SLC25A32

solute carrier family 25 member 32

Summary

This gene encodes a member of the P(I/L)W subfamily of mitochondrial carrier family transport proteins. The encoded protein transports folate across the inner mitochondrial membrane. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2013]

Known Variants145 total

rsidPosition (GRCh37)AllelesClassClinVar
rs22417778:104,412,388C/A3 prime UTR variantbenign
rs352252638:104,412,517A/T—benign
rs749348758:104,412,635G/A—likely benign
rs7608225628:104,412,654T/C—likely benign
rs21304340228:104,412,660G/A—likely benign
rs7641931038:104,412,673T/C—uncertain significance
rs14362445568:104,412,675T/C—likely benign
rs7651040678:104,412,685T/G—uncertain significance
rs1418563988:104,412,688T/C—likely benign
rs24881865408:104,412,726A/C—uncertain significance
rs1420867908:104,412,728T/A—uncertain significance
rs1445308928:104,412,761C/T—benign
rs3691018458:104,412,764C/T—conflicting classifications of pathogenicity
rs1919490478:104,412,765G/A—likely benign
rs24881866838:104,412,780G/C—uncertain significance
rs101037398:104,412,830C/T—benign
rs22417788:104,412,935C/T—benign
rs1173664178:104,413,501C/T—benign
rs592839788:104,413,724G/T—likely benign
rs3695825818:104,413,728T/C—likely benign
rs3742704498:104,413,733C/T—likely benign
rs1159686738:104,413,734G/A—likely benign
rs24881884918:104,413,746C/G—uncertain significance
rs7627810548:104,413,754T/C—uncertain significance
rs2019520678:104,413,755T/C—likely benign
rs1413670188:104,413,814C/T—likely benign
rs3715927388:104,413,833T/C—likely benign
rs7482965988:104,413,838C/T—uncertain significance
rs3725323408:104,413,839G/A—uncertain significance
rs7777768028:104,413,841C/T—uncertain significance
rs1437759408:104,413,847A/G—uncertain significance
rs1457851578:104,413,858A/G—uncertain significance
rs7592324268:104,413,861G/A—uncertain significance
rs3766645358:104,413,863T/C—likely benign
rs7637101138:104,413,869A/G—likely benign
rs24881889098:104,413,871A/G—uncertain significance
rs7635850568:104,413,874T/C—uncertain significance
rs14906142098:104,413,875A/G—likely benign
rs7815406868:104,413,903A/G—likely benign
rs7613828038:104,414,163T/C—uncertain significance
rs24881896738:104,414,174G/C—uncertain significance
rs7747136688:104,414,176G/A—uncertain significance
rs7530702528:104,414,182G/C—uncertain significance
rs24881896958:104,414,184T/C—likely benign
rs24881897048:104,414,190A/G—likely benign
rs5328405038:104,414,253C/T—likely benign
rs7582887818:104,414,254G/A—uncertain significance
rs18162290568:104,414,257G/A—uncertain significance
rs7797440598:104,414,262A/C—uncertain significance
rs10158957488:104,414,281C/T—uncertain significance
rs14544690228:104,414,286C/T—likely benign
rs5509803228:104,414,289G/A—benign
rs7727167938:104,414,293A/G—likely benign
rs1487688508:104,414,295G/T—benign
rs1173996288:104,414,338T/C—benign
rs726754498:104,414,593A/G—benign
rs31338108:104,415,118C/T—benign
rs24881917628:104,415,372A/C—likely benign
rs12430358158:104,415,373T/C—likely benign
rs7513481168:104,415,375T/C—likely benign
rs8646220288:104,415,396T/C—uncertain significance
rs24881918218:104,415,398T/C—likely benign
rs5549254248:104,415,405C/T—uncertain significance
rs3740257898:104,415,406G/A—uncertain significance
rs9290338168:104,415,407C/T—likely benign
rs7769147588:104,415,438G/A—uncertain significance
rs24881921578:104,415,443A/C—uncertain significance
rs1480869778:104,415,456T/C—uncertain significance
rs3707231558:104,415,463G/A—uncertain significance
rs1999963238:104,415,472A/C—uncertain significance
rs24881922658:104,415,482A/T—likely benign
rs8951171428:104,415,499T/G—uncertain significance
rs7524968638:104,415,502G/C—uncertain significance
rs1423290988:104,415,504C/Tmissense variantpathogenic
rs1470148558:104,415,519C/Tstop gainedpathogenic
rs7801353388:104,415,523A/C—uncertain significance
rs1999038518:104,415,524T/C—likely benign
rs13551550488:104,415,537C/A—uncertain significance
rs24881924008:104,415,539G/A—likely benign
rs9023843508:104,415,542G/C—likely benign
rs7621420838:104,415,547T/C—uncertain significance
rs21304393388:104,415,548G/A—likely benign
rs7699469298:104,415,553C/T—uncertain significance
rs5553717118:104,415,569A/G—likely benign
rs18658548:104,416,785C/T—benign
rs715208128:104,416,801C/T—benign
rs18658558:104,416,833C/A—benign
rs14456563998:104,416,994A/G—likely benign
rs7555278208:104,416,995T/C—likely benign
rs5585617548:104,417,020G/A—likely benign
rs1381937968:104,417,038C/T—benign
rs178034418:104,417,045C/T—benign
rs1505619168:104,417,046G/A—uncertain significance
rs12439159738:104,417,052C/T—uncertain significance
rs7604732568:104,417,064T/C—uncertain significance
rs7535362078:104,417,070A/G—uncertain significance
rs7499734728:104,417,093A/G—likely benign
rs12147608038:104,417,104T/C—likely benign
rs14526755348:104,417,108A/C—likely benign
rs794445598:104,417,167C/T—likely benign

Showing 100 of 145 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.