TAS1R3

taste 1 receptor member 3

Summary

The protein encoded by this gene is a G-protein coupled receptor involved in taste responses. The encoded protein can form a heterodimeric receptor with TAS1R1 to elicit the umami taste response, or it can bind with TAS1R2 to form a receptor for the sweet taste response. [provided by RefSeq, Nov 2015]

Known Variants127 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs307355	1:1,265,154	C/T	upstream gene variant	—
rs307377	1:1,266,660	C/T	missense variant	—
rs2523090854	1:1,266,783	G/A	—	uncertain significance
rs373388210	1:1,266,822	G/C	—	uncertain significance
rs377350793	1:1,266,846	T/A	—	uncertain significance
rs372727451	1:1,266,863	C/T	—	benign
rs368532955	1:1,266,880	G/A	—	uncertain significance
rs746044880	1:1,266,886	G/A	—	uncertain significance
rs371880423	1:1,267,064	G/A	—	uncertain significance
rs374712712	1:1,267,081	C/G	—	uncertain significance
rs201655269	1:1,267,086	C/T	—	uncertain significance
rs867182117	1:1,267,088	G/A	—	uncertain significance
rs776847816	1:1,267,110	T/C	—	uncertain significance
rs764093530	1:1,267,121	C/T	—	uncertain significance
rs770154322	1:1,267,167	T/C	—	uncertain significance
rs753252214	1:1,267,178	G/A	—	uncertain significance
rs1028200144	1:1,267,199	A/G	—	uncertain significance
rs780598354	1:1,267,205	G/A	—	uncertain significance
rs375171209	1:1,267,221	C/T	—	uncertain significance
rs779276757	1:1,267,270	G/C	—	uncertain significance
rs2523093940	1:1,267,280	G/A	—	likely benign
rs769741462	1:1,267,281	T/C	—	uncertain significance
rs773061284	1:1,267,419	A/T	—	uncertain significance
rs111858626	1:1,267,437	G/A	—	uncertain significance
rs542634007	1:1,267,440	C/T	—	uncertain significance
rs373399503	1:1,267,441	G/A	—	uncertain significance
rs201534184	1:1,267,495	C/T	—	uncertain significance
rs368284939	1:1,267,500	G/A	—	uncertain significance
rs111428041	1:1,267,504	C/T	—	likely benign
rs1442761922	1:1,267,532	C/G	—	uncertain significance
rs755139378	1:1,267,557	G/A	—	uncertain significance
rs780910059	1:1,267,560	G/A	—	uncertain significance
rs779804992	1:1,267,566	G/A	—	uncertain significance
rs755889188	1:1,267,603	C/T	—	uncertain significance
rs1446807517	1:1,267,605	G/A	—	uncertain significance
rs754595900	1:1,267,609	G/A	—	uncertain significance
rs1163713078	1:1,267,612	G/T	—	uncertain significance
rs752921589	1:1,267,642	C/T	—	uncertain significance
rs754670134	1:1,267,647	C/A	—	uncertain significance
rs544429799	1:1,267,663	C/T	—	likely benign
rs373879203	1:1,267,666	G/A	—	uncertain significance
rs752361983	1:1,267,692	C/T	—	uncertain significance
rs370117959	1:1,267,729	T/C	—	uncertain significance
rs374355734	1:1,267,789	C/T	—	uncertain significance
rs748427491	1:1,267,797	G/A	—	uncertain significance
rs150848527	1:1,267,827	T/C	—	uncertain significance
rs768334149	1:1,267,842	G/C	—	uncertain significance
rs531793804	1:1,267,848	C/G	—	uncertain significance
rs201607183	1:1,267,870	C/T	—	uncertain significance
rs777986883	1:1,267,897	C/G	—	uncertain significance
rs200087307	1:1,267,908	G/A	—	likely benign
rs148558246	1:1,267,923	G/A	—	uncertain significance
rs2523099602	1:1,267,944	G/A	—	uncertain significance
rs138056288	1:1,267,968	G/A	—	uncertain significance
rs776220108	1:1,267,975	G/A	—	likely benign
rs138858544	1:1,267,977	G/A	—	uncertain significance
rs200764612	1:1,268,000	G/C	—	uncertain significance
rs147600530	1:1,268,010	G/T	—	benign
rs1280813075	1:1,268,026	A/G	—	uncertain significance
rs750447360	1:1,268,031	G/T	—	uncertain significance
rs752614857	1:1,268,041	C/T	—	uncertain significance
rs139374386	1:1,268,057	C/T	—	benign
rs746111424	1:1,268,058	G/A	—	uncertain significance
rs143959072	1:1,268,093	C/T	—	likely benign
rs780884469	1:1,268,094	G/A	—	uncertain significance
rs779608337	1:1,268,106	A/G	—	uncertain significance
rs142077967	1:1,268,145	G/A	—	uncertain significance
rs1010090465	1:1,268,155	G/A	—	uncertain significance
rs1557656886	1:1,268,173	T/G	—	uncertain significance
rs111703380	1:1,268,348	G/A	—	benign
rs200305103	1:1,268,352	C/T	—	uncertain significance
rs748811798	1:1,268,358	G/A	—	likely benign
rs143311630	1:1,268,367	G/A	—	uncertain significance
rs755284382	1:1,268,368	G/C	—	uncertain significance
rs146208824	1:1,268,371	A/G	—	uncertain significance
rs149099807	1:1,268,388	G/A	—	uncertain significance
rs761183119	1:1,268,398	T/C	—	uncertain significance
rs745746312	1:1,268,426	G/C	—	uncertain significance
rs144635443	1:1,268,433	G/A	—	uncertain significance
rs768355198	1:1,268,435	C/T	—	likely benign
rs141557900	1:1,268,461	G/A	—	uncertain significance
rs138915131	1:1,268,462	G/A	—	benign
rs758710569	1:1,268,463	A/T	—	uncertain significance
rs746577629	1:1,268,497	A/G	—	likely benign
rs748396729	1:1,268,645	G/A	—	uncertain significance
rs370629720	1:1,268,652	G/A	—	likely benign
rs2523104321	1:1,268,655	G/T	—	uncertain significance
rs755606520	1:1,268,684	C/T	—	uncertain significance
rs145196342	1:1,268,688	G/A	—	uncertain significance
rs1460062717	1:1,268,717	G/A	—	uncertain significance
rs774178597	1:1,268,721	G/A	—	uncertain significance
rs371035684	1:1,268,723	G/A	—	uncertain significance
rs750033775	1:1,268,729	T/C	—	uncertain significance
rs374466982	1:1,268,737	G/A	—	likely benign
rs201407678	1:1,268,747	C/T	—	uncertain significance
rs1043750401	1:1,268,748	G/A	—	likely benign
rs2523105356	1:1,268,752	A/T	—	uncertain significance
rs746607242	1:1,268,888	G/C	—	uncertain significance
rs750836058	1:1,268,934	G/A	—	uncertain significance
rs144259160	1:1,268,942	C/T	—	uncertain significance

Showing 100 of 127 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.