| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ANKRD13C, LOC126805756 (H58R) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (G20R) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (V85L) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (P72L) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (N71S) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (L80V) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (Y114H) | Single nucleotide variant (missense variant) | not specified | |
| | ANKRD13C, LOC126805756 (G26R) | Single nucleotide variant (missense variant) | not specified | |
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