| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCNC3, LOC130064972 (W192C +1 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Microsatellite (inframe_deletion) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | KCNC3, LOC130064972 (P257T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | KCNC3, LOC130064972 (A178V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KCNC3, LOC130064972 (G177D +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
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