TFG

trafficking from ER to golgi regulator

Summary

There are several documented fusion oncoproteins encoded partially by this gene. This gene also participates in several oncogenic rearrangements resulting in anaplastic lymphoma and mixoid chondrosarcoma, and may play a role in the NF-kappaB pathway. Multiple transcript variants have been found for this gene. [provided by RefSeq, Sep 2010]

Known Variants332 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs75268146	3:100,428,061	T/C	—	benign
rs1143776	3:100,428,118	G/A	—	benign
rs72919417	3:100,428,286	G/T	—	benign
rs114124529	3:100,428,356	G/A	—	benign
rs1059363	3:100,428,460	C/G	—	benign
rs141580409	3:100,428,644	T/C	—	benign
rs142048727	3:100,432,326	A/G	—	likely benign
rs771836549	3:100,432,535	C/T	—	likely benign
rs2472056460	3:100,432,546	A/C	—	uncertain significance
rs1553699512	3:100,432,553	T/G	—	uncertain significance
rs200716443	3:100,432,554	G/A	—	uncertain significance
rs369343773	3:100,432,562	A/T	—	likely benign
rs2149057606	3:100,432,563	A/G	—	uncertain significance
rs200695895	3:100,432,566	A/G	—	uncertain significance
rs745478256	3:100,432,582	G/C	—	uncertain significance
rs1576353054	3:100,432,586	G/A	—	likely benign
rs377136610	3:100,432,590	A/T	—	uncertain significance
rs989357227	3:100,432,593	C/T	—	pathogenic
rs774808090	3:100,432,597	G/A	—	uncertain significance
rs2472056888	3:100,432,609	A/G	—	uncertain significance
rs2095037556	3:100,432,626	T/C	—	uncertain significance
rs763523148	3:100,432,627	A/G	—	uncertain significance
rs769041703	3:100,432,628	T/A	—	uncertain significance
rs2472057133	3:100,432,630	A/T	—	uncertain significance
rs2149057725	3:100,432,654	G/A	—	uncertain significance
rs2472057244	3:100,432,662	A/C	—	likely benign
rs2472057284	3:100,432,674	C/A	—	uncertain significance
rs767892218	3:100,432,689	G/A	—	uncertain significance
rs200195571	3:100,432,691	A/C	—	likely benign
rs1406625923	3:100,432,695	A/G	—	uncertain significance
rs201326908	3:100,432,700	G/A	—	likely benign
rs2472057486	3:100,432,702	A/G	—	uncertain significance
rs1291270880	3:100,432,703	T/C	—	likely benign
rs1232918261	3:100,432,704	A/G	—	uncertain significance
rs766483726	3:100,432,706	A/G	—	likely benign
rs2095037817	3:100,432,712	A/C	—	uncertain significance
rs2472057622	3:100,432,718	G/A	—	uncertain significance
rs2472057641	3:100,432,719	A/C	—	uncertain significance
rs200924045	3:100,432,724	T/C	—	benign
rs758417817	3:100,432,726	T/C	—	likely benign
rs9824942	3:100,432,752	A/T	—	benign
rs772577601	3:100,432,753	A/T	—	benign
rs773643503	3:100,432,754	A/T	—	likely benign
rs9825075	3:100,432,767	A/G	—	benign
rs13059686	3:100,432,975	C/T	—	benign
rs78081928	3:100,438,762	C/T	—	likely benign
rs1503838	3:100,438,784	A/G	—	benign
rs2472074122	3:100,438,806	T/C	—	likely benign
rs79631225	3:100,438,809	T/A	—	likely benign
rs778438842	3:100,438,810	A/T	—	likely benign
rs2149066367	3:100,438,828	T/G	—	uncertain significance
rs2095056321	3:100,438,830	A/G	—	uncertain significance
rs1295139107	3:100,438,831	T/C	—	uncertain significance
rs2095056339	3:100,438,832	A/G	—	uncertain significance
rs773769795	3:100,438,847	T/C	—	likely benign
rs2472074393	3:100,438,849	C/G	—	uncertain significance
rs2149066401	3:100,438,853	C/T	—	likely benign
rs747353898	3:100,438,859	C/G	—	likely benign
rs2095056400	3:100,438,864	C/T	—	uncertain significance
rs771223027	3:100,438,865	A/G	—	likely benign
rs147546544	3:100,438,868	T/A	—	likely benign
rs1173009495	3:100,438,871	G/T	—	uncertain significance
rs1335010812	3:100,438,888	A/C	—	uncertain significance
rs140174542	3:100,438,890	C/G	—	uncertain significance
rs150620449	3:100,438,892	G/T	—	likely benign
rs2149066459	3:100,438,895	A/G	—	likely benign
rs775485992	3:100,438,898	A/G	—	likely benign
rs1468380372	3:100,438,902	G/A	—	uncertain significance
rs1325276402	3:100,438,909	A/G	—	likely benign
rs1227137986	3:100,438,910	G/A	—	likely benign
rs2149066494	3:100,438,914	A/G	—	likely benign
rs767431238	3:100,438,920	T/A	—	likely benign
rs755835566	3:100,438,922	A/T	—	likely benign
rs9833043	3:100,439,191	A/G	—	benign
rs13317522	3:100,447,318	C/G	—	benign
rs181800796	3:100,447,415	T/A	—	likely benign
rs1143775	3:100,447,416	T/A	—	benign
rs377094635	3:100,447,417	A/T	—	likely benign
rs184425200	3:100,447,446	T/C	—	likely benign
rs2472097321	3:100,447,543	G/A	—	likely benign
rs2095082752	3:100,447,551	T/C	—	likely benign
rs1234041059	3:100,447,563	C/T	—	likely benign
rs1282207535	3:100,447,567	C/A	—	uncertain significance
rs1435777080	3:100,447,573	C/T	—	uncertain significance
rs1180461235	3:100,447,575	C/G	—	likely benign
rs1576366321	3:100,447,577	T/A	—	uncertain significance
rs2095082870	3:100,447,580	A/C	—	uncertain significance
rs1576366326	3:100,447,589	A/G	—	uncertain significance
rs746086227	3:100,447,590	G/C	—	uncertain significance
rs369508900	3:100,447,596	A/G	—	likely benign
rs775608477	3:100,447,597	T/C	—	conflicting classifications of pathogenicity
rs587777175	3:100,447,603	C/T	missense variant	pathogenic
rs376971794	3:100,447,604	G/A	—	conflicting classifications of pathogenicity
rs373307369	3:100,447,607	G/C	—	uncertain significance
rs145735377	3:100,447,611	A/G	—	likely benign
rs759168672	3:100,447,612	C/T	—	conflicting classifications of pathogenicity
rs1434913178	3:100,447,617	A/G	—	uncertain significance
rs2472097616	3:100,447,619	A/C	—	uncertain significance
rs764959531	3:100,447,624	C/A	synonymous variant	likely benign
rs1423123429	3:100,447,625	G/T	—	uncertain significance

Showing 100 of 332 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.