| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126806226, TMEM17 (R172H) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (R180Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (R180W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (R172S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (D177G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (R172C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (L124I) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806226, TMEM17 (W114R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129933873, TMEM17 (D5E) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
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