ClinVar Miner

List of variants in gene SLC2A10 reported as likely benign for Arterial tortuosity syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP
NM_030777.4(SLC2A10):c.*1141G>A
NM_030777.4(SLC2A10):c.*1272G>C rs562491351
NM_030777.4(SLC2A10):c.*1340G>A rs78189695
NM_030777.4(SLC2A10):c.*1449T>C
NM_030777.4(SLC2A10):c.*194G>T
NM_030777.4(SLC2A10):c.*2150C>A rs6012025
NM_030777.4(SLC2A10):c.*29C>G rs34965637
NM_030777.4(SLC2A10):c.*410A>C
NM_030777.4(SLC2A10):c.1008C>T (p.Thr336=) rs370173604
NM_030777.4(SLC2A10):c.1010G>C (p.Gly337Ala) rs150745395
NM_030777.4(SLC2A10):c.1032C>T (p.Asp344=) rs1301992983
NM_030777.4(SLC2A10):c.1079A>G (p.Asn360Ser)
NM_030777.4(SLC2A10):c.1185C>T (p.Leu395=)
NM_030777.4(SLC2A10):c.1187C>T (p.Pro396Leu) rs755654519
NM_030777.4(SLC2A10):c.1203C>T (p.Pro401=) rs368021257
NM_030777.4(SLC2A10):c.1233C>T (p.Thr411=) rs778452693
NM_030777.4(SLC2A10):c.1234G>A (p.Ala412Thr) rs746203433
NM_030777.4(SLC2A10):c.1269C>T (p.Phe423=) rs1057524067
NM_030777.4(SLC2A10):c.1289-6C>T rs199967429
NM_030777.4(SLC2A10):c.1299T>C (p.Leu433=) rs879632885
NM_030777.4(SLC2A10):c.1305C>T (p.Leu435=) rs201159437
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val) rs201393026
NM_030777.4(SLC2A10):c.1371G>A (p.Ala457=) rs558894862
NM_030777.4(SLC2A10):c.1377C>T (p.Asn459=) rs756207829
NM_030777.4(SLC2A10):c.1401C>T (p.Leu467=) rs774586341
NM_030777.4(SLC2A10):c.1446C>T (p.Tyr482=) rs150398871
NM_030777.4(SLC2A10):c.1455C>T (p.Thr485=) rs1285063741
NM_030777.4(SLC2A10):c.1464C>T (p.Leu488=) rs142639587
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=) rs117587497
NM_030777.4(SLC2A10):c.1536C>T (p.Phe512=) rs745307904
NM_030777.4(SLC2A10):c.1548G>T (p.Arg516=) rs116344406
NM_030777.4(SLC2A10):c.1559G>A (p.Ser520Asn) rs573480396
NM_030777.4(SLC2A10):c.1566C>T (p.Gly522=)
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys) rs370141550
NM_030777.4(SLC2A10):c.1593G>A (p.Pro531=) rs148424607
NM_030777.4(SLC2A10):c.1605C>T (p.Ile535=) rs148470005
NM_030777.4(SLC2A10):c.180C>T (p.Leu60=) rs371988251
NM_030777.4(SLC2A10):c.189G>C (p.Leu63=) rs890578209
NM_030777.4(SLC2A10):c.237C>T (p.Leu79=) rs201323237
NM_030777.4(SLC2A10):c.264C>G (p.Gly88=) rs768512276
NM_030777.4(SLC2A10):c.267C>T (p.Ser89=) rs747559824
NM_030777.4(SLC2A10):c.306C>T (p.Val102=) rs530216827
NM_030777.4(SLC2A10):c.315C>T (p.Arg105=) rs150800734
NM_030777.4(SLC2A10):c.316G>A (p.Ala106Thr) rs6094438
NM_030777.4(SLC2A10):c.317C>G (p.Ala106Gly) rs144095826
NM_030777.4(SLC2A10):c.330C>T (p.Phe110=) rs199848479
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=) rs34990188
NM_030777.4(SLC2A10):c.4+10G>A
NM_030777.4(SLC2A10):c.432C>T (p.Thr144=) rs371344477
NM_030777.4(SLC2A10):c.5-9_5-7del rs1600666288
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile) rs143301610
NM_030777.4(SLC2A10):c.581C>T (p.Thr194Ile) rs763889166
NM_030777.4(SLC2A10):c.599C>G (p.Pro200Arg) rs75218052
NM_030777.4(SLC2A10):c.621C>G (p.Pro207=)
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=) rs748662135
NM_030777.4(SLC2A10):c.630C>T (p.Gly210=) rs142431229
NM_030777.4(SLC2A10):c.645G>C (p.Arg215=)
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His) rs34295241
NM_030777.4(SLC2A10):c.681C>T (p.Asn227=)
NM_030777.4(SLC2A10):c.696C>G (p.Thr232=) rs138679634
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=) rs142106322
NM_030777.4(SLC2A10):c.780C>T (p.Ser260=) rs181500247
NM_030777.4(SLC2A10):c.792T>C (p.His264=) rs377031320
NM_030777.4(SLC2A10):c.810G>C (p.Val270=) rs774452914
NM_030777.4(SLC2A10):c.816C>G (p.Ala272=) rs148058006
NM_030777.4(SLC2A10):c.831C>A (p.Gly277=)
NM_030777.4(SLC2A10):c.831C>T (p.Gly277=)
NM_030777.4(SLC2A10):c.858C>T (p.Thr286=) rs758420381
NM_030777.4(SLC2A10):c.876C>A (p.Asp292Glu) rs777604168
NM_030777.4(SLC2A10):c.924C>T (p.Ala308=) rs377173165
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041
NM_030777.4(SLC2A10):c.948C>T (p.Leu316=) rs755109002
NM_030777.4(SLC2A10):c.960C>T (p.Ala320=)
NM_030777.4(SLC2A10):c.961G>A (p.Val321Met) rs372596900
NM_030777.4(SLC2A10):c.9C>T (p.His3=) rs1423610543

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.