ClinVar Miner

List of variants in gene FGF3 studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_005247.4(FGF3):c.255del (p.Ile85fs) rs281860302
NM_005247.4(FGF3):c.270dup (p.Leu91fs) rs1554981083
NM_005247.4(FGF3):c.283C>T (p.Arg95Trp) rs281860303
NM_005247.4(FGF3):c.310C>T (p.Arg104Ter) rs121917704
NM_005247.4(FGF3):c.317A>G (p.Tyr106Cys) rs281860306
NM_005247.4(FGF3):c.394del (p.Arg132fs) rs281860304
NM_005247.4(FGF3):c.457_458del (p.Trp153fs) rs281860307
NM_005247.4(FGF3):c.462C>G (p.Tyr154Ter) rs782712529
NM_005247.4(FGF3):c.466T>C (p.Ser156Pro) rs121917703
NM_005247.4(FGF3):c.616del (p.Val206fs) rs281860305

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