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

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.248A>G (p.Tyr83Cys)	rs373646414	0.00006
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.1377-18T>A	rs1032236740	0.00002
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_001042492.3(NF1):c.1888G>A (p.Val630Ile)	rs751795238
NM_177438.3(DICER1):c.1908-138_2804+645del
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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