List of variants in gene SLC2A1 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_006516.4(SLC2A1):c.894C>T (p.Phe298=)	rs140825318	0.00073
NM_006516.4(SLC2A1):c.777C>T (p.Ile259=)	rs78388808	0.00068
NM_006516.4(SLC2A1):c.276-7T>C	rs369273744	0.00063
NM_006516.4(SLC2A1):c.498C>T (p.Val166=)	rs150971143	0.00036
NM_006516.4(SLC2A1):c.972+7del	rs531385270	0.00016
NM_006516.4(SLC2A1):c.987G>A (p.Glu329=)	rs201989024	0.00008
NM_006516.4(SLC2A1):c.258C>T (p.Phe86=)	rs147319894	0.00007
NM_006516.4(SLC2A1):c.1016T>C (p.Ile339Thr)	rs141619735	0.00006
NM_006516.4(SLC2A1):c.1034C>T (p.Ala345Val)	rs769943554	0.00004
NM_006516.4(SLC2A1):c.179C>T (p.Thr60Met)	rs142986731	0.00004
NM_006516.4(SLC2A1):c.321C>T (p.Ala107=)	rs398124230	0.00004
NM_006516.4(SLC2A1):c.906G>T (p.Gly302=)	rs55693364	0.00004
NM_006516.4(SLC2A1):c.652C>T (p.Arg218Cys)	rs147249343	0.00003
NM_006516.4(SLC2A1):c.322G>A (p.Val108Met)	rs74323945	0.00002
NM_006516.4(SLC2A1):c.790C>T (p.Arg264Cys)	rs766376173	0.00002
NM_006516.4(SLC2A1):c.1171G>A (p.Val391Met)	rs764168088	0.00001
NM_006516.4(SLC2A1):c.1446G>C (p.Leu482=)	rs794726996	0.00001
NM_006516.4(SLC2A1):c.19-4G>A	rs398124229	0.00001
NM_006516.4(SLC2A1):c.567G>C (p.Leu189=)	rs794727721	0.00001
NM_006516.4(SLC2A1):c.1006C>G (p.Leu336Val)	rs755946345
NM_006516.4(SLC2A1):c.114+7A>G	rs80301843
NM_006516.4(SLC2A1):c.164G>C (p.Ser55Thr)	rs794727508
NM_006516.4(SLC2A1):c.274C>A (p.Arg92=)	rs202060209
NM_006516.4(SLC2A1):c.458G>A (p.Arg153His)	rs794727642
NM_006516.4(SLC2A1):c.679+4C>T	rs139492241
NM_006516.4(SLC2A1):c.80G>A (p.Gly27Asp)	rs794727283
NM_006516.4(SLC2A1):c.938C>A (p.Ser313Tyr)	rs794727870

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