| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CRTC3, CRTC3-AS1 +1 more (G523D) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CRTC3, CRTC3-AS1 +1 more (Q528H) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CRTC3, CRTC3-AS1 +1 more (P537L) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CRTC3, CRTC3-AS1 +1 more (G542R) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
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