ClinVar Miner

List of variants in gene SLC2A9 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020041.3(SLC2A9):c.1114-89G>C rs114361719 0.02226
NM_020041.3(SLC2A9):c.1215+95T>C rs28571073 0.00731
NM_020041.3(SLC2A9):c.1420-167C>T rs139913518 0.00548
NM_020041.3(SLC2A9):c.899G>A (p.Arg300His) rs145688560 0.00315
NM_020041.3(SLC2A9):c.1545C>T (p.Ser515=) rs144428359 0.00298
NM_020041.3(SLC2A9):c.883G>A (p.Val295Met) rs75088806 0.00272
NM_020041.3(SLC2A9):c.410+211C>T rs558711638 0.00259
NM_020041.3(SLC2A9):c.107G>A (p.Cys36Tyr) rs144053854 0.00130
NM_020041.3(SLC2A9):c.1299C>T (p.Ile433=) rs147534794 0.00088
NM_020041.3(SLC2A9):c.30G>A (p.Lys10=) rs147368076 0.00058
NM_020041.3(SLC2A9):c.726C>T (p.Ala242=) rs147545113 0.00022
NM_020041.3(SLC2A9):c.198C>G (p.Gly66=) rs374679729 0.00016
NM_020041.3(SLC2A9):c.1221C>T (p.His407=) rs369754879 0.00013
NM_020041.3(SLC2A9):c.1002+16C>T rs753237840 0.00011
NM_020041.3(SLC2A9):c.666C>T (p.Pro222=) rs139449249 0.00010
NM_020041.3(SLC2A9):c.250-9T>C rs770788275 0.00005
NM_020041.3(SLC2A9):c.825G>A (p.Thr275=) rs375484164 0.00005
NM_020041.3(SLC2A9):c.957C>T (p.Thr319=) rs770758004 0.00005
NM_020041.3(SLC2A9):c.909C>T (p.Ser303=) rs371313593 0.00004
NM_020041.3(SLC2A9):c.1419+16del rs762153562 0.00003
NM_020041.3(SLC2A9):c.536-18T>A rs796931938 0.00002
NM_020041.3(SLC2A9):c.795C>T (p.Asn265=) rs112580274 0.00002
NM_020041.3(SLC2A9):c.843C>T (p.Asp281=) rs374095603 0.00002
NM_020041.3(SLC2A9):c.1215+7C>T rs780348287 0.00001
NM_020041.3(SLC2A9):c.1344G>A (p.Pro448=) rs368484282 0.00001
NM_020041.3(SLC2A9):c.1518C>G (p.Thr506=) rs771866622 0.00001
NM_020041.3(SLC2A9):c.168C>G (p.Leu56=) rs931819754 0.00001
NM_001001290.2(SLC2A9):c.21C>T (p.Asp7=)
NM_020041.3(SLC2A9):c.1002+11G>A rs2110083239
NM_020041.3(SLC2A9):c.1002+17G>A
NM_020041.3(SLC2A9):c.105G>A (p.Glu35=)
NM_020041.3(SLC2A9):c.1065C>T (p.Tyr355=)
NM_020041.3(SLC2A9):c.1113+16G>A
NM_020041.3(SLC2A9):c.1114-19C>T
NM_020041.3(SLC2A9):c.1114-29CT[8] rs141838570
NM_020041.3(SLC2A9):c.1152C>T (p.Leu384=)
NM_020041.3(SLC2A9):c.1197C>G (p.Thr399=)
NM_020041.3(SLC2A9):c.1291+16C>A
NM_020041.3(SLC2A9):c.1291+9C>T
NM_020041.3(SLC2A9):c.1302G>A (p.Pro434=) rs556085300
NM_020041.3(SLC2A9):c.1380C>T (p.Leu460=)
NM_020041.3(SLC2A9):c.1383C>T (p.Ser461=)
NM_020041.3(SLC2A9):c.1420-6C>T
NM_020041.3(SLC2A9):c.150+15C>G
NM_020041.3(SLC2A9):c.150+16T>C
NM_020041.3(SLC2A9):c.150+8C>T
NM_020041.3(SLC2A9):c.168C>T (p.Leu56=)
NM_020041.3(SLC2A9):c.186G>T (p.Ala62=)
NM_020041.3(SLC2A9):c.195C>T (p.Phe65=)
NM_020041.3(SLC2A9):c.250-213del
NM_020041.3(SLC2A9):c.363A>C (p.Gly121=)
NM_020041.3(SLC2A9):c.411-14T>C
NM_020041.3(SLC2A9):c.411-19A>T
NM_020041.3(SLC2A9):c.535+10C>A
NM_020041.3(SLC2A9):c.535+18C>T
NM_020041.3(SLC2A9):c.535+19G>A
NM_020041.3(SLC2A9):c.536-7T>C
NM_020041.3(SLC2A9):c.537C>T (p.Gly179=)
NM_020041.3(SLC2A9):c.540C>T (p.Val180=)
NM_020041.3(SLC2A9):c.546C>T (p.Leu182=)
NM_020041.3(SLC2A9):c.564C>T (p.Tyr188=)
NM_020041.3(SLC2A9):c.567T>A (p.Leu189=)
NM_020041.3(SLC2A9):c.612G>A (p.Val204=)
NM_020041.3(SLC2A9):c.682-19G>A
NM_020041.3(SLC2A9):c.723T>A (p.Pro241=)
NM_020041.3(SLC2A9):c.72C>T (p.Ala24=) rs138916724
NM_020041.3(SLC2A9):c.72_73delinsGA (p.Gly25Arg)
NM_020041.3(SLC2A9):c.756C>T (p.Leu252=)
NM_020041.3(SLC2A9):c.768A>C (p.Pro256=)
NM_020041.3(SLC2A9):c.780C>G (p.Leu260=)
NM_020041.3(SLC2A9):c.802A>C (p.Arg268=)
NM_020041.3(SLC2A9):c.815-16G>A
NM_020041.3(SLC2A9):c.84G>A (p.Gly28=)
NM_020041.3(SLC2A9):c.864G>A (p.Glu288=) rs1743740032
NM_020041.3(SLC2A9):c.882C>T (p.Arg294=)

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.