Sf3a1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

32 records found for search term Sf3a1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15203051	CV778479	single nucleotide variant	NM_005877.6(SF3A1):c.651+8G>C	not provided [RCV000958190]	benign	22	30344925	30344925	Human		name
156390732	CV2383362	single nucleotide variant	NM_005877.6(SF3A1):c.29C>T (p.Pro10Leu)	not specified [RCV004222394]	uncertain significance	22	30356764	30356764	Human		name
405763257	CV3321391	single nucleotide variant	NM_005877.6(SF3A1):c.38C>T (p.Pro13Leu)	not specified [RCV004455683]	uncertain significance	22	30356755	30356755	Human		name
405763269	CV3321393	single nucleotide variant	NM_005877.6(SF3A1):c.77A>C (p.Glu26Ala)	not specified [RCV004455685]	uncertain significance	22	30353059	30353059	Human		name
407450786	CV3483980	single nucleotide variant	NM_005877.6(SF3A1):c.50C>T (p.Thr17Met)	not specified [RCV004666154]	uncertain significance	22	30356743	30356743	Human		name
156087188	CV2299103	single nucleotide variant	NM_005877.6(SF3A1):c.287A>G (p.His96Arg)	not specified [RCV004152461]	uncertain significance	22	30346418	30346418	Human		name
401912500	CV2822119	single nucleotide variant	NM_005877.6(SF3A1):c.226A>T (p.Ile76Phe)	not provided [RCV003427219]	uncertain significance	22	30346479	30346479	Human		name
597672009	CV3595501	single nucleotide variant	NM_005877.6(SF3A1):c.255C>A (p.Asn85Lys)	not specified [RCV004856478]	uncertain significance	22	30346450	30346450	Human		name
155972332	CV2238774	single nucleotide variant	NM_005877.6(SF3A1):c.670G>T (p.Gly224Cys)	not specified [RCV004109698]	uncertain significance	22	30342861	30342861	Human		name
156172772	CV2286970	single nucleotide variant	NM_005877.6(SF3A1):c.688A>C (p.Lys230Gln)	not specified [RCV004144571]	uncertain significance	22	30342843	30342843	Human		name
329398710	CV2471296	single nucleotide variant	NM_005877.6(SF3A1):c.575A>G (p.Asn192Ser)	not specified [RCV004280315]	uncertain significance	22	30345009	30345009	Human		name
401870798	CV2792415	single nucleotide variant	NM_005877.6(SF3A1):c.869A>G (p.Asn290Ser)	not specified [RCV004363168]	uncertain significance	22	30342208	30342208	Human		name
401940549	CV2839414	deletion	NM_005877.6(SF3A1):c.1641del (p.Ser548fs)	Malignant lymphoma, large B-cell, diffuse [RCV003449009]	pathogenic	22	30338891	30338891	Human	1	name
405763263	CV3321392	single nucleotide variant	NM_005877.6(SF3A1):c.686T>C (p.Leu229Pro)	not specified [RCV004455684]	uncertain significance	22	30342845	30342845	Human		name
405763280	CV3321395	single nucleotide variant	NM_005877.6(SF3A1):c.876A>C (p.Gln292His)	not specified [RCV004455687]	uncertain significance	22	30342201	30342201	Human		name
407490091	CV3483976	single nucleotide variant	NM_005877.6(SF3A1):c.791A>G (p.Lys264Arg)	not specified [RCV004666150]	uncertain significance	22	30342286	30342286	Human		name
597672002	CV3595500	single nucleotide variant	NM_005877.6(SF3A1):c.654C>G (p.Ile218Met)	not specified [RCV004856477]	uncertain significance	22	30342877	30342877	Human		name
597672025	CV3595503	single nucleotide variant	NM_005877.6(SF3A1):c.714A>T (p.Glu238Asp)	not specified [RCV004856480]	uncertain significance	22	30342817	30342817	Human		name
155991042	CV2384115	single nucleotide variant	NM_005877.6(SF3A1):c.1652A>G (p.Asn551Ser)	not specified [RCV004227520]	uncertain significance	22	30338880	30338880	Human		name
329397717	CV2463946	single nucleotide variant	NM_005877.6(SF3A1):c.1703G>A (p.Ser568Asn)	not specified [RCV004280009]	uncertain significance	22	30338829	30338829	Human		name
401773616	CV2695304	single nucleotide variant	NM_005877.6(SF3A1):c.1634T>G (p.Ile545Ser)	not specified [RCV004303428]	uncertain significance	22	30338898	30338898	Human		name
401888372	CV2788403	single nucleotide variant	NM_005877.6(SF3A1):c.1783C>T (p.Pro595Ser)	not specified [RCV004354937]	uncertain significance	22	30337858	30337858	Human		name
405763237	CV3321388	single nucleotide variant	NM_005877.6(SF3A1):c.1673C>T (p.Pro558Leu)	not specified [RCV004455680]	uncertain significance	22	30338859	30338859	Human		name
405763246	CV3321389	single nucleotide variant	NM_005877.6(SF3A1):c.1891A>G (p.Met631Val)	not specified [RCV004455681]	uncertain significance	22	30337750	30337750	Human		name
405763251	CV3321390	single nucleotide variant	NM_005877.6(SF3A1):c.1936A>G (p.Met646Val)	not specified [RCV004455682]	uncertain significance	22	30337705	30337705	Human		name
407490087	CV3483977	single nucleotide variant	NM_005877.6(SF3A1):c.1349A>G (p.Gln450Arg)	not specified [RCV004666151]	uncertain significance	22	30340222	30340222	Human		name
597671996	CV3595499	single nucleotide variant	NM_005877.6(SF3A1):c.2020C>G (p.Pro674Ala)	not specified [RCV004856476]	uncertain significance	22	30337112	30337112	Human		name
597672017	CV3595502	single nucleotide variant	NM_005877.6(SF3A1):c.2024C>A (p.Pro675His)	not specified [RCV004856479]	uncertain significance	22	30337108	30337108	Human		name
597672033	CV3595504	single nucleotide variant	NM_005877.6(SF3A1):c.1414C>T (p.Arg472Trp)	not specified [RCV004856481]	uncertain significance	22	30339213	30339213	Human		name
598198008	CV3900756	single nucleotide variant	NM_005877.6(SF3A1):c.1210G>A (p.Ala404Thr)	not specified [RCV005268192]	uncertain significance	22	30340361	30340361	Human		name
598198018	CV3900757	single nucleotide variant	NM_005877.6(SF3A1):c.1150C>T (p.Pro384Ser)	not specified [RCV005268193]	uncertain significance	22	30340734	30340734	Human		name
8637613	CV92839	single nucleotide variant	NM_005877.5(SF3A1):c.1759C>T (p.Arg587Cys)	Malignant melanoma [RCV000072937]	not provided	22	30337882	30337882	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