ClinVar Miner

List of variants in gene SLC2A10 reported as pathogenic by GeneReviews

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Gene type:
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Total variants: 20
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HGVS dbSNP
NM_030777.4(SLC2A10):c.1276G>T (p.Gly426Trp) rs121908172
NM_030777.4(SLC2A10):c.1309G>A (p.Glu437Lys) rs763220502
NM_030777.4(SLC2A10):c.1330C>T (p.Arg444Ter) rs370547023
NM_030777.4(SLC2A10):c.1334G>A (p.Gly445Glu) rs753723351
NM_030777.4(SLC2A10):c.1334del (p.Gly445fs) rs587776600
NM_030777.4(SLC2A10):c.1411+1G>A rs864309479
NM_030777.4(SLC2A10):c.1411+480_1547+299del
NM_030777.4(SLC2A10):c.243C>G (p.Ser81Arg) rs80358230
NM_030777.4(SLC2A10):c.313C>T (p.Arg105Cys) rs767864243
NM_030777.4(SLC2A10):c.394C>T (p.Arg132Trp) rs121908173
NM_030777.4(SLC2A10):c.417T>A (p.Tyr139Ter) rs572620317
NM_030777.4(SLC2A10):c.425G>T (p.Gly142Val) rs864309480
NM_030777.4(SLC2A10):c.510G>A (p.Trp170Ter) rs80358229
NM_030777.4(SLC2A10):c.685C>T (p.Arg229Ter) rs756457861
NM_030777.4(SLC2A10):c.691C>T (p.Arg231Trp) rs146579504
NM_030777.4(SLC2A10):c.692G>A (p.Arg231Gln) rs771028960
NM_030777.4(SLC2A10):c.731_734del (p.Leu244fs) rs864309481
NM_030777.4(SLC2A10):c.737G>A (p.Gly246Glu) rs564317065
NM_030777.4(SLC2A10):c.756C>A (p.Cys252Ter) rs864309478
NM_030777.4(SLC2A10):c.961del (p.Val321fs) rs587776599

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