ClinVar Miner

List of variants in gene IFT140 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_014714.4(IFT140):c.1542C>A (p.Leu514=) rs141542834
NM_014714.4(IFT140):c.1682G>A (p.Ser561Asn) rs8050974
NM_014714.4(IFT140):c.1918G>A (p.Asp640Asn) rs61742753
NM_014714.4(IFT140):c.2008C>T (p.Pro670Ser) rs34900355
NM_014714.4(IFT140):c.2330T>G (p.Leu777Arg) rs34535263
NM_014714.4(IFT140):c.2454C>T (p.Asp818=) rs34668993
NM_014714.4(IFT140):c.2550C>T (p.Ala850=) rs2745180
NM_014714.4(IFT140):c.2569G>A (p.Gly857Ser) rs200876696
NM_014714.4(IFT140):c.2661G>A (p.Glu887=) rs1287846996
NM_014714.4(IFT140):c.2694G>A (p.Val898=) rs1555478342
NM_014714.4(IFT140):c.3079G>A (p.Gly1027Arg) rs137995818
NM_014714.4(IFT140):c.3336C>T (p.Leu1112=) rs372114503
NM_014714.4(IFT140):c.3693G>A (p.Thr1231=) rs144028766
NM_014714.4(IFT140):c.3711C>T (p.Phe1237=) rs146172074
NM_014714.4(IFT140):c.3743T>C (p.Ile1248Thr) rs79494390
NM_014714.4(IFT140):c.3990G>A (p.Ala1330=) rs61745103
NM_014714.4(IFT140):c.4380C>T (p.Asp1460=) rs61749517

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.