List of variants reported as pathogenic for Severe combined immunodeficiency due to LCK deficiency

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005356.5(LCK):c.1022T>C (p.Leu341Pro)	rs587777335
NM_005356.5(LCK):c.1126del (p.Thr375_Leu376insTer)
NM_005356.5(LCK):c.1129dup (p.Ser377fs)	rs1569967422
NM_005356.5(LCK):c.115C>T (p.Arg39Ter)
NM_005356.5(LCK):c.1201A>T (p.Lys401Ter)	rs1640406042
NM_005356.5(LCK):c.1318C>T (p.Pro440Ser)
NM_005356.5(LCK):c.1393T>C (p.Cys465Arg)
NM_005356.5(LCK):c.188-2A>G
NM_005356.5(LCK):c.415del (p.Arg139fs)	rs1640237880
NM_005356.5(LCK):c.477del (p.Ala160fs)	rs2124355238

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