Usp15 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

50 records found for search term Usp15

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
408365742	CV3509392	single nucleotide variant	NM_001252078.2(USP15):c.1652+10A>G	USP15-related disorder [RCV004755213]	likely benign	12	62389709	62389709	Human		name , trait , alternate_id
405287801	CV3217967	single nucleotide variant	NM_001252078.2(USP15):c.246C>T (p.His82=)	USP15-related disorder [RCV003982090]	benign	12	62302818	62302818	Human		name , trait , alternate_id
405258105	CV3208130	single nucleotide variant	NM_001252078.2(USP15):c.801A>G (p.Ser267=)	USP15-related disorder [RCV003941577]	likely benign	12	62355361	62355361	Human		name , trait , alternate_id
8654126	CV130701	single nucleotide variant	NM_001252078.1(USP15):c.2487A>T (p.Pro829=)	Lung cancer [RCV000111188]	uncertain significance	12	62393119	62393119	Human		name
156366993	CV2203441	single nucleotide variant	NM_001252078.2(USP15):c.187G>A (p.Gly63Arg)	not specified [RCV004072656]	uncertain significance	12	62294276	62294276	Human		name
405284589	CV3190475	single nucleotide variant	NM_001252078.2(USP15):c.1371A>G (p.Thr457=)	USP15-related disorder [RCV003909284]	likely benign	12	62384200	62384200	Human		name , trait , alternate_id
405274393	CV3211732	single nucleotide variant	NM_001252078.2(USP15):c.1602C>T (p.Phe534=)	USP15-related disorder [RCV003951532]	likely benign	12	62389649	62389649	Human		name , trait , alternate_id
405262166	CV3216704	single nucleotide variant	NM_001252078.2(USP15):c.1572T>C (p.Asp524=)	USP15-related disorder [RCV003944683]	likely benign	12	62389619	62389619	Human		name , trait , alternate_id
405277252	CV3217709	single nucleotide variant	NM_001252078.2(USP15):c.2301T>C (p.Ala767=)	USP15-related disorder [RCV003974774]	benign	12	62391883	62391883	Human		name , trait , alternate_id
405287822	CV3217978	single nucleotide variant	NM_001252078.2(USP15):c.1455A>G (p.Pro485=)	USP15-related disorder [RCV003982102]	benign	12	62384284	62384284	Human		name , trait , alternate_id
407455238	CV3487424	single nucleotide variant	NM_001252078.2(USP15):c.220G>A (p.Gly74Ser)	not specified [RCV004685436]	uncertain significance	12	62302792	62302792	Human		name
597722462	CV3626115	single nucleotide variant	NM_001252078.2(USP15):c.182A>G (p.Tyr61Cys)	not specified [RCV004888022]	uncertain significance	12	62294271	62294271	Human		name
156058775	CV2239262	single nucleotide variant	NM_001252078.2(USP15):c.499A>G (p.Lys167Glu)	not specified [RCV004112230]	uncertain significance	12	62321487	62321487	Human		name
156038863	CV2384213	single nucleotide variant	NM_001252078.2(USP15):c.673T>C (p.Ser225Pro)	not specified [RCV004227607]	uncertain significance	12	62325923	62325923	Human		name
329388383	CV2437359	single nucleotide variant	NM_001252078.2(USP15):c.853C>G (p.Gln285Glu)	not specified [RCV004256230]	uncertain significance	12	62355413	62355413	Human		name
405814664	CV3341644	single nucleotide variant	NM_001252078.2(USP15):c.651T>A (p.Asp217Glu)	not specified [RCV004484530]	uncertain significance	12	62325901	62325901	Human		name
597722436	CV3626110	single nucleotide variant	NM_001252078.2(USP15):c.446C>T (p.Thr149Ile)	not specified [RCV004888020]	uncertain significance	12	62314887	62314887	Human		name
598275142	CV3936459	single nucleotide variant	NM_001252078.2(USP15):c.552G>A (p.Met184Ile)	not specified [RCV005304280]	uncertain significance	12	62321540	62321540	Human		name
155920921	CV2240440	single nucleotide variant	NM_001252078.2(USP15):c.1901G>T (p.Cys634Phe)	not specified [RCV004117329]	uncertain significance	12	62390920	62390920	Human		name
156334479	CV2263296	single nucleotide variant	NM_001252078.2(USP15):c.1693G>A (p.Val565Met)	not specified [RCV004133574]	uncertain significance	12	62389837	62389837	Human		name
155982451	CV2272971	single nucleotide variant	NM_001252078.2(USP15):c.2902A>G (p.Asn968Asp)	not specified [RCV004137640]	uncertain significance	12	62404331	62404331	Human		name
155991506	CV2276599	single nucleotide variant	NM_001252078.2(USP15):c.1512T>A (p.Asp504Glu)	not specified [RCV004146086]	uncertain significance	12	62389469	62389469	Human		name
156245564	CV2283431	single nucleotide variant	NM_001252078.2(USP15):c.2620C>A (p.Arg874Ser)	not specified [RCV004139654]	uncertain significance	12	62396344	62396344	Human		name
155959971	CV2285345	single nucleotide variant	NM_001252078.2(USP15):c.1939A>T (p.Ile647Leu)	not specified [RCV004139219]	uncertain significance	12	62390958	62390958	Human		name
155908172	CV2302369	single nucleotide variant	NM_001252078.2(USP15):c.2497G>A (p.Val833Ile)	not specified [RCV004161121]	uncertain significance	12	62393129	62393129	Human		name
156274841	CV2330629	single nucleotide variant	NM_001252078.2(USP15):c.1852G>A (p.Val618Ile)	not specified [RCV004183658]	uncertain significance	12	62390871	62390871	Human		name
156284708	CV2349040	single nucleotide variant	NM_001252078.2(USP15):c.1310T>C (p.Ile437Thr)	USP15-related disorder [RCV003946392]\|not specified [RCV004205481]	likely benign\|uncertain significance	12	62384139	62384139	Human		name , trait , alternate_id
156284719	CV2349041	single nucleotide variant	NM_001252078.2(USP15):c.2061T>G (p.Asp687Glu)	USP15-related disorder [RCV003946393]\|not specified [RCV004205482]	likely benign\|uncertain significance	12	62391257	62391257	Human		name , trait , alternate_id
329379764	CV2443545	single nucleotide variant	NM_001252078.2(USP15):c.1069G>A (p.Val357Ile)	not specified [RCV004262373]	uncertain significance	12	62381643	62381643	Human		name
329379938	CV2452848	single nucleotide variant	NM_001252078.2(USP15):c.2446C>G (p.Gln816Glu)	not specified [RCV004277499]	uncertain significance	12	62393078	62393078	Human		name
329372237	CV2455121	single nucleotide variant	NM_001252078.2(USP15):c.1291G>T (p.Asp431Tyr)	not specified [RCV004272365]	uncertain significance	12	62384120	62384120	Human		name
329395283	CV2457905	single nucleotide variant	NM_001252078.2(USP15):c.1922G>A (p.Gly641Glu)	not specified [RCV004271495]	uncertain significance	12	62390941	62390941	Human		name
401878176	CV2777784	single nucleotide variant	NM_001252078.2(USP15):c.1562T>C (p.Ile521Thr)	not specified [RCV004345612]	uncertain significance	12	62389609	62389609	Human		name
401880426	CV2780085	single nucleotide variant	NM_001252078.2(USP15):c.2014C>G (p.Pro672Ala)	not specified [RCV004355747]	uncertain significance	12	62391210	62391210	Human		name
401926693	CV2798729	single nucleotide variant	NM_001252078.2(USP15):c.1506A>G (p.Ile502Met)	USP15-related disorder [RCV003406017]	uncertain significance	12	62389463	62389463	Human		name , trait , alternate_id
405814657	CV3341640	single nucleotide variant	NM_001252078.2(USP15):c.1093C>G (p.Gln365Glu)	not specified [RCV004484526]	uncertain significance	12	62383843	62383843	Human		name
405814661	CV3341642	single nucleotide variant	NM_001252078.2(USP15):c.2897A>G (p.Asn966Ser)	not specified [RCV004484528]	uncertain significance	12	62404326	62404326	Human		name
405814663	CV3341643	single nucleotide variant	NM_001252078.2(USP15):c.2933T>G (p.Met978Arg)	not specified [RCV004484529]	uncertain significance	12	62404362	62404362	Human		name
407455242	CV3487422	single nucleotide variant	NM_001252078.2(USP15):c.2620C>T (p.Arg874Cys)	not specified [RCV004685434]	uncertain significance	12	62396344	62396344	Human		name
407455240	CV3487423	single nucleotide variant	NM_001252078.2(USP15):c.1994C>A (p.Ser665Tyr)	not specified [RCV004685435]	uncertain significance	12	62391190	62391190	Human		name
407455236	CV3487425	single nucleotide variant	NM_001252078.2(USP15):c.2240C>G (p.Ser747Cys)	not specified [RCV004685437]	uncertain significance	12	62391822	62391822	Human		name
597798384	CV3626111	single nucleotide variant	NM_001252078.2(USP15):c.1729C>T (p.His577Tyr)	not specified [RCV004879160]	uncertain significance	12	62389873	62389873	Human		name
597798387	CV3626112	single nucleotide variant	NM_001252078.2(USP15):c.1492A>C (p.Lys498Gln)	not specified [RCV004879161]	uncertain significance	12	62389449	62389449	Human		name
597723156	CV3626113	single nucleotide variant	NM_001252078.2(USP15):c.2837G>A (p.Arg946Gln)	not specified [RCV004888021]	uncertain significance	12	62404266	62404266	Human		name
597798390	CV3626114	single nucleotide variant	NM_001252078.2(USP15):c.2129G>A (p.Arg710Gln)	not specified [RCV004879162]	uncertain significance	12	62391325	62391325	Human		name
597722472	CV3626116	single nucleotide variant	NM_001252078.2(USP15):c.2180T>A (p.Ile727Asn)	not specified [RCV004888023]	uncertain significance	12	62391376	62391376	Human		name
597798392	CV3626118	single nucleotide variant	NM_001252078.2(USP15):c.2939C>G (p.Thr980Ser)	not specified [RCV004879163]	uncertain significance	12	62404368	62404368	Human		name
597798395	CV3626119	single nucleotide variant	NM_001252078.2(USP15):c.2060A>T (p.Asp687Val)	not specified [RCV004879164]	uncertain significance	12	62391256	62391256	Human		name
598203545	CV3936458	single nucleotide variant	NM_001252078.2(USP15):c.1573A>G (p.Ile525Val)	not specified [RCV005290551]	uncertain significance	12	62389620	62389620	Human		name
598203550	CV3936460	single nucleotide variant	NM_001252078.2(USP15):c.2248G>A (p.Ala750Thr)	not specified [RCV005290552]	uncertain significance	12	62391830	62391830	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