List of variants in gene SLC2A10 reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_030777.4(SLC2A10):c.616G>A (p.Ala206Thr)	rs2235491	0.12280
NM_030777.4(SLC2A10):c.1541A>G (p.Lys514Arg)	rs41283344	0.05817
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.394C>T (p.Arg132Trp)	rs121908173	0.00009
NM_030777.4(SLC2A10):c.1276G>T (p.Gly426Trp)	rs121908172	0.00004
NM_030777.4(SLC2A10):c.685C>T (p.Arg229Ter)	rs756457861	0.00001
NM_030777.4(SLC2A10):c.1334del (p.Gly445fs)	rs587776600

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