ClinVar Miner

List of variants in gene MYCN studied for Feingold syndrome type 1

Included ClinVar conditions (2):
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_005378.6(MYCN):c.429C>T (p.Ala143=) rs532543210 0.00069
NM_005378.6(MYCN):c.1062G>A (p.Ala354=) rs201114632 0.00055
NM_005378.6(MYCN):c.1380C>T (p.His460=) rs150023769 0.00024
NM_005378.6(MYCN):c.612C>T (p.Pro204=) rs767651526 0.00002
NM_005378.6(MYCN):c.854G>T (p.Arg285Leu) rs747134309 0.00002
NM_005378.6(MYCN):c.718G>A (p.Gly240Ser) rs1397907417 0.00001
NM_005378.6(MYCN):c.1014C>A (p.Tyr338Ter) rs367962377
NM_005378.6(MYCN):c.1037del (p.Pro346fs)
NM_005378.6(MYCN):c.1060G>T (p.Ala354Ser)
NM_005378.6(MYCN):c.1061dup (p.Ser355fs) rs1553370963
NM_005378.6(MYCN):c.1105_1106dup (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.1171C>A (p.Arg391Ser) rs1662856733
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.1181G>T (p.Arg394Leu) rs104893648
NM_005378.6(MYCN):c.1211T>G (p.Leu404Arg)
NM_005378.6(MYCN):c.1274_1283del (p.Lys425fs)
NM_005378.6(MYCN):c.1319T>C (p.Leu440Pro)
NM_005378.6(MYCN):c.1384C>T (p.Arg462Trp)
NM_005378.6(MYCN):c.403C>T (p.Gln135Ter)
NM_005378.6(MYCN):c.559del (p.Val187fs) rs2103325472
NM_005378.6(MYCN):c.621dup (p.Ala208fs)
NM_005378.6(MYCN):c.626dup (p.Ala210fs) rs1558534266
NM_005378.6(MYCN):c.633_634dup (p.Ala212fs)
NM_005378.6(MYCN):c.727C>T (p.Gln243Ter)
NM_005378.6(MYCN):c.796G>T (p.Glu266Ter) rs2103330255
NM_005378.6(MYCN):c.801_809del rs794727504
NM_005378.6(MYCN):c.845_846del (p.Val282fs) rs1572220856
NM_005378.6(MYCN):c.902_903del (p.Val301fs) rs1553370918
NM_005378.6(MYCN):c.964C>T (p.Arg322Ter) rs759103701

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