ClinVar Miner

List of variants reported as pathogenic for Feingold syndrome

Included ClinVar conditions (2):
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Total variants: 15
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HGVS dbSNP
NC_000013.11:g.(?_90698351)_(90699137_?)del
NM_005378.6(MYCN):c.1014C>A (p.Tyr338Ter) rs367962377
NM_005378.6(MYCN):c.1061dup (p.Ser355fs) rs1553370963
NM_005378.6(MYCN):c.1103_1104AG[3] (p.Ser369fs) rs1572221400
NM_005378.6(MYCN):c.1117C>T (p.Arg373Ter) rs754137452
NM_005378.6(MYCN):c.1145G>A (p.Arg382His) rs121913666
NM_005378.6(MYCN):c.1177C>A (p.Arg393Ser) rs104893647
NM_005378.6(MYCN):c.1178G>A (p.Arg393His) rs104893646
NM_005378.6(MYCN):c.1181G>A (p.Arg394His) rs104893648
NM_005378.6(MYCN):c.217G>T (p.Glu73Ter) rs113994115
NM_005378.6(MYCN):c.231G>A (p.Trp77Ter) rs121913667
NM_005378.6(MYCN):c.626dup (p.Ala210fs) rs1558534266
NM_005378.6(MYCN):c.68_71dup (p.Gln25fs) rs1553370260
NM_005378.6(MYCN):c.900_901TG[1] (p.Val301fs) rs1553370918
NM_005378.6(MYCN):c.964C>T (p.Arg322Ter) rs759103701

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