| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CACNA1G, CACNA1G-AS1 (E5Q) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | CACNA1G, CACNA1G-AS1 (D24N) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | CACNA1G, CACNA1G-AS1 (D24E) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | CACNA1G, CACNA1G-AS1 (G30D) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | CACNA1G, CACNA1G-AS1 (A55V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
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