ClinVar Miner

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

Included ClinVar conditions (137):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
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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