ClinVar Miner

List of variants in gene combination IFT80, TRIM59-IFT80 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: 8
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HGVS dbSNP
NM_020800.3(IFT80):c.-40C>T rs79756374
NM_020800.3(IFT80):c.1076C>T (p.Ser359Phe) rs144099135
NM_020800.3(IFT80):c.1326C>G (p.Leu442=)
NM_020800.3(IFT80):c.1926+13T>C rs3737214
NM_020800.3(IFT80):c.2224-10del rs58665245
NM_020800.3(IFT80):c.440-12T>G
NM_020800.3(IFT80):c.462G>A (p.Ala154=) rs34182424
NM_020800.3(IFT80):c.777+20A>G

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