| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126805697, MAP7D1 (W231C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126805697, MAP7D1 (R193H) | Single nucleotide variant (missense variant) | not specified | |
| | LOC121725012, MAP7D1 (K696E +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126805697, MAP7D1 (K221R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126805697, MAP7D1 (K220R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126805697, MAP7D1 (R199W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC121725012, MAP7D1 (E656V +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126805697, MAP7D1 (R210C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126805697, MAP7D1 (R192C) | Single nucleotide variant (missense variant) | not specified | |
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