ClinVar Miner

List of variants in gene DOCK6 reported as uncertain significance for Adams-Oliver syndrome 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020812.4(DOCK6):c.2104G>A (p.Gly702Ser) rs199838752 0.00102
NM_020812.4(DOCK6):c.5216A>T (p.His1739Leu) rs200792145 0.00042
NM_020812.4(DOCK6):c.3052C>T (p.Arg1018Trp) rs200261463 0.00029
NM_020812.4(DOCK6):c.2629C>T (p.Arg877Cys) rs199553475 0.00019
NM_020812.4(DOCK6):c.6128G>A (p.Arg2043Gln) rs746117967 0.00016
NM_020812.4(DOCK6):c.4216T>G (p.Ser1406Ala) rs34479977 0.00014
NM_020812.4(DOCK6):c.2506G>A (p.Val836Ile) rs200935357 0.00011
NM_020812.4(DOCK6):c.2767G>A (p.Val923Ile) rs143194982 0.00011
NM_020812.4(DOCK6):c.4198G>A (p.Val1400Met) rs201255040 0.00006
NM_020812.4(DOCK6):c.6014G>A (p.Arg2005His) rs768594454 0.00003
NM_020812.4(DOCK6):c.449C>T (p.Pro150Leu) rs781180338 0.00002
NM_020812.4(DOCK6):c.281C>T (p.Thr94Ile) rs747666106 0.00001
NM_020812.4(DOCK6):c.100C>G (p.His34Asp) rs201065561
NM_020812.4(DOCK6):c.292G>A (p.Gly98Arg)
NM_020812.4(DOCK6):c.3125T>A (p.Met1042Lys)
NM_020812.4(DOCK6):c.3616A>G (p.Ile1206Val)
NM_020812.4(DOCK6):c.4339-8G>A
NM_020812.4(DOCK6):c.521G>A (p.Arg174His)
NM_020812.4(DOCK6):c.5272G>A (p.Gly1758Ser)
NM_020812.4(DOCK6):c.5345T>C (p.Ile1782Thr) rs866624292
NM_020812.4(DOCK6):c.5615G>C (p.Arg1872Pro)
NM_020812.4(DOCK6):c.804C>T (p.Leu268=)

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.