ClinVar Miner

List of variants reported as likely pathogenic for Lymphoma

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.743G>A (p.Arg248Gln) rs11540652 0.00002
NM_002468.5(MYD88):c.755T>C (p.Leu252Pro) rs387907272 0.00001
NM_003482.4(KMT2D):c.10624_10625del (p.Leu3542fs) rs1592123162
NM_003482.4(KMT2D):c.11897_11911del (p.Phe3966_Gln3971delinsTer) rs1592119138
NM_004456.5(EZH2):c.1936T>A (p.Tyr646Asn) rs267601395
NM_004456.5(EZH2):c.1936T>C (p.Tyr646His) rs267601395
NM_004456.5(EZH2):c.1937A>C (p.Tyr646Ser) rs267601394
NM_004456.5(EZH2):c.1937A>T (p.Tyr646Phe) rs267601394
NM_004456.5(EZH2):c.2045C>G (p.Ala682Gly) rs1057519833
NM_015559.3(SETBP1):c.1703G>T (p.Ser568Ile) rs1599367044

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