ClinVar Miner

List of variants studied for Galloway-Mowat syndrome 7

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020401.4(NUP107):c.1998+14G>T rs7976871 0.25758
NM_020401.4(NUP107):c.1998+15G>T rs7976876 0.21375
NM_020401.4(NUP107):c.1063C>T (p.Arg355Cys) rs1165860389 0.00001
NM_020401.4(NUP107):c.303G>A (p.Met101Ile) rs730882216 0.00001
NM_020401.4(NUP107):c.1325G>A (p.Cys442Tyr) rs745342141
NM_020401.4(NUP107):c.2347A>G (p.Thr783Ala)
NM_020401.4(NUP107):c.72G>A (p.Arg24=) rs2259588

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.