List of variants reported as likely pathogenic for B-cell neoplasm by Wasik Lab, Fox Chase Cancer Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002468.5(MYD88):c.755T>C (p.Leu252Pro)	rs387907272	0.00001
NM_000626.4(CD79B):c.586T>C (p.Tyr196His)
NM_001987.5(ETV6):c.33+1G>A
NM_024665.7(TBL1XR1):c.1192A>T (p.Lys398Ter)
NM_024665.7(TBL1XR1):c.1337A>G (p.Tyr446Cys)	rs878854402

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