List of variants in gene TFG reported as likely benign for Charcot-Marie-Tooth disease

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 18

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HGVS	dbSNP
NM_006070.6(TFG):c.1048G>A (p.Ala350Thr)	rs543542721
NM_006070.6(TFG):c.1060C>G (p.Pro354Ala)	rs111356679
NM_006070.6(TFG):c.1116C>T (p.Thr372=)	rs1576389880
NM_006070.6(TFG):c.1146G>A (p.Ala382=)	rs761808737
NM_006070.6(TFG):c.1199G>A (p.Arg400Gln)	rs963151000
NM_006070.6(TFG):c.185-10T>A	rs79631225
NM_006070.6(TFG):c.185-9A>T	rs778438842
NM_006070.6(TFG):c.457T>G (p.Ser153Ala)	rs140466338
NM_006070.6(TFG):c.57G>A (p.Glu19=)	rs1576353054
NM_006070.6(TFG):c.621C>T (p.Pro207=)	rs141786985
NM_006070.6(TFG):c.663C>T (p.Gly221=)	rs140669729
NM_006070.6(TFG):c.672A>C (p.Pro224=)	rs141412018
NM_006070.6(TFG):c.741C>T (p.Tyr247=)	rs1576379547
NM_006070.6(TFG):c.771G>A (p.Gln257=)	rs374006808
NM_006070.6(TFG):c.774G>A (p.Pro258=)	rs1367793822
NM_006070.6(TFG):c.908C>T (p.Ala303Val)	rs1576389064
NM_006070.6(TFG):c.988A>G (p.Thr330Ala)	rs145835282
Single allele

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