List of variants reported as pathogenic for Severe combined immunodeficiency due to LCK deficiency by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005356.5(LCK):c.1126del (p.Thr375_Leu376insTer)
NM_005356.5(LCK):c.115C>T (p.Arg39Ter)
NM_005356.5(LCK):c.1201A>T (p.Lys401Ter)	rs1640406042
NM_005356.5(LCK):c.415del (p.Arg139fs)	rs1640237880
NM_005356.5(LCK):c.477del (p.Ala160fs)	rs2124355238

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