| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FAM117B, LOC129935440 (P153H) | Single nucleotide variant (missense variant) | not specified | |
| | FAM117B, LOC129935440 (S180F) | Single nucleotide variant (missense variant) | not specified | |
| | FAM117B, LOC129935440 (P181L) | Single nucleotide variant (missense variant) | not specified | |
| | FAM117B, LOC129935440 (S184R) | Single nucleotide variant (missense variant) | not specified | |
| | FAM117B, LOC129935440 (P188S) | Single nucleotide variant (missense variant) | not specified | |
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