| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129994610, SHROOM1 (S133G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (E130K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (Q127R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (A126V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (A125T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (L115P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (T103I) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (T98A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (R92P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (A91T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129994610, SHROOM1 (A90V) | Single nucleotide variant (missense variant) | not specified | |
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