ClinVar Miner

List of variants in gene MYL4 studied for atrial fibrillation (disease)

Included ClinVar conditions (37):
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Gene type:
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Total variants: 66
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HGVS dbSNP
NC_000017.10:g.(?_45297260)_(45300418_?)del
NM_002476.2(MYL4):c.100_102dup (p.Pro34dup)
NM_002476.2(MYL4):c.113C>A (p.Ala38Asp) rs780020430
NM_002476.2(MYL4):c.113C>G (p.Ala38Gly)
NM_002476.2(MYL4):c.128G>A (p.Ser43Asn)
NM_002476.2(MYL4):c.131T>C (p.Val44Ala)
NM_002476.2(MYL4):c.135G>A (p.Lys45=)
NM_002476.2(MYL4):c.136A>G (p.Ile46Val)
NM_002476.2(MYL4):c.137T>C (p.Ile46Thr)
NM_002476.2(MYL4):c.150C>T (p.Ala50=) rs143234546
NM_002476.2(MYL4):c.153C>G (p.Asp51Glu)
NM_002476.2(MYL4):c.159T>G (p.Ile53Met)
NM_002476.2(MYL4):c.164-8C>T
NM_002476.2(MYL4):c.167T>C (p.Phe56Ser) rs144870368
NM_002476.2(MYL4):c.194G>A (p.Arg65Gln)
NM_002476.2(MYL4):c.201G>A (p.Pro67=) rs149036573
NM_002476.2(MYL4):c.210G>T (p.Glu70Asp)
NM_002476.2(MYL4):c.211A>G (p.Met71Val)
NM_002476.2(MYL4):c.212T>G (p.Met71Arg)
NM_002476.2(MYL4):c.23C>T (p.Pro8Leu) rs957196759
NM_002476.2(MYL4):c.248G>T (p.Arg83Leu)
NM_002476.2(MYL4):c.251C>T (p.Ala84Val)
NM_002476.2(MYL4):c.252C>T (p.Ala84=) rs1598659253
NM_002476.2(MYL4):c.276C>T (p.Ala92=)
NM_002476.2(MYL4):c.277G>A (p.Glu93Lys) rs369894969
NM_002476.2(MYL4):c.286C>T (p.Arg96Cys)
NM_002476.2(MYL4):c.287G>A (p.Arg96His)
NM_002476.2(MYL4):c.304A>G (p.Lys102Glu)
NM_002476.2(MYL4):c.313+8C>A rs372826462
NM_002476.2(MYL4):c.313+8C>T
NM_002476.2(MYL4):c.314-4G>A rs114024716
NM_002476.2(MYL4):c.318G>A (p.Met106Ile)
NM_002476.2(MYL4):c.31G>A (p.Glu11Lys) rs886037778
NM_002476.2(MYL4):c.339T>G (p.Phe113Leu) rs200195383
NM_002476.2(MYL4):c.344C>T (p.Thr115Met)
NM_002476.2(MYL4):c.345G>A (p.Thr115=) rs372522881
NM_002476.2(MYL4):c.352C>T (p.Pro118Ser)
NM_002476.2(MYL4):c.353C>G (p.Pro118Arg)
NM_002476.2(MYL4):c.365A>G (p.His122Arg) rs376695433
NM_002476.2(MYL4):c.374G>A (p.Arg125His)
NM_002476.2(MYL4):c.381G>A (p.Lys127=)
NM_002476.2(MYL4):c.405C>T (p.Phe135=) rs150593274
NM_002476.2(MYL4):c.406G>A (p.Val136Met) rs375241929
NM_002476.2(MYL4):c.418C>T (p.Arg140Cys) rs767035280
NM_002476.2(MYL4):c.419G>A (p.Arg140His) rs374127769
NM_002476.2(MYL4):c.446C>T (p.Thr149Met) rs200236286
NM_002476.2(MYL4):c.447G>A (p.Thr149=) rs371944933
NM_002476.2(MYL4):c.466C>T (p.Arg156Trp)
NM_002476.2(MYL4):c.471C>T (p.His157=)
NM_002476.2(MYL4):c.487+1G>C rs769405762
NM_002476.2(MYL4):c.487+4T>C rs1443330356
NM_002476.2(MYL4):c.488-1G>A rs770372675
NM_002476.2(MYL4):c.488-4G>A rs146859926
NM_002476.2(MYL4):c.488-5C>T rs376118927
NM_002476.2(MYL4):c.48TCCAGC[2] (p.16AP[7])
NM_002476.2(MYL4):c.48TCCAGC[4] (p.16AP[9])
NM_002476.2(MYL4):c.522G>A (p.Leu174=) rs767533462
NM_002476.2(MYL4):c.537G>A (p.Glu179=) rs181540609
NM_002476.2(MYL4):c.544A>G (p.Asn182Asp)
NM_002476.2(MYL4):c.556A>T (p.Asn186Tyr) rs16941677
NM_002476.2(MYL4):c.557A>G (p.Asn186Ser)
NM_002476.2(MYL4):c.565+2T>C
NM_002476.2(MYL4):c.566-4C>T rs2071439
NM_002476.2(MYL4):c.567C>T (p.Ala189=)
NM_002476.2(MYL4):c.582C>A (p.Ile194=) rs1405716390
NM_002476.2(MYL4):c.68C>T (p.Pro23Leu)

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