| P10-Organoid | CEP104 | 1 | 3754070 | A | G | Missense_Mutation | ENST00000378230.3:c.905T>C | ENSP00000367476.3:NA | 0.49137931 |
| P10-Organoid | CATSPER4 | 1 | 26517899 | G | A | Missense_Mutation | ENST00000456354.2:c.335G>A | ENSP00000390423.2:NA | 0.48201438 |
| P10-Organoid | ASH1L | 1 | 155308000 | T | C | Missense_Mutation | ENST00000392403.3:c.8683A>G | ENSP00000376204.3:p.Thr2895Ala | 0.04390243 |
| P10-Organoid | SMG5 | 1 | 156242115 | G | A | Missense_Mutation | ENST00000368267.5:c.709C>T | ENSP00000357250.4:p.Arg237Cys | 0.032 |
| P10-Organoid | CACNA1S | 1 | 201081373 | A | T | Missense_Mutation | ENST00000367338.3:c.95T>A | ENSP00000356307.3:p.Phe32Tyr | 0.03947368 |
| P10-Organoid | OR14K1 | 1 | 247902100 | C | T | Nonsense_Mutation | ENST00000283225.2:c.184C>T | ENSP00000283225.2:p.Arg62Ter | 0.02839116 |
| P10-Organoid | ASAP2 | 2 | 9347277 | A | T | Missense_Mutation | ENST00000315273.4:c.44A>T | ENSP00000316404.4:p.His15Leu | 0.07352941 |
| P10-Organoid | TEKT4 | 2 | 95542476 | C | T | Missense_Mutation | ENST00000295201.4:c.1270C>T | ENSP00000295201.4:p.Arg424Cys | 0.02894736 |
| P10-Organoid | TTN | 2 | 179639033 | G | A | Missense_Mutation | ENST00000591111.1:c.6958C>T | ENSP00000465570.1:p.Arg2320Cys | 0.03301886 |
| P10-Organoid | PARD3B | 2 | 206305254 | G | A | Missense_Mutation | ENST00000406610.2:c.2902G>A | ENSP00000385848.2:p.Val968Ile | 0.02622950 |
| P10-Organoid | IQCF3 | 3 | 51864572 | C | A | Missense_Mutation | ENST00000444293.1:c.110C>A | ENSP00000402530.1:p.Thr37Lys | 0.41747572 |
| P10-Organoid | LRRC66 | 4 | 52860862 | GT | G | Frame_Shift_Del | ENST00000343457.3:c.2325del | ENSP00000341944.3:p.Lys775AsnfsTer40 | 0.40514469 |
| P10-Organoid | FRAS1 | 4 | 79205620 | A | C | Missense_Mutation | ENST00000325942.6:c.1317A>C | ENSP00000326330.6:p.Gln439His | 0.03041825 |
| P10-Organoid | NLN | 5 | 65105883 | G | C | Missense_Mutation | ENST00000502464.1:c.1422G>C | ENSP00000423214.1:p.Gln474His | 0.02659574 |
| P10-Organoid | CMYA5 | 5 | 79034640 | G | A | Missense_Mutation | ENST00000446378.2:c.10052G>A | ENSP00000394770.2:p.Arg3351His | 0.44493392 |
| P10-Organoid | PCDH12 | 5 | 141336818 | T | G | Missense_Mutation | ENST00000231484.3:c.599A>C | ENSP00000231484.3:p.Lys200Thr | 0.42028985 |
| P10-Organoid | SLC29A1 | 6 | 44197363 | C | T | Missense_Mutation | ENST00000427851.2:c.149C>T | ENSP00000392668.2:p.Ser50Phe | 0.02359882 |
| P10-Organoid | PREP | 6 | 105726047 | C | T | Missense_Mutation | ENST00000369110.3:c.2105G>A | ENSP00000358106.3:p.Arg702Gln | 0.03716216 |
| P10-Organoid | GRM1 | 6 | 146755216 | G | A | Missense_Mutation | ENST00000361719.2:c.2869G>A | ENSP00000354896.2:p.Val957Ile | 0.39426523 |
| P10-Organoid | AUTS2 | 7 | 70231133 | G | A | Missense_Mutation | ENST00000406775.2:c.1502G>A | ENSP00000385263.2:p.Arg501His | 0.01907356 |
| P10-Organoid | POM121 | 7 | 72413723 | T | TCTC | In_Frame_Ins | ENST00000446813.1:c.2398_2399insCCT | ENSP00000393020.1:p.Phe799_Phe800insSer | 0.04562737 |
| P10-Organoid | GJC3 | 7 | 99527179 | C | A | Missense_Mutation | ENST00000312891.2:c.65G>T | ENSP00000325775.2:p.Arg22Leu | 0.05932203 |
| P10-Organoid | ZNF3 | 7 | 99669202 | T | C | Missense_Mutation | ENST00000424697.1:c.905A>G | ENSP00000415358.1:p.His302Arg | 0.46818181 |
| P10-Organoid | CTTNBP2 | 7 | 117513457 | C | T | Missense_Mutation | ENST00000160373.3:c.13G>A | ENSP00000160373.3:p.Gly5Ser | 0.04395604 |
| P10-Organoid | GIMAP6 | 7 | 150325441 | C | T | Missense_Mutation | ENST00000328902.5:c.245G>A | ENSP00000330374.5:p.Arg82Gln | 0.02310231 |
| P10-Organoid | ZFHX4 | 8 | 77763746 | C | T | Missense_Mutation | ENST00000521891.2:c.4589C>T | ENSP00000430497.2:p.Thr1530Met | 0.03225806 |
| P10-Organoid | GLIS3 | 9 | 4118236 | CT | C | Frame_Shift_Del | ENST00000381971.3:c.1241del | ENSP00000371398.3:p.Gln414ArgfsTer28 | 0.01851851 |
| P10-Organoid | TAF1L | 9 | 32632543 | G | T | Missense_Mutation | ENST00000242310.4:c.3035C>A | ENSP00000418379.1:p.Ala1012Glu | 0.03950617 |
| P10-Organoid | COL15A1 | 9 | 101748020 | G | A | Missense_Mutation | ENST00000375001.3:c.274G>A | ENSP00000364140.3:p.Ala92Thr | 0.36904761 |
| P10-Organoid | GRIN1 | 9 | 140040199 | C | T | Missense_Mutation | ENST00000371561.3:c.415C>T | ENSP00000360616.3:p.Arg139Cys | 0.34265734 |
| P10-Organoid | ADARB2 | 10 | 1284350 | C | T | Missense_Mutation | ENST00000381312.1:c.1205G>A | ENSP00000370713.1:p.Arg402Gln | 0.04375 |
| P10-Organoid | FRMD4A | 10 | 13708300 | C | T | Missense_Mutation | ENST00000378503.1:c.1400G>A | ENSP00000367764.1:p.Arg467Gln | 0.47682119 |
| P10-Organoid | ZNF503 | 10 | 77158605 | C | T | Missense_Mutation | ENST00000535216.1:c.1843G>A | ENSP00000438988.1:p.Ala615Thr | 0.04424778 |
| P10-Organoid | OR5F1 | 11 | 55762069 | C | A | Missense_Mutation | ENST00000278409.1:c.33G>T | ENSP00000278409.1:p.Glu11Asp | 0.53846153 |
| P10-Organoid | PCNXL3 | 11 | 65387314 | TGCTCACCCGG | T | Frame_Shift_Del | ENST00000355703.3:c.1922_1931del | ENSP00000347931.3:p.Leu641ProfsTer45 | 0.23529411 |
| P10-Organoid | KRAS | 12 | 25398284 | C | T | Missense_Mutation | ENST00000557334.1:c.35G>A | ENSP00000452512.1:p.Gly12Asp | 0.44444444 |
| P10-Organoid | ADAMTS20 | 12 | 43828109 | A | G | Missense_Mutation | ENST00000553158.1:c.2659T>C | ENSP00000448341.1:p.Cys887Arg | 0.45751634 |
| P10-Organoid | RAPGEF3 | 12 | 48151822 | C | G | Missense_Mutation | ENST00000449771.2:c.46G>C | ENSP00000395708.2:p.Ala16Pro | 0.50549450 |
| P10-Organoid | ADCY6 | 12 | 49171426 | T | A | Missense_Mutation | ENST00000550422.1:c.1108A>T | ENSP00000446730.1:p.Ile370Phe | 0.38031914 |
| P10-Organoid | TMEM132D | 12 | 130184839 | C | T | Missense_Mutation | ENST00000422113.2:c.484G>A | ENSP00000408581.2:p.Gly162Arg | 0.02747252 |
| P10-Organoid | AKAP6 | 14 | 33291275 | G | A | Missense_Mutation | ENST00000280979.4:c.4256G>A | ENSP00000280979.4:p.Ser1419Asn | 0.04838709 |
| P10-Organoid | ATP6V1D | 14 | 67807202 | T | C | Missense_Mutation | ENST00000555474.1:c.260A>G | ENSP00000450885.1:p.Tyr87Cys | 0.53658536 |
| P10-Organoid | SAMD15 | 14 | 77845271 | T | A | Missense_Mutation | ENST00000216471.4:c.1510T>A | ENSP00000216471.4:p.Leu504Ile | 0.06875 |
| P10-Organoid | NPAP1 | 15 | 24921511 | C | T | Missense_Mutation | ENST00000329468.2:c.497C>T | ENSP00000333735.2:p.Pro166Leu | 0.40425531 |
| P10-Organoid | MGA | 15 | 41988341 | A | G | Missense_Mutation | ENST00000570161.1:c.1133A>G | ENSP00000457035.1:p.Asn378Ser | 0.03181818 |
| P10-Organoid | HERC1 | 15 | 63986583 | C | A | Missense_Mutation | ENST00000443617.2:c.5408G>T | ENSP00000390158.2:p.Gly1803Val | 0.04347826 |
| P10-Organoid | ZSCAN32 | 16 | 3433651 | A | G | Missense_Mutation | ENST00000439568.2:c.428T>C | ENSP00000391787.2:p.Val143Ala | 0.43103448 |
| P10-Organoid | ZP2 | 16 | 21213466 | G | A | Missense_Mutation | ENST00000574091.1:c.1246C>T | ENSP00000458991.1:p.Arg416Trp | 0.08374384 |
| P10-Organoid | OTOA | 16 | 21698755 | G | A | Missense_Mutation | ENST00000388958.3:c.421G>A | ENSP00000373610.3:p.Asp141Asn | 0.5 |
| P10-Organoid | CNGB1 | 16 | 57996879 | T | A | Missense_Mutation | ENST00000564448.1:c.380A>T | ENSP00000454633.1:p.Gln127Leu | 0.37593985 |
| P10-Organoid | RNF43 | 17 | 56436026 | G | A | Nonsense_Mutation | ENST00000584437.1:c.1111C>T | ENSP00000463069.1:p.Arg371Ter | 0.42391304 |
| P10-Organoid | RNF43 | 17 | 56492894 | C | T | Nonsense_Mutation | ENST00000584437.1:c.45G>A | ENSP00000463069.1:p.Trp15Ter | 0.36 |
| P10-Organoid | TANC2 | 17 | 61315295 | C | G | Missense_Mutation | ENST00000424789.2:c.668C>G | ENSP00000387593.2:p.Ser223Cys | 0.5 |
| P10-Organoid | RPTOR | 17 | 78866552 | C | G | Missense_Mutation | ENST00000544334.2:c.1651C>G | ENSP00000442479.2:p.Arg551Gly | 0.04347826 |
| P10-Organoid | COLEC12 | 18 | 480713 | G | A | Missense_Mutation | ENST00000400256.3:c.52C>T | ENSP00000383115.3:p.Arg18Trp | 0.45725646 |
| P10-Organoid | STARD6 | 18 | 51851163 | T | C | Missense_Mutation | ENST00000581310.1:c.562A>G | ENSP00000462349.1:p.Met188Val | 0.42477876 |
| P10-Organoid | ELANE | 19 | 856061 | C | T | Missense_Mutation | ENST00000590230.1:c.701C>T | ENSP00000466090.1:p.Pro234Leu | 0.42679900 |
| P10-Organoid | DNM2 | 19 | 10940937 | T | C | Missense_Mutation | ENST00000585892.1:c.2426T>C | ENSP00000468734.1:p.Ile809Thr | 0.50115473 |
| P10-Organoid | ABHD8 | 19 | 17412043 | T | A | Missense_Mutation | ENST00000247706.3:c.383A>T | ENSP00000247706.2:p.Asp128Val | 0.02197802 |
| P10-Organoid | HAS1 | 19 | 52216816 | C | T | Missense_Mutation | ENST00000601714.1:c.1622G>A | ENSP00000472821.1:p.Arg541His | 0.40372670 |
| P10-Organoid | LILRB1 | 19 | 55147987 | GA | CC | Missense_Mutation | ENST00000434867.2:c.1690_1691delinsCC | ENSP00000405243.2:p.Glu564Pro | 0.11864406 |
| P10-Organoid | ZNFX1 | 20 | 47887343 | T | C | Missense_Mutation | ENST00000396105.1:c.1006A>G | ENSP00000379412.1:p.Met336Val | 0.35260115 |
| P10-Organoid | GNAS | 20 | 57484421 | G | A | Missense_Mutation | ENST00000371102.4:c.2489G>A | ENSP00000360143.4:p.Arg830His | 0.46857142 |
| P10-Organoid | HRH3 | 20 | 60791235 | C | T | Missense_Mutation | ENST00000340177.5:c.1165G>A | ENSP00000342560.5:p.Val389Ile | 0.02402402 |
| P10-Organoid | KRTAP10-6 | 21 | 46012231 | G | GCT | Frame_Shift_Ins | ENST00000400368.1:c.134_135insAG | ENSP00000383219.1:p.Cys46AlafsTer9 | 0.00934579 |
| P10-Organoid | MICAL3 | 22 | 18300558 | C | T | Missense_Mutation | ENST00000441493.2:c.4869G>A | ENSP00000416015.2:p.Met1623Ile | 0.56129032 |
| P10-Organoid | PKDREJ | 22 | 46657950 | T | TA | Frame_Shift_Ins | ENST00000253255.5:c.1269dup | ENSP00000253255.5:p.Lys424Ter | 0.47945205 |
| P10-Organoid | PKDREJ | 22 | 46657953 | G | A | Missense_Mutation | ENST00000253255.5:c.1267C>T | ENSP00000253255.5:p.Leu423Phe | 0.5 |
| P10-Organoid | PLXNB2 | 22 | 50728527 | C | T | Missense_Mutation | ENST00000449103.1:c.487G>A | ENSP00000409171.1:p.Gly163Ser | 0.41922290 |
| P10-Organoid | TBL1X | X | 9656079 | G | A | Missense_Mutation | ENST00000536365.1:c.227G>A | ENSP00000445317.1:p.Arg76His | 0.98173516 |
| P10-Organoid | SHROOM2 | X | 9905361 | C | T | Missense_Mutation | ENST00000418909.2:c.280C>T | ENSP00000415229.2:p.Arg94Cys | 0.06727828 |
| P10-Organoid | RBM10 | X | 47045136 | C | T | Nonsense_Mutation | ENST00000377604.3:c.2377C>T | ENSP00000366829.3:p.Arg793Ter | 0.05166051 |
| P10-Organoid | BRCC3 | X | 154299812 | C | T | Nonsense_Mutation | ENST00000399042.1:c.10C>T | ENSP00000381998.1:p.Gln4Ter | 1 |