ClinVar Miner

List of variants in gene MYH7 reported by OMIM

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Total variants: 43
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HGVS dbSNP
NM_000257.2(MYH7):c.1208G>T (p.Arg403Leu) rs121913624
NM_000257.2(MYH7):c.2845G>A (p.Glu949Lys) rs121913629
NM_000257.2(MYH7):c.5378T>C (p.Leu1793Pro) rs121913654
NM_000257.2(MYH7):c.5647G>A (p.Glu1883Lys) rs121913652
NM_000257.2(MYH7):c.5754C>R (p.Asn1918Lys) rs138110910
NM_000257.3(MYH7):c.1046T>C (p.Met349Thr) rs121913640
NM_000257.3(MYH7):c.1322C>T (p.Thr441Met) rs121913653
NM_000257.3(MYH7):c.1357C>A (p.Arg453Ser) rs121913625
NM_000257.3(MYH7):c.1447G>A (p.Glu483Lys) rs121913651
NM_000257.3(MYH7):c.1491G>T (p.Glu497Asp) rs267606911
NM_000257.3(MYH7):c.1538T>G (p.Phe513Cys) rs121913636
NM_000257.3(MYH7):c.1816G>A (p.Val606Met) rs121913627
NM_000257.3(MYH7):c.1925C>T (p.Ser642Leu) rs121913646
NM_000257.3(MYH7):c.2229G>C (p.Glu743Asp) rs397516139
NM_000257.3(MYH7):c.2292C>G (p.Phe764Leu) rs121913643
NM_000257.3(MYH7):c.2333A>G (p.Asp778Gly) rs121913634
NM_000257.3(MYH7):c.2770G>A (p.Glu924Lys) rs121913628
NM_000257.3(MYH7):c.2803G>A (p.Glu935Lys) rs121913639
NM_000257.3(MYH7):c.5296G>A (p.Ala1766Thr) rs267606909
NM_000257.3(MYH7):c.5458C>T (p.Arg1820Trp) rs145734640
NM_000257.3(MYH7):c.5533C>T (p.Arg1845Trp) rs28933098
NM_000257.3(MYH7):c.5702A>T (p.His1901Leu) rs121913649
NM_000257.3(MYH7):c.667G>A (p.Ala223Thr) rs121913645
NM_000257.3(MYH7):c.728G>A (p.Arg243His) rs267606910
NM_000257.3(MYH7):c.732+1G>A rs730880850
NM_000257.3(MYH7):c.746G>A (p.Arg249Gln) rs3218713
NM_000257.3(MYH7):c.767G>A (p.Gly256Glu) rs121913633
NM_000257.3(MYH7):c.847T>G (p.Tyr283Asp) rs397515482
NM_000257.3(MYH7):c.[1816G>A;2183C>T]
NM_000257.4(MYH7):c.1207C>T (p.Arg403Trp) rs3218714
NM_000257.4(MYH7):c.1208G>A (p.Arg403Gln) rs121913624
NM_000257.4(MYH7):c.1357C>T (p.Arg453Cys) rs121913625
NM_000257.4(MYH7):c.1594T>C (p.Ser532Pro) rs121913642
NM_000257.4(MYH7):c.1750G>C (p.Gly584Arg) rs121913626
NM_000257.4(MYH7):c.2146G>A (p.Gly716Arg) rs121913638
NM_000257.4(MYH7):c.2155C>T (p.Arg719Trp) rs121913637
NM_000257.4(MYH7):c.2156G>A (p.Arg719Gln) rs121913641
NM_000257.4(MYH7):c.2167C>T (p.Arg723Cys) rs121913630
NM_000257.4(MYH7):c.2221G>C (p.Gly741Arg) rs121913632
NM_000257.4(MYH7):c.2609G>A (p.Arg870His) rs36211715
NM_000257.4(MYH7):c.2717A>G (p.Asp906Gly) rs267606908
NM_000257.4(MYH7):c.2722C>G (p.Leu908Val) rs121913631
nsv513807

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