List of variants reported as likely benign for immune system cancer by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002609.4(PDGFRB):c.946G>A (p.Val316Met)	rs41287112	0.00287
NM_002609.4(PDGFRB):c.2523G>A (p.Lys841=)	rs41287108	0.00236
NM_198253.3(TERT):c.572G>C (p.Ser191Thr)	rs11952056	0.00100
NM_198253.3(TERT):c.1836C>G (p.Ala612=)	rs34170122	0.00056
NM_005188.4(CBL):c.12C>T (p.Asn4=)	rs371567712	0.00036
NM_198253.3(TERT):c.2582+11C>T	rs180675821	0.00036
NM_198253.3(TERT):c.1932G>A (p.Thr644=)	rs148582238	0.00031
NM_198253.3(TERT):c.2991G>A (p.Val997=)	rs376266401	0.00030
NM_198253.3(TERT):c.838G>A (p.Glu280Lys)	rs199701877	0.00018
NM_001754.5(RUNX1):c.1005G>T (p.Gln335His)	rs80314254	0.00011
NM_005188.4(CBL):c.873T>C (p.Tyr291=)	rs756526812	0.00009
NM_001754.5(RUNX1):c.492C>T (p.Val164=)	rs200907577	0.00008
NM_005188.4(CBL):c.6C>G (p.Ala2=)	rs770473070	0.00006
NM_198253.3(TERT):c.2262C>T (p.His754=)	rs778622091	0.00003
NM_198253.3(TERT):c.729C>T (p.Ala243=)	rs762491880	0.00001
NM_198253.3(TERT):c.1662C>T (p.Val554=)	rs200539091

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