Skip to main content

Table 3 Sequences of the primers used to confirm the mutation by Sanger sequencing

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′