SLC25A42

solute carrier family 25 member 42

Summary

This gene encodes a solute carrier family 25 protein. Solute carrier family 25 proteins are localized to mitochondria and play critical roles in the transport of molecules across the inner mitochondrial membrane. The encoded protein is a mitochondrial transporter for coenzyme A (CoA) and adenosine 3',5'-diphosphate. [provided by RefSeq, Feb 2012]

Known Variants131 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5710200219:19,200,345T/Aintron variant—
rs205976370519:19,206,937G/T—uncertain significance
rs11794012119:19,206,959C/T—uncertain significance
rs37015322919:19,206,960G/A—likely benign
rs76125883519:19,206,965G/A—uncertain significance
rs75419293019:19,206,981T/C—likely benign
rs205976420419:19,206,996C/G—likely benign
rs74839435019:19,206,998C/T—uncertain significance
rs75848474719:19,206,999G/A—likely benign
rs52749803819:19,207,002C/T—likely benign
rs74576828419:19,207,003G/A—uncertain significance
rs77535354419:19,207,005C/T—likely benign
rs74909573819:19,207,013A/C—uncertain significance
rs97660349219:19,207,020T/G—uncertain significance
rs37482882619:19,207,026G/A—likely benign
rs11296871919:19,207,117T/A—benign
rs53320474319:19,212,573C/G—likely benign
rs57591784319:19,212,576A/G—likely benign
rs205979766819:19,212,578G/A—likely benign
rs118470173419:19,212,586G/A—likely benign
rs11274293119:19,212,591G/A—uncertain significance
rs13851793319:19,212,617C/T—likely benign
rs118532813019:19,212,619G/T—likely benign
rs53290696219:19,212,622G/C—likely benign
rs251410278719:19,212,631C/T—likely benign
rs5614412619:19,212,658G/A—benign
rs103537721519:19,212,679C/T—likely benign
rs75367429519:19,212,712C/T—likely benign
rs75496013119:19,212,713C/T—likely benign
rs95595057419:19,212,715A/T—likely benign
rs11124976919:19,215,550A/G—benign
rs136261740119:19,215,705G/C—likely benign
rs75056038819:19,215,713T/G—likely benign
rs36775669119:19,215,715T/C—likely benign
rs132066311819:19,215,718C/G—likely benign
rs75811968619:19,215,765C/T—likely benign
rs37055215919:19,215,766G/A—likely benign
rs76191386519:19,216,357C/T—likely benign
rs76785139819:19,216,358G/A—likely benign
rs171673197219:19,216,359C/T—likely benign
rs205982168719:19,216,406G/A—uncertain significance
rs205982192219:19,216,448G/C—uncertain significance
rs14555205619:19,216,450G/T—likely benign
rs13803628719:19,216,454G/A—uncertain significance
rs156852393519:19,216,465C/G—likely pathogenic
rs130079247019:19,216,468C/T—likely benign
rs76091527819:19,216,477G/A—likely benign
rs77673860019:19,216,485C/T—uncertain significance
rs144246492719:19,216,495G/A—likely benign
rs75588338319:19,216,502C/A—uncertain significance
rs74860414019:19,216,514A/C—uncertain significance
rs103772994419:19,216,525C/T—likely benign
rs124742443219:19,216,538T/A—pathogenic
rs77668749119:19,216,545C/G—likely benign
rs133869013219:19,216,546C/T—likely benign
rs96776841619:19,216,547G/A—likely benign
rs480892019:19,216,613T/C—benign
rs1297706919:19,216,728G/A—benign
rs74744026319:19,217,064C/T—likely benign
rs144744070519:19,217,079G/T—uncertain significance
rs205982713819:19,217,080C/A—uncertain significance
rs6174050619:19,217,081C/G—likely benign
rs251410949419:19,217,084G/A—likely benign
rs251410949619:19,217,086C/T—uncertain significance
rs19963409719:19,217,088C/G—likely benign
rs74809037419:19,217,094C/T—uncertain significance
rs205982740619:19,217,106G/A—uncertain significance
rs76049143219:19,217,108C/T—likely benign
rs75218714219:19,217,123A/G—likely benign
rs75757800019:19,217,139C/G—uncertain significance
rs20127078519:19,217,150C/G—likely benign
rs14811226319:19,217,177C/T—likely benign
rs37222940919:19,217,201C/T—likely benign
rs77505084419:19,217,210G/C—likely benign
rs36989554619:19,217,214A/T—likely benign
rs1166862019:19,218,490C/G—benign
rs251411264219:19,218,699G/A—likely benign
rs76725752519:19,218,709C/T—uncertain significance
rs14958511919:19,218,731C/T—uncertain significance
rs251411273019:19,218,737T/C—uncertain significance
rs56841466419:19,218,739G/A—benign
rs134131804219:19,218,749G/A—uncertain significance
rs36800721119:19,218,769T/C—likely benign
rs251411283819:19,218,774T/C—uncertain significance
rs14425636019:19,218,779C/T—uncertain significance
rs77384086519:19,218,785G/A—uncertain significance
rs251411289719:19,218,793G/C—likely benign
rs76117370919:19,218,797A/C—uncertain significance
rs14071131819:19,218,800C/G—uncertain significance
rs37219910319:19,218,801C/T—uncertain significance
rs14492912819:19,218,805C/T—likely benign
rs53157776019:19,218,806G/T—uncertain significance
rs92558710119:19,218,807C/G—uncertain significance
rs76662635319:19,218,829T/C—likely benign
rs75982546519:19,218,835G/A—likely benign
rs76561105319:19,218,836C/T—uncertain significance
rs92137405219:19,218,849A/G—uncertain significance
rs4554693619:19,218,853A/G—uncertain significance
rs37655065119:19,218,861A/G—likely benign
rs251411306219:19,218,866T/C—likely benign

Showing 100 of 131 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.