Mutations
| Gene name | Gene | Transcript | AA syntax | CDS syntax | Mutation type | Pubmed ID |
|---|---|---|---|---|---|---|
| ZNF23 | ENSG00000167377 | ENST00000393539 | p.H302Q | c.906C>G | Missense_Mutation | - |
| PCDHA3 | ENSG00000255408 | ENST00000522353 | p.A540A | c.1620G>C | Silent | - |
| CLEC4A | ENSG00000111729 | ENST00000229332 | p.K93fs | c.276_277insA | Frame_Shift_Ins | - |
| LAT2 | ENSG00000086730 | ENST00000460943 | p.P184P | c.552G>A | Silent | - |
| THOC3 | ENSG00000051596 | ENST00000265097 | p.N221N | c.663C>T | Silent | - |
| NEB | ENSG00000183091 | ENST00000604864 | p.K3279Q | c.9835A>C | Missense_Mutation | - |
| NKTR | ENSG00000114857 | ENST00000232978 | p.E1113fs | c.3337_3338insA | Frame_Shift_Ins | - |
| CENPC | ENSG00000145241 | ENST00000273853 | p.S684N | c.2051G>A | Splice_Site | - |
| RRP12 | ENSG00000052749 | ENST00000370992 | p.A461A | c.1383C>G | Silent | - |
| C19orf25 | ENSG00000119559 | ENST00000436106 | p.A79V | c.236C>T | Missense_Mutation | - |