| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062297, TTC39C
+1 more (R12Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130062297, TTC39C
+1 more (S4L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
Click to view in NCBI Gene