| P5-Organoid | CSMD2 | 1 | 34011696 | G | A | Missense_Mutation | ENST00000373381.4:c.9041C>T | ENSP00000362479.4:p.Ser2870Leu | 0.19463087 |
| P5-Organoid | COL8A2 | 1 | 36563720 | G | A | Missense_Mutation | ENST00000481785.1:c.1367C>T | ENSP00000436433.1:NA | 0.13259668 |
| P5-Organoid | RIMS3 | 1 | 41094559 | T | A | Missense_Mutation | ENST00000372684.3:c.637A>T | ENSP00000361769.3:NA | 0.15533980 |
| P5-Organoid | KCNA2 | 1 | 111146840 | G | A | Missense_Mutation | ENST00000485317.1:c.565C>T | ENSP00000433109.1:p.Arg189Trp | 0.23880597 |
| P5-Organoid | DENND2C | 1 | 115168468 | A | T | Missense_Mutation | ENST00000393277.1:c.138T>A | ENSP00000376958.1:NA | 0.05633802 |
| P5-Organoid | LINGO4 | 1 | 151774193 | C | A | Missense_Mutation | ENST00000368820.3:c.988G>T | ENSP00000357810.3:p.Asp330Tyr | 0.02325581 |
| P5-Organoid | BCAN | 1 | 156617855 | A | G | Missense_Mutation | ENST00000361588.5:c.722A>G | ENSP00000354925.5:p.Asp241Gly | 0.04794520 |
| P5-Organoid | BRINP3 | 1 | 190067654 | TC | T | Frame_Shift_Del | ENST00000534846.1:c.1488del | ENSP00000438022.1:p.Thr497LeufsTer14 | 0.04310344 |
| P5-Organoid | KCNK2 | 1 | 215179287 | G | T | Missense_Mutation | ENST00000391895.2:c.23G>T | ENSP00000375765.2:p.Arg8Met | 0.07692307 |
| P5-Organoid | KCNS3 | 2 | 18112885 | G | A | Missense_Mutation | ENST00000403915.1:c.610G>A | ENSP00000385968.1:p.Val204Ile | 0.07209302 |
| P5-Organoid | KCNS3 | 2 | 18112957 | G | A | Missense_Mutation | ENST00000403915.1:c.682G>A | ENSP00000385968.1:p.Ala228Thr | 0.02898550 |
| P5-Organoid | DPYSL5 | 2 | 27157527 | C | T | Missense_Mutation | ENST00000401478.1:c.872C>T | ENSP00000385549.1:p.Ala291Val | 0.08130081 |
| P5-Organoid | GPR45 | 2 | 105858853 | C | T | Missense_Mutation | ENST00000258456.1:c.538C>T | ENSP00000258456.1:p.Pro180Ser | 0.05483871 |
| P5-Organoid | CCDC174 | 3 | 14709664 | G | A | Missense_Mutation | ENST00000383794.3:c.928G>A | ENSP00000373304.3:p.Gly310Ser | 0.16666666 |
| P5-Organoid | TNNC1 | 3 | 52485854 | C | T | Missense_Mutation | ENST00000232975.3:c.223G>A | ENSP00000232975.3:p.Asp75Asn | 0.3 |
| P5-Organoid | PDZRN3 | 3 | 73433783 | C | T | Missense_Mutation | ENST00000535920.1:c.1100G>A | ENSP00000442026.1:p.Arg367His | 0.04676259 |
| P5-Organoid | MAATS1 | 3 | 119445155 | G | A | Missense_Mutation | ENST00000273390.5:c.820G>A | ENSP00000273390.5:p.Glu274Lys | 0.12371134 |
| P5-Organoid | ALDH1L1 | 3 | 125854502 | T | C | Missense_Mutation | ENST00000472186.1:c.1348A>G | ENSP00000420293.1:p.Ile450Val | 0.06698564 |
| P5-Organoid | IFT80 | 3 | 160025475 | G | A | Missense_Mutation | ENST00000496589.1:c.641C>T | ENSP00000420646.1:p.Thr214Met | 0.10526315 |
| P5-Organoid | KCTD8 | 4 | 44177010 | G | A | Missense_Mutation | ENST00000360029.3:c.1219C>T | ENSP00000353129.3:p.Arg407Cys | 0.08947368 |
| P5-Organoid | FRYL | 4 | 48608515 | T | A | Missense_Mutation | ENST00000537810.1:c.681A>T | ENSP00000441114.1:p.Lys227Asn | 0.10084033 |
| P5-Organoid | HSD17B4 | 5 | 118832319 | C | T | Missense_Mutation | ENST00000515320.1:c.896C>T | ENSP00000424613.1:p.Thr299Met | 0.08860759 |
| P5-Organoid | LOX | 5 | 121413238 | G | A | Missense_Mutation | ENST00000231004.4:c.443C>T | ENSP00000231004.4:p.Pro148Leu | 0.03030303 |
| P5-Organoid | MZB1 | 5 | 138723794 | A | C | Missense_Mutation | ENST00000412103.2:c.53T>G | ENSP00000414565.2:p.Val18Gly | 0.08450704 |
| P5-Organoid | PCDHA9 | 5 | 140230122 | G | A | Missense_Mutation | ENST00000532602.1:c.2042G>A | ENSP00000436042.1:p.Arg681Gln | 0.27568922 |
| P5-Organoid | PCDHB8 | 5 | 140558171 | C | T | Missense_Mutation | ENST00000239444.2:c.556C>T | ENSP00000239444.2:p.Arg186Cys | 0.11065573 |
| P5-Organoid | DSP | 6 | 7584376 | C | A | Missense_Mutation | ENST00000418664.2:c.5084C>A | ENSP00000396591.2:p.Ala1695Asp | 0.04 |
| P5-Organoid | RGS17 | 6 | 153365078 | T | G | Missense_Mutation | ENST00000367225.2:c.76A>C | ENSP00000356194.1:p.Asn26His | 0.20588235 |
| P5-Organoid | SMOC2 | 6 | 168999654 | C | T | Missense_Mutation | ENST00000356284.2:c.794C>T | ENSP00000348630.2:p.Thr265Met | 0.07874015 |
| P5-Organoid | SNX13 | 7 | 17841230 | G | A | Missense_Mutation | ENST00000428135.3:c.2279C>T | ENSP00000398789.2:p.Ser760Leu | 0.10588235 |
| P5-Organoid | HECW1 | 7 | 43484504 | C | T | Missense_Mutation | ENST00000453890.1:c.1733C>T | ENSP00000407774.1:p.Ala578Val | 0.09138381 |
| P5-Organoid | SPDYE1 | 7 | 44046934 | G | A | Missense_Mutation | ENST00000258704.3:c.700G>A | ENSP00000258704.3:p.Gly234Arg | 0.04966887 |
| P5-Organoid | SMURF1 | 7 | 98648560 | G | T | Missense_Mutation | ENST00000361125.1:c.862C>A | ENSP00000354621.1:p.Gln288Lys | 0.16981132 |
| P5-Organoid | TMEM168 | 7 | 112424237 | G | GA | Frame_Shift_Ins | ENST00000454074.1:c.643dup | ENSP00000390696.1:p.Ser215PhefsTer22 | 0.125 |
| P5-Organoid | PLXNA4 | 7 | 131866930 | C | T | Missense_Mutation | ENST00000359827.3:c.3178G>A | ENSP00000352882.3:p.Val1060Ile | 0.17037037 |
| P5-Organoid | TRBC2 | 7 | 142498959 | G | A | Missense_Mutation | ENST00000466254.1:c.235G>A | ENSP00000417300.1:p.Arg79His | 0.1121673 |
| P5-Organoid | KAT6A | 8 | 41844990 | G | T | Missense_Mutation | ENST00000485568.1:c.692C>A | ENSP00000430606.1:p.Ala231Asp | 0.12 |
| P5-Organoid | AARD | 8 | 117950501 | C | T | Missense_Mutation | ENST00000378279.3:c.19C>T | ENSP00000367528.3:p.Arg7Cys | 0.1 |
| P5-Organoid | FAM135B | 8 | 139163572 | T | C | Missense_Mutation | ENST00000395297.1:c.3146A>G | ENSP00000378710.1:p.Lys1049Arg | 0.09890109 |
| P5-Organoid | ARID3C | 9 | 34623622 | C | T | Missense_Mutation | ENST00000378909.2:c.665G>A | ENSP00000368189.2:p.Arg222His | 0.24880382 |
| P5-Organoid | C9orf129 | 9 | 96097804 | C | T | Missense_Mutation | ENST00000375419.1:c.217G>A | ENSP00000364568.1:p.Glu73Lys | 0.02643171 |
| P5-Organoid | COL27A1 | 9 | 116930880 | C | T | Missense_Mutation | ENST00000356083.3:c.1045C>T | ENSP00000348385.3:p.Arg349Cys | 0.21568627 |
| P5-Organoid | GOLGA2 | 9 | 131023841 | C | T | Splice_Site | ENST00000609374.1:c.1108-1G>A | | 0.27160493 |
| P5-Organoid | PRRC2B | 9 | 134330507 | G | T | Missense_Mutation | ENST00000458550.1:c.1165G>T | ENSP00000398853.1:p.Asp389Tyr | 0.26168224 |
| P5-Organoid | SVIL | 10 | 29811448 | C | A | Nonsense_Mutation | ENST00000375400.3:c.2002G>T | ENSP00000364549.3:p.Glu668Ter | 0.06989247 |
| P5-Organoid | ARHGAP22 | 10 | 49687765 | G | A | Missense_Mutation | ENST00000435790.2:c.383C>T | ENSP00000416701.2:p.Ala128Val | 0.15702479 |
| P5-Organoid | ZNF503 | 10 | 77159052 | ATCCGGACTTCAGCG | A | Frame_Shift_Del | ENST00000535216.1:c.1382_1395del | ENSP00000438988.1:p.Ala461ValfsTer44 | 0.07983193 |
| P5-Organoid | GLUD1 | 10 | 88834343 | C | A | Missense_Mutation | ENST00000544149.1:c.212G>T | ENSP00000444732.1:p.Arg71Met | 0.125 |
| P5-Organoid | SORCS3 | 10 | 107005354 | G | C | Missense_Mutation | ENST00000369701.3:c.2923G>C | ENSP00000358715.3:p.Asp975His | 0.16379310 |
| P5-Organoid | VWA2 | 10 | 116048814 | T | C | Missense_Mutation | ENST00000603594.1:c.1688T>C | ENSP00000473752.1:p.Val563Ala | 0.11650485 |
| P5-Organoid | DCHS1 | 11 | 6661869 | G | A | Missense_Mutation | ENST00000299441.3:c.976C>T | ENSP00000299441.3:p.Arg326Trp | 0.12977099 |
| P5-Organoid | CCDC73 | 11 | 32657248 | C | G | Missense_Mutation | ENST00000335185.5:c.1179G>C | ENSP00000335325.5:p.Lys393Asn | 0.13333333 |
| P5-Organoid | KIAA1549L | 11 | 33581396 | C | A | Missense_Mutation | ENST00000389726.3:c.3084C>A | ENSP00000374376.3:p.Ser1028Arg | 0.14942528 |
| P5-Organoid | TTC12 | 11 | 113211403 | T | A | Missense_Mutation | ENST00000529221.1:c.844T>A | ENSP00000433757.1:p.Phe282Ile | 0.02580645 |
| P5-Organoid | HTR3B | 11 | 113802589 | T | A | Missense_Mutation | ENST00000537778.1:c.335T>A | ENSP00000443118.1:p.Phe112Tyr | 0.06161137 |
| P5-Organoid | SLC6A12 | 12 | 304450 | C | T | Missense_Mutation | ENST00000536824.1:c.1370G>A | ENSP00000444268.1:p.Ser457Asn | 0.05113636 |
| P5-Organoid | KRAS | 12 | 25398284 | C | T | Missense_Mutation | ENST00000557334.1:c.35G>A | ENSP00000452512.1:p.Gly12Asp | 0.21052631 |
| P5-Organoid | CACNB3 | 12 | 49221471 | C | T | Missense_Mutation | ENST00000547392.1:c.1163C>T | ENSP00000446529.1:p.Thr388Ile | 0.13863216 |
| P5-Organoid | GRASP | 12 | 52404706 | G | A | Missense_Mutation | ENST00000293662.4:c.338G>A | ENSP00000293662.4:p.Gly113Asp | 0.23152709 |
| P5-Organoid | SLC17A8 | 12 | 100774715 | G | A | Missense_Mutation | ENST00000392989.3:c.338G>A | ENSP00000376715.3:p.Gly113Glu | 0.14814814 |
| P5-Organoid | ACADS | 12 | 121176633 | C | T | Missense_Mutation | ENST00000411593.2:c.932C>T | ENSP00000401045.2:p.Ala311Val | 0.03825136 |
| P5-Organoid | SLC15A4 | 12 | 129285547 | CA | C | Frame_Shift_Del | ENST00000544112.1:c.254del | ENSP00000439946.1:p.Leu85TrpfsTer6 | 0.26050420 |
| P5-Organoid | TOX4 | 14 | 21960767 | CAA | C | Frame_Shift_Del | ENST00000448790.2:c.924_925del | ENSP00000393080.2:p.Ile309ArgfsTer12 | 0.04938271 |
| P5-Organoid | TOX4 | 14 | 21960770 | T | C | Missense_Mutation | ENST00000448790.2:c.926T>C | ENSP00000393080.2:p.Ile309Thr | 0.04938271 |
| P5-Organoid | OXA1L | 14 | 23236470 | C | T | Missense_Mutation | ENST00000604262.1:c.77C>T | ENSP00000474623.1:p.Ala26Val | 0.04562737 |
| P5-Organoid | AKAP6 | 14 | 33004853 | G | A | Missense_Mutation | ENST00000557354.1:c.418G>A | ENSP00000450531.1:p.Val140Met | 0.06811145 |
| P5-Organoid | AHNAK2 | 14 | 105411396 | C | G | Missense_Mutation | ENST00000333244.5:c.10392G>C | ENSP00000353114.4:p.Lys3464Asn | 0.19125683 |
| P5-Organoid | SNURF | 15 | 25207326 | G | C | Missense_Mutation | ENST00000577949.1:c.80G>C | ENSP00000463201.1:p.Arg27Pro | 0.10526315 |
| P5-Organoid | USP8 | 15 | 50754515 | G | GAA | Frame_Shift_Ins | ENST00000433963.1:c.539_540dup | ENSP00000405537.1:p.Gly181LysfsTer12 | 0.10526315 |
| P5-Organoid | AKAP13 | 15 | 86198910 | C | T | Missense_Mutation | ENST00000394518.2:c.4637C>T | ENSP00000378026.2:p.Ala1546Val | 0.07547169 |
| P5-Organoid | GLYR1 | 16 | 4882093 | C | G | Missense_Mutation | ENST00000591451.1:c.424G>C | ENSP00000468328.1:p.Glu142Gln | 0.07359307 |
| P5-Organoid | SLC5A11 | 16 | 24881226 | G | T | Missense_Mutation | ENST00000569071.1:c.20G>T | ENSP00000456376.1:p.Gly7Val | 0.05882352 |
| P5-Organoid | ESRP2 | 16 | 68266492 | A | T | Missense_Mutation | ENST00000565858.1:c.839T>A | ENSP00000454554.1:p.Leu280His | 0.12842105 |
| P5-Organoid | FUK | 16 | 70507098 | C | T | Missense_Mutation | ENST00000571514.1:c.98C>T | ENSP00000462584.1:p.Ala33Val | 0.23140495 |
| P5-Organoid | PKD1L2 | 16 | 81167189 | C | A | Missense_Mutation | ENST00000533478.1:c.3781G>T | ENSP00000434644.1:p.Ala1261Ser | 0.12568306 |
| P5-Organoid | POLR2A | 17 | 7414827 | G | A | Missense_Mutation | ENST00000322644.6:c.4021G>A | ENSP00000314949.6:p.Val1341Met | 0.08717948 |
| P5-Organoid | TP53 | 17 | 7578406 | C | T | Missense_Mutation | ENST00000455263.2:c.524G>A | ENSP00000398846.2:p.Arg175His | 0.375 |
| P5-Organoid | CYB5D1 | 17 | 7762829 | ATCCGG | A | Frame_Shift_Del | ENST00000570446.1:c.203_207del | ENSP00000461852.1:p.Ile68ArgfsTer2 | 0.07017543 |
| P5-Organoid | CCDC42 | 17 | 8647882 | G | A | Missense_Mutation | ENST00000539522.2:c.46C>T | ENSP00000444359.2:p.Arg16Trp | 0.05633802 |
| P5-Organoid | DNAH9 | 17 | 11684458 | C | T | Missense_Mutation | ENST00000454412.2:c.7685C>T | ENSP00000414874.2:p.Thr2562Ile | 0.07894736 |
| P5-Organoid | SPPL2C | 17 | 43924263 | C | T | Missense_Mutation | ENST00000329196.5:c.1991C>T | ENSP00000332488.5:p.Ala664Val | 0.22704081 |
| P5-Organoid | SDK2 | 17 | 71344846 | G | T | Missense_Mutation | ENST00000392650.3:c.6057C>A | ENSP00000376421.3:p.Ser2019Arg | 0.29931972 |
| P5-Organoid | CBLN2 | 18 | 70205952 | G | T | Missense_Mutation | ENST00000585159.1:c.413C>A | ENSP00000463771.1:p.Pro138Gln | 0.12612612 |
| P5-Organoid | ZFR2 | 19 | 3827531 | C | T | Missense_Mutation | ENST00000262961.4:c.973G>A | ENSP00000262961.3:p.Ala325Thr | 0.05882352 |
| P5-Organoid | ZNF625 | 19 | 12256195 | C | T | Missense_Mutation | ENST00000542938.1:c.838G>A | ENSP00000438436.1:p.Val280Ile | 0.05479452 |
| P5-Organoid | EXOSC5 | 19 | 41897867 | C | T | Missense_Mutation | ENST00000596905.1:c.149G>A | ENSP00000471002.1:p.Gly50Asp | 0.085 |
| P5-Organoid | LILRB1 | 19 | 55147987 | GA | CC | Missense_Mutation | ENST00000434867.2:c.1690_1691delinsCC | ENSP00000405243.2:p.Glu564Pro | 0.13333333 |
| P5-Organoid | NLRP5 | 19 | 56561882 | C | T | Missense_Mutation | ENST00000390649.3:c.3056C>T | ENSP00000375063.3:p.Pro1019Leu | 0.02 |
| P5-Organoid | ADRA1D | 20 | 4228688 | A | G | Missense_Mutation | ENST00000379453.4:c.917T>C | ENSP00000368766.4:p.Ile306Thr | 0.03143418 |
| P5-Organoid | PROKR2 | 20 | 5282708 | A | G | Missense_Mutation | ENST00000546004.1:c.1133T>C | ENSP00000440790.1:p.Val378Ala | 0.03070175 |
| P5-Organoid | JAG1 | 20 | 10629308 | TC | CT | Missense_Mutation | ENST00000423891.2:c.980_981delinsAG | ENSP00000389519.2:p.Arg327Lys | 0.10169491 |
| P5-Organoid | KIAA1755 | 20 | 36869597 | C | A | Missense_Mutation | ENST00000279024.4:c.936G>T | ENSP00000279024.4:p.Lys312Asn | 0.19921875 |
| P5-Organoid | ADNP | 20 | 49508046 | T | C | Missense_Mutation | ENST00000396032.3:c.3205A>G | ENSP00000379349.2:p.Ile1069Val | 0.07352941 |
| P5-Organoid | NFATC2 | 20 | 50092093 | G | C | Missense_Mutation | ENST00000610033.1:c.780C>G | ENSP00000477142.1:p.Ile260Met | 0.09848484 |
| P5-Organoid | ZNF831 | 20 | 57769069 | G | A | Missense_Mutation | ENST00000371030.2:c.2995G>A | ENSP00000360069.2:p.Gly999Ser | 0.07291666 |
| P5-Organoid | KRTAP13-3 | 21 | 31797791 | C | A | Missense_Mutation | ENST00000390690.2:c.440G>T | ENSP00000375109.2:p.Cys147Phe | 0.15107913 |
| P5-Organoid | DOPEY2 | 21 | 37660356 | G | A | Missense_Mutation | ENST00000399151.3:c.6205G>A | ENSP00000382104.3:p.Ala2069Thr | 0.03809523 |
| P5-Organoid | KRTAP10-4 | 21 | 45994110 | A | G | Missense_Mutation | ENST00000400374.3:c.475A>G | ENSP00000383225.3:p.Ile159Val | 0.31956912 |
| P5-Organoid | SAMM50 | 22 | 44392219 | A | G | Missense_Mutation | ENST00000396202.3:c.736A>G | ENSP00000379505.3:p.Ile246Val | 0.02734375 |
| P5-Organoid | FRMPD4 | X | 12736390 | C | T | Missense_Mutation | ENST00000380682.1:c.3445C>T | ENSP00000370057.1:p.Arg1149Cys | 0.20338983 |
| P5-Organoid | HEPH | X | 65486401 | G | A | Missense_Mutation | ENST00000519389.1:c.3526G>A | ENSP00000430620.1:p.Val1176Ile | 0.40540540 |
| P5-Organoid | CXorf40B | X | 149101881 | A | G | Missense_Mutation | ENST00000462691.1:c.212T>C | ENSP00000417546.1:p.Leu71Ser | 0.03547297 |