Table 1.

PCR primers used for the mutation profiling of GNAQ, GNA11, and BAP1.

Gene	Exon	Forward primer sequence 5′–3′	Reverse primer sequence 5′–3′
GNAQ	5	TTTCCCTAAGTTTGTAAGTAGTGCT	AAGTTCACTCCATTCCCCAC
GNA11	5	AGCCGATGTCAGTCTGGTGT	AAGGCAGAGGGAATCAGAGG
BAP1	4	AGTGATGACGCAGTGCAAAG	CTCCATTTCCACTTCCCAAG
	5	TGTCCAGATATGACTGACCTG	ATGTGGTAGCATTCCCAGTG
	6–7	TCTGAAGCTTTGCCTTCCAC	GCCACTGGGTACCACATACC
	8	TGTCTTCCTTCCCACTCCTG	TGGATACTCTCTGTCCCTCCC
	9	CTCAACCTGATGGCGGG	AATGCAGGGAGGGTTGG
	10	TTCCTTTAGGTCCTCAGCCC	AAAAGACTTTCCCTGTTTAGG
	11	TCTCTGGGAAGTGCTGGTTC	CATGGGAAAATTGCCTGTTG
	12	CCGAGCAGCACTTGTTTG	GATCCGAAGCACCTAGAACC
	13	AGCCATTCTGGGTACTGCTG	GAGTGCAGGACACTTTGTGG
	15–16	CTGCCTATTGCTCGTGGG	CAAGGTCTGCTCAAGCCTC
	17	ACAGGGAGGGCCATGAG	TACTGGGAAAAGGGGAAGTG