ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by ClinGen Inherited Cardiomyopathy Variant Curation Expert Panel,

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 12
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NM_000257.4(MYH7):c.1477_1478del (p.Met493fs) rs727504336
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.3169G>A (p.Gly1057Ser) rs397516179
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr) rs45478699
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
NM_000257.4(MYH7):c.3578G>A (p.Arg1193His) rs397516187
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.5302G>A (p.Glu1768Lys) rs397516241
NM_000257.4(MYH7):c.5326A>G (p.Ser1776Gly) rs369437262
NM_000257.4(MYH7):c.5329G>A (p.Ala1777Thr) rs200939753
NM_000257.4(MYH7):c.5588G>A (p.Arg1863Gln) rs45520836
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln) rs187073962

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