ClinVar Miner

List of variants in gene MYH7 reported as likely benign for not provided

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Total variants: 44
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HGVS dbSNP
NM_000257.4(MYH7):c.*1C>T rs1566520659
NM_000257.4(MYH7):c.-8-104T>C
NM_000257.4(MYH7):c.1000-164_1000-134del
NM_000257.4(MYH7):c.1332T>C (p.Asn444=) rs397516099
NM_000257.4(MYH7):c.1491G>A (p.Glu497=)
NM_000257.4(MYH7):c.1578+187T>A
NM_000257.4(MYH7):c.1579-71T>C
NM_000257.4(MYH7):c.1878G>A (p.Gly626=)
NM_000257.4(MYH7):c.1956+120G>A
NM_000257.4(MYH7):c.2044+122T>C
NM_000257.4(MYH7):c.2162+17A>C
NM_000257.4(MYH7):c.2183C>T (p.Ala728Val) rs121913644
NM_000257.4(MYH7):c.2349C>T (p.Arg783=) rs139882431
NM_000257.4(MYH7):c.2424-58G>A
NM_000257.4(MYH7):c.2679+260C>G
NM_000257.4(MYH7):c.2868T>C (p.Asp956=) rs140718120
NM_000257.4(MYH7):c.28G>C (p.Gly10Arg) rs199577321
NM_000257.4(MYH7):c.2922+62C>T
NM_000257.4(MYH7):c.3100-102G>A
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=) rs45540831
NM_000257.4(MYH7):c.3337-316C>A
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
NM_000257.4(MYH7):c.3777C>T (p.His1259=) rs149103761
NM_000257.4(MYH7):c.3854-50G>A
NM_000257.4(MYH7):c.3854-76C>T
NM_000257.4(MYH7):c.3936G>T (p.Leu1312=)
NM_000257.4(MYH7):c.3973-176C>T
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4077C>T (p.Arg1359=) rs45523835
NM_000257.4(MYH7):c.4170-215C>T
NM_000257.4(MYH7):c.4191G>A (p.Leu1397=)
NM_000257.4(MYH7):c.4197A>T (p.Glu1399Asp) rs730880725
NM_000257.4(MYH7):c.456C>G (p.Pro152=)
NM_000257.4(MYH7):c.530+243G>A
NM_000257.4(MYH7):c.530+294C>A
NM_000257.4(MYH7):c.531-144G>A
NM_000257.4(MYH7):c.5655+21C>T
NM_000257.4(MYH7):c.5730G>A (p.Ala1910=) rs776940948
NM_000257.4(MYH7):c.5791-162A>C
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570
NM_000257.4(MYH7):c.801T>C (p.Leu267=)
NM_000257.4(MYH7):c.999+154G>A
NM_000257.4(MYH7):c.999+175G>A
NM_000257.4(MYH7):c.999+60G>T

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