List of variants in gene SLC2A1 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.1395C>T (p.Ser465=)	rs75852730	0.00008
NM_006516.4(SLC2A1):c.1016T>C (p.Ile339Thr)	rs141619735	0.00006
NM_006516.4(SLC2A1):c.1396G>A (p.Gly466Ser)	rs138139624	0.00004
NM_006516.4(SLC2A1):c.179C>T (p.Thr60Met)	rs142986731	0.00004
NM_006516.4(SLC2A1):c.103G>T (p.Ala35Ser)	rs796053245	0.00002
NM_006516.4(SLC2A1):c.278G>A (p.Arg93Gln)	rs80359815	0.00001
NM_006516.4(SLC2A1):c.1023C>G (p.Leu341=)	rs143588685
NM_006516.4(SLC2A1):c.1084C>T (p.Pro362Ser)
NM_006516.4(SLC2A1):c.1261T>C (p.Cys421Arg)	rs1557644984
NM_006516.4(SLC2A1):c.274C>A (p.Arg92=)	rs202060209
NM_006516.4(SLC2A1):c.472A>C (p.Thr158Pro)	rs1553156155
NM_006516.4(SLC2A1):c.516+7T>G	rs1325285163
NM_006516.4(SLC2A1):c.73C>A (p.Gln25Lys)	rs1165759782
NM_006516.4(SLC2A1):c.766_767delinsGT (p.Lys256Val)	rs80359822
NM_006516.4(SLC2A1):c.945C>G (p.Ile315Met)	rs780528770

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