ClinVar Miner

List of variants in gene VCL studied for Familial hypertrophic cardiomyopathy 15

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Total variants: 5
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HGVS dbSNP
NM_014000.2(VCL):c.1531G>T (p.Asp511Tyr) rs863225121
NM_014000.2(VCL):c.2828_2829del (p.Pro943fs) rs781036800
NM_014000.2(VCL):c.2923C>T (p.Arg975Trp) rs121917776
NM_014000.2(VCL):c.625A>T (p.Met209Leu) rs144683137
NM_014000.2(VCL):c.829C>A (p.Leu277Met) rs71579353

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