List of variants reported as likely pathogenic for adenocarcinoma by Genome Sciences Centre, British Columbia Cancer Agency

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001123385.2(BCOR):c.398_399insAC (p.Ala134fs)	rs1555919960
NM_001123385.2(BCOR):c.4063G>T (p.Glu1355Ter)	rs780712297
NM_001123385.2(BCOR):c.4787_4802del (p.Gly1596fs)	rs1555913337
NM_004985.5(KRAS):c.182A>T (p.Gln61Leu)	rs121913240
NM_017617.5(NOTCH1):c.2825G>A (p.Cys942Tyr)	rs1554728658
NM_017617.5(NOTCH1):c.4045_4052del (p.Ala1349fs)	rs1554728034
NM_152641.4(ARID2):c.2989C>T (p.Gln997Ter)	rs1555155110

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