List of variants reported as uncertain significance for anaplastic cancer by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001754.5(RUNX1):c.155T>A (p.Met52Lys)	rs200431130	0.00028
NM_177438.3(DICER1):c.248A>G (p.Tyr83Cys)	rs373646414	0.00006
NM_024675.4(PALB2):c.3249G>C (p.Glu1083Asp)	rs147045425	0.00005
NM_177438.3(DICER1):c.1410G>C (p.Glu470Asp)	rs774271782	0.00004
NM_177438.3(DICER1):c.1801A>G (p.Ile601Val)	rs564224919	0.00004
NM_177438.3(DICER1):c.3422C>T (p.Ser1141Phe)	rs780815020	0.00004
NM_177438.3(DICER1):c.2378A>G (p.Tyr793Cys)	rs527568726	0.00002
NM_177438.3(DICER1):c.3229G>A (p.Asp1077Asn)	rs373412959	0.00001
NM_177438.3(DICER1):c.4675A>G (p.Ile1559Val)	rs377409989	0.00001
NM_177438.3(DICER1):c.925G>A (p.Val309Ile)	rs1181141404	0.00001
NM_177438.3(DICER1):c.1908-138_2804+645del
NM_177438.3(DICER1):c.2026C>T (p.Arg676Ter)	rs878855246
NM_177438.3(DICER1):c.2154G>C (p.Glu718Asp)	rs1555371628
NM_177438.3(DICER1):c.3357T>A (p.Asp1119Glu)
NM_177438.3(DICER1):c.4374G>A (p.Met1458Ile)	rs1488281692
NM_177438.3(DICER1):c.968G>T (p.Gly323Val)	rs906299601

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