| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129936566, NKTR
+1 more (R701H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129936566, NKTR
+1 more (S707C +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129936566, NKTR
+1 more (N969D +2 more) | Single nucleotide variant (missense variant) | not specified | |
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