Dtx4 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

56 records found for search term Dtx4

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156266359	CV2312332	single nucleotide variant	NM_015177.2(DTX4):c.43G>A (p.Glu15Lys)	not specified [RCV004167038]	uncertain significance	11	59172638	59172638	Human		name
156068987	CV2381208	single nucleotide variant	NM_015177.2(DTX4):c.68G>A (p.Ser23Asn)	not specified [RCV004227278]	uncertain significance	11	59172663	59172663	Human		name
15162197	CV712895	single nucleotide variant	NM_015177.2(DTX4):c.852C>T (p.Thr284=)	not provided [RCV000970228]	benign	11	59182379	59182379	Human		name
155924442	CV2220320	single nucleotide variant	NM_015177.2(DTX4):c.238T>C (p.Tyr80His)	not specified [RCV004095742]	uncertain significance	11	59181765	59181765	Human		name
401730487	CV2711347	single nucleotide variant	NM_015177.2(DTX4):c.295A>C (p.Asn99His)	not specified [RCV004313110]	uncertain significance	11	59181822	59181822	Human		name
401897172	CV2793373	single nucleotide variant	NM_015177.2(DTX4):c.208A>T (p.Thr70Ser)	not specified [RCV004362179]	uncertain significance	11	59172803	59172803	Human		name
405733608	CV3244986	single nucleotide variant	NM_015177.2(DTX4):c.100G>A (p.Val34Ile)	not specified [RCV004379529]	uncertain significance	11	59172695	59172695	Human		name
405733625	CV3244988	single nucleotide variant	NM_015177.2(DTX4):c.154C>G (p.Arg52Gly)	not specified [RCV004379531]	uncertain significance	11	59172749	59172749	Human		name
405733641	CV3244990	single nucleotide variant	NM_015177.2(DTX4):c.209C>G (p.Thr70Arg)	not specified [RCV004379533]	uncertain significance	11	59172804	59172804	Human		name
405733648	CV3244991	single nucleotide variant	NM_015177.2(DTX4):c.233G>C (p.Arg78Pro)	not specified [RCV004379534]	uncertain significance	11	59181760	59181760	Human		name
405733656	CV3244992	single nucleotide variant	NM_015177.2(DTX4):c.254C>T (p.Ser85Leu)	not specified [RCV004379535]	uncertain significance	11	59181781	59181781	Human		name
407490079	CV3431033	single nucleotide variant	NM_015177.2(DTX4):c.113C>T (p.Pro38Leu)	not specified [RCV004620077]	uncertain significance	11	59172708	59172708	Human		name
597683485	CV3673900	single nucleotide variant	NM_015177.2(DTX4):c.206A>T (p.Asp69Val)	not specified [RCV004914587]	uncertain significance	11	59172801	59172801	Human		name
597683514	CV3673904	single nucleotide variant	NM_015177.2(DTX4):c.221G>A (p.Arg74His)	not specified [RCV004914590]	uncertain significance	11	59181748	59181748	Human		name
15196028	CV724501	single nucleotide variant	NM_015177.2(DTX4):c.1026G>A (p.Ala342=)	not provided [RCV000889667]	benign	11	59189190	59189190	Human		name
15180908	CV724502	single nucleotide variant	NM_015177.2(DTX4):c.1065C>T (p.Val355=)	not provided [RCV000885641]	benign	11	59189229	59189229	Human		name
153001865	CV1682718	single nucleotide variant	NM_015177.2(DTX4):c.974G>A (p.Ser325Asn)	not provided [RCV002251797]	uncertain significance	11	59188773	59188773	Human		name
156066317	CV2193317	single nucleotide variant	NM_015177.2(DTX4):c.464G>A (p.Arg155Gln)	not specified [RCV004072823]	uncertain significance	11	59181991	59181991	Human		name
155912194	CV2235534	single nucleotide variant	NM_015177.2(DTX4):c.862G>C (p.Ala288Pro)	not specified [RCV004109568]	uncertain significance	11	59182389	59182389	Human		name
156154335	CV2266067	single nucleotide variant	NM_015177.2(DTX4):c.454C>T (p.Arg152Cys)	not specified [RCV004126880]	uncertain significance	11	59181981	59181981	Human		name
156351148	CV2316354	single nucleotide variant	NM_015177.2(DTX4):c.302C>G (p.Ser101Cys)	not specified [RCV004174363]	uncertain significance	11	59181829	59181829	Human		name
156048694	CV2382702	single nucleotide variant	NM_015177.2(DTX4):c.594G>A (p.Met198Ile)	not specified [RCV004233012]	uncertain significance	11	59182121	59182121	Human		name
329369286	CV2450593	single nucleotide variant	NM_015177.2(DTX4):c.697C>T (p.Pro233Ser)	not specified [RCV004265491]	uncertain significance	11	59182224	59182224	Human		name
401759988	CV2698699	single nucleotide variant	NM_015177.2(DTX4):c.511G>A (p.Ala171Thr)	not specified [RCV004301161]	uncertain significance	11	59182038	59182038	Human		name
401752756	CV2707115	single nucleotide variant	NM_015177.2(DTX4):c.580T>C (p.Cys194Arg)	not specified [RCV004321695]	uncertain significance	11	59182107	59182107	Human		name
401773500	CV2709342	single nucleotide variant	NM_015177.2(DTX4):c.887A>C (p.Asn296Thr)	not specified [RCV004316487]	uncertain significance	11	59182414	59182414	Human		name
401857272	CV2758964	single nucleotide variant	NM_015177.2(DTX4):c.463C>T (p.Arg155Trp)	not specified [RCV004342279]	uncertain significance	11	59181990	59181990	Human		name
405733661	CV3244993	single nucleotide variant	NM_015177.2(DTX4):c.308C>T (p.Thr103Met)	not specified [RCV004379536]	uncertain significance	11	59181835	59181835	Human		name
405733668	CV3244994	single nucleotide variant	NM_015177.2(DTX4):c.434G>A (p.Arg145His)	not specified [RCV004379537]	uncertain significance	11	59181961	59181961	Human		name
405733686	CV3244996	single nucleotide variant	NM_015177.2(DTX4):c.478A>G (p.Ile160Val)	not specified [RCV004379539]	uncertain significance	11	59182005	59182005	Human		name
405733695	CV3244997	single nucleotide variant	NM_015177.2(DTX4):c.719T>C (p.Leu240Pro)	not specified [RCV004379540]	uncertain significance	11	59182246	59182246	Human		name
405733704	CV3244998	single nucleotide variant	NM_015177.2(DTX4):c.853G>A (p.Gly285Arg)	not specified [RCV004379541]	uncertain significance	11	59182380	59182380	Human		name
407490090	CV3431035	single nucleotide variant	NM_015177.2(DTX4):c.460C>T (p.Arg154Cys)	not specified [RCV004620079]	uncertain significance	11	59181987	59181987	Human		name
597683474	CV3673899	single nucleotide variant	NM_015177.2(DTX4):c.550C>A (p.Pro184Thr)	not specified [RCV004914586]	uncertain significance	11	59182077	59182077	Human		name
597683533	CV3673906	single nucleotide variant	NM_015177.2(DTX4):c.533C>T (p.Pro178Leu)	not specified [RCV004914592]	uncertain significance	11	59182060	59182060	Human		name
598189878	CV3957426	single nucleotide variant	NM_015177.2(DTX4):c.652C>T (p.Arg218Cys)	not specified [RCV005334613]	uncertain significance	11	59182179	59182179	Human		name
598189896	CV3957428	single nucleotide variant	NM_015177.2(DTX4):c.617A>C (p.Asn206Thr)	not specified [RCV005334615]	uncertain significance	11	59182144	59182144	Human		name
598266834	CV3957433	single nucleotide variant	NM_015177.2(DTX4):c.314A>G (p.Tyr105Cys)	not specified [RCV005326731]	uncertain significance	11	59181841	59181841	Human		name
15196024	CV724500	single nucleotide variant	NM_015177.2(DTX4):c.770T>G (p.Val257Gly)	not provided [RCV000889666]	benign	11	59182297	59182297	Human		name
156340804	CV2225689	single nucleotide variant	NM_015177.2(DTX4):c.1699G>A (p.Glu567Lys)	not specified [RCV004103112]	uncertain significance	11	59204748	59204748	Human		name
155960589	CV2285417	single nucleotide variant	NM_015177.2(DTX4):c.1657C>T (p.Arg553Cys)	not specified [RCV004139276]	uncertain significance	11	59204706	59204706	Human		name
156258576	CV2366115	single nucleotide variant	NM_015177.2(DTX4):c.1573G>A (p.Ala525Thr)	not specified [RCV004210150]	uncertain significance	11	59199720	59199720	Human		name
329374201	CV2463431	single nucleotide variant	NM_015177.2(DTX4):c.1057A>C (p.Lys353Gln)	not specified [RCV004277265]	uncertain significance	11	59189221	59189221	Human		name
401886450	CV2771285	single nucleotide variant	NM_015177.2(DTX4):c.1838G>A (p.Ser613Asn)	not specified [RCV004346259]	uncertain significance	11	59204887	59204887	Human		name
401864761	CV2791348	single nucleotide variant	NM_015177.2(DTX4):c.1174G>C (p.Glu392Gln)	not specified [RCV004358757]	uncertain significance	11	59191128	59191128	Human		name
405733616	CV3244987	single nucleotide variant	NM_015177.2(DTX4):c.1458C>A (p.His486Gln)	not specified [RCV004379530]	uncertain significance	11	59195291	59195291	Human		name
405733632	CV3244989	single nucleotide variant	NM_015177.2(DTX4):c.1711G>A (p.Val571Ile)	not specified [RCV004379532]	uncertain significance	11	59204760	59204760	Human		name
407490085	CV3431034	single nucleotide variant	NM_015177.2(DTX4):c.1472C>A (p.Ser491Tyr)	not specified [RCV004620078]	uncertain significance	11	59195305	59195305	Human		name
597683464	CV3673898	single nucleotide variant	NM_015177.2(DTX4):c.1130G>A (p.Arg377His)	not specified [RCV004914585]	uncertain significance	11	59189294	59189294	Human		name
597683495	CV3673901	single nucleotide variant	NM_015177.2(DTX4):c.1336A>C (p.Ile446Leu)	not specified [RCV004914588]	uncertain significance	11	59192212	59192212	Human		name
597735108	CV3673902	single nucleotide variant	NM_015177.2(DTX4):c.1789C>G (p.Leu597Val)	not specified [RCV004920405]	uncertain significance	11	59204838	59204838	Human		name
597683525	CV3673905	single nucleotide variant	NM_015177.2(DTX4):c.1097T>C (p.Ile366Thr)	not specified [RCV004914591]	uncertain significance	11	59189261	59189261	Human		name
598189888	CV3957427	single nucleotide variant	NM_015177.2(DTX4):c.1486C>A (p.Pro496Thr)	not specified [RCV005334614]	uncertain significance	11	59195319	59195319	Human		name
598189902	CV3957429	single nucleotide variant	NM_015177.2(DTX4):c.1436C>T (p.Pro479Leu)	not specified [RCV005334616]	uncertain significance	11	59195269	59195269	Human		name
598189917	CV3957431	single nucleotide variant	NM_015177.2(DTX4):c.1807G>C (p.Glu603Gln)	not specified [RCV005334618]	uncertain significance	11	59204856	59204856	Human		name
598189925	CV3957432	single nucleotide variant	NM_015177.2(DTX4):c.1220A>G (p.Glu407Gly)	not specified [RCV005334619]	uncertain significance	11	59191174	59191174	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