| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +2 more | |
| | MCPH1, MCPH1-AS1 (A761V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified +2 more | |
| | MCPH1-AS1, MCPH1 (S801G +1 more) | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | MCPH1-AS1, MCPH1 (P828S +2 more) | Single nucleotide variant (missense variant) | not specified +2 more | |
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