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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 63

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile)	rs143301610	0.00100
NM_030777.4(SLC2A10):c.1010G>C (p.Gly337Ala)	rs150745395	0.00071
NM_030777.4(SLC2A10):c.1415C>T (p.Thr472Ile)	rs563376340	0.00061
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile)	rs139932041	0.00026
NM_030777.4(SLC2A10):c.1079A>G (p.Asn360Ser)	rs139117495	0.00024
NM_030777.4(SLC2A10):c.317C>G (p.Ala106Gly)	rs144095826	0.00023
NM_030777.4(SLC2A10):c.1481A>G (p.Tyr494Cys)	rs374854180	0.00021
NM_030777.4(SLC2A10):c.388C>T (p.Arg130Trp)	rs201150247	0.00019
NM_030777.4(SLC2A10):c.781G>A (p.Val261Ile)	rs372561968	0.00019
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val)	rs201393026	0.00015
NM_030777.4(SLC2A10):c.808G>A (p.Val270Met)	rs749220947	0.00015
NM_030777.4(SLC2A10):c.1324G>C (p.Glu442Gln)	rs143265363	0.00014
NM_030777.4(SLC2A10):c.1600C>T (p.Arg534Cys)	rs142577271	0.00014
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys)	rs370141550	0.00012
NM_030777.4(SLC2A10):c.238G>A (p.Gly80Arg)	rs369865870	0.00010
NM_030777.4(SLC2A10):c.1225C>T (p.Arg409Cys)	rs562212724	0.00009
NM_030777.4(SLC2A10):c.212G>T (p.Cys71Phe)	rs377305511	0.00006
NM_030777.4(SLC2A10):c.484T>C (p.Trp162Arg)	rs755925085	0.00006
NM_030777.4(SLC2A10):c.797G>T (p.Gly266Val)	rs369484751	0.00006
NM_030777.4(SLC2A10):c.395G>A (p.Arg132Gln)	rs376346077	0.00005
NM_030777.4(SLC2A10):c.878G>A (p.Arg293His)	rs770882223	0.00005
NM_030777.4(SLC2A10):c.443T>C (p.Leu148Pro)	rs863223732	0.00004
NM_030777.4(SLC2A10):c.1402G>A (p.Asp468Asn)	rs768345011	0.00003
NM_030777.4(SLC2A10):c.322G>A (p.Val108Ile)	rs373375540	0.00003
NM_030777.4(SLC2A10):c.920T>A (p.Met307Lys)	rs768142427	0.00003
NM_030777.4(SLC2A10):c.929C>T (p.Ser310Phe)	rs763521707	0.00003
NM_030777.4(SLC2A10):c.1163G>A (p.Arg388Gln)	rs780660981	0.00002
NM_030777.4(SLC2A10):c.1616C>T (p.Ala539Val)	rs140312420	0.00002
NM_030777.4(SLC2A10):c.416A>G (p.Tyr139Cys)	rs139858464	0.00002
NM_030777.4(SLC2A10):c.562G>C (p.Gly188Arg)	rs374246708	0.00002
NM_030777.4(SLC2A10):c.859G>A (p.Ala287Thr)	rs780058786	0.00002
NM_030777.4(SLC2A10):c.876C>A (p.Asp292Glu)	rs777604168	0.00002
NM_030777.4(SLC2A10):c.1014G>C (p.Gln338His)	rs35833600	0.00001
NM_030777.4(SLC2A10):c.1096C>T (p.Pro366Ser)	rs774664650	0.00001
NM_030777.4(SLC2A10):c.1175G>A (p.Ser392Asn)	rs863223733	0.00001
NM_030777.4(SLC2A10):c.1423T>G (p.Leu475Val)	rs754355572	0.00001
NM_030777.4(SLC2A10):c.142G>C (p.Glu48Gln)	rs1252274574	0.00001
NM_030777.4(SLC2A10):c.163C>T (p.Leu55Phe)	rs745611450	0.00001
NM_030777.4(SLC2A10):c.170G>T (p.Gly57Val)	rs369796310	0.00001
NM_030777.4(SLC2A10):c.260C>T (p.Ala87Val)	rs746966441	0.00001
NM_030777.4(SLC2A10):c.455C>T (p.Ala152Val)	rs775987124	0.00001
NM_030777.4(SLC2A10):c.462C>G (p.Asn154Lys)	rs769340563	0.00001
NM_030777.4(SLC2A10):c.646T>A (p.Tyr216Asn)	rs1269438372	0.00001
NM_030777.4(SLC2A10):c.712C>G (p.Leu238Val)	rs761633200	0.00001
NM_030777.4(SLC2A10):c.995T>C (p.Val332Ala)	rs570363463	0.00001
NM_030777.4(SLC2A10):c.1057C>G (p.Leu353Val)	rs200196034
NM_030777.4(SLC2A10):c.1210G>C (p.Gly404Arg)
NM_030777.4(SLC2A10):c.129C>G (p.Ser43Arg)	rs863223734
NM_030777.4(SLC2A10):c.1360T>A (p.Phe454Ile)	rs1980003027
NM_030777.4(SLC2A10):c.1387A>C (p.Ser463Arg)	rs771091234
NM_030777.4(SLC2A10):c.1411+4_1411+5del	rs1980009887
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.254T>C (p.Leu85Pro)	rs754120063
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.430A>T (p.Thr144Ser)	rs748746893
NM_030777.4(SLC2A10):c.464A>C (p.Tyr155Ser)	rs1015767771
NM_030777.4(SLC2A10):c.504C>A (p.Phe168Leu)	rs540023880
NM_030777.4(SLC2A10):c.632C>T (p.Pro211Leu)	rs151324893
NM_030777.4(SLC2A10):c.673C>T (p.Arg225Cys)	rs199659394
NM_030777.4(SLC2A10):c.815C>T (p.Ala272Val)
NM_030777.4(SLC2A10):c.952A>G (p.Ser318Gly)

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