| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126807163, SLC7A11 (P25T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807163, SLC7A11 (V2F) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807163, SLC7A11 (T73A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807163, SLC7A11 (I58T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807163, SLC7A11 (K37T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807163, SLC7A11 (N19S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807163, SLC7A11 (P32T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC132089068, LOC132089069 +1051 more | Copy number gain | See cases | |
| | LOC126807210, LOC126807211 +1102 more | Copy number gain | See cases | |
| | LOC126807213, LOC126807214 +1068 more | Copy number gain | See cases | |
| | LINC00616, LOC126807163 +4 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LINC02479, LINC02485 +185 more | Copy number loss | See cases | |
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