ClinVar Miner

List of variants in gene FGF10 studied for EEC syndrome and related syndrome

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_004465.1(FGF10):c.*5A>T rs111763965
NM_004465.1(FGF10):c.144G>A (p.Glu48=) rs886060655
NM_004465.1(FGF10):c.186C>A (p.Ser62Arg) rs886060654
NM_004465.1(FGF10):c.1A>G (p.Met1Val) rs1554040396
NM_004465.1(FGF10):c.232delC (p.Arg78Alafs) rs1554040364
NM_004465.1(FGF10):c.240A>C (p.Arg80Ser) rs104893888
NM_004465.1(FGF10):c.256delA (p.Thr86Profs) rs1554040361
NM_004465.1(FGF10):c.261G>A (p.Lys87=) rs545941601
NM_004465.1(FGF10):c.317G>T (p.Cys106Phe) rs104893885
NM_004465.1(FGF10):c.356delG (p.Gly119Glufs) rs1554035763
NM_004465.1(FGF10):c.401T>A (p.Met134Lys) rs1554035757
NM_004465.1(FGF10):c.409A>T (p.Lys137Ter) rs104893887
NM_004465.1(FGF10):c.426C>T (p.Gly142=) rs149851674
NM_004465.1(FGF10):c.430-15G>C rs2290070
NM_004465.1(FGF10):c.467T>G (p.Ile156Arg) rs104893886
NM_004465.1(FGF10):c.541A>C (p.Asn181His) rs1332768200
NM_004465.1(FGF10):c.550G>A (p.Gly184Arg) rs1554035469
NM_004465.1(FGF10):c.591C>T (p.Thr197=) rs17234639
NM_004465.1(FGF10):c.620A>C (p.His207Pro) rs147715509
NM_004465.1(FGF10):c.624A>G (p.Ser208=) rs886060653

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