Aqp8 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

34 records found for search term Aqp8

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15102253	CV703573	single nucleotide variant	NM_001169.3(AQP8):c.60G>A (p.Pro20=)	not provided [RCV000959255]	benign	16	25217245	25217245	Human		name
15111503	CV755046	single nucleotide variant	NM_001169.3(AQP8):c.63C>T (p.Ser21=)	not provided [RCV000916741]	likely benign	16	25217248	25217248	Human		name
405673544	CV3286075	single nucleotide variant	NM_001169.3(AQP8):c.29C>G (p.Pro10Arg)	not specified [RCV004420055]	uncertain significance	16	25217214	25217214	Human		name
405673552	CV3286077	single nucleotide variant	NM_001169.3(AQP8):c.738G>A (p.Arg246=)	not specified [RCV004420057]	likely benign	16	25228444	25228444	Human		name
407482591	CV3471342	single nucleotide variant	NM_001169.3(AQP8):c.59C>T (p.Pro20Leu)	not specified [RCV004664795]	uncertain significance	16	25217244	25217244	Human		name
598228475	CV3894632	single nucleotide variant	NM_001169.3(AQP8):c.471G>A (p.Ala157=)	not provided [RCV005257876]	likely benign	16	25224445	25224445	Human		name
15161508	CV703574	single nucleotide variant	NM_001169.3(AQP8):c.429G>A (p.Ala143=)	not provided [RCV000947685]	benign	16	25224403	25224403	Human		name
15104779	CV703575	single nucleotide variant	NM_001169.3(AQP8):c.654G>A (p.Ala218=)	not provided [RCV000959754]	benign	16	25227119	25227119	Human		name
156302406	CV2319584	single nucleotide variant	NM_001169.3(AQP8):c.220C>A (p.Leu74Met)	not specified [RCV004185140]	uncertain significance	16	25217405	25217405	Human		name
156157625	CV2363718	single nucleotide variant	NM_001169.3(AQP8):c.182C>T (p.Thr61Met)	not specified [RCV004216662]	uncertain significance	16	25217367	25217367	Human		name
329375733	CV2431484	single nucleotide variant	NM_001169.3(AQP8):c.203C>T (p.Pro68Leu)	not specified [RCV004254646]	uncertain significance	16	25217388	25217388	Human		name
401765016	CV2728190	single nucleotide variant	NM_001169.3(AQP8):c.188C>T (p.Thr63Ile)	not specified [RCV004324234]	uncertain significance	16	25217373	25217373	Human		name
401864107	CV2781496	single nucleotide variant	NM_001169.3(AQP8):c.245C>T (p.Thr82Met)	not specified [RCV004354729]	uncertain significance	16	25217430	25217430	Human		name
405673537	CV3286073	single nucleotide variant	NM_001169.3(AQP8):c.178G>A (p.Gly60Arg)	not specified [RCV004420053]	uncertain significance	16	25217363	25217363	Human		name
405673540	CV3286074	single nucleotide variant	NM_001169.3(AQP8):c.223G>A (p.Ala75Thr)	not specified [RCV004420054]	uncertain significance	16	25217408	25217408	Human		name
597701046	CV3572448	single nucleotide variant	NM_001169.3(AQP8):c.169A>G (p.Ile57Val)	not specified [RCV004839777]	uncertain significance	16	25217354	25217354	Human		name
598166090	CV4002430	single nucleotide variant	NM_001169.3(AQP8):c.119T>C (p.Val40Ala)	not specified [RCV005391568]	uncertain significance	16	25217304	25217304	Human		name
598166114	CV4002436	single nucleotide variant	NM_001169.3(AQP8):c.114T>G (p.Cys38Trp)	not specified [RCV005391573]	uncertain significance	16	25217299	25217299	Human		name
156237442	CV2193559	single nucleotide variant	NM_001169.3(AQP8):c.586G>A (p.Val196Met)	not specified [RCV004073033]	uncertain significance	16	25224560	25224560	Human		name
156336096	CV2228491	single nucleotide variant	NM_001169.3(AQP8):c.370G>A (p.Gly124Arg)	not specified [RCV004092738]	uncertain significance	16	25221566	25221566	Human		name
156054857	CV2320493	single nucleotide variant	NM_001169.3(AQP8):c.484A>G (p.Ile162Val)	not specified [RCV004172127]	uncertain significance	16	25224458	25224458	Human		name
156074987	CV2331710	single nucleotide variant	NM_001169.3(AQP8):c.571G>A (p.Gly191Ser)	not specified [RCV004184338]	uncertain significance	16	25224545	25224545	Human		name
156031825	CV2376411	single nucleotide variant	NM_001169.3(AQP8):c.470C>T (p.Ala157Val)	not specified [RCV004220595]	uncertain significance	16	25224444	25224444	Human		name
156261321	CV2381330	single nucleotide variant	NM_001169.3(AQP8):c.418G>T (p.Ala140Ser)	not specified [RCV004227389]	uncertain significance	16	25224392	25224392	Human		name
405673549	CV3286076	single nucleotide variant	NM_001169.3(AQP8):c.443T>C (p.Val148Ala)	not specified [RCV004420056]	uncertain significance	16	25224417	25224417	Human		name
407529527	CV3471353	single nucleotide variant	NM_001169.3(AQP8):c.455G>A (p.Gly152Glu)	not specified [RCV004656085]	uncertain significance	16	25224429	25224429	Human		name
407482638	CV3471364	single nucleotide variant	NM_001169.3(AQP8):c.497C>T (p.Thr166Met)	not specified [RCV004664803]	uncertain significance	16	25224471	25224471	Human		name
407529553	CV3471375	single nucleotide variant	NM_001169.3(AQP8):c.407G>C (p.Arg136Thr)	not specified [RCV004656099]	uncertain significance	16	25224381	25224381	Human		name
407529563	CV3471386	single nucleotide variant	NM_001169.3(AQP8):c.542C>T (p.Thr181Ile)	not specified [RCV004656104]	uncertain significance	16	25224516	25224516	Human		name
597701030	CV3572433	single nucleotide variant	NM_001169.3(AQP8):c.524G>T (p.Gly175Val)	not specified [RCV004839775]	uncertain significance	16	25224498	25224498	Human		name
597701039	CV3572441	single nucleotide variant	NM_001169.3(AQP8):c.626T>C (p.Met209Thr)	not specified [RCV004839776]	uncertain significance	16	25227091	25227091	Human		name
598196216	CV4002408	single nucleotide variant	NM_001169.3(AQP8):c.397C>T (p.Pro133Ser)	not specified [RCV005397673]	uncertain significance	16	25224371	25224371	Human		name
598196230	CV4002415	single nucleotide variant	NM_001169.3(AQP8):c.335C>T (p.Pro112Leu)	not specified [RCV005397676]	uncertain significance	16	25221531	25221531	Human		name
598166069	CV4002423	single nucleotide variant	NM_001169.3(AQP8):c.542C>A (p.Thr181Lys)	not specified [RCV005391563]	uncertain significance	16	25224516	25224516	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