Pipox Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

37 records found for search term Pipox

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
152979575	CV1676623	single nucleotide variant	NM_016518.3(PIPOX):c.5C>T (p.Ala2Val)	Low-frequency hearing loss [RCV002246212]	uncertain significance	17	29043230	29043230	Human	1	name
155999537	CV2378600	single nucleotide variant	NM_016518.3(PIPOX):c.173C>T (p.Ala58Val)	not specified [RCV004231080]	uncertain significance	17	29044917	29044917	Human		name
401783775	CV2720420	single nucleotide variant	NM_016518.3(PIPOX):c.151C>G (p.Gln51Glu)	not specified [RCV004327846]	uncertain significance	17	29044895	29044895	Human		name
401885773	CV2774516	single nucleotide variant	NM_016518.3(PIPOX):c.241G>A (p.Glu81Lys)	not specified [RCV004350005]	uncertain significance	17	29044985	29044985	Human		name
597741200	CV3576093	single nucleotide variant	NM_016518.3(PIPOX):c.260A>G (p.His87Arg)	not specified [RCV004844656]	uncertain significance	17	29045004	29045004	Human		name
597767436	CV3576097	single nucleotide variant	NM_016518.3(PIPOX):c.124C>A (p.Pro42Thr)	not specified [RCV004850467]	uncertain significance	17	29044868	29044868	Human		name
156282725	CV2252429	single nucleotide variant	NM_016518.3(PIPOX):c.940G>A (p.Ala314Thr)	not specified [RCV004116267]	uncertain significance	17	29055195	29055195	Human		name
156141378	CV2260497	single nucleotide variant	NM_016518.3(PIPOX):c.410G>C (p.Gly137Ala)	not specified [RCV004123285]	uncertain significance	17	29053066	29053066	Human		name
156233871	CV2271026	single nucleotide variant	NM_016518.3(PIPOX):c.877G>A (p.Gly293Arg)	not specified [RCV004134430]	likely benign	17	29055132	29055132	Human		name
156071454	CV2295883	single nucleotide variant	NM_016518.3(PIPOX):c.998G>A (p.Arg333His)	not specified [RCV004151790]	uncertain significance	17	29055844	29055844	Human		name
156164780	CV2323700	single nucleotide variant	NM_016518.3(PIPOX):c.541G>A (p.Gly181Arg)	not specified [RCV004165875]	uncertain significance	17	29053476	29053476	Human		name
155909135	CV2369461	single nucleotide variant	NM_016518.3(PIPOX):c.475C>G (p.Gln159Glu)	not specified [RCV004210399]	uncertain significance	17	29053131	29053131	Human		name
329383886	CV2434905	single nucleotide variant	NM_016518.3(PIPOX):c.509G>A (p.Arg170His)	not specified [RCV004250779]	likely benign	17	29053444	29053444	Human		name
401867795	CV2767086	single nucleotide variant	NM_016518.3(PIPOX):c.871G>T (p.Asp291Tyr)	not specified [RCV004347488]	uncertain significance	17	29055126	29055126	Human		name
401858934	CV2774987	single nucleotide variant	NM_016518.3(PIPOX):c.457A>G (p.Lys153Glu)	not specified [RCV004346382]	uncertain significance	17	29053113	29053113	Human		name
405791619	CV3368851	single nucleotide variant	NM_016518.3(PIPOX):c.436G>A (p.Gly146Arg)	not specified [RCV004506103]	uncertain significance	17	29053092	29053092	Human		name
405791623	CV3368852	single nucleotide variant	NM_016518.3(PIPOX):c.755G>A (p.Cys252Tyr)	not specified [RCV004506104]	likely benign	17	29054639	29054639	Human		name
405791626	CV3368853	single nucleotide variant	NM_016518.3(PIPOX):c.962A>G (p.Tyr321Cys)	not specified [RCV004506105]	uncertain significance	17	29055217	29055217	Human		name
407512164	CV3463698	single nucleotide variant	NM_016518.3(PIPOX):c.994G>A (p.Asp332Asn)	not specified [RCV004648302]	uncertain significance	17	29055840	29055840	Human		name
407512167	CV3463699	single nucleotide variant	NM_016518.3(PIPOX):c.785G>T (p.Gly262Val)	not specified [RCV004648303]	uncertain significance	17	29054669	29054669	Human		name
407530848	CV3463700	single nucleotide variant	NM_016518.3(PIPOX):c.626T>C (p.Leu209Pro)	not specified [RCV004657268]	uncertain significance	17	29053561	29053561	Human		name
597767426	CV3576089	single nucleotide variant	NM_016518.3(PIPOX):c.554C>T (p.Thr185Met)	not specified [RCV004850465]	uncertain significance	17	29053489	29053489	Human		name
597741188	CV3576090	single nucleotide variant	NM_016518.3(PIPOX):c.503T>C (p.Ile168Thr)	not specified [RCV004844654]	uncertain significance	17	29053438	29053438	Human		name
597741194	CV3576091	single nucleotide variant	NM_016518.3(PIPOX):c.427G>A (p.Asp143Asn)	not specified [RCV004844655]	uncertain significance	17	29053083	29053083	Human		name
597767431	CV3576092	single nucleotide variant	NM_016518.3(PIPOX):c.731C>T (p.Pro244Leu)	not specified [RCV004850466]	uncertain significance	17	29054615	29054615	Human		name
597741205	CV3576094	single nucleotide variant	NM_016518.3(PIPOX):c.536A>G (p.Asn179Ser)	not specified [RCV004844657]	uncertain significance	17	29053471	29053471	Human		name
597741209	CV3576095	single nucleotide variant	NM_016518.3(PIPOX):c.445A>G (p.Ile149Val)	not specified [RCV004844658]	uncertain significance	17	29053101	29053101	Human		name
597741225	CV3576099	single nucleotide variant	NM_016518.3(PIPOX):c.328C>A (p.Leu110Met)	not specified [RCV004844661]	uncertain significance	17	29052984	29052984	Human		name
597741231	CV3576100	single nucleotide variant	NM_016518.3(PIPOX):c.696G>T (p.Met232Ile)	not specified [RCV004844662]	uncertain significance	17	29054580	29054580	Human		name
156090019	CV2256471	single nucleotide variant	NM_016518.3(PIPOX):c.1048G>A (p.Gly350Arg)	not specified [RCV004118680]	uncertain significance	17	29056180	29056180	Human		name
156147709	CV2265225	single nucleotide variant	NM_016518.3(PIPOX):c.1072G>A (p.Gly358Arg)	not specified [RCV004126338]	uncertain significance	17	29056204	29056204	Human		name
156014032	CV2368656	single nucleotide variant	NM_016518.3(PIPOX):c.1133G>A (p.Arg378Gln)	not specified [RCV004214552]	uncertain significance	17	29056265	29056265	Human		name
155936610	CV2379864	single nucleotide variant	NM_016518.3(PIPOX):c.1066G>A (p.Val356Met)	not specified [RCV004219971]	uncertain significance	17	29056198	29056198	Human		name
405791616	CV3368850	single nucleotide variant	NM_016518.3(PIPOX):c.1060G>A (p.Ala354Thr)	not specified [RCV004506102]	uncertain significance	17	29056192	29056192	Human		name
597741214	CV3576096	single nucleotide variant	NM_016518.3(PIPOX):c.1127C>A (p.Pro376His)	not specified [RCV004844659]	uncertain significance	17	29056259	29056259	Human		name
598205272	CV4002849	single nucleotide variant	NM_016518.3(PIPOX):c.1142G>A (p.Arg381His)	not specified [RCV005399439]	uncertain significance	17	29056274	29056274	Human		name
598273073	CV4002850	single nucleotide variant	NM_016518.3(PIPOX):c.1014C>G (p.Asp338Glu)	not specified [RCV005389553]	uncertain significance	17	29055860	29055860	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