ClinVar Miner

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

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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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

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