| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CMTM3, CMTM4
+1 more (E48D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CMTM3, CMTM4
+1 more (R28C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CMTM3, CMTM4
+1 more (P14T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CMTM3, CMTM4
+1 more (A29T) | Single nucleotide variant (missense variant +1 more) | not specified | |
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