Tas2r39 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

28 records found for search term Tas2r39

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156099767	CV2250699	single nucleotide variant	NM_176881.2(TAS2R39):c.12A>C (p.Arg4Ser)	not specified [RCV004129319]	uncertain significance	7	143183430	143183430	Human		name
401781309	CV2681961	single nucleotide variant	NM_176881.2(TAS2R39):c.70C>A (p.Pro24Thr)	not specified [RCV004296945]	uncertain significance	7	143183488	143183488	Human		name
8632414	CV87622	single nucleotide variant	NM_176881.2(TAS2R39):c.699C>T (p.Leu233=)	Malignant melanoma [RCV000067714]	not provided	7	143184117	143184117	Human		name
401880115	CV2766130	single nucleotide variant	NM_176881.2(TAS2R39):c.181G>A (p.Ala61Thr)	not specified [RCV004340584]	uncertain significance	7	143183599	143183599	Human		name
405777980	CV3324301	single nucleotide variant	NM_176881.2(TAS2R39):c.295A>G (p.Thr99Ala)	not specified [RCV004471449]	uncertain significance	7	143183713	143183713	Human		name
407511912	CV3475299	single nucleotide variant	NM_176881.2(TAS2R39):c.112T>G (p.Leu38Val)	not specified [RCV004673268]	uncertain significance	7	143183530	143183530	Human		name
156278268	CV2286755	single nucleotide variant	NM_176881.2(TAS2R39):c.697C>A (p.Leu233Ile)	not specified [RCV004142568]	likely benign	7	143184115	143184115	Human		name
156087576	CV2299154	single nucleotide variant	NM_176881.2(TAS2R39):c.460A>G (p.Ile154Val)	not specified [RCV004152497]	uncertain significance	7	143183878	143183878	Human		name
156094414	CV2300298	single nucleotide variant	NM_176881.2(TAS2R39):c.521T>G (p.Met174Arg)	not specified [RCV004153252]	uncertain significance	7	143183939	143183939	Human		name
156156233	CV2328864	single nucleotide variant	NM_176881.2(TAS2R39):c.570C>G (p.Ile190Met)	not specified [RCV004179867]	uncertain significance	7	143183988	143183988	Human		name
155918062	CV2332931	single nucleotide variant	NM_176881.2(TAS2R39):c.830C>T (p.Ala277Val)	not specified [RCV004192188]	uncertain significance	7	143184248	143184248	Human		name
156091696	CV2384768	single nucleotide variant	NM_176881.2(TAS2R39):c.970C>T (p.Arg324Trp)	not specified [RCV004232533]	uncertain significance	7	143184388	143184388	Human		name
405777986	CV3324302	single nucleotide variant	NM_176881.2(TAS2R39):c.419C>T (p.Ala140Val)	not specified [RCV004471450]	uncertain significance	7	143183837	143183837	Human		name
405777999	CV3324304	single nucleotide variant	NM_176881.2(TAS2R39):c.622G>A (p.Gly208Ser)	not specified [RCV004471452]	likely benign	7	143184040	143184040	Human		name
405778005	CV3324305	single nucleotide variant	NM_176881.2(TAS2R39):c.808C>T (p.Leu270Phe)	not specified [RCV004471453]	uncertain significance	7	143184226	143184226	Human		name
405778011	CV3324306	single nucleotide variant	NM_176881.2(TAS2R39):c.921C>G (p.His307Gln)	not specified [RCV004471454]	uncertain significance	7	143184339	143184339	Human		name
407511908	CV3475298	single nucleotide variant	NM_176881.2(TAS2R39):c.610A>T (p.Ile204Phe)	not specified [RCV004673267]	uncertain significance	7	143184028	143184028	Human		name
407530541	CV3475300	single nucleotide variant	NM_176881.2(TAS2R39):c.511A>C (p.Ser171Arg)	not specified [RCV004681964]	uncertain significance	7	143183929	143183929	Human		name
407511915	CV3475301	single nucleotide variant	NM_176881.2(TAS2R39):c.668T>A (p.Met223Lys)	not specified [RCV004673269]	uncertain significance	7	143184086	143184086	Human		name
407530542	CV3475302	single nucleotide variant	NM_176881.2(TAS2R39):c.551G>A (p.Cys184Tyr)	not specified [RCV004681965]	uncertain significance	7	143183969	143183969	Human		name
597749872	CV3612575	single nucleotide variant	NM_176881.2(TAS2R39):c.458G>T (p.Arg153Ile)	not specified [RCV004866579]	uncertain significance	7	143183876	143183876	Human		name
597749876	CV3612576	single nucleotide variant	NM_176881.2(TAS2R39):c.461T>A (p.Ile154Asn)	not specified [RCV004866580]	uncertain significance	7	143183879	143183879	Human		name
598195135	CV3916407	single nucleotide variant	NM_176881.2(TAS2R39):c.925A>G (p.Ile309Val)	not specified [RCV005289189]	likely benign	7	143184343	143184343	Human		name
598195140	CV3916408	single nucleotide variant	NM_176881.2(TAS2R39):c.499T>A (p.Phe167Ile)	not specified [RCV005289190]	uncertain significance	7	143183917	143183917	Human		name
598195146	CV3916409	single nucleotide variant	NM_176881.2(TAS2R39):c.559T>A (p.Ser187Thr)	not specified [RCV005289191]	uncertain significance	7	143183977	143183977	Human		name
598195152	CV3916410	single nucleotide variant	NM_176881.2(TAS2R39):c.868A>G (p.Ser290Gly)	not specified [RCV005289192]	uncertain significance	7	143184286	143184286	Human		name
598195158	CV3916411	single nucleotide variant	NM_176881.2(TAS2R39):c.385G>C (p.Ala129Pro)	not specified [RCV005289193]	uncertain significance	7	143183803	143183803	Human		name
8626356	CV81500	single nucleotide variant	NM_176881.2(TAS2R39):c.646G>T (p.Gly216Trp)	Malignant melanoma [RCV000061578]	not provided	7	143184064	143184064	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