| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862572, TMEM101 (I95N +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862572, TMEM101 (A34T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862572, TMEM101 (A24V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126862572, TMEM101 (G30C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862572, TMEM101 (C26Y) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862572, TMEM101 (L22P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862572, TMEM101 (I15F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862572, TMEM101 (G6R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862572, TMEM101 (G6S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862572, TMEM101 (K4N) | Single nucleotide variant (missense variant +1 more) | not specified | |
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