| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | C14orf28, LOC101927418 (S148F) | Single nucleotide variant (missense variant) | not specified | |
| | C14orf28, LOC101927418 (L282F) | Single nucleotide variant (missense variant) | not specified | |
| | C14orf28, LOC101927418 (E309D) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | C14orf28, LOC101927418 (S234F) | Single nucleotide variant (missense variant) | not provided | |
| | C14orf28, LOC101927418 (P177L) | Single nucleotide variant (missense variant) | not provided | |
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