| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ATP11A, LOC126861868 (S1038L) | Single nucleotide variant (missense variant) | not provided | |
| | ATP11A, LOC130010167 (L9V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATP11A, LOC128772390 (A1113T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hearing loss, autosomal dominant 84 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | ATP11A, LOC128772390 (R1117Q +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ATP11A, LOC126861868 (A1021T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATP11A, LOC126861868 (H1025Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ATP11A, LOC130010167 (S4N) | Single nucleotide variant (missense variant) | Hearing loss, autosomal dominant 84 | |
| | ATP11A, LOC128772390 (T1123S) | Single nucleotide variant (missense variant +1 more) | not provided | |
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