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Fig. 1 | BMC Cancer

Fig. 1

From: Detection of mutations in SF3B1, EIF1AX and GNAQ in primary orbital melanoma by candidate gene analysis

Fig. 1

Point mutations identified in tumour tissue of primary orbital melanoma. a Two cases (patients 4 and 5) harboured a heterozygous mutation in GNAQ (c.A626T, p.Q209L). b A recurrent heterozygous mutation in SF3B1 (c.G1874A, p.R625H) was identified in four patients with favourable prognoses (cases 4, 9, 11, 12). c One patient, case 10, carried a heterozygous change in EIF1AX (c.A11T, p.N4S)

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BMC Cancer

ISSN: 1471-2407

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