SLC25A24

solute carrier family 25 member 24

Summary

This gene encodes a carrier protein that transports ATP-Mg exchanging it for phosphate. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]

Known Variants119 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs17021096	1:108,679,151	G/A	—	benign
rs964682263	1:108,679,276	C/A	—	uncertain significance
rs2524003711	1:108,679,319	C/A	—	uncertain significance
rs377138462	1:108,679,320	C/A	—	likely benign
rs2101592553	1:108,679,324	T/C	—	uncertain significance
rs1419247169	1:108,679,349	C/T	—	uncertain significance
rs749266397	1:108,679,363	G/A	—	uncertain significance
rs1210521223	1:108,679,372	C/T	—	uncertain significance
rs772402918	1:108,679,393	C/A	—	uncertain significance
rs149670605	1:108,679,411	C/T	—	uncertain significance
rs376157270	1:108,679,415	G/A	—	likely benign
rs2101592710	1:108,679,423	C/T	—	uncertain significance
rs780069314	1:108,679,436	G/T	—	uncertain significance
rs778125454	1:108,679,455	C/A	—	uncertain significance
rs1245516372	1:108,679,460	C/T	—	uncertain significance
rs1679304153	1:108,679,462	A/G	—	likely benign
rs17513812	1:108,679,532	C/T	—	benign
rs11185282	1:108,681,482	G/T	—	benign
rs34563977	1:108,681,600	T/C	—	benign
rs781747926	1:108,681,694	C/T	—	uncertain significance
rs2524009417	1:108,681,700	C/T	—	benign
rs768776765	1:108,681,718	T/A	—	uncertain significance
rs145479430	1:108,681,795	T/G	—	conflicting classifications of pathogenicity
rs376390270	1:108,681,805	T/G	—	uncertain significance
rs756530511	1:108,681,826	A/G	—	uncertain significance
rs12076095	1:108,681,944	A/G	—	benign
rs12071569	1:108,682,022	A/G	—	benign
rs2524020442	1:108,686,187	C/A	—	uncertain significance
rs757904663	1:108,686,191	C/T	—	uncertain significance
rs1026780755	1:108,686,223	T/C	—	uncertain significance
rs1338033505	1:108,686,239	C/G	—	uncertain significance
rs151069768	1:108,686,241	C/T	—	uncertain significance
rs2524021114	1:108,686,332	C/A	—	uncertain significance
rs150195740	1:108,690,906	T/C	—	likely benign
rs1364005877	1:108,690,913	T/C	—	benign
rs1198269918	1:108,690,942	T/C	—	uncertain significance
rs1679662322	1:108,690,944	G/C	—	uncertain significance
rs879578204	1:108,690,962	T/C	—	uncertain significance
rs2524034247	1:108,690,965	A/G	—	uncertain significance
rs775932085	1:108,690,985	T/G	—	conflicting classifications of pathogenicity
rs761350702	1:108,690,999	A/G	—	likely benign
rs767044567	1:108,691,001	T/C	—	uncertain significance
rs202000976	1:108,691,018	C/A	—	benign
rs1048734028	1:108,697,604	C/T	—	uncertain significance
rs888765978	1:108,697,614	T/C	—	likely benign
rs1679856843	1:108,697,661	T/C	—	uncertain significance
rs1571285932	1:108,697,669	C/G	—	likely pathogenic
rs200993204	1:108,697,685	G/A	—	uncertain significance
rs147531188	1:108,697,712	G/A	—	uncertain significance
rs2524049977	1:108,697,720	C/T	—	uncertain significance
rs931596898	1:108,697,726	A/G	—	uncertain significance
rs369827745	1:108,697,731	C/T	—	uncertain significance
rs7555964	1:108,697,845	C/G	—	benign
rs17021146	1:108,697,900	A/G	—	benign
rs200470374	1:108,700,078	G/C	—	likely benign
rs769914346	1:108,700,096	T/C	—	benign
rs1553253989	1:108,700,103	C/T	—	pathogenic
rs1553253990	1:108,700,104	G/A	—	pathogenic
rs145306696	1:108,700,128	G/A	—	likely benign
rs755037648	1:108,700,140	C/G	—	uncertain significance
rs778013594	1:108,700,179	C/T	—	uncertain significance
rs829002	1:108,700,316	G/C	—	benign
rs151259113	1:108,703,824	G/A	—	likely benign
rs2524068323	1:108,703,830	T/C	—	uncertain significance
rs11185293	1:108,703,834	T/C	—	benign
rs149281325	1:108,703,852	A/C	—	conflicting classifications of pathogenicity
rs368829753	1:108,703,878	C/T	—	uncertain significance
rs1291591276	1:108,703,885	G/T	—	uncertain significance
rs2101618595	1:108,703,890	C/T	—	uncertain significance
rs2524068772	1:108,703,933	T/C	—	likely benign
rs149486864	1:108,720,614	G/A	intron variant	—
rs490680	1:108,724,518	G/A	—	benign
rs148035477	1:108,724,552	G/A	—	benign
rs143444253	1:108,724,588	G/T	—	likely benign
rs749551277	1:108,724,604	A/G	—	likely benign
rs373754515	1:108,724,669	G/A	—	likely benign
rs1400300251	1:108,724,670	G/A	—	likely benign
rs491785	1:108,724,693	A/G	—	benign
rs492601	1:108,724,766	G/A	—	benign
rs694667	1:108,728,347	T/C	—	benign
rs144824377	1:108,728,446	A/G	—	likely benign
rs1392041479	1:108,728,470	C/G	—	benign
rs862493	1:108,728,484	T/C	—	benign
rs551037811	1:108,728,500	T/C	—	uncertain significance
rs763613175	1:108,728,502	G/A	—	likely benign
rs767354896	1:108,728,526	T/G	—	uncertain significance
rs146823029	1:108,728,544	A/G	—	likely benign
rs2524135975	1:108,728,558	C/G	—	likely benign
rs779318679	1:108,728,561	C/T	—	uncertain significance
rs114771768	1:108,728,562	A/T	—	benign
rs521545	1:108,734,993	G/C	—	benign
rs199601855	1:108,735,152	T/A	—	benign
rs79735952	1:108,735,212	T/C	—	benign
rs7514794	1:108,735,311	A/G	—	benign
rs41278472	1:108,735,383	T/C	—	benign
rs524504	1:108,735,388	T/A	—	benign
rs116515973	1:108,735,575	T/C	—	benign
rs370060381	1:108,742,561	C/A	—	benign
rs373023235	1:108,742,571	G/A	—	benign
rs2101652360	1:108,742,587	G/A	—	likely benign

Showing 100 of 119 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.