| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CMPK2, LOC129933018 (G151A) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (G151D) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (E148Q) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (D138A) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (F131S) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (L99M) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (T80I) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (A63V) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (A51T) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (A49S) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (L35V) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (A24G) | Single nucleotide variant (missense variant) | not specified | |
| | CMPK2, LOC129933018 (R20P) | Single nucleotide variant (missense variant) | not specified | |
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