TRPM3

transient receptor potential cation channel subfamily M member 3

Summary

The product of this gene belongs to the family of transient receptor potential (TRP) channels. TRP channels are cation-selective channels important for cellular calcium signaling and homeostasis. The protein encoded by this gene mediates calcium entry, and this entry is potentiated by calcium store depletion. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Known Variants201 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs895354230	9:73,150,906	G/A	—	uncertain significance
rs150876089	9:73,150,942	C/T	—	uncertain significance
rs768647446	9:73,150,959	G/C	—	likely benign
rs6560142	9:73,150,984	T/C	—	benign
rs756713006	9:73,151,002	C/T	—	uncertain significance
rs41287375	9:73,151,003	G/A	—	conflicting classifications of pathogenicity
rs768982135	9:73,151,024	T/G	—	uncertain significance
rs148848073	9:73,151,059	G/T	—	uncertain significance
rs2537996631	9:73,151,086	T/C	—	uncertain significance
rs765557409	9:73,151,091	G/A	—	likely benign
rs748273171	9:73,151,107	A/C	—	uncertain significance
rs13440436	9:73,151,110	G/A	—	benign
rs2041696318	9:73,151,116	T/C	—	likely pathogenic
rs77177051	9:73,151,140	T/A	—	benign
rs551255724	9:73,151,167	A/G	—	uncertain significance
rs1220275139	9:73,151,261	C/A	—	uncertain significance
rs371292628	9:73,151,331	C/A	—	uncertain significance
rs2538002091	9:73,151,342	T/C	—	uncertain significance
rs769122112	9:73,151,344	C/T	—	likely benign
rs148192709	9:73,151,387	C/T	—	likely benign
rs2041783872	9:73,151,392	T/C	—	uncertain significance
rs377423818	9:73,151,462	G/C	—	uncertain significance
rs774052094	9:73,151,485	C/T	—	uncertain significance
rs2041829797	9:73,151,536	C/G	—	uncertain significance
rs150378459	9:73,151,552	C/G	—	likely benign
rs182290052	9:73,151,589	G/A	—	likely benign
rs776544359	9:73,151,617	A/G	—	uncertain significance
rs761562359	9:73,151,618	T/C	—	uncertain significance
rs765032665	9:73,151,623	C/A	—	conflicting classifications of pathogenicity
rs763169990	9:73,151,625	G/T	—	uncertain significance
rs1264484958	9:73,151,644	G/A	—	uncertain significance
rs144707364	9:73,151,653	G/T	—	uncertain significance
rs746588506	9:73,151,677	G/A	—	uncertain significance
rs2538009208	9:73,151,695	G/A	—	uncertain significance
rs188032279	9:73,151,712	G/A	—	likely benign
rs7033976	9:73,151,715	C/T	—	benign
rs1185656430	9:73,151,722	A/G	—	uncertain significance
rs757556760	9:73,151,732	C/T	—	likely benign
rs138081538	9:73,151,733	G/A	—	likely benign
rs2538010557	9:73,151,743	A/G	—	uncertain significance
rs769831095	9:73,151,752	A/G	—	uncertain significance
rs2131583890	9:73,151,768	C/G	—	uncertain significance
rs1477490960	9:73,151,800	G/C	—	uncertain significance
rs2538012047	9:73,151,809	C/T	—	uncertain significance
rs2538012248	9:73,151,821	G/A	—	uncertain significance
rs201390941	9:73,151,828	T/C	—	uncertain significance
rs754568676	9:73,151,829	G/A	—	likely benign
rs2041917397	9:73,151,842	G/T	—	uncertain significance
rs2538014637	9:73,151,929	C/G	—	uncertain significance
rs1345311078	9:73,151,937	C/A	—	uncertain significance
rs752272878	9:73,151,951	C/T	—	uncertain significance
rs2538015328	9:73,151,958	T/A	—	uncertain significance
rs755675741	9:73,151,961	C/T	—	uncertain significance
rs3739776	9:73,151,970	T/C	—	benign
rs766607935	9:73,152,030	C/A	—	likely benign
rs1386465651	9:73,152,038	C/A	—	uncertain significance
rs2041978314	9:73,152,052	C/T	—	uncertain significance
rs184424910	9:73,152,062	G/T	—	conflicting classifications of pathogenicity
rs2041988493	9:73,152,091	A/G	—	uncertain significance
rs751378692	9:73,152,148	C/T	—	uncertain significance
rs148061413	9:73,152,149	G/A	—	uncertain significance
rs538584258	9:73,152,164	C/T	—	uncertain significance
rs141399885	9:73,152,169	C/T	—	likely benign
rs138205746	9:73,152,198	C/A	—	benign
rs578035531	9:73,152,219	G/T	—	likely benign
rs374070652	9:73,152,232	G/A	—	conflicting classifications of pathogenicity
rs760461668	9:73,152,248	C/T	—	uncertain significance
rs1162521187	9:73,152,327	C/T	—	likely benign
rs201691726	9:73,152,328	G/A	—	likely benign
rs10780944	9:73,157,416	G/C	—	—
rs2131814076	9:73,164,555	G/A	—	uncertain significance
rs2538307490	9:73,167,778	C/T	—	likely benign
rs144823346	9:73,167,783	G/A	—	uncertain significance
rs377602208	9:73,167,793	C/T	—	uncertain significance
rs764458021	9:73,167,807	C/T	—	uncertain significance
rs2538309346	9:73,167,903	T/C	—	likely pathogenic
rs2131863502	9:73,167,906	C/T	—	likely pathogenic
rs2538309680	9:73,167,937	A/G	—	likely pathogenic
rs2131863747	9:73,167,958	T/C	—	pathogenic
rs2538312900	9:73,168,080	A/C	—	uncertain significance
rs143219293	9:73,168,144	C/T	—	benign
rs1564292436	9:73,168,145	G/T	—	uncertain significance
rs929984630	9:73,168,166	T/C	—	uncertain significance
rs1319189898	9:73,168,205	G/T	—	likely benign
rs763369558	9:73,168,224	G/A	—	uncertain significance
rs200861574	9:73,168,234	G/T	—	likely benign
rs760339927	9:73,205,946	C/T	—	uncertain significance
rs2538910734	9:73,205,952	A/G	—	uncertain significance
rs116330117	9:73,205,960	C/T	—	benign
rs2538911332	9:73,205,995	T/C	—	uncertain significance
rs12337271	9:73,206,014	C/T	—	benign
rs1036752298	9:73,206,061	C/T	—	uncertain significance
rs34054081	9:73,213,359	C/T	—	likely benign
rs1564493599	9:73,213,379	C/T	—	pathogenic
rs34994337	9:73,213,386	G/A	—	benign
rs1459726819	9:73,213,427	A/T	—	uncertain significance
rs2538998935	9:73,213,442	C/A	—	uncertain significance
rs778849121	9:73,213,505	C/T	—	uncertain significance
rs931648453	9:73,213,508	T/C	—	uncertain significance
rs1355173307	9:73,213,516	G/A	—	uncertain significance

Showing 100 of 201 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.