ClinVar Miner

List of variants in gene FGF10 studied for LADD syndrome

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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NM_004465.1(FGF10):c.*5A>T rs111763965
NM_004465.2(FGF10):c.1A>G (p.Met1Val) rs1554040396
NM_004465.2(FGF10):c.232del (p.Arg78fs) rs1554040364
NM_004465.2(FGF10):c.240A>C (p.Arg80Ser) rs104893888
NM_004465.2(FGF10):c.256del (p.Thr86fs) rs1554040361
NM_004465.2(FGF10):c.317G>T (p.Cys106Phe) rs104893885
NM_004465.2(FGF10):c.356del (p.Gly119fs) rs1554035763
NM_004465.2(FGF10):c.401T>A (p.Met134Lys) rs1554035757
NM_004465.2(FGF10):c.409A>T (p.Lys137Ter) rs104893887
NM_004465.2(FGF10):c.467T>G (p.Ile156Arg) rs104893886
NM_004465.2(FGF10):c.541A>C (p.Asn181His) rs1332768200
NM_004465.2(FGF10):c.550G>A (p.Gly184Arg) rs1554035469
NM_004465.2(FGF10):c.624A>G (p.Ser208=) rs886060653

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