List of variants reported as uncertain significance for Adrenal cortex carcinoma by Genome Sciences Centre, British Columbia Cancer Agency

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.1837_1839del (p.Val613del)	rs2135353566
NM_000179.3(MSH6):c.3644T>A (p.Leu1215Ter)	rs2104526529
NM_000249.4(MLH1):c.884G>T (p.Ser295Ile)	rs63750144
NM_000489.6(ATRX):c.3904del (p.Arg1302fs)	rs2148497062
NM_000489.6(ATRX):c.6235C>T (p.Arg2079Ter)	rs2148020083
NM_001197104.2(KMT2A):c.2318dup (p.Ser774fs)	rs782297546
NM_001374828.1(ARID1B):c.4453C>T (p.Gln1485Ter)	rs2128366503
NM_003072.5(SMARCA4):c.276G>C (p.Gln92His)	rs1555752030
NM_004972.4(JAK2):c.2385G>T (p.Arg795Ser)	rs1819621092
NM_006218.4(PIK3CA):c.2086G>A (p.Gly696Arg)	rs2108413471
Single allele
t(12;16)(q13.13;p11.2)
t(17;19)(q25.1;p13.3)

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