ClinVar Miner

List of variants in gene SLC2A10 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_030777.3(SLC2A10):c.-321C>A rs73115554 0.03270
NM_030777.4(SLC2A10):c.1547+153T>G rs1430966603 0.02383
NM_030777.3(SLC2A10):c.-273C>T rs137938281 0.02020
NM_030777.4(SLC2A10):c.1547+255G>A rs6012024 0.01450
NM_030777.4(SLC2A10):c.*280C>T rs6018009 0.01365
NM_030777.4(SLC2A10):c.1547+152T>G rs1358271407 0.01072
NM_030777.4(SLC2A10):c.*32T>C rs78864327 0.00746
NM_030777.4(SLC2A10):c.1548-61C>G rs113249258 0.00738
NM_030777.4(SLC2A10):c.1547+156T>G rs1244723248 0.00707
NM_030777.4(SLC2A10):c.5-116A>G rs183563269 0.00672
NM_030777.4(SLC2A10):c.5-135_5-131del rs375425716 0.00651
NM_030777.4(SLC2A10):c.4+228C>T rs181896882 0.00509
NM_030777.4(SLC2A10):c.1411+23C>T rs61516789 0.00372
NM_030777.4(SLC2A10):c.*29C>G rs34965637 0.00241
NM_030777.4(SLC2A10):c.630C>T (p.Gly210=) rs142431229 0.00113
NM_030777.4(SLC2A10):c.696C>G (p.Thr232=) rs138679634 0.00029
NM_030777.4(SLC2A10):c.*8G>A rs375282462 0.00025
NM_030777.4(SLC2A10):c.315C>T (p.Arg105=) rs150800734 0.00015
NM_030777.4(SLC2A10):c.1547+19G>A rs546525339 0.00011
NM_030777.4(SLC2A10):c.1208G>A (p.Arg403Gln) rs199912561 0.00010
NM_030777.4(SLC2A10):c.330C>T (p.Phe110=) rs199848479 0.00010
NM_030777.4(SLC2A10):c.1412-3C>T rs374857656 0.00009
NM_030777.4(SLC2A10):c.1559G>A (p.Ser520Asn) rs573480396 0.00007
NM_030777.4(SLC2A10):c.792T>C (p.His264=) rs377031320 0.00007
NM_030777.4(SLC2A10):c.1464C>T (p.Leu488=) rs142639587 0.00006
NM_030777.4(SLC2A10):c.1605C>T (p.Ile535=) rs148470005 0.00006
NM_030777.4(SLC2A10):c.644G>A (p.Arg215Gln) rs774497964 0.00006
NM_030777.4(SLC2A10):c.961G>A (p.Val321Met) rs372596900 0.00006
NM_030777.4(SLC2A10):c.1234G>A (p.Ala412Thr) rs746203433 0.00004
NM_030777.4(SLC2A10):c.807C>T (p.Ala269=) rs144705080 0.00004
NM_030777.4(SLC2A10):c.1446C>T (p.Tyr482=) rs150398871 0.00003
NM_030777.4(SLC2A10):c.189G>C (p.Leu63=) rs890578209 0.00003
NM_030777.4(SLC2A10):c.306C>T (p.Val102=) rs530216827 0.00003
NM_030777.4(SLC2A10):c.948C>T (p.Leu316=) rs755109002 0.00003
NM_030777.4(SLC2A10):c.1299T>C (p.Leu433=) rs879632885 0.00002
NM_030777.4(SLC2A10):c.1412-13C>T rs371888996 0.00002
NM_030777.4(SLC2A10):c.1110T>C (p.Thr370=) rs760859018 0.00001
NM_030777.4(SLC2A10):c.120T>C (p.Phe40=) rs202176956 0.00001
NM_030777.4(SLC2A10):c.1269C>T (p.Phe423=) rs1057524067 0.00001
NM_030777.4(SLC2A10):c.1305C>T (p.Leu435=) rs201159437 0.00001
NM_030777.4(SLC2A10):c.1371G>A (p.Ala457=) rs558894862 0.00001
NM_030777.4(SLC2A10):c.1497A>G (p.Glu499=) rs780076629 0.00001
NM_030777.4(SLC2A10):c.1518A>G (p.Ala506=) rs548796220 0.00001
NM_030777.4(SLC2A10):c.1547+18del rs771439306 0.00001
NM_030777.4(SLC2A10):c.180C>T (p.Leu60=) rs371988251 0.00001
NM_030777.4(SLC2A10):c.195T>A (p.Gly65=) rs1002286842 0.00001
NM_030777.4(SLC2A10):c.252G>A (p.Val84=) rs878855129 0.00001
NM_030777.4(SLC2A10):c.587A>T (p.Lys196Met) rs145446653 0.00001
NM_030777.4(SLC2A10):c.720C>A (p.Leu240=) rs374985824 0.00001
NM_030777.4(SLC2A10):c.810G>C (p.Val270=) rs774452914 0.00001
NM_030777.4(SLC2A10):c.873G>A (p.Val291=) rs755197578 0.00001
NM_030777.4(SLC2A10):c.*269del rs113206025
NM_030777.4(SLC2A10):c.-26dup rs1335581409
NM_030777.4(SLC2A10):c.1191G>A (p.Gly397=) rs750216918
NM_030777.4(SLC2A10):c.1461C>T (p.Val487=) rs1555888585
NM_030777.4(SLC2A10):c.237C>A (p.Leu79=) rs201323237
NM_030777.4(SLC2A10):c.369G>C (p.Val123=) rs1555887891
NM_030777.4(SLC2A10):c.4+9C>G rs1057521373
NM_030777.4(SLC2A10):c.5-121dup rs879560987
NM_030777.4(SLC2A10):c.5-163_5-162insCGGATGGA rs1555887757
NM_030777.4(SLC2A10):c.504C>T (p.Phe168=) rs540023880
NM_030777.4(SLC2A10):c.54T>C (p.Gly18=) rs772186491
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=) rs748662135
NM_030777.4(SLC2A10):c.635G>C (p.Gly212Ala) rs863223730
NM_030777.4(SLC2A10):c.645G>C (p.Arg215=) rs367742782
NM_030777.4(SLC2A10):c.794G>C (p.Gly265Ala) rs863223731
NM_030777.4(SLC2A10):c.831C>T (p.Gly277=) rs142697617

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