ClinVar Miner

List of variants in gene SLC25A13 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014251.3(SLC25A13):c.328+6A>G rs6957975 0.67687
NM_014251.3(SLC25A13):c.1194A>G (p.Leu398=) rs2301629 0.34968
NM_014251.3(SLC25A13):c.93T>C (p.Gly31=) rs78430478 0.01089
NM_014251.3(SLC25A13):c.1311+3A>G rs180844972 0.00092
NM_014251.3(SLC25A13):c.1910T>C (p.Val637Ala) rs148962110 0.00075
NM_014251.3(SLC25A13):c.1618C>T (p.Pro540Ser) rs75622628 0.00052
NM_014251.3(SLC25A13):c.882T>C (p.Ala294=) rs138094550 0.00024
NM_014251.3(SLC25A13):c.408A>G (p.Leu136=) rs188486690 0.00015
NM_014251.3(SLC25A13):c.1275G>A (p.Ser425=) rs376416252 0.00014
NM_014251.3(SLC25A13):c.849-4A>G rs368491877 0.00012
NM_014251.3(SLC25A13):c.483G>A (p.Glu161=) rs762752651 0.00009
NM_014251.3(SLC25A13):c.1451A>G (p.Lys484Arg) rs367988218 0.00008
NM_014251.3(SLC25A13):c.1751-4_1751-3insT rs765170811 0.00006
NM_014251.3(SLC25A13):c.534C>T (p.Val178=) rs776288888 0.00006
NM_014251.3(SLC25A13):c.551G>A (p.Arg184Gln) rs142427515 0.00005
NM_014251.3(SLC25A13):c.960A>G (p.Pro320=) rs765358773 0.00005
NM_014251.3(SLC25A13):c.1336A>C (p.Thr446Pro) rs200237622 0.00004
NM_014251.3(SLC25A13):c.1505C>T (p.Pro502Leu) rs139149160 0.00003
NM_014251.3(SLC25A13):c.1711C>T (p.Arg571Cys) rs753626243 0.00003
NM_014251.3(SLC25A13):c.615+5G>A rs80338717 0.00003
NM_014251.3(SLC25A13):c.1344T>C (p.Pro448=) rs1037190907 0.00002
NM_014251.3(SLC25A13):c.1236C>T (p.Asn412=) rs747257110 0.00001
NM_014251.3(SLC25A13):c.1637C>G (p.Thr546Arg) rs548769905 0.00001
NM_014251.3(SLC25A13):c.1665C>T (p.Gly555=) rs199735534 0.00001
NM_014251.3(SLC25A13):c.1896G>A (p.Pro632=) rs764388459 0.00001
NM_014251.3(SLC25A13):c.576C>G (p.Pro192=) rs753114158 0.00001
NM_014251.3(SLC25A13):c.848+1G>T rs761370420 0.00001
NM_014251.3(SLC25A13):c.1075C>T (p.Gln359Ter) rs1794541339
NM_014251.3(SLC25A13):c.1083A>C (p.Ser361=)
NM_014251.3(SLC25A13):c.1274C>T (p.Ser425Leu)
NM_014251.3(SLC25A13):c.1424G>A (p.Arg475Gln)
NM_014251.3(SLC25A13):c.1452+5C>G
NM_014251.3(SLC25A13):c.1453-1G>A rs1792048079
NM_014251.3(SLC25A13):c.1464A>C (p.Ala488=) rs1244207348
NM_014251.3(SLC25A13):c.1544A>T (p.Asp515Val)
NM_014251.3(SLC25A13):c.1564A>T (p.Ser522Cys)
NM_014251.3(SLC25A13):c.1653_1655del (p.Ala552del) rs781077173
NM_014251.3(SLC25A13):c.1657C>T (p.Arg553Trp)
NM_014251.3(SLC25A13):c.1740G>A (p.Lys580=) rs1791522939
NM_014251.3(SLC25A13):c.306T>C (p.Ala102=) rs565008080
NM_014251.3(SLC25A13):c.755-8C>A
NM_014251.3(SLC25A13):c.848+9G>T rs201395793
NM_014251.3(SLC25A13):c.848G>C (p.Gly283Ala)
NM_014251.3(SLC25A13):c.852_855del (p.Met285fs) rs80338720

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.