| 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 | |
| | | Copy number loss | not provided | |
| | 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 | |
| | | Copy number loss | not provided | |
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