ClinVar Miner

List of variants in gene SLC2A10 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
Download table as spreadsheet
HGVS dbSNP
NM_030777.4(SLC2A10):c.1010G>C (p.Gly337Ala) rs150745395
NM_030777.4(SLC2A10):c.1014G>C (p.Gln338His) rs35833600
NM_030777.4(SLC2A10):c.1057C>G (p.Leu353Val) rs200196034
NM_030777.4(SLC2A10):c.1096C>T (p.Pro366Ser) rs774664650
NM_030777.4(SLC2A10):c.1175G>A (p.Ser392Asn) rs863223733
NM_030777.4(SLC2A10):c.129C>G (p.Ser43Arg) rs863223734
NM_030777.4(SLC2A10):c.1324G>C (p.Glu442Gln) rs143265363
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val) rs201393026
NM_030777.4(SLC2A10):c.1387A>C (p.Ser463Arg) rs771091234
NM_030777.4(SLC2A10):c.1402G>A (p.Asp468Asn) rs768345011
NM_030777.4(SLC2A10):c.1415C>T (p.Thr472Ile) rs563376340
NM_030777.4(SLC2A10):c.1423T>G (p.Leu475Val) rs754355572
NM_030777.4(SLC2A10):c.1456G>A (p.Ala486Thr) rs759205774
NM_030777.4(SLC2A10):c.145T>A (p.Phe49Ile) rs863223729
NM_030777.4(SLC2A10):c.1481A>G (p.Tyr494Cys) rs374854180
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys) rs370141550
NM_030777.4(SLC2A10):c.1600C>T (p.Arg534Cys) rs142577271
NM_030777.4(SLC2A10):c.1616C>T (p.Ala539Val) rs140312420
NM_030777.4(SLC2A10):c.163C>T (p.Leu55Phe) rs745611450
NM_030777.4(SLC2A10):c.212G>T (p.Cys71Phe) rs377305511
NM_030777.4(SLC2A10):c.238G>A (p.Gly80Arg) rs369865870
NM_030777.4(SLC2A10):c.316G>A (p.Ala106Thr) rs6094438
NM_030777.4(SLC2A10):c.371C>T (p.Ser124Leu) rs774076515
NM_030777.4(SLC2A10):c.416A>G (p.Tyr139Cys) rs139858464
NM_030777.4(SLC2A10):c.430A>T (p.Thr144Ser) rs748746893
NM_030777.4(SLC2A10):c.443T>C (p.Leu148Pro) rs863223732
NM_030777.4(SLC2A10):c.455C>T (p.Ala152Val) rs775987124
NM_030777.4(SLC2A10):c.484T>C (p.Trp162Arg) rs755925085
NM_030777.4(SLC2A10):c.504C>A (p.Phe168Leu) rs540023880
NM_030777.4(SLC2A10):c.673C>T (p.Arg225Cys) rs199659394
NM_030777.4(SLC2A10):c.797G>T (p.Gly266Val) rs369484751
NM_030777.4(SLC2A10):c.859G>A (p.Ala287Thr) rs780058786
NM_030777.4(SLC2A10):c.876C>A (p.Asp292Glu) rs777604168
NM_030777.4(SLC2A10):c.878G>A (p.Arg293His) rs770882223
NM_030777.4(SLC2A10):c.920T>A (p.Met307Lys) rs768142427
NM_030777.4(SLC2A10):c.929C>T (p.Ser310Phe) rs763521707
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041
NM_030777.4(SLC2A10):c.961G>A (p.Val321Met) rs372596900
NM_030777.4(SLC2A10):c.995T>C (p.Val332Ala) rs570363463

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.