Gdpd4 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

54 records found for search term Gdpd4

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401905480	CV2813568	single nucleotide variant	NM_182833.3(GDPD4):c.*274A>G	not provided [RCV003395931]	likely benign	11	77217003	77217003	Human		name
405786156	CV3258146	single nucleotide variant	NM_182833.3(GDPD4):c.19A>C (p.Ile7Leu)	not specified [RCV004387649]	uncertain significance	11	77285119	77285119	Human		name
401762998	CV2710402	single nucleotide variant	NM_182833.3(GDPD4):c.71C>G (p.Thr24Arg)	not specified [RCV004317561]	uncertain significance	11	77279382	77279382	Human		name
598219394	CV3970610	single nucleotide variant	NM_182833.3(GDPD4):c.625T>C (p.Leu209=)	not specified [RCV005340288]	likely benign	11	77268539	77268539	Human		name
8627128	CV82272	single nucleotide variant	NM_182833.1(GDPD4):c.354C>T (p.Ile118=)	Malignant melanoma [RCV000062351]	not provided	11	77271176	77271176	Human		name
401888820	CV2764754	single nucleotide variant	NM_182833.3(GDPD4):c.271A>G (p.Lys91Glu)	not specified [RCV004334863]	uncertain significance	11	77271330	77271330	Human		name
405786150	CV3258147	single nucleotide variant	NM_182833.3(GDPD4):c.247A>G (p.Met83Val)	not specified [RCV004387650]	uncertain significance	11	77271354	77271354	Human		name
8634385	CV89605	single nucleotide variant	NM_182833.1(GDPD4):c.1419C>T (p.Leu473=)	Malignant melanoma [RCV000069702]	not provided	11	77229203	77229203	Human		name
150467261	CV1269201	duplication	NM_182833.3(GDPD4):c.1191dup (p.Ile398fs)	not provided [RCV001694609]	benign	11	77243743	77243744	Human		name
156074300	CV2294745	single nucleotide variant	NM_182833.3(GDPD4):c.764T>G (p.Ile255Ser)	not specified [RCV004161982]	uncertain significance	11	77258486	77258486	Human		name
155967836	CV2329969	single nucleotide variant	NM_182833.3(GDPD4):c.743A>G (p.Asp248Gly)	not specified [RCV004183421]	uncertain significance	11	77258507	77258507	Human		name
329354561	CV2448413	single nucleotide variant	NM_182833.3(GDPD4):c.470G>A (p.Arg157Lys)	not specified [RCV004256697]	likely benign	11	77269891	77269891	Human		name
401736205	CV2689284	single nucleotide variant	NM_182833.3(GDPD4):c.778C>T (p.Pro260Ser)	not specified [RCV004306121]	uncertain significance	11	77258472	77258472	Human		name
401735031	CV2706636	single nucleotide variant	NM_182833.3(GDPD4):c.487G>A (p.Val163Met)	not specified [RCV004319214]	uncertain significance	11	77269061	77269061	Human		name
401871436	CV2783503	single nucleotide variant	NM_182833.3(GDPD4):c.988T>A (p.Phe330Ile)	not specified [RCV004365837]	uncertain significance	11	77245379	77245379	Human		name
405786144	CV3258148	single nucleotide variant	NM_182833.3(GDPD4):c.557C>T (p.Pro186Leu)	not specified [RCV004387651]	uncertain significance	11	77268991	77268991	Human		name
405786139	CV3258149	single nucleotide variant	NM_182833.3(GDPD4):c.667G>A (p.Glu223Lys)	not specified [RCV004387652]	uncertain significance	11	77268497	77268497	Human		name
405786134	CV3258150	single nucleotide variant	NM_182833.3(GDPD4):c.731T>A (p.Met244Lys)	not specified [RCV004387653]	uncertain significance	11	77258519	77258519	Human		name
405786129	CV3258151	single nucleotide variant	NM_182833.3(GDPD4):c.806T>C (p.Phe269Ser)	not specified [RCV004387654]	uncertain significance	11	77258444	77258444	Human		name
407512647	CV3432947	single nucleotide variant	NM_182833.3(GDPD4):c.335G>A (p.Ser112Asn)	not specified [RCV004626868]	uncertain significance	11	77271195	77271195	Human		name
407512656	CV3432950	single nucleotide variant	NM_182833.3(GDPD4):c.620C>T (p.Pro207Leu)	not specified [RCV004626871]	uncertain significance	11	77268928	77268928	Human		name
597703645	CV3687782	single nucleotide variant	NM_182833.3(GDPD4):c.407T>C (p.Met136Thr)	not specified [RCV004916729]	uncertain significance	11	77269954	77269954	Human		name
597758444	CV3687785	single nucleotide variant	NM_182833.3(GDPD4):c.956C>T (p.Thr319Ile)	not specified [RCV004925291]	uncertain significance	11	77245411	77245411	Human		name
597758449	CV3687786	single nucleotide variant	NM_182833.3(GDPD4):c.323T>G (p.Val108Gly)	not specified [RCV004925292]	uncertain significance	11	77271207	77271207	Human		name
597703687	CV3687789	single nucleotide variant	NM_182833.3(GDPD4):c.887A>T (p.Lys296Ile)	not specified [RCV004916734]	uncertain significance	11	77245480	77245480	Human		name
598219358	CV3970605	single nucleotide variant	NM_182833.3(GDPD4):c.304C>A (p.Gln102Lys)	not specified [RCV005340283]	likely benign	11	77271297	77271297	Human		name
598219365	CV3970606	single nucleotide variant	NM_182833.3(GDPD4):c.379G>A (p.Val127Met)	not specified [RCV005340284]	uncertain significance	11	77271151	77271151	Human		name
598219380	CV3970608	single nucleotide variant	NM_182833.3(GDPD4):c.827C>G (p.Ser276Trp)	not specified [RCV005340286]	uncertain significance	11	77258423	77258423	Human		name
598219387	CV3970609	single nucleotide variant	NM_182833.3(GDPD4):c.367G>A (p.Val123Met)	not specified [RCV005340287]	uncertain significance	11	77271163	77271163	Human		name
155923301	CV2215567	single nucleotide variant	NM_182833.3(GDPD4):c.1025G>C (p.Arg342Thr)	not specified [RCV004089336]	uncertain significance	11	77245342	77245342	Human		name
156145626	CV2265066	single nucleotide variant	NM_182833.3(GDPD4):c.1063G>T (p.Ala355Ser)	not specified [RCV004126217]	uncertain significance	11	77245304	77245304	Human		name
156286587	CV2288315	single nucleotide variant	NM_182833.3(GDPD4):c.1469A>G (p.His490Arg)	not specified [RCV004150089]	uncertain significance	11	77229153	77229153	Human		name
155965991	CV2330627	single nucleotide variant	NM_182833.3(GDPD4):c.1285A>G (p.Asn429Asp)	not specified [RCV004183222]	uncertain significance	11	77233129	77233129	Human		name
156102875	CV2352324	single nucleotide variant	NM_182833.3(GDPD4):c.1129G>T (p.Val377Leu)	not specified [RCV004200798]	uncertain significance	11	77243806	77243806	Human		name
156207230	CV2382330	single nucleotide variant	NM_182833.3(GDPD4):c.1039C>T (p.Arg347Cys)	not specified [RCV004230676]	uncertain significance	11	77245328	77245328	Human		name
329376760	CV2460483	single nucleotide variant	NM_182833.3(GDPD4):c.1286A>G (p.Asn429Ser)	not specified [RCV004268776]	uncertain significance	11	77233128	77233128	Human		name
329398350	CV2465037	single nucleotide variant	NM_182833.3(GDPD4):c.1138G>T (p.Gly380Cys)	not specified [RCV004286772]	uncertain significance	11	77243797	77243797	Human		name
401740742	CV2702609	single nucleotide variant	NM_182833.3(GDPD4):c.1078C>A (p.Gln360Lys)	not specified [RCV004317091]	uncertain significance	11	77245289	77245289	Human		name
401888088	CV2791235	single nucleotide variant	NM_182833.3(GDPD4):c.1111A>G (p.Arg371Gly)	not specified [RCV004356872]	uncertain significance	11	77243824	77243824	Human		name
405786187	CV3258140	single nucleotide variant	NM_182833.3(GDPD4):c.1156C>T (p.Arg386Cys)	not specified [RCV004387643]	uncertain significance	11	77243779	77243779	Human		name
405786182	CV3258141	single nucleotide variant	NM_182833.3(GDPD4):c.1214A>G (p.Tyr405Cys)	not specified [RCV004387644]	uncertain significance	11	77243721	77243721	Human		name
405786177	CV3258142	single nucleotide variant	NM_182833.3(GDPD4):c.1253C>G (p.Ala418Gly)	not specified [RCV004387645]	uncertain significance	11	77233161	77233161	Human		name
405786173	CV3258143	single nucleotide variant	NM_182833.3(GDPD4):c.1273G>A (p.Val425Ile)	not specified [RCV004387646]	uncertain significance	11	77233141	77233141	Human		name
405786167	CV3258144	single nucleotide variant	NM_182833.3(GDPD4):c.1450G>T (p.Val484Phe)	not specified [RCV004387647]	uncertain significance	11	77229172	77229172	Human		name
405786162	CV3258145	single nucleotide variant	NM_182833.3(GDPD4):c.1475G>A (p.Arg492Gln)	not specified [RCV004387648]	uncertain significance	11	77227914	77227914	Human		name
407512650	CV3432948	single nucleotide variant	NM_182833.3(GDPD4):c.1036G>T (p.Val346Phe)	not specified [RCV004626869]	uncertain significance	11	77245331	77245331	Human		name
407512659	CV3432951	single nucleotide variant	NM_182833.3(GDPD4):c.1048G>A (p.Val350Ile)	not specified [RCV004626872]	uncertain significance	11	77245319	77245319	Human		name
597704437	CV3687781	single nucleotide variant	NM_182833.3(GDPD4):c.1120G>A (p.Val374Ile)	not specified [RCV004916728]	uncertain significance	11	77243815	77243815	Human		name
597703652	CV3687783	single nucleotide variant	NM_182833.3(GDPD4):c.1208T>C (p.Val403Ala)	not specified [RCV004916730]	uncertain significance	11	77243727	77243727	Human		name
597703670	CV3687787	single nucleotide variant	NM_182833.3(GDPD4):c.1528A>G (p.Thr510Ala)	not specified [RCV004916732]	uncertain significance	11	77217312	77217312	Human		name
597703679	CV3687788	single nucleotide variant	NM_182833.3(GDPD4):c.1244A>G (p.Asp415Gly)	not specified [RCV004916733]	uncertain significance	11	77233170	77233170	Human		name
597703694	CV3687790	single nucleotide variant	NM_182833.3(GDPD4):c.1180G>A (p.Ala394Thr)	not specified [RCV004916735]	likely benign	11	77243755	77243755	Human		name
598219349	CV3970604	single nucleotide variant	NM_182833.3(GDPD4):c.1040G>A (p.Arg347His)	not specified [RCV005340282]	uncertain significance	11	77245327	77245327	Human		name
598219372	CV3970607	single nucleotide variant	NM_182833.3(GDPD4):c.1286A>C (p.Asn429Thr)	not specified [RCV005340285]	uncertain significance	11	77233128	77233128	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