| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129929950, TMEM200B (H111Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (E100Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (A89V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (P159L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (P178H) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (R113L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (M94R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (G105S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129929950, TMEM200B (P92R) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene