| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129935164, LOC129935165 +697 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | HOXD8, LOC100129455 (S11P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | HOXD8, LOC100129455 (T30P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | HOXD8, LOC100129455 (V40I) | Single nucleotide variant (non-coding transcript variant +2 more) | not specified | |
| | HOXD8, LOC100129455 (R43C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | HOXD8, LOC100129455 (H44Y) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | HOXD8, LOC100129455 (H44D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | HOXD8, LOC100129455 (A47S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | HOXD8, LOC100129455 (A48E) | Single nucleotide variant (missense variant +1 more) | not specified | |
Click to view in NCBI Gene