ClinVar Miner

List of variants in gene combination IFT80, TRIM59-IFT80 reported as 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: 8
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HGVS dbSNP
NM_020800.2(IFT80):c.2224-10delT rs58665245
NM_020800.3(IFT80):c.*42G>A rs16831149
NM_020800.3(IFT80):c.1076C>T (p.Ser359Phe) rs144099135
NM_020800.3(IFT80):c.1756A>T (p.Thr586Ser) rs6778728
NM_020800.3(IFT80):c.2224-19dup rs58665245
NM_020800.3(IFT80):c.371-10C>A rs188321058
NM_020800.3(IFT80):c.462G>A (p.Ala154=) rs34182424
NM_020800.3(IFT80):c.933A>G (p.Thr311=) rs138798955

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