List of variants in gene SLC2A10 reported as uncertain significance by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.*8G>A	rs375282462	0.00025
NM_030777.4(SLC2A10):c.317C>G (p.Ala106Gly)	rs144095826	0.00023
NM_030777.4(SLC2A10):c.1600C>T (p.Arg534Cys)	rs142577271	0.00014
NM_030777.4(SLC2A10):c.1204G>A (p.Ala402Thr)	rs147710229	0.00011
NM_030777.4(SLC2A10):c.1208G>A (p.Arg403Gln)	rs199912561	0.00010
NM_030777.4(SLC2A10):c.1331G>A (p.Arg444Gln)	rs148324236	0.00003
NM_030777.4(SLC2A10):c.322G>A (p.Val108Ile)	rs373375540	0.00003
NM_030777.4(SLC2A10):c.923C>T (p.Ala308Val)	rs776373143	0.00003
NM_030777.4(SLC2A10):c.929C>T (p.Ser310Phe)	rs763521707	0.00003
NM_030777.4(SLC2A10):c.1274T>C (p.Phe425Ser)	rs546176728	0.00001
NM_030777.4(SLC2A10):c.142G>C (p.Glu48Gln)	rs1252274574	0.00001
NM_030777.4(SLC2A10):c.1080T>G (p.Asn360Lys)	rs772874942
NM_030777.4(SLC2A10):c.1411+5G>A
NM_030777.4(SLC2A10):c.152T>C (p.Val51Ala)
NM_030777.4(SLC2A10):c.4+6T>A
NM_030777.4(SLC2A10):c.590A>G (p.Asp197Gly)	rs1158420839
NM_030777.4(SLC2A10):c.673C>T (p.Arg225Cys)	rs199659394

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