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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′