List of variants in gene SLC2A10 reported as likely benign 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: 21

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.366C>T (p.Tyr122=)	rs34990188	0.00411
NM_030777.4(SLC2A10):c.674G>A (p.Arg225His)	rs34295241	0.00302
NM_030777.4(SLC2A10):c.-15C>T	rs377142129	0.00164
NM_030777.4(SLC2A10):c.1512G>A (p.Ser504=)	rs117587497	0.00128
NM_030777.4(SLC2A10):c.515C>T (p.Thr172Ile)	rs143301610	0.00100
NM_030777.4(SLC2A10):c.816C>G (p.Ala272=)	rs148058006	0.00077
NM_030777.4(SLC2A10):c.765C>T (p.Ser255=)	rs142106322	0.00060
NM_030777.4(SLC2A10):c.931G>A (p.Val311Ile)	rs139932041	0.00026
NM_030777.4(SLC2A10):c.1008C>T (p.Thr336=)	rs370173604	0.00019
NM_030777.4(SLC2A10):c.780C>T (p.Ser260=)	rs181500247	0.00017
NM_030777.4(SLC2A10):c.1559G>A (p.Ser520Asn)	rs573480396	0.00015
NM_030777.4(SLC2A10):c.315C>T (p.Arg105=)	rs150800734	0.00015
NM_030777.4(SLC2A10):c.1571G>A (p.Arg524Lys)	rs370141550	0.00012
NM_030777.4(SLC2A10):c.1464C>T (p.Leu488=)	rs142639587	0.00006
NM_030777.4(SLC2A10):c.924C>T (p.Ala308=)	rs377173165	0.00004
NM_030777.4(SLC2A10):c.1371G>A (p.Ala457=)	rs558894862	0.00001
NM_030777.4(SLC2A10):c.1518A>G (p.Ala506=)	rs548796220	0.00001
NM_030777.4(SLC2A10):c.1110T>C (p.Thr370=)	rs760859018
NM_030777.4(SLC2A10):c.1206T>A (p.Ala402=)	rs764278693
NM_030777.4(SLC2A10):c.624G>A (p.Lys208=)
NM_030777.4(SLC2A10):c.939C>G (p.Gly313=)	rs2123048967

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