| P12-Organoid | ASXL2 | 2 | 25972742 | C | A | Missense_Mutation | ENST00000435504.4:c.1683G>T | ENSP00000391447.3:p.Gln561His | 0.03100775 |
| P12-Organoid | B3GNT2 | 2 | 62450083 | A | G | Missense_Mutation | ENST00000405767.1:c.728A>G | ENSP00000384692.1:p.Lys243Arg | 0.03436426 |
| P12-Organoid | POLR1B | 2 | 113310289 | A | C | Missense_Mutation | ENST00000541869.1:c.1168A>C | ENSP00000444136.1:p.Lys390Gln | 0.04545454 |
| P12-Organoid | ERBB4 | 2 | 212576871 | A | G | Missense_Mutation | ENST00000436443.1:c.1028T>C | ENSP00000403204.1:p.Met343Thr | 0.05027933 |
| P12-Organoid | SCN11A | 3 | 38936183 | C | A | Missense_Mutation | ENST00000456224.3:c.2676G>T | ENSP00000416757.3:p.Glu892Asp | 0.02816901 |
| P12-Organoid | KPNA4 | 3 | 160225993 | G | A | Missense_Mutation | ENST00000334256.4:c.1274C>T | ENSP00000334373.4:p.Ala425Val | 0.12844036 |
| P12-Organoid | SEPT11 | 4 | 77941786 | G | T | Missense_Mutation | ENST00000541121.1:c.946G>T | ENSP00000443701.1:p.Gly316Trp | 0.01760563 |
| P12-Organoid | SLC9B1 | 4 | 103822431 | G | T | Missense_Mutation | ENST00000296422.7:c.1391C>A | ENSP00000296422.7:p.Pro464Gln | 0.1875 |
| P12-Organoid | TENM3 | 4 | 183694720 | T | C | Missense_Mutation | ENST00000511685.1:c.4988T>C | ENSP00000424226.1:p.Ile1663Thr | 0.03323262 |
| P12-Organoid | SORBS2 | 4 | 186548093 | T | C | Missense_Mutation | ENST00000449407.2:c.1028A>G | ENSP00000397262.2:p.Gln343Arg | 0.08467741 |
| P12-Organoid | SLC36A1 | 5 | 150867631 | C | A | Missense_Mutation | ENST00000520701.1:c.1247C>A | ENSP00000428140.1:p.Pro416Gln | 0.00775193 |
| P12-Organoid | TRERF1 | 6 | 42236862 | C | A | Missense_Mutation | ENST00000541110.1:c.467G>T | ENSP00000439689.1:p.Arg156Leu | 0.02419354 |
| P12-Organoid | C7orf63 | 7 | 89917578 | G | A | Missense_Mutation | ENST00000497910.1:c.1633G>A | ENSP00000419549.1:p.Val545Ile | 0.18032786 |
| P12-Organoid | SNTG1 | 8 | 51617181 | C | T | Missense_Mutation | ENST00000522124.1:c.1060C>T | ENSP00000429842.1:p.Arg354Trp | 0.05050505 |
| P12-Organoid | C10orf2 | 10 | 102750687 | C | A | Missense_Mutation | ENST00000370228.1:c.1654C>A | ENSP00000359248.1:p.His552Asn | 0.04219409 |
| P12-Organoid | COL17A1 | 10 | 105793794 | C | T | Missense_Mutation | ENST00000369733.3:c.3819G>A | ENSP00000358748.3:p.Met1273Ile | 0.06796116 |
| P12-Organoid | DMBT1 | 10 | 124389946 | C | G | Missense_Mutation | ENST00000368956.2:c.3694C>G | ENSP00000357952.2:p.Arg1232Gly | 0.15695067 |
| P12-Organoid | DEAF1 | 11 | 694961 | GGCCGCCGCCGCCACAGCGGCCGCGGCC | G | In_Frame_Del | ENST00000382409.3:c.60_86del | ENSP00000371846.3:p.Val25_Ala33del | 0.09803921 |
| P12-Organoid | INSC | 11 | 15260560 | G | A | Missense_Mutation | ENST00000530161.1:c.1333G>A | ENSP00000436194.1:p.Val445Met | 0.02832861 |
| P12-Organoid | OR5R1 | 11 | 56185579 | C | A | Missense_Mutation | ENST00000312253.1:c.130G>T | ENSP00000308595.1:p.Gly44Trp | 0.01209677 |
| P12-Organoid | TRIM29 | 11 | 120008421 | C | A | Missense_Mutation | ENST00000341846.5:c.319G>T | ENSP00000343129.5:p.Ala107Ser | 0.01851851 |
| P12-Organoid | KCNH3 | 12 | 49937058 | G | T | Missense_Mutation | ENST00000257981.6:c.580G>T | ENSP00000257981.5:p.Gly194Trp | 0.03947368 |
| P12-Organoid | NACA | 12 | 57114788 | A | T | Missense_Mutation | ENST00000550952.1:c.526T>A | ENSP00000448035.1:p.Ser176Thr | 0.03030303 |
| P12-Organoid | ARHGAP9 | 12 | 57867929 | C | A | Missense_Mutation | ENST00000550288.1:c.2051G>T | ENSP00000473445.1:p.Trp684Leu | 0.02469135 |
| P12-Organoid | USP8 | 15 | 50784950 | C | T | Missense_Mutation | ENST00000433963.1:c.2287C>T | ENSP00000405537.1:p.Arg763Trp | 0.16363636 |
| P12-Organoid | USP8 | 15 | 50784955 | C | A | Missense_Mutation | ENST00000433963.1:c.2292C>A | ENSP00000405537.1:p.Asn764Lys | 0.16574585 |
| P12-Organoid | WFIKKN1 | 16 | 683474 | C | A | Missense_Mutation | ENST00000319070.2:c.1064C>A | ENSP00000324763.2:p.Pro355His | 0.01648351 |
| P12-Organoid | MED1 | 17 | 37604067 | A | C | Missense_Mutation | ENST00000394287.3:c.116T>G | ENSP00000377828.3:p.Leu39Arg | 0.08955223 |
| P12-Organoid | MUC16 | 19 | 9066866 | C | A | Missense_Mutation | ENST00000397910.4:c.20580G>T | ENSP00000381008.2:p.Leu6860Phe | 0.03252032 |
| P12-Organoid | LRFN1 | 19 | 39804790 | G | A | Missense_Mutation | ENST00000248668.4:c.1187C>T | ENSP00000248668.4:p.Pro396Leu | 0.04333333 |
| P12-Organoid | LILRB1 | 19 | 55147987 | GA | CC | Missense_Mutation | ENST00000434867.2:c.1690_1691delinsCC | ENSP00000405243.2:p.Glu564Pro | 0.35952848 |
| P12-Organoid | ELMO2 | 20 | 45002114 | TC | AA | Missense_Mutation | ENST00000454865.2:c.535_536delinsTT | ENSP00000415641.2:p.Glu179Leu | 0.01298701 |
| P12-Organoid | NTSR1 | 20 | 61341261 | G | T | Missense_Mutation | ENST00000370501.3:c.702G>T | ENSP00000359532.3:p.Lys234Asn | 0.01724137 |
| P12-Organoid | DYRK1A | 21 | 38845110 | G | T | Missense_Mutation | ENST00000451934.1:c.135G>T | ENSP00000416089.1:p.Gln45His | 0.14393939 |
| P12-Organoid | RBMX2 | X | 129546749 | C | A | Missense_Mutation | ENST00000305536.6:c.896C>A | ENSP00000339090.4:p.Ser299Tyr | 0.025 |
| P12-Organoid | PLXNA3 | X | 153689836 | C | A | Missense_Mutation | ENST00000369682.3:c.992C>A | ENSP00000358696.3:p.Pro331Gln | 0.08163265 |