Tas2r39 Variant Search Result - Rat Genome Database

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28 records found for search term Tas2r39

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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

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