| P3-Organoid | BAI2 | 1 | 32198577 | C | T | Missense_Mutation | ENST00000527361.1:c.3521G>A | ENSP00000435397.1:NA | 0.45263157 |
| P3-Organoid | KIF2C | 1 | 45216159 | G | A | Missense_Mutation | ENST00000372224.4:c.362G>A | ENSP00000361298.4:p.Arg121His | 0.27272727 |
| P3-Organoid | DMRTA2 | 1 | 50887013 | G | A | Missense_Mutation | ENST00000418121.1:c.196C>T | ENSP00000399370.1:NA | 0.24479166 |
| P3-Organoid | LRRIQ3 | 1 | 74506901 | C | CT | Frame_Shift_Ins | ENST00000395089.1:c.1713dup | ENSP00000378524.1:NA | 0.29629629 |
| P3-Organoid | HS2ST1 | 1 | 87570165 | A | G | Missense_Mutation | ENST00000370550.5:c.857A>G | ENSP00000359581.4:NA | 0.21487603 |
| P3-Organoid | RBM15 | 1 | 110882980 | C | A | Missense_Mutation | ENST00000602849.1:c.953C>A | ENSP00000473638.1:p.Pro318Gln | 0.50554323 |
| P3-Organoid | PEX11B | 1 | 145518256 | G | T | Missense_Mutation | ENST00000537888.1:c.316G>T | ENSP00000437510.1:NA | 0.56976744 |
| P3-Organoid | LCE1C | 1 | 152777707 | C | T | Missense_Mutation | ENST00000607093.1:c.248G>A | ENSP00000475270.1:p.Arg83His | 0.41904761 |
| P3-Organoid | OR10X1 | 1 | 158549687 | C | T | Translation_Start_Site | ENST00000368150.1:c.3G>A | ENSP00000357132.1:p.Met1? | 0.47692307 |
| P3-Organoid | FCRLB | 1 | 161696729 | A | G | Missense_Mutation | ENST00000392158.1:c.811A>G | ENSP00000375999.1:p.Thr271Ala | 0.45045045 |
| P3-Organoid | ATP1B1 | 1 | 169076157 | CAGTTGGTGTA | C | Splice_Site | ENST00000367816.1:c.94_97+6del | | 0.125 |
| P3-Organoid | USH2A | 1 | 215799151 | C | T | Missense_Mutation | ENST00000366943.2:c.15653G>A | ENSP00000355910.2:p.Arg5218His | 0.14606741 |
| P3-Organoid | OR6F1 | 1 | 247875319 | C | T | Missense_Mutation | ENST00000302084.2:c.739G>A | ENSP00000305640.2:p.Val247Met | 0.48849104 |
| P3-Organoid | CCDC85A | 2 | 56603013 | C | A | Missense_Mutation | ENST00000407595.2:c.1515C>A | ENSP00000384040.2:p.Ser505Arg | 0.44 |
| P3-Organoid | MAT2A | 2 | 85766481 | C | T | Missense_Mutation | ENST00000306434.3:c.71C>T | ENSP00000303147.3:p.Ser24Leu | 0.53186274 |
| P3-Organoid | NEB | 2 | 152512803 | A | T | Missense_Mutation | ENST00000604864.1:c.6359T>A | ENSP00000474498.1:p.Leu2120His | 0.01935483 |
| P3-Organoid | GRM2 | 3 | 51746586 | G | A | Missense_Mutation | ENST00000442933.2:c.548G>A | ENSP00000408906.2:p.Arg183His | 0.29866666 |
| P3-Organoid | CD200 | 3 | 112054863 | A | G | Missense_Mutation | ENST00000473539.1:c.86A>G | ENSP00000420298.1:p.Gln29Arg | 0.54385964 |
| P3-Organoid | EPHB1 | 3 | 134960039 | G | A | Missense_Mutation | ENST00000493838.1:c.1079G>A | ENSP00000419574.1:p.Arg360His | 0.37201365 |
| P3-Organoid | CAMK2D | 4 | 114426173 | C | T | Missense_Mutation | ENST00000511664.1:c.1003G>A | ENSP00000425824.1:p.Val335Met | 0.62376237 |
| P3-Organoid | AADAT | 4 | 170988477 | C | T | Splice_Site | ENST00000515480.1:c.962+1G>A | | 0.29670329 |
| P3-Organoid | SGTB | 5 | 65004322 | C | A | Missense_Mutation | ENST00000381007.4:c.268G>T | ENSP00000370395.4:p.Asp90Tyr | 0.17272727 |
| P3-Organoid | PIK3R1 | 5 | 67589274 | A | T | Missense_Mutation | ENST00000523872.1:c.173A>T | ENSP00000430098.1:p.Asp58Val | 0.56756756 |
| P3-Organoid | NKX2-5 | 5 | 172659685 | C | T | Missense_Mutation | ENST00000329198.4:c.862G>A | ENSP00000327758.4:p.Ala288Thr | 0.50282485 |
| P3-Organoid | RING1 | 6 | 33177715 | G | T | Missense_Mutation | ENST00000374656.4:c.263G>T | ENSP00000363787.4:p.Arg88Leu | 0.59090909 |
| P3-Organoid | MDFI | 6 | 41621204 | ACTGCGACCTGCC | A | In_Frame_Del | ENST00000373050.4:c.460_471del | ENSP00000362141.4:p.Pro154_Leu157del | 0.46956521 |
| P3-Organoid | TTBK1 | 6 | 43214466 | T | G | Missense_Mutation | ENST00000259750.4:c.68T>G | ENSP00000259750.4:p.Ile23Ser | 0.63529411 |
| P3-Organoid | COL12A1 | 6 | 75816171 | C | G | Missense_Mutation | ENST00000483888.2:c.8142G>C | ENSP00000421216.1:p.Trp2714Cys | 0.65408805 |
| P3-Organoid | MDN1 | 6 | 90359882 | C | T | Missense_Mutation | ENST00000428876.1:c.16067G>A | ENSP00000413970.1:p.Arg5356Gln | 0.07738095 |
| P3-Organoid | NUP43 | 6 | 150063660 | C | T | Missense_Mutation | ENST00000460354.2:c.368G>A | ENSP00000432401.2:p.Gly123Asp | 0.37301587 |
| P3-Organoid | SLC22A2 | 6 | 160670366 | G | A | Nonsense_Mutation | ENST00000366953.3:c.724C>T | ENSP00000355920.3:p.Gln242Ter | 0.66115702 |
| P3-Organoid | UNC93A | 6 | 167708152 | G | A | Missense_Mutation | ENST00000366829.2:c.235G>A | ENSP00000355794.2:p.Val79Met | 0.31617647 |
| P3-Organoid | SDK1 | 7 | 4088988 | G | A | Missense_Mutation | ENST00000404826.2:c.2611G>A | ENSP00000385899.2:p.Ala871Thr | 0.22262773 |
| P3-Organoid | MOGAT3 | 7 | 100841617 | C | T | Missense_Mutation | ENST00000440203.2:c.523G>A | ENSP00000403756.2:p.Asp175Asn | 0.49275362 |
| P3-Organoid | KMT2C | 7 | 151882672 | C | A | Missense_Mutation | ENST00000355193.2:c.5053G>T | ENSP00000347325.2:p.Ala1685Ser | 0.12903225 |
| P3-Organoid | GRHL2 | 8 | 102643864 | G | C | Splice_Site | ENST00000395927.1:c.1210-1G>C | | 0.62222222 |
| P3-Organoid | FOXD4 | 9 | 117371 | C | G | Missense_Mutation | ENST00000382500.2:c.749G>C | ENSP00000371940.2:p.Gly250Ala | 1 |
| P3-Organoid | CDKN2A | 9 | 21971120 | G | A | Nonsense_Mutation | ENST00000579122.1:c.238C>T | ENSP00000464202.1:p.Arg80Ter | 0.99342105 |
| P3-Organoid | APBA1 | 9 | 72131199 | G | A | Missense_Mutation | ENST00000265381.4:c.928C>T | ENSP00000265381.3:p.Arg310Cys | 0.45454545 |
| P3-Organoid | SLC2A6 | 9 | 136340162 | C | T | Missense_Mutation | ENST00000371899.4:c.848G>A | ENSP00000360966.4:p.Arg283His | 0.3671875 |
| P3-Organoid | MYO3A | 10 | 26385322 | T | A | Missense_Mutation | ENST00000543632.1:c.1575T>A | ENSP00000445909.1:p.Asn525Lys | 0.51612903 |
| P3-Organoid | DNHD1 | 11 | 6541027 | G | T | Missense_Mutation | ENST00000527990.2:c.1590G>T | ENSP00000436180.2:p.Gln530His | 0.01591511 |
| P3-Organoid | NAV2 | 11 | 20066793 | G | A | Missense_Mutation | ENST00000540292.1:c.3341G>A | ENSP00000443489.1:p.Ser1114Asn | 0.39295393 |
| P3-Organoid | ALX4 | 11 | 44331215 | G | A | Missense_Mutation | ENST00000329255.3:c.398C>T | ENSP00000332744.3:p.Pro133Leu | 0.10227272 |
| P3-Organoid | OR8K1 | 11 | 56113669 | T | A | Missense_Mutation | ENST00000279783.2:c.155T>A | ENSP00000279783.2:p.Val52Asp | 0.32984293 |
| P3-Organoid | OR9G1 | 11 | 56468212 | G | A | Missense_Mutation | ENST00000312153.1:c.349G>A | ENSP00000309012.1:p.Val117Met | 0.63194444 |
| P3-Organoid | OR9G4 | 11 | 56510657 | C | T | Missense_Mutation | ENST00000302957.3:c.631G>A | ENSP00000307515.3:p.Glu211Lys | 0.62992126 |
| P3-Organoid | FAM111A | 11 | 58919557 | A | G | Missense_Mutation | ENST00000533703.1:c.416A>G | ENSP00000433154.1:p.Asn139Ser | 0.33613445 |
| P3-Organoid | RASGRP2 | 11 | 64506875 | C | T | Missense_Mutation | ENST00000394432.3:c.770G>A | ENSP00000377953.3:p.Arg257His | 0.64233576 |
| P3-Organoid | GUCY1A2 | 11 | 106681104 | C | T | Missense_Mutation | ENST00000526355.2:c.1307G>A | ENSP00000431245.1:p.Arg436Gln | 0.62857142 |
| P3-Organoid | PDE3A | 12 | 20522547 | G | A | Missense_Mutation | ENST00000359062.3:c.329G>A | ENSP00000351957.3:p.Gly110Asp | 0.98148148 |
| P3-Organoid | KRAS | 12 | 25398284 | C | T | Missense_Mutation | ENST00000557334.1:c.35G>A | ENSP00000452512.1:p.Gly12Asp | 1 |
| P3-Organoid | SPERT | 13 | 46287581 | C | T | Missense_Mutation | ENST00000378966.3:c.313C>T | ENSP00000368249.3:p.Arg105Cys | 0.30191458 |
| P3-Organoid | SPTB | 14 | 65259941 | G | A | Missense_Mutation | ENST00000556626.1:c.2440C>T | ENSP00000451752.1:p.Arg814Trp | 0.35645933 |
| P3-Organoid | ZNF839 | 14 | 102793048 | G | A | Missense_Mutation | ENST00000559185.1:c.667G>A | ENSP00000453109.1:p.Gly223Ser | 0.31775700 |
| P3-Organoid | AKT1 | 14 | 105246533 | G | A | Missense_Mutation | ENST00000555528.1:c.67C>T | ENSP00000450688.1:p.Arg23Trp | 0.70642201 |
| P3-Organoid | LCTL | 15 | 66853402 | G | A | Missense_Mutation | ENST00000537670.1:c.128C>T | ENSP00000445419.1:p.Ala43Val | 0.27979274 |
| P3-Organoid | IL16 | 15 | 81589273 | C | T | Missense_Mutation | ENST00000394660.2:c.1907C>T | ENSP00000378155.2:p.Ala636Val | 0.67441860 |
| P3-Organoid | TEKT5 | 16 | 10729724 | A | C | Missense_Mutation | ENST00000283025.2:c.1138T>G | ENSP00000283025.2:p.Ser380Ala | 0.05844155 |
| P3-Organoid | TP53 | 17 | 7577121 | G | A | Missense_Mutation | ENST00000455263.2:c.817C>T | ENSP00000398846.2:p.Arg273Cys | 1 |
| P3-Organoid | ARHGAP27 | 17 | 43481661 | C | T | Missense_Mutation | ENST00000528384.1:c.349G>A | ENSP00000431591.1:p.Val117Ile | 0.29770992 |
| P3-Organoid | RNF43 | 17 | 56448395 | C | A | Splice_Site | ENST00000584437.1:c.253-1G>T | | 0.57295373 |
| P3-Organoid | ACTG1 | 17 | 79478217 | G | T | Missense_Mutation | ENST00000575842.1:c.799C>A | ENSP00000458162.1:p.Leu267Met | 0.41418764 |
| P3-Organoid | STK11 | 19 | 1221226 | C | T | Missense_Mutation | ENST00000326873.7:c.749C>T | ENSP00000324856.6:p.Thr250Met | 0.43478260 |
| P3-Organoid | TBXA2R | 19 | 3599929 | C | T | Missense_Mutation | ENST00000411851.3:c.704G>A | ENSP00000393333.2:p.Arg235His | 0.42696629 |
| P3-Organoid | PDE4A | 19 | 10561287 | C | T | Missense_Mutation | ENST00000592685.1:c.563C>T | ENSP00000468507.1:p.Pro188Leu | 0.43055555 |
| P3-Organoid | FKBP8 | 19 | 18643527 | T | C | Missense_Mutation | ENST00000610101.1:c.622A>G | ENSP00000476586.1:p.Met208Val | 0.34275618 |
| P3-Organoid | ZNF91 | 19 | 23542902 | TGAATTATCTTATGTGTA | T | Frame_Shift_Del | ENST00000397082.2:c.2766_2782del | ENSP00000380272.2:p.Thr923TyrfsTer9 | 0.18709677 |
| P3-Organoid | ZNF536 | 19 | 31039824 | G | A | Missense_Mutation | ENST00000355537.3:c.3298G>A | ENSP00000347730.1:p.Val1100Met | 0.74520547 |
| P3-Organoid | IFNL3 | 19 | 39734787 | C | T | Missense_Mutation | ENST00000413851.2:c.269G>A | ENSP00000409000.2:p.Arg90His | 0.43699187 |
| P3-Organoid | PSG2 | 19 | 43579505 | C | T | Splice_Site | ENST00000406487.1:c.709+1G>A | | 0.17915309 |
| P3-Organoid | RRAS | 19 | 50140383 | T | C | Missense_Mutation | ENST00000246792.3:c.158A>G | ENSP00000246792.2:p.Tyr53Cys | 0.76515151 |
| P3-Organoid | MYBPC2 | 19 | 50962189 | C | T | Missense_Mutation | ENST00000357701.5:c.2521C>T | ENSP00000350332.4:p.Arg841Trp | 0.17277486 |
| P3-Organoid | RP4-576H24.4 | 20 | 1559023 | CCA | C | Frame_Shift_Del | ENST00000564763.1:c.392_393del | ENSP00000457944.1:p.Val131GlyfsTer3 | 0.01988636 |
| P3-Organoid | MAGEB18 | X | 26157473 | C | T | Missense_Mutation | ENST00000325250.1:c.371C>T | ENSP00000314543.1:p.Thr124Met | 0.55056179 |