435863	single nucleotide variant	NM_007076.3(FICD):c.768G>T (p.Lys256Asn)	not specified [RCV004623507]	uncertain significance	12	108518866	108518866	Human		name
597753226	CV3669565	single nucleotide variant	NM_007076.3(FICD):c.946G>A (p.Val316Ile)	not specified [RCV004924083]	uncertain significance	12	108519044	108519044	Human		name
597753231	CV3669566	single nucleotide variant	NM_007076.3(FICD):c.757G>A (p.Val253Met)	not specified [RCV004924084]	uncertain significance	12	108518855	108518855	Human		name
597753240	CV3669568	single nucleotide variant	NM_007076.3(FICD):c.410C>T (p.Pro137Leu)	not specified [RCV004924086]	uncertain significance	12	108518508	108518508	Human		name
597753254	CV3669572	single nucleotide variant	NM_007076.3(FICD):c.386T>C (p.Phe129Ser)	not specified [RCV004924089]	uncertain significance	12	108518484	108518484	Human		name
597753259	CV3669573	single nucleotide variant	NM_007076.3(FICD):c.347T>C (p.Met116Thr)	not specified [RCV004924090]	uncertain significance	12	108518445	108518445	Human		name
597753264	CV3669574	single nucleotide variant	NM_007076.3(FICD):c.847G>A (p.Gly283Ser)	not specified [RCV004924091]	uncertain significance	12	108518945	108518945	Human		name
597753269	CV3669575	single nucleotide variant	NM_007076.3(FICD):c.548C>G (p.Thr183Arg)	not specified [RCV004924092]	uncertain significance	12	108518646	108518646	Human		name
598200068	CV3955773	single nucleotide variant	NM_007076.3(FICD):c.506T>C (p.Ile169Thr)	not specified [RCV005336598]	uncertain significance	12	108518604	108518604	Human		name
598200096	CV3955777	single nucleotide variant	NM_007076.3(FICD):c.495A>T (p.Arg165Ser)	not specified [RCV005336602]	uncertain significance	12	108518593	108518593	Human		name
598200104	CV3955778	single nucleotide variant	NM_007076.3(FICD):c.926T>C (p.Phe309Ser)	not specified [RCV005336603]	uncertain significance	12	108519024	108519024	Human		name
15182415	CV713308	single nucleotide variant	NM_007076.3(FICD):c.524A>C (p.Lys175Thr)	not provided [RCV000974626]	benign	12	108518622	108518622	Human		name
156152845	CV2209398	single nucleotide variant	NM_007076.3(FICD):c.1330C>G (p.Gln444Glu)	not specified [RCV004093563]	uncertain significance	12	108519428	108519428	Human		name
156129377	CV2279672	single nucleotide variant	NM_007076.3(FICD):c.1198T>C (p.Tyr400His)	not specified [RCV004144296]	uncertain significance	12	108519296	108519296	Human		name
156209088	CV2298176	single nucleotide variant	NM_007076.3(FICD):c.1304A>C (p.Glu435Ala)	not specified [RCV004159834]	uncertain significance	12	108519402	108519402	Human		name
156190573	CV2391126	single nucleotide variant	NM_007076.3(FICD):c.1174C>T (p.Arg392Cys)	not specified [RCV004235105]	uncertain significance	12	108519272	108519272	Human		name
401891161	CV2778677	single nucleotide variant	NM_007076.3(FICD):c.1238C>T (p.Pro413Leu)	not specified [RCV004346315]	uncertain significance	12	108519336	108519336	Human		name
597753251	CV3669571	single nucleotide variant	NM_007076.3(FICD):c.1120C>A (p.Arg374Ser)	not specified [RCV004924088]	uncertain significance	12	108519218	108519218	Human		name
597753274	CV3669576	single nucleotide variant	NM_007076.3(FICD):c.1282A>C (p.Thr428Pro)	not specified [RCV004924093]	uncertain significance	12	108519380	108519380	Human		name
598200083	CV3955775	single nucleotide variant	NM_007076.3(FICD):c.1363C>G (p.Pro455Ala)	not specified [RCV005336600]	uncertain significance	12	108519461	108519461	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