Sfxn1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

27 records found for search term Sfxn1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15191850	CV735017	single nucleotide variant	NM_022754.7(SFXN1):c.141G>A (p.Ala47=)	not provided [RCV000910367]	benign	5	175492244	175492244	Human		name
401868602	CV2788278	single nucleotide variant	NM_022754.7(SFXN1):c.38A>G (p.Glu13Gly)	not specified [RCV004352868]	uncertain significance	5	175492141	175492141	Human		name
597672724	CV3595659	single nucleotide variant	NM_022754.7(SFXN1):c.29A>G (p.Asn10Ser)	not specified [RCV004856599]	uncertain significance	5	175492132	175492132	Human		name
598166651	CV3921186	single nucleotide variant	NM_022754.7(SFXN1):c.666G>A (p.Ala222=)	not specified [RCV005283701]	likely benign	5	175513532	175513532	Human		name
15133688	CV709833	single nucleotide variant	NM_022754.7(SFXN1):c.77A>G (p.Asn26Ser)	not provided [RCV000964996]	benign	5	175492180	175492180	Human		name
329362224	CV2448436	single nucleotide variant	NM_022754.7(SFXN1):c.229T>G (p.Ser77Ala)	not specified [RCV004256718]	uncertain significance	5	175509096	175509096	Human		name
405764253	CV3321559	single nucleotide variant	NM_022754.7(SFXN1):c.224A>G (p.Tyr75Cys)	not specified [RCV004455851]	uncertain significance	5	175509091	175509091	Human		name
405764259	CV3321560	single nucleotide variant	NM_022754.7(SFXN1):c.240T>A (p.His80Gln)	not specified [RCV004455852]	uncertain significance	5	175509107	175509107	Human		name
405764266	CV3321561	single nucleotide variant	NM_022754.7(SFXN1):c.242C>T (p.Pro81Leu)	not specified [RCV004455853]	uncertain significance	5	175509109	175509109	Human		name
407489991	CV3484051	single nucleotide variant	NM_022754.7(SFXN1):c.211G>C (p.Ala71Pro)	not specified [RCV004666204]	uncertain significance	5	175509078	175509078	Human		name
597672717	CV3595658	single nucleotide variant	NM_022754.7(SFXN1):c.181C>G (p.Pro61Ala)	not specified [RCV004856598]	uncertain significance	5	175509048	175509048	Human		name
598198564	CV3921185	single nucleotide variant	NM_022754.7(SFXN1):c.212C>T (p.Ala71Val)	not specified [RCV005268266]	uncertain significance	5	175509079	175509079	Human		name
8631555	CV86759	single nucleotide variant	NM_022754.5(SFXN1):c.124G>A (p.Glu42Lys)	Malignant melanoma [RCV000066850]	not provided	5	175492227	175492227	Human		name
156233332	CV2197111	single nucleotide variant	NM_022754.7(SFXN1):c.475G>A (p.Val159Ile)	not specified [RCV004071543]	uncertain significance	5	175511491	175511491	Human		name
156252636	CV2212464	single nucleotide variant	NM_022754.7(SFXN1):c.587T>C (p.Met196Thr)	not specified [RCV004091362]	uncertain significance	5	175512187	175512187	Human		name
156241061	CV2246064	single nucleotide variant	NM_022754.7(SFXN1):c.565A>C (p.Asn189His)	not specified [RCV004113975]	uncertain significance	5	175512165	175512165	Human		name
156289360	CV2299338	single nucleotide variant	NM_022754.7(SFXN1):c.472G>A (p.Ala158Thr)	not specified [RCV004152651]	uncertain significance	5	175511488	175511488	Human		name
156152120	CV2318866	single nucleotide variant	NM_022754.7(SFXN1):c.364T>C (p.Trp122Arg)	not specified [RCV004175771]	uncertain significance	5	175510137	175510137	Human		name
156256834	CV2322021	single nucleotide variant	NM_022754.7(SFXN1):c.829G>A (p.Val277Met)	not specified [RCV004173774]	uncertain significance	5	175522379	175522379	Human		name
156326109	CV2335414	single nucleotide variant	NM_022754.7(SFXN1):c.898G>A (p.Ala300Thr)	not specified [RCV004186966]	uncertain significance	5	175526663	175526663	Human		name
329366026	CV2438015	single nucleotide variant	NM_022754.7(SFXN1):c.653C>T (p.Ser218Leu)	not specified [RCV004263722]	uncertain significance	5	175513519	175513519	Human		name
401762449	CV2696130	single nucleotide variant	NM_022754.7(SFXN1):c.764C>T (p.Ala255Val)	not specified [RCV004310190]	uncertain significance	5	175516653	175516653	Human		name
401768095	CV2727380	single nucleotide variant	NM_022754.7(SFXN1):c.578T>C (p.Ile193Thr)	not specified [RCV004327479]	uncertain significance	5	175512178	175512178	Human		name
401890299	CV2768064	single nucleotide variant	NM_022754.7(SFXN1):c.656C>T (p.Ala219Val)	not specified [RCV004348300]	uncertain significance	5	175513522	175513522	Human		name
401895810	CV2772126	single nucleotide variant	NM_022754.7(SFXN1):c.415G>C (p.Asp139His)	not specified [RCV004344777]	uncertain significance	5	175510188	175510188	Human		name
405764273	CV3321562	single nucleotide variant	NM_022754.7(SFXN1):c.692T>C (p.Val231Ala)	not specified [RCV004455854]	uncertain significance	5	175513558	175513558	Human		name
597672732	CV3595660	single nucleotide variant	NM_022754.7(SFXN1):c.713C>G (p.Ala238Gly)	not specified [RCV004856600]	uncertain significance	5	175513579	175513579	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