| P2-Organoid | HSPG2 | 1 | 22188550 | C | G | Missense_Mutation | ENST00000374695.3:c.4799G>C | ENSP00000363827.3:NA | 1 |
| P2-Organoid | TMEM53 | 1 | 45120448 | G | A | Missense_Mutation | ENST00000372237.3:c.617C>T | ENSP00000361311.3:NA | 0.26595744 |
| P2-Organoid | MIER1 | 1 | 67411908 | G | A | Missense_Mutation | ENST00000401042.3:c.110G>A | ENSP00000383821.3:p.Arg37Gln | 1 |
| P2-Organoid | ASPM | 1 | 197059118 | C | G | Missense_Mutation | ENST00000367409.4:c.9926G>C | ENSP00000356379.4:p.Ser3309Thr | 0.35802469 |
| P2-Organoid | PPFIA4 | 1 | 203024615 | C | T | Missense_Mutation | ENST00000599966.1:c.367C>T | ENSP00000471264.1:p.Arg123Cys | 0.30582010 |
| P2-Organoid | USH2A | 1 | 216419944 | C | T | Missense_Mutation | ENST00000366943.2:c.2792G>A | ENSP00000355910.2:p.Cys931Tyr | 0.02463054 |
| P2-Organoid | OR6F1 | 1 | 247875926 | AG | A | Frame_Shift_Del | ENST00000302084.2:c.131del | ENSP00000305640.2:p.Ala44ValfsTer3 | 0.23938223 |
| P2-Organoid | ASAP2 | 2 | 9347277 | A | T | Missense_Mutation | ENST00000315273.4:c.44A>T | ENSP00000316404.4:p.His15Leu | 0.05027173 |
| P2-Organoid | IFT172 | 2 | 27684338 | A | C | Missense_Mutation | ENST00000260570.3:c.2240T>G | ENSP00000260570.3:p.Leu747Arg | 0.47839506 |
| P2-Organoid | CLASP1 | 2 | 122285420 | C | T | Missense_Mutation | ENST00000541377.1:c.425G>A | ENSP00000441625.1:p.Arg142His | 0.44827586 |
| P2-Organoid | TTN | 2 | 179498672 | C | T | Missense_Mutation | ENST00000591111.1:c.37631G>A | ENSP00000465570.1:p.Arg12544Lys | 0.14948453 |
| P2-Organoid | RAPH1 | 2 | 204355961 | G | C | Missense_Mutation | ENST00000457812.1:c.202C>G | ENSP00000392854.1:p.Arg68Gly | 0.28846153 |
| P2-Organoid | ERBB4 | 2 | 212522706 | T | G | Missense_Mutation | ENST00000402597.1:c.1885A>C | ENSP00000385565.1:p.Ser629Arg | 0.54615384 |
| P2-Organoid | TTLL4 | 2 | 219602823 | G | GA | Frame_Shift_Ins | ENST00000442769.1:c.430dup | ENSP00000396555.1:p.Ser144LysfsTer71 | 0.37272727 |
| P2-Organoid | SLC4A3 | 2 | 220502893 | G | A | Missense_Mutation | ENST00000373762.3:c.2855G>A | ENSP00000362867.3:p.Arg952His | 0.49418604 |
| P2-Organoid | KPNA1 | 3 | 122156036 | C | T | Missense_Mutation | ENST00000344337.6:c.1103G>A | ENSP00000343701.6:p.Gly368Glu | 0.60869565 |
| P2-Organoid | DEPDC1B | 5 | 59899244 | G | A | Missense_Mutation | ENST00000545085.1:c.1135C>T | ENSP00000438320.1:p.Arg379Cys | 0.46341463 |
| P2-Organoid | EPHA7 | 6 | 93967847 | C | T | Missense_Mutation | ENST00000369303.4:c.2080G>A | ENSP00000358309.4:p.Val694Ile | 0.43786982 |
| P2-Organoid | SUGCT | 7 | 40900005 | T | G | Missense_Mutation | ENST00000401647.2:c.1121T>G | ENSP00000385222.2:p.Val374Gly | 0.43674698 |
| P2-Organoid | KCNK9 | 8 | 140630863 | G | A | Missense_Mutation | ENST00000520439.1:c.763C>T | ENSP00000430676.1:p.Arg255Trp | 0.95 |
| P2-Organoid | BAI1 | 8 | 143558817 | C | T | Missense_Mutation | ENST00000517894.1:c.1294C>T | ENSP00000430945.1:p.Arg432Cys | 0.33462282 |
| P2-Organoid | CYP11B2 | 8 | 143996298 | G | A | Missense_Mutation | ENST00000323110.2:c.622C>T | ENSP00000325822.2:p.Arg208Trp | 0.46166950 |
| P2-Organoid | CEL | 9 | 135946015 | T | C | Missense_Mutation | ENST00000372080.4:c.1463T>C | ENSP00000361151.4:p.Ile488Thr | 0.08984375 |
| P2-Organoid | MUC5B | 11 | 1268488 | C | T | Missense_Mutation | ENST00000529681.1:c.10378C>T | ENSP00000436812.1:p.Pro3460Ser | 0.16521739 |
| P2-Organoid | OR5T3 | 11 | 56019901 | G | C | Missense_Mutation | ENST00000303059.3:c.226G>C | ENSP00000305403.3:p.Val76Leu | 0.46305418 |
| P2-Organoid | OR8D4 | 11 | 123777232 | T | G | Missense_Mutation | ENST00000321355.2:c.94T>G | ENSP00000325381.2:p.Leu32Val | 0.52173913 |
| P2-Organoid | GLB1L3 | 11 | 134163054 | A | G | Missense_Mutation | ENST00000431683.2:c.827A>G | ENSP00000396615.2:p.Asn276Ser | 0.44660194 |
| P2-Organoid | ACRBP | 12 | 6756507 | A | C | Missense_Mutation | ENST00000536350.1:c.26T>G | ENSP00000443153.1:p.Leu9Arg | 0.61904761 |
| P2-Organoid | KRAS | 12 | 25398284 | C | T | Missense_Mutation | ENST00000557334.1:c.35G>A | ENSP00000452512.1:p.Gly12Asp | 0.3 |
| P2-Organoid | KMT2D | 12 | 49445979 | GGA | G | Frame_Shift_Del | ENST00000301067.7:c.1485_1486del | ENSP00000301067.7:p.Pro496AlafsTer3 | 0.42211055 |
| P2-Organoid | DUOX1 | 15 | 45427329 | G | C | Missense_Mutation | ENST00000389037.3:c.335G>C | ENSP00000373689.3:p.Ser112Thr | 0.46045918 |
| P2-Organoid | DMXL2 | 15 | 51772927 | G | A | Missense_Mutation | ENST00000543779.2:c.6376C>T | ENSP00000441858.2:p.Arg2126Cys | 0.48958333 |
| P2-Organoid | CLEC16A | 16 | 11260318 | C | A | Missense_Mutation | ENST00000409790.1:c.2715C>A | ENSP00000387122.1:p.Ser905Arg | 0.12186379 |
| P2-Organoid | TP53 | 17 | 7577539 | G | A | Missense_Mutation | ENST00000455263.2:c.742C>T | ENSP00000398846.2:p.Arg248Trp | 1 |
| P2-Organoid | TBX2 | 17 | 59482881 | C | T | Missense_Mutation | ENST00000240328.3:c.1370C>T | ENSP00000240328.3:p.Ala457Val | 0.55121951 |
| P2-Organoid | ARID3A | 19 | 932476 | G | A | Missense_Mutation | ENST00000263620.3:c.427G>A | ENSP00000263620.2:p.Glu143Lys | 0.55405405 |
| P2-Organoid | XAB2 | 19 | 7688662 | G | C | Missense_Mutation | ENST00000534844.1:c.1065C>G | ENSP00000438225.1:p.His355Gln | 0.49264705 |
| P2-Organoid | GPATCH1 | 19 | 33581694 | C | T | Missense_Mutation | ENST00000170564.2:c.217C>T | ENSP00000170564.1:p.Pro73Ser | 0.41346153 |
| P2-Organoid | IRGC | 19 | 44223415 | C | A | Missense_Mutation | ENST00000244314.5:c.705C>A | ENSP00000244314.5:p.Asp235Glu | 0.49014778 |
| P2-Organoid | BCR | 22 | 23653975 | T | TCCGG | Frame_Shift_Ins | ENST00000359540.3:c.3143_3146dup | ENSP00000352535.3:p.Val1050ArgfsTer17 | 0.5 |
| P2-Organoid | TCEAL2 | X | 101382371 | C | T | Missense_Mutation | ENST00000372780.1:c.569C>T | ENSP00000361866.1:p.Ala190Val | 1 |
| P2-Organoid | MECP2 | X | 153363111 | G | GGCGGCGGTGGCGGCA | In_Frame_Ins | ENST00000453960.2:c.11_12insTGCCGCCACCGCCGC | ENSP00000395535.2:p.Ala6_Ala7insThrAlaAlaAlaAla | 0.01212121 |