List of variants reported as uncertain significance for combined immunodeficiency due to DOCK8 deficiency by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.4087C>T (p.Arg1363Trp)	rs142093178	0.00004
NM_203447.4(DOCK8):c.4659G>T (p.Met1553Ile)
NM_203447.4(DOCK8):c.5431_5433delinsCAA (p.Glu1811Gln)
NM_203447.4(DOCK8):c.5693C>T (p.Pro1898Leu)	rs2057264393
NM_203447.4(DOCK8):c.5962G>C (p.Gly1988Arg)	rs1482237306
NM_203447.4(DOCK8):c.6146del (p.Asn2049fs)

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