List of variants reported as pathogenic for B-cell neoplasm by Department Of Pathology & Laboratory Medicine, University Of Pennsylvania

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.517C>T (p.Arg173Cys)	rs121913293	0.00001
NM_139276.3(STAT3):c.1919A>T (p.Tyr640Phe)	rs769031989	0.00001
NM_000059.4(BRCA2):c.9097dup (p.Thr3033fs)	rs397507419
NM_000314.8(PTEN):c.800del (p.Lys267fs)	rs121913289
NM_000314.8(PTEN):c.968del (p.Asn323fs)	rs121913291
NM_000535.7(PMS2):c.163+2T>G
NM_000546.6(TP53):c.776A>C (p.Asp259Ala)
NM_002485.5(NBN):c.1396del (p.Arg466fs)	rs1349928568
NM_003745.2(SOCS1):c.462C>A (p.Tyr154Ter)
NM_004380.3(CREBBP):c.4268del (p.Pro1423fs)
NM_005877.6(SF3A1):c.1641del (p.Ser548fs)
NM_022552.5(DNMT3A):c.2204A>G (p.Tyr735Cys)	rs147828672

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