| | LOC129934333, TMEM127 (I41V) | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | LOC129934333, TMEM127 (I41fs) | Deletion (frameshift variant) | Hereditary pheochromocytoma-paraganglioma +3 more | |
| | LOC129934333, TMEM127 (A38S) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +2 more | |
| | LOC129934333, TMEM127 (G37D) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +3 more | |
| | LOC129934333, TMEM127 (A34G) | Single nucleotide variant (missense variant) | Pheochromocytoma +2 more | |
| | LOC129934333, TMEM127 (S30G) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | LOC129934333, TMEM127 (P27L) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +3 more | |
| | LOC129934333, TMEM127 (L23M) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | LOC129934333, TMEM127 (S21N) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | LOC129934333, TMEM127 (S21C) | Single nucleotide variant (missense variant +1 more) | Pheochromocytoma | |
| | LOC129934333, TMEM127 (P18S) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | LOC129934333, TMEM127 (S17I) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +2 more | |
| | LOC129934333, TMEM127 (S17G) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +2 more | |
| | LOC129934333, TMEM127 (R15L) | Single nucleotide variant (missense variant) | Pheochromocytoma +1 more | |
| | LOC129934333, TMEM127 (R13C) | Single nucleotide variant (missense variant) | Pheochromocytoma +1 more | |
| | | Deletion (inframe_deletion) | Hereditary cancer-predisposing syndrome +2 more | |
| | LOC129934333, TMEM127 (P10L) | Single nucleotide variant (missense variant +1 more) | Pheochromocytoma | |
| | LOC129934333, TMEM127 (G6V) | Single nucleotide variant (missense variant) | Pheochromocytoma +1 more | |
| | LOC129934333, TMEM127 (G5R) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +2 more | |
| | LOC129934333, TMEM127 (P4S) | Single nucleotide variant (missense variant) | Hereditary pheochromocytoma-paraganglioma +2 more | |