ClinVar Miner

List of variants in gene MYL4 reported as likely benign for Atrial fibrillation, familial, 18

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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_002476.2(MYL4):c.167T>C (p.Phe56Ser) rs144870368 0.00147
NM_002476.2(MYL4):c.565+12C>T rs144326821 0.00066
NM_002476.2(MYL4):c.565+19C>T rs145181954 0.00014
NM_002476.2(MYL4):c.201G>A (p.Pro67=) rs149036573 0.00011
NM_002476.2(MYL4):c.405C>T (p.Phe135=) rs150593274 0.00011
NM_002476.2(MYL4):c.339T>G (p.Phe113Leu) rs200195383 0.00009
NM_002476.2(MYL4):c.565+13G>A rs374440892 0.00006
NM_002476.2(MYL4):c.565+17T>C rs576910138 0.00006
NM_002476.2(MYL4):c.313+16T>C rs376080778 0.00004
NM_002476.2(MYL4):c.313+9G>A rs1418767431 0.00004
NM_002476.2(MYL4):c.447G>A (p.Thr149=) rs371944933 0.00004
NM_002476.2(MYL4):c.471C>T (p.His157=) rs781162398 0.00004
NM_002476.2(MYL4):c.234C>T (p.Cys78=) rs138710476 0.00002
NM_002476.2(MYL4):c.345G>A (p.Thr115=) rs372522881 0.00002
NM_002476.2(MYL4):c.381G>A (p.Lys127=) rs557505985 0.00002
NM_002476.2(MYL4):c.72A>C (p.Ala24=) rs370547497 0.00002
NM_002476.2(MYL4):c.164-13C>G rs770170911 0.00001
NM_002476.2(MYL4):c.276C>T (p.Ala92=) rs1343489917 0.00001
NM_002476.2(MYL4):c.487+14G>A rs1282938957 0.00001
NM_002476.2(MYL4):c.522G>A (p.Leu174=) rs767533462 0.00001
NM_002476.2(MYL4):c.537G>A (p.Glu179=) rs181540609 0.00001
NM_002476.2(MYL4):c.565+10C>T rs778856429 0.00001
NM_002476.2(MYL4):c.567C>T (p.Ala189=) rs777538559 0.00001
NM_002476.2(MYL4):c.57A>G (p.Pro19=) rs765876288 0.00001
NM_002476.2(MYL4):c.102C>T (p.Pro34=)
NM_002476.2(MYL4):c.135+14A>G
NM_002476.2(MYL4):c.150C>G (p.Ala50=)
NM_002476.2(MYL4):c.163+16C>T
NM_002476.2(MYL4):c.163+17C>A
NM_002476.2(MYL4):c.163+17C>G
NM_002476.2(MYL4):c.164-16G>A
NM_002476.2(MYL4):c.164-20G>A
NM_002476.2(MYL4):c.164-4A>C rs2149047338
NM_002476.2(MYL4):c.164-8C>T rs893225315
NM_002476.2(MYL4):c.184T>C (p.Leu62=)
NM_002476.2(MYL4):c.207A>T (p.Gly69=)
NM_002476.2(MYL4):c.225C>T (p.Tyr75=)
NM_002476.2(MYL4):c.252C>T (p.Ala84=) rs1598659253
NM_002476.2(MYL4):c.291G>T (p.Val97=)
NM_002476.2(MYL4):c.300G>A (p.Lys100=) rs2064844083
NM_002476.2(MYL4):c.313+19C>T
NM_002476.2(MYL4):c.313+8C>A rs372826462
NM_002476.2(MYL4):c.313+8C>T rs372826462
NM_002476.2(MYL4):c.314-16C>T
NM_002476.2(MYL4):c.314-6C>T rs2149048609
NM_002476.2(MYL4):c.314-9T>C
NM_002476.2(MYL4):c.315G>A (p.Glu105=)
NM_002476.2(MYL4):c.348C>T (p.Phe116=)
NM_002476.2(MYL4):c.351G>A (p.Leu117=)
NM_002476.2(MYL4):c.396T>C (p.Tyr132=)
NM_002476.2(MYL4):c.429C>T (p.Asp143=)
NM_002476.2(MYL4):c.441T>C (p.Asn147=)
NM_002476.2(MYL4):c.474C>T (p.Val158=) rs2149048808
NM_002476.2(MYL4):c.487+13G>A rs1223343679
NM_002476.2(MYL4):c.487+20A>C rs2149048835
NM_002476.2(MYL4):c.488-10C>A
NM_002476.2(MYL4):c.504G>A (p.Glu168=)
NM_002476.2(MYL4):c.549C>T (p.Gly183=)
NM_002476.2(MYL4):c.565+11G>T
NM_002476.2(MYL4):c.565+12C>A
NM_002476.2(MYL4):c.565+7A>G
NM_002476.2(MYL4):c.576G>A (p.Lys192=)
NM_002476.2(MYL4):c.582C>A (p.Ile194=) rs1405716390
NM_002476.2(MYL4):c.588A>G (p.Ser196=)
NM_002476.2(MYL4):c.66C>T (p.Ala22=)
NM_002476.2(MYL4):c.6T>C (p.Ala2=)
NM_002476.2(MYL4):c.72A>G (p.Ala24=)

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