List of variants in gene SLC2A10 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His)	rs34295241	0.00302
NM_030777.4(SLC2A10):c.1370C>T (p.Ala457Val)	rs201393026	0.00015
NM_030777.4(SLC2A10):c.314G>A (p.Arg105His)	rs753280877	0.00004
NM_030777.4(SLC2A10):c.322G>A (p.Val108Ile)	rs373375540	0.00003
NM_030777.4(SLC2A10):c.1601G>A (p.Arg534His)	rs746480018	0.00002
NM_030777.4(SLC2A10):c.110_121del (p.Gln37_Gly41delinsArg)	rs767211470	0.00001
NM_030777.4(SLC2A10):c.367G>A (p.Val123Met)	rs770619266	0.00001
NM_030777.4(SLC2A10):c.383G>A (p.Gly128Glu)	rs1226198239	0.00001
NM_030777.4(SLC2A10):c.475G>T (p.Gly159Cys)	rs761947206	0.00001
NM_030777.4(SLC2A10):c.505G>A (p.Gly169Ser)	rs35151194	0.00001
NM_030777.4(SLC2A10):c.1016C>T (p.Thr339Ile)	rs1213099627
NM_030777.4(SLC2A10):c.316G>A (p.Ala106Thr)	rs6094438
NM_030777.4(SLC2A10):c.476G>T (p.Gly159Val)
NM_030777.4(SLC2A10):c.647A>G (p.Tyr216Cys)	rs111525892

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