| P1-Organoid | ATAD3B | 1 | 1431060 | T | C | Missense_Mutation | ENST00000308647.7:c.1810T>C | ENSP00000311766.7:p.Tyr604His | 0.25 |
| P1-Organoid | ATAD3B | 1 | 1431165 | C | T | Missense_Mutation | ENST00000308647.7:c.1915C>T | ENSP00000311766.7:p.Pro639Ser | 0.43035714 |
| P1-Organoid | PRAMEF1 | 1 | 12855774 | A | G | Missense_Mutation | ENST00000400814.3:c.319A>G | ENSP00000383616.3:p.Lys352Glu | 0.10849056 |
| P1-Organoid | CLCNKA | 1 | 16354394 | C | T | Missense_Mutation | ENST00000439316.2:c.731C>T | ENSP00000414445.2:p.Ala287Val | 0.46101694 |
| P1-Organoid | ADC | 1 | 33563691 | A | G | Missense_Mutation | ENST00000398167.1:c.1000A>G | ENSP00000381233.1:NA | 0.39606741 |
| P1-Organoid | HIVEP3 | 1 | 42049181 | C | T | Missense_Mutation | ENST00000429157.2:c.1288G>A | ENSP00000410828.2:NA | 0.24 |
| P1-Organoid | LCE1D | 1 | 152770503 | G | A | Missense_Mutation | ENST00000326233.6:c.233G>A | ENSP00000316737.6:p.Arg78His | 0.09282700 |
| P1-Organoid | LCE1D | 1 | 152770521 | G | A | Missense_Mutation | ENST00000326233.6:c.251G>A | ENSP00000316737.6:p.Arg84His | 0.17073170 |
| P1-Organoid | AQP10 | 1 | 154294464 | A | G | Missense_Mutation | ENST00000484864.1:c.161A>G | ENSP00000420341.1:p.Asn54Ser | 0.19305019 |
| P1-Organoid | DAP3 | 1 | 155699069 | C | A | Missense_Mutation | ENST00000535183.1:c.632C>A | ENSP00000445003.1:p.Ser211Tyr | 0.28767123 |
| P1-Organoid | BLZF1 | 1 | 169347575 | G | A | Missense_Mutation | ENST00000367808.3:c.476G>A | ENSP00000356782.3:p.Arg159His | 0.53763440 |
| P1-Organoid | BRE | 2 | 28460164 | A | G | Missense_Mutation | ENST00000379632.2:c.776A>G | ENSP00000368953.2:p.Asn259Ser | 1 |
| P1-Organoid | VWA3B | 2 | 98779374 | C | T | Missense_Mutation | ENST00000477737.1:c.1049C>T | ENSP00000417955.1:p.Thr350Met | 0.43925233 |
| P1-Organoid | ANAPC1 | 2 | 112614429 | G | A | Nonsense_Mutation | ENST00000341068.3:c.1393C>T | ENSP00000339109.3:p.Gln465Ter | 0.25130890 |
| P1-Organoid | TUBA3E | 2 | 130951894 | G | T | Missense_Mutation | ENST00000312988.7:c.521C>A | ENSP00000318197.7:p.Ala174Asp | 0.21052631 |
| P1-Organoid | LRP1B | 2 | 141079606 | G | A | Missense_Mutation | ENST00000389484.3:c.12566C>T | ENSP00000374135.3:p.Pro4189Leu | 0.17263843 |
| P1-Organoid | BAZ2B | 2 | 160205653 | A | G | Missense_Mutation | ENST00000392783.2:c.5002T>C | ENSP00000376534.2:p.Phe1668Leu | 0.456 |
| P1-Organoid | VILL | 3 | 38043268 | G | A | Missense_Mutation | ENST00000465644.1:c.550G>A | ENSP00000422096.1:p.Val184Ile | 0.03333333 |
| P1-Organoid | COL7A1 | 3 | 48629354 | C | T | Missense_Mutation | ENST00000454817.1:c.1334G>A | ENSP00000412569.1:p.Arg445Gln | 0.64102564 |
| P1-Organoid | MST1 | 3 | 49722905 | T | TGG | Frame_Shift_Ins | ENST00000449682.2:c.1420_1421dup | ENSP00000414287.2:p.Asp475GlnfsTer52 | 0.09240924 |
| P1-Organoid | SLC33A1 | 3 | 155571270 | TTC | T | Frame_Shift_Del | ENST00000392845.3:c.515_516del | ENSP00000376587.2:p.Arg172AsnfsTer15 | 0.58139534 |
| P1-Organoid | MYOZ2 | 4 | 120107249 | G | T | Missense_Mutation | ENST00000307128.5:c.689G>T | ENSP00000306997.5:p.Arg230Leu | 0.03157894 |
| P1-Organoid | WDR17 | 4 | 177067184 | G | A | Missense_Mutation | ENST00000508596.1:c.1568G>A | ENSP00000422763.1:p.Arg523His | 0.39316239 |
| P1-Organoid | ARSB | 5 | 78135181 | G | A | Missense_Mutation | ENST00000565165.1:c.1211C>T | ENSP00000456339.1:p.Pro404Leu | 0.24679487 |
| P1-Organoid | AP3S1 | 5 | 115249078 | C | T | Missense_Mutation | ENST00000316788.7:c.473C>T | ENSP00000325369.7:p.Pro158Leu | 0.35793357 |
| P1-Organoid | TMEM14B | 6 | 10756712 | C | T | Missense_Mutation | ENST00000473276.1:c.127C>T | ENSP00000420580.1:p.Arg43Cys | 0.05821917 |
| P1-Organoid | TNXB | 6 | 32035705 | C | T | Missense_Mutation | ENST00000375247.2:c.6277G>A | ENSP00000364396.2:p.Ala2093Thr | 0.41689373 |
| P1-Organoid | BRD2 | 6 | 32943223 | CAAT | C | In_Frame_Del | ENST00000449085.2:c.256_258del | ENSP00000409145.2:p.Asn86del | 0.66666666 |
| P1-Organoid | GNA12 | 7 | 2802374 | C | T | Missense_Mutation | ENST00000407653.1:c.149G>A | ENSP00000386054.1:p.Arg50Gln | 0.29927007 |
| P1-Organoid | RADIL | 7 | 4917673 | C | T | Missense_Mutation | ENST00000536091.1:c.98G>A | ENSP00000442533.1:p.Ser33Asn | 0.24489795 |
| P1-Organoid | USP42 | 7 | 6194003 | G | T | Nonsense_Mutation | ENST00000306177.5:c.2818G>T | ENSP00000301962.5:p.Glu940Ter | 0.04255319 |
| P1-Organoid | TNS3 | 7 | 47317793 | G | A | Nonsense_Mutation | ENST00000398879.1:c.4219C>T | ENSP00000381854.1:p.Gln1407Ter | 0.27559055 |
| P1-Organoid | FIGNL1 | 7 | 50514478 | G | A | Nonsense_Mutation | ENST00000433017.1:c.508C>T | ENSP00000399997.1:p.Arg170Ter | 0.29333333 |
| P1-Organoid | SLC12A9 | 7 | 100463991 | G | A | Missense_Mutation | ENST00000354161.3:c.2509G>A | ENSP00000275730.4:p.Ala837Thr | 0.45161290 |
| P1-Organoid | SLC35G5 | 8 | 11188922 | T | C | Missense_Mutation | ENST00000382435.4:c.307T>C | ENSP00000371872.4:p.Trp103Arg | 0.08637873 |
| P1-Organoid | GRHL2 | 8 | 102589721 | CGGCGAAGCAGA | C | Frame_Shift_Del | ENST00000395927.1:c.932_942del | ENSP00000379260.1:p.Ala311GlyfsTer3 | 0.63636363 |
| P1-Organoid | GLIS3 | 9 | 4118415 | G | A | Missense_Mutation | ENST00000381971.3:c.1063C>T | ENSP00000371398.3:p.Arg355Cys | 0.30769230 |
| P1-Organoid | ANKRD20A2 | 9 | 42368614 | A | G | Missense_Mutation | ENST00000377601.2:c.200A>G | ENSP00000366826.2:p.His67Arg | 0.47982062 |
| P1-Organoid | PTCH1 | 9 | 98270531 | C | G | Missense_Mutation | ENST00000331920.6:c.113G>C | ENSP00000332353.6:p.Gly38Ala | 0.45098039 |
| P1-Organoid | TRIM32 | 9 | 119461721 | ACTT | A | In_Frame_Del | ENST00000450136.1:c.1706_1708del | ENSP00000408292.1:p.Phe569del | 0.58646616 |
| P1-Organoid | RALGPS1 | 9 | 129812376 | G | C | Missense_Mutation | ENST00000424082.2:c.355G>C | ENSP00000415630.2:p.Ala119Pro | 0.13714285 |
| P1-Organoid | LOXL4 | 10 | 100015394 | C | T | Missense_Mutation | ENST00000260702.3:c.1531G>A | ENSP00000260702.3:p.Gly511Arg | 0.34408602 |
| P1-Organoid | TMEM138 | 11 | 61131879 | A | G | Missense_Mutation | ENST00000542946.1:c.17A>G | ENSP00000445792.1:p.Asn6Ser | 0.01734104 |
| P1-Organoid | KRAS | 12 | 25398284 | C | T | Missense_Mutation | ENST00000557334.1:c.35G>A | ENSP00000452512.1:p.Gly12Asp | 0.44 |
| P1-Organoid | DDX11 | 12 | 31237978 | C | T | Missense_Mutation | ENST00000545668.1:c.556C>T | ENSP00000440402.1:p.Arg186Trp | 0.17760617 |
| P1-Organoid | DDX11 | 12 | 31250875 | G | C | Missense_Mutation | ENST00000545668.1:c.1819G>C | ENSP00000440402.1:p.Ala607Pro | 0.18119266 |
| P1-Organoid | PABPC3 | 13 | 25671585 | TA | CC | Missense_Mutation | ENST00000281589.3:c.1249_1250delinsCC | ENSP00000281589.3:p.Tyr417Pro | 0.04467354 |
| P1-Organoid | PCCA | 13 | 101020827 | C | T | Missense_Mutation | ENST00000376286.4:c.1667C>T | ENSP00000365463.4:p.Ser556Leu | 0.43697479 |
| P1-Organoid | NOP9 | 14 | 24769311 | C | T | Missense_Mutation | ENST00000396802.3:c.151C>T | ENSP00000380020.3:p.Pro51Ser | 0.67407407 |
| P1-Organoid | GZMH | 14 | 25076877 | G | C | Missense_Mutation | ENST00000382548.4:c.280C>G | ENSP00000371988.4:p.Pro94Ala | 0.13839285 |
| P1-Organoid | RP11-176H8.1 | 14 | 31926584 | G | A | Missense_Mutation | ENST00000547378.1:c.16C>T | ENSP00000447056.1:p.Arg6Trp | 0.35 |
| P1-Organoid | YLPM1 | 14 | 75248907 | G | A | Missense_Mutation | ENST00000552421.1:c.2161G>A | ENSP00000447921.1:p.Gly721Arg | 0.73275862 |
| P1-Organoid | DYNC1H1 | 14 | 102445804 | A | AT | Frame_Shift_Ins | ENST00000360184.4:c.495dup | ENSP00000348965.4:p.Arg166Ter | 0.39442231 |
| P1-Organoid | TECPR2 | 14 | 102918775 | G | A | Missense_Mutation | ENST00000558678.1:c.3451G>A | ENSP00000453671.1:p.Val1151Ile | 0.27325581 |
| P1-Organoid | WDR24 | 16 | 739642 | G | A | Missense_Mutation | ENST00000248142.6:c.185C>T | ENSP00000248142.6:p.Ala62Val | 0.55555555 |
| P1-Organoid | HAGHL | 16 | 778956 | G | T | Missense_Mutation | ENST00000341413.4:c.661G>T | ENSP00000341952.4:p.Gly221Trp | 0.0625 |
| P1-Organoid | HAGHL | 16 | 778962 | G | T | Missense_Mutation | ENST00000341413.4:c.667G>T | ENSP00000341952.4:p.Ala223Ser | 0.06666666 |
| P1-Organoid | C16orf58 | 16 | 31519193 | CAAACGCCTGGAGAAGA | C | Splice_Site | ENST00000570164.1:c.301-10_306del | | 0.23622047 |
| P1-Organoid | IRX5 | 16 | 54967174 | G | A | Missense_Mutation | ENST00000558597.1:c.643G>A | ENSP00000453725.1:p.Ala215Thr | 0.40384615 |
| P1-Organoid | MARVELD3 | 16 | 71668212 | T | C | Missense_Mutation | ENST00000567501.1:c.152T>C | ENSP00000455814.1:p.Leu51Pro | 0.47142857 |
| P1-Organoid | TP53 | 17 | 7578406 | C | T | Missense_Mutation | ENST00000455263.2:c.524G>A | ENSP00000398846.2:p.Arg175His | 1 |
| P1-Organoid | NCOR1 | 17 | 15952173 | C | A | Missense_Mutation | ENST00000395857.3:c.2274G>T | ENSP00000379198.3:p.Glu758Asp | 0.02684563 |
| P1-Organoid | TBC1D29 | 17 | 28890301 | G | A | Missense_Mutation | ENST00000580161.1:c.311G>A | ENSP00000462799.1:p.Ser104Asn | 0.09022556 |
| P1-Organoid | CCL4L2 | 17 | 34641494 | A | C | Missense_Mutation | ENST00000394465.2:c.236A>C | ENSP00000377978.2:p.Glu79Ala | 0.05882352 |
| P1-Organoid | EVPL | 17 | 74005146 | C | A | Missense_Mutation | ENST00000586740.1:c.4206G>T | ENSP00000465630.1:p.Lys1402Asn | 0.01724137 |
| P1-Organoid | SMAD4 | 18 | 48573649 | TG | T | Frame_Shift_Del | ENST00000588745.1:c.235del | ENSP00000464901.1:p.Asp79MetfsTer15 | 0.88888888 |
| P1-Organoid | RPS15 | 19 | 1440068 | G | C | Missense_Mutation | ENST00000593052.1:c.161G>C | ENSP00000466010.1:p.Arg54Pro | 0.14814814 |
| P1-Organoid | ZNF441 | 19 | 11891163 | C | T | Missense_Mutation | ENST00000454339.2:c.323C>T | ENSP00000403738.2:p.Ala108Val | 0.04705882 |
| P1-Organoid | CCDC105 | 19 | 15121794 | G | A | Missense_Mutation | ENST00000292574.3:c.157G>A | ENSP00000292574.2:p.Val53Met | 0.68421052 |
| P1-Organoid | PDCD2L | 19 | 34900211 | G | A | Missense_Mutation | ENST00000246535.3:c.482G>A | ENSP00000246535.1:p.Arg161Gln | 0.13175675 |
| P1-Organoid | PRX | 19 | 40901570 | G | A | Nonsense_Mutation | ENST00000324001.7:c.2689C>T | ENSP00000326018.6:p.Arg897Ter | 0.11519607 |
| P1-Organoid | NLRP12 | 19 | 54312910 | G | A | Missense_Mutation | ENST00000535162.1:c.2003C>T | ENSP00000438030.1:p.Ala668Val | 0.63928571 |
| P1-Organoid | ZNF580 | 19 | 56154275 | A | C | Missense_Mutation | ENST00000545125.1:c.401A>C | ENSP00000446126.1:p.His134Pro | 0.72777777 |
| P1-Organoid | SYNDIG1 | 20 | 24524031 | C | T | Missense_Mutation | ENST00000376862.3:c.298C>T | ENSP00000366058.3:p.Arg100Cys | 0.09803921 |
| P1-Organoid | TTLL9 | 20 | 30530746 | A | G | Splice_Site | ENST00000535842.1:c.1244-2A>G | | 0.51785714 |
| P1-Organoid | PPDPF | 20 | 62152689 | C | T | Missense_Mutation | ENST00000370179.3:c.28C>T | ENSP00000359198.3:p.Leu10Phe | 0.46909090 |
| P1-Organoid | CBR3 | 21 | 37518742 | C | A | Missense_Mutation | ENST00000290354.5:c.766C>A | ENSP00000290354.5:p.Leu256Ile | 0.01875 |
| P1-Organoid | RIPK4 | 21 | 43176822 | A | AT | Frame_Shift_Ins | ENST00000544709.1:c.147dup | ENSP00000441754.1:p.Leu50IlefsTer49 | 0.875 |
| P1-Organoid | MXRA5 | X | 3236044 | C | G | Missense_Mutation | ENST00000217939.6:c.5678G>C | ENSP00000217939.5:p.Gly1893Ala | 0.68316831 |
| P1-Organoid | CLCN4 | X | 10176601 | G | A | Missense_Mutation | ENST00000421085.2:c.1078G>A | ENSP00000405754.2:p.Val360Ile | 0.64359861 |
| P1-Organoid | ATP6AP2 | X | 40464996 | C | T | Nonsense_Mutation | ENST00000544975.1:c.814C>T | ENSP00000440459.1:p.Arg272Ter | 0.06072874 |
| P1-Organoid | MED14 | X | 40542109 | C | CATTAAGTG | Frame_Shift_Ins | ENST00000324817.1:c.2189_2196dup | ENSP00000323720.1:p.Gly733HisfsTer18 | 0.43730886 |
| P1-Organoid | DLG3 | X | 69665197 | C | T | Missense_Mutation | ENST00000374360.3:c.146C>T | ENSP00000363480.3:p.Ala49Val | 0.325 |
| P1-Organoid | LONRF3 | X | 118124436 | C | T | Missense_Mutation | ENST00000422289.2:c.560C>T | ENSP00000408894.2:p.Pro187Leu | 0.33079847 |