List of variants in gene DOCK8 reported by Revvity Omics, Revvity

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.1193G>A (p.Arg398Gln)	rs147287319	0.00040
NM_203447.4(DOCK8):c.54-1G>T	rs192864327	0.00036
NM_203447.4(DOCK8):c.1588G>A (p.Val530Met)	rs373187839	0.00013
NM_203447.4(DOCK8):c.3234+2T>C	rs756871628	0.00010
NM_203447.4(DOCK8):c.4904A>G (p.Gln1635Arg)	rs200869192	0.00007
NM_203447.4(DOCK8):c.4346C>T (p.Ser1449Leu)	rs370123223	0.00006
NM_203447.4(DOCK8):c.2350C>T (p.Arg784Cys)	rs1251716138	0.00002
NM_203447.4(DOCK8):c.1787A>G (p.Asn596Ser)	rs367602254	0.00001
NM_203447.4(DOCK8):c.3044G>A (p.Arg1015His)	rs200494857	0.00001
NM_203447.4(DOCK8):c.*1031G>A	rs149002313
NM_203447.4(DOCK8):c.1964A>G (p.Gln655Arg)	rs750213861
NM_203447.4(DOCK8):c.2017A>T (p.Ile673Phe)	rs372858877
NM_203447.4(DOCK8):c.4268C>G (p.Ala1423Gly)	rs750589703
NM_203447.4(DOCK8):c.4474-26C>T
NM_203447.4(DOCK8):c.5205C>T (p.Ala1735=)	rs150682688
NM_203447.4(DOCK8):c.6147C>G (p.Asn2049Lys)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.