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Table 1 Coverage of known HCM and HCM-phenocopy genes in the WES data

From: Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy

Gene

Proportion of coding region covered at given level

1x

10x

20x

MYBPC3

1

1

0.9663

MYH7

1

1

1

TNNT2

1

1

0.9989

TNNI3

1

1

0.8674

TPM1

1

0.9993

0.9289

ACTC1

1

1

1

MYL2

1

1

1

MYL3

1

1

1

FH11

1

1

1

NEXN

1

1

1

PLN

1

0.9983

0.9883

GLA

1

1

1

LAMP2

1

1

1

PRKAG2

1

1

0.9589