ClinVar Miner

Variants in gene IFT122 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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HGVS dbSNP
NM_052989.3(IFT122):c.1026C>T (p.Asp342=) rs79187669
NM_052989.3(IFT122):c.1526T>C (p.Val509Ala) rs191420441
NM_052989.3(IFT122):c.2181C>T (p.Thr727=) rs545131069
NM_052989.3(IFT122):c.3129C>T (p.Arg1043=) rs76881473
NM_052989.3(IFT122):c.978G>A (p.Thr326=) rs781409395

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