ClinVar Miner

List of variants in gene SLC2A10 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NM_030777.4(SLC2A10):c.*1000C>T rs886056733
NM_030777.4(SLC2A10):c.*1064G>A
NM_030777.4(SLC2A10):c.*1143G>T rs545129749
NM_030777.4(SLC2A10):c.*1162C>T rs185898725
NM_030777.4(SLC2A10):c.*116C>T
NM_030777.4(SLC2A10):c.*1230C>T
NM_030777.4(SLC2A10):c.*1249G>A
NM_030777.4(SLC2A10):c.*1394G>A rs775775371
NM_030777.4(SLC2A10):c.*1502C>T
NM_030777.4(SLC2A10):c.*1628T>A rs886056734
NM_030777.4(SLC2A10):c.*1715G>A
NM_030777.4(SLC2A10):c.*171C>T rs886056728
NM_030777.4(SLC2A10):c.*1731C>T rs762351956
NM_030777.4(SLC2A10):c.*1758A>C
NM_030777.4(SLC2A10):c.*180A>G rs188370349
NM_030777.4(SLC2A10):c.*182T>G rs886056729
NM_030777.4(SLC2A10):c.*1858T>G rs886056735
NM_030777.4(SLC2A10):c.*191C>T
NM_030777.4(SLC2A10):c.*194G>A
NM_030777.4(SLC2A10):c.*2018C>T rs886056736
NM_030777.4(SLC2A10):c.*2098A>G
NM_030777.4(SLC2A10):c.*2137C>G
NM_030777.4(SLC2A10):c.*214T>G
NM_030777.4(SLC2A10):c.*2203C>A rs528071290
NM_030777.4(SLC2A10):c.*2254del rs886056737
NM_030777.4(SLC2A10):c.*2316C>T rs757116033
NM_030777.4(SLC2A10):c.*2409A>G
NM_030777.4(SLC2A10):c.*2416_*2418del rs528431199
NM_030777.4(SLC2A10):c.*2482T>A
NM_030777.4(SLC2A10):c.*269del rs113206025
NM_030777.4(SLC2A10):c.*389C>G rs147684335
NM_030777.4(SLC2A10):c.*401C>A rs142547155
NM_030777.4(SLC2A10):c.*414G>T
NM_030777.4(SLC2A10):c.*470_*472del rs3091691
NM_030777.4(SLC2A10):c.*472dup rs3091691
NM_030777.4(SLC2A10):c.*579G>C
NM_030777.4(SLC2A10):c.*608C>A
NM_030777.4(SLC2A10):c.*659G>A
NM_030777.4(SLC2A10):c.*712A>G rs886056732
NM_030777.4(SLC2A10):c.*852T>C
NM_030777.4(SLC2A10):c.*898A>C
NM_030777.4(SLC2A10):c.*926C>T
NM_030777.4(SLC2A10):c.-15C>T rs377142129
NM_030777.4(SLC2A10):c.-22A>G rs886056723
NM_030777.4(SLC2A10):c.-55G>T
NM_030777.4(SLC2A10):c.-60G>T rs886056722
NM_030777.4(SLC2A10):c.1014G>C (p.Gln338His) rs35833600
NM_030777.4(SLC2A10):c.1032C>T (p.Asp344=) rs1301992983
NM_030777.4(SLC2A10):c.1057C>G (p.Leu353Val) rs200196034
NM_030777.4(SLC2A10):c.1225C>G (p.Arg409Gly)
NM_030777.4(SLC2A10):c.1225C>T (p.Arg409Cys) rs562212724
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.1489G>A (p.Val497Ile) rs758538766
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=) rs117587497
NM_030777.4(SLC2A10):c.1596C>T (p.Tyr532=) rs886056727
NM_030777.4(SLC2A10):c.1605C>T (p.Ile535=) rs148470005
NM_030777.4(SLC2A10):c.173C>T (p.Ala58Val)
NM_030777.4(SLC2A10):c.300G>C (p.Trp100Cys) rs886056725
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.365A>G (p.Tyr122Cys)
NM_030777.4(SLC2A10):c.432C>T (p.Thr144=) rs371344477
NM_030777.4(SLC2A10):c.501G>A (p.Met167Ile)
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile) rs143301610
NM_030777.4(SLC2A10):c.599C>G (p.Pro200Arg) rs75218052
NM_030777.4(SLC2A10):c.617C>T (p.Ala206Val)
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=) rs748662135
NM_030777.4(SLC2A10):c.632C>T (p.Pro211Leu)
NM_030777.4(SLC2A10):c.673C>T (p.Arg225Cys) rs199659394
NM_030777.4(SLC2A10):c.692G>A (p.Arg231Gln) rs771028960
NM_030777.4(SLC2A10):c.71A>T (p.Tyr24Phe) rs886056724
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.781G>A (p.Val261Ile) rs372561968
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.920T>A (p.Met307Lys) rs768142427
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile) rs139932041
NM_030777.4(SLC2A10):c.961G>A (p.Val321Met) rs372596900
NM_030777.4(SLC2A10):c.965C>T (p.Pro322Leu) rs886056726

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