ClinVar Miner

List of variants in gene VIPAS39 studied for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_022067.4(VIPAS39):c.1179+1G>A
NM_022067.4(VIPAS39):c.1184G>A (p.Trp395Ter) rs1555364979
NM_022067.4(VIPAS39):c.1455C>A (p.Ser485Arg) rs145453157
NM_022067.4(VIPAS39):c.20del (p.Asp7fs)
NM_022067.4(VIPAS39):c.2T>G (p.Met1Arg) rs267607172
NM_022067.4(VIPAS39):c.535C>T (p.Gln179Ter) rs267607173
NM_022067.4(VIPAS39):c.618_626dup (p.Arg206_Leu208dup)
NM_022067.4(VIPAS39):c.658C>T (p.Arg220Ter) rs200370925
NM_022067.4(VIPAS39):c.677A>G (p.His226Arg) rs1555366438
NM_022067.4(VIPAS39):c.749_753del (p.Thr250fs) rs794726653
NM_022067.4(VIPAS39):c.871C>T (p.Gln291Ter) rs267607171

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.