From: Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease
Patient ID
Gene
Variant
Primers
SH1190831
MYH6
c.3835C > T
(p.R1279X)
F 5′-CACACTCACCCTTCCTGTCT-3′
R 5′-CTGAAATGAGGGGCTTGTGG-3′