List of variants in gene DOCK8 reported by Genome-Nilou Lab

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.4491T>C (p.Phe1497=)	rs7854035	0.99726
NM_203447.4(DOCK8):c.2605+30T>C	rs10758420	0.93542
NM_203447.4(DOCK8):c.5961+133A>G	rs10121936	0.83292
NM_203447.4(DOCK8):c.5433G>A (p.Glu1811=)	rs1887957	0.75495
NM_203447.4(DOCK8):c.5356-48C>T	rs10974467	0.71940
NM_203447.4(DOCK8):c.4785+6C>G	rs7036567	0.70190
NM_203447.4(DOCK8):c.4886+3A>G	rs2360712	0.69369
NM_203447.4(DOCK8):c.4627-85T>C	rs1329377	0.68824
NM_203447.4(DOCK8):c.894+74_894+75insC	rs3831138	0.67848
NM_203447.4(DOCK8):c.895-16T>C	rs2296828	0.66765
NM_203447.4(DOCK8):c.895-84G>C	rs2296825	0.63039
NM_203447.4(DOCK8):c.4241+22T>C	rs10217719	0.57971
NM_203447.4(DOCK8):c.5223+65G>C	rs10758598	0.57714
NM_203447.4(DOCK8):c.2206-48A>G	rs7020921	0.53910
NM_203447.4(DOCK8):c.4107C>G (p.Leu1369=)	rs2297079	0.44487
NM_203447.4(DOCK8):c.4154-68T>A	rs2297081	0.43281
NM_203447.4(DOCK8):c.895-65T>G	rs2296826	0.36072
NM_203447.4(DOCK8):c.65C>T (p.Ala22Val)	rs506121	0.32449
NM_203447.4(DOCK8):c.1238A>G (p.Asn413Ser)	rs10970979	0.24995
NM_203447.4(DOCK8):c.1423-100G>A	rs12340920	0.21365
NM_203447.4(DOCK8):c.6068+32G>C	rs16909246	0.12477
NM_203447.4(DOCK8):c.5080-143G>C	rs10733508
NM_203447.4(DOCK8):c.5223+79A>C	rs10217568
NM_203447.4(DOCK8):c.5490+21C>T	rs1887958
NM_203447.4(DOCK8):c.5581-18G>C	rs10814952
NM_203447.4(DOCK8):c.699T>C (p.Asn233=)	rs2039045

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