ClinVar Miner

List of variants in gene SLC2A10 reported as likely benign for not provided

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Gene type:
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Total variants: 66
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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.1154C>G (p.Ala385Gly) rs79849424 0.01835
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.366C>T (p.Tyr122=) rs34990188 0.00411
NM_030777.4(SLC2A10):c.1411+23C>T rs61516789 0.00372
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His) rs34295241 0.00302
NM_030777.4(SLC2A10):c.*29C>G rs34965637 0.00241
NM_030777.4(SLC2A10):c.-15C>T rs377142129 0.00166
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=) rs117587497 0.00128
NM_030777.4(SLC2A10):c.630C>T (p.Gly210=) rs142431229 0.00113
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile) rs143301610 0.00100
NM_030777.4(SLC2A10):c.816C>G (p.Ala272=) rs148058006 0.00077
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=) rs142106322 0.00065
NM_030777.4(SLC2A10):c.696C>G (p.Thr232=) rs138679634 0.00029
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041 0.00026
NM_030777.4(SLC2A10):c.1008C>T (p.Thr336=) rs370173604 0.00019
NM_030777.4(SLC2A10):c.780C>T (p.Ser260=) rs181500247 0.00016
NM_030777.4(SLC2A10):c.315C>T (p.Arg105=) rs150800734 0.00015
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys) rs370141550 0.00012
NM_030777.4(SLC2A10):c.330C>T (p.Phe110=) rs199848479 0.00010
NM_030777.4(SLC2A10):c.1559G>A (p.Ser520Asn) rs573480396 0.00007
NM_030777.4(SLC2A10):c.581C>T (p.Thr194Ile) rs763889166 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.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.924C>T (p.Ala308=) rs377173165 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.120T>C (p.Phe40=) rs202176956 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.297C>T (p.Ala99=) rs1390850910 0.00001
NM_030777.4(SLC2A10):c.57C>T (p.Gly19=) rs1600666379 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.1191G>A (p.Gly397=) rs750216918
NM_030777.4(SLC2A10):c.1206T>A (p.Ala402=) rs764278693
NM_030777.4(SLC2A10):c.363C>T (p.Ile121=) rs1164117855
NM_030777.4(SLC2A10):c.5-121dup rs879560987
NM_030777.4(SLC2A10):c.5-163_5-162insCGGATGGA rs1555887757
NM_030777.4(SLC2A10):c.519A>G (p.Ala173=) rs747333286
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=) rs748662135
NM_030777.4(SLC2A10):c.645G>C (p.Arg215=) rs367742782
NM_030777.4(SLC2A10):c.663C>A (p.Leu221=) rs768433086
NM_030777.4(SLC2A10):c.831C>T (p.Gly277=) rs142697617
NM_030777.4(SLC2A10):c.918C>T (p.Leu306=) rs1979909437
NM_030777.4(SLC2A10):c.939C>G (p.Gly313=) rs2123048967

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