Organoidomics
Please contact Prof. Semin Lee, Jinho Jang or Web-master for any inquires.
3D Organoids
3D OrganoidsRAMP
RAMPClinical Information
| ID | Diagnosis | Stage | Age | BMI | Sex | CA19-9 |
| P8 | PDAC | 3 | 68 | 15 | Male | 292.88 |
Mutation Profiles
Primary Tumor
| ID | Gene | CHROM | POS | REF | ALT | Consequence | HGVSc | HGVSp | VAF |
| P8-Tissue | CLCNKA | 1 | 16353849 | C | T | Missense_Mutation | ENST00000439316.2:c.571C>T | ENSP00000414445.2:p.Arg234Trp | 0.06726457 |
| P8-Tissue | HECTD3 | 1 | 45472676 | C | T | Missense_Mutation | ENST00000372172.4:c.1568G>A | ENSP00000361245.4:p.Arg523His | 0.05860805 |
| P8-Tissue | PBXIP1 | 1 | 154918357 | TCC | AAG | Missense_Mutation | ENST00000542459.1:c.1326_1328delinsCTT | ENSP00000438584.1:p.Gln597_Glu598delinsHisLeu | 0.00649350 |
| P8-Tissue | PBXIP1 | 1 | 154918361 | G | A | Nonsense_Mutation | ENST00000542459.1:c.1324C>T | ENSP00000438584.1:p.Gln597Ter | 0.00636942 |
| P8-Tissue | GBA | 1 | 155207287 | C | T | Missense_Mutation | ENST00000536770.1:c.505G>A | ENSP00000445560.1:p.Gly282Arg | 0.04477611 |
| P8-Tissue | CCDC181 | 1 | 169390821 | G | T | Nonsense_Mutation | ENST00000545005.1:c.848C>A | ENSP00000442297.1:p.Ser283Ter | 0.06493506 |
| P8-Tissue | TNR | 1 | 175365809 | G | T | Missense_Mutation | ENST00000367674.2:c.1111C>A | ENSP00000356646.1:p.Gln371Lys | 0.18115942 |
| P8-Tissue | LYST | 1 | 235884106 | G | T | Missense_Mutation | ENST00000389794.3:c.9415C>A | ENSP00000374444.3:p.Gln3139Lys | 0.08994709 |
| P8-Tissue | TEKT4 | 2 | 95540690 | C | T | Missense_Mutation | ENST00000295201.4:c.883C>T | ENSP00000295201.4:p.Arg295Cys | 0.04090909 |
| P8-Tissue | KCNH7 | 2 | 163228461 | G | A | Missense_Mutation | ENST00000332142.5:c.3469C>T | ENSP00000331727.5:p.Arg1157Trp | 0.05970149 |
| P8-Tissue | GALNT3 | 2 | 166611543 | C | A | Nonsense_Mutation | ENST00000409882.1:c.637G>T | ENSP00000386955.1:p.Glu213Ter | 0.16666666 |
| P8-Tissue | TTN | 2 | 179396259 | G | A | Missense_Mutation | ENST00000591111.1:c.100160C>T | ENSP00000465570.1:p.Thr33387Met | 0.10091743 |
| P8-Tissue | CCDC141 | 2 | 179732758 | G | A | Missense_Mutation | ENST00000420890.2:c.2569C>T | ENSP00000395995.2:p.Arg857Trp | 0.05109489 |
| P8-Tissue | PTH1R | 3 | 46944904 | C | A | Missense_Mutation | ENST00000449590.1:c.1540C>A | ENSP00000402723.1:p.Leu514Ile | 0.06338028 |
| P8-Tissue | BSN | 3 | 49690629 | G | A | Missense_Mutation | ENST00000296452.4:c.3640G>A | ENSP00000296452.4:p.Gly1214Ser | 0.08333333 |
| P8-Tissue | HTR1F | 3 | 88040765 | G | A | Missense_Mutation | ENST00000319595.4:c.866G>A | ENSP00000322924.4:p.Arg289Gln | 0.10062893 |
| P8-Tissue | DLG1 | 3 | 196842906 | G | C | Missense_Mutation | ENST00000452595.1:c.1086C>G | ENSP00000398939.1:p.Phe362Leu | 0.04580152 |
| P8-Tissue | FGG | 4 | 155533284 | C | A | Missense_Mutation | ENST00000407946.1:c.193G>T | ENSP00000384552.1:p.Asp65Tyr | 0.06428571 |
| P8-Tissue | PDZD2 | 5 | 31995725 | C | T | Missense_Mutation | ENST00000438447.1:c.1022C>T | ENSP00000402033.1:p.Ser341Leu | 0.09216589 |
| P8-Tissue | DAB2 | 5 | 39382803 | C | A | Missense_Mutation | ENST00000545653.1:c.1195G>T | ENSP00000439919.1:p.Val399Phe | 0.10176991 |
| P8-Tissue | CD14 | 5 | 140012123 | A | C | Missense_Mutation | ENST00000401743.2:c.446T>G | ENSP00000385519.2:p.Leu149Arg | 0.08247422 |
| P8-Tissue | GABBR1 | 6 | 29595382 | C | T | Missense_Mutation | ENST00000377034.4:c.538G>A | ENSP00000366233.4:p.Gly180Arg | 0.09183673 |
| P8-Tissue | HLA-DRB5 | 6 | 32487338 | C | G | Missense_Mutation | ENST00000374975.3:c.461G>C | ENSP00000364114.3:p.Gly154Ala | 0.04794520 |
| P8-Tissue | HLA-DRB5 | 6 | 32487344 | T | C | Missense_Mutation | ENST00000374975.3:c.455A>G | ENSP00000364114.3:p.Tyr152Cys | 0.04861111 |
| P8-Tissue | GLO1 | 6 | 38645160 | CT | AG | Splice_Site | ENST00000373365.4:c.467-2_467-1inv | 0.05813953 | |
| P8-Tissue | DAAM2 | 6 | 39867880 | C | T | Missense_Mutation | ENST00000538976.1:c.2704C>T | ENSP00000437808.1:p.Arg902Trp | 0.07931034 |
| P8-Tissue | MTRF1L | 6 | 153323607 | TC | T | Frame_Shift_Del | ENST00000367233.5:c.213del | ENSP00000356202.5:p.Asn72ThrfsTer21 | 0.04838709 |
| P8-Tissue | MTRF1L | 6 | 153323609 | A | G | Missense_Mutation | ENST00000367233.5:c.212T>C | ENSP00000356202.5:p.Leu71Pro | 0.04761904 |
| P8-Tissue | INTS1 | 7 | 1539635 | C | T | Missense_Mutation | ENST00000404767.3:c.569G>A | ENSP00000385722.3:p.Arg190Gln | 0.08015267 |
| P8-Tissue | SLC4A2 | 7 | 150773113 | G | A | Missense_Mutation | ENST00000485713.1:c.3485G>A | ENSP00000419412.1:p.Arg1162His | 0.13888888 |
| P8-Tissue | TNKS | 8 | 9627661 | G | T | Missense_Mutation | ENST00000518281.1:c.3075G>T | ENSP00000429890.1:p.Gln1025His | 0.09523809 |
| P8-Tissue | SLCO5A1 | 8 | 70585409 | C | T | Missense_Mutation | ENST00000530307.1:c.2077G>A | ENSP00000431611.1:p.Val693Ile | 0.07977208 |
| P8-Tissue | RIMS2 | 8 | 105001597 | C | T | Nonsense_Mutation | ENST00000507740.1:c.2368C>T | ENSP00000423559.1:p.Arg790Ter | 0.18571428 |
| P8-Tissue | CSMD3 | 8 | 113240986 | T | A | Missense_Mutation | ENST00000455883.2:c.10456A>T | ENSP00000412263.2:p.Arg3486Trp | 0.07407407 |
| P8-Tissue | CSMD3 | 8 | 113303747 | T | G | Missense_Mutation | ENST00000455883.2:c.8459A>C | ENSP00000412263.2:p.Glu2820Ala | 0.07258064 |
| P8-Tissue | COL15A1 | 9 | 101767303 | G | A | Missense_Mutation | ENST00000375001.3:c.1324G>A | ENSP00000364140.3:p.Ala442Thr | 0.05325443 |
| P8-Tissue | BSPRY | 9 | 116122925 | C | T | Missense_Mutation | ENST00000374183.4:c.439C>T | ENSP00000363298.4:p.Arg147Trp | 0.08745247 |
| P8-Tissue | ABCA2 | 9 | 139902941 | C | A | Missense_Mutation | ENST00000371605.3:c.7199G>T | ENSP00000360666.3:p.Arg2400Leu | 0.04455445 |
| P8-Tissue | ZNF33A | 10 | 38343552 | C | A | Missense_Mutation | ENST00000458705.2:c.497C>A | ENSP00000387713.2:p.Ser166Tyr | 0.09259259 |
| P8-Tissue | IFITM3 | 11 | 320606 | G | T | Missense_Mutation | ENST00000602735.1:c.145C>A | ENSP00000473544.1:p.Pro49Thr | 0.08923884 |
| P8-Tissue | CCDC87 | 11 | 66358943 | A | G | Missense_Mutation | ENST00000333861.3:c.1544T>C | ENSP00000328487.3:p.Val515Ala | 0.08982035 |
| P8-Tissue | CACNA1C | 12 | 2676932 | C | T | Missense_Mutation | ENST00000480911.1:c.1867C>T | ENSP00000437936.1:p.Arg623Trp | 0.11304347 |
| P8-Tissue | KIAA1467 | 12 | 13208617 | C | T | Missense_Mutation | ENST00000197268.8:c.170C>T | ENSP00000197268.8:p.Ala57Val | 0.05325443 |
| P8-Tissue | KRAS | 12 | 25398284 | C | A | Missense_Mutation | ENST00000557334.1:c.35G>T | ENSP00000452512.1:p.Gly12Val | 0.05696202 |
| P8-Tissue | TDG | 12 | 104359839 | G | C | Splice_Site | ENST00000544861.1:c.-264+1G>C | 0.016 | |
| P8-Tissue | MYH7 | 14 | 23887458 | G | A | Missense_Mutation | ENST00000355349.3:c.4130C>T | ENSP00000347507.3:p.Thr1377Met | 0.06030150 |
| P8-Tissue | REC8 | 14 | 24642136 | C | T | Nonsense_Mutation | ENST00000559919.1:c.154C>T | ENSP00000453242.1:p.Arg52Ter | 0.08778626 |
| P8-Tissue | ALPK3 | 15 | 85400031 | G | A | Missense_Mutation | ENST00000258888.5:c.2668G>A | ENSP00000258888.5:p.Ala890Thr | 0.04761904 |
| P8-Tissue | ADCY9 | 16 | 4016815 | T | A | Missense_Mutation | ENST00000294016.3:c.3023A>T | ENSP00000294016.3:p.Tyr1008Phe | 0.00588235 |
| P8-Tissue | MMP15 | 16 | 58077528 | G | A | Missense_Mutation | ENST00000219271.3:c.1567G>A | ENSP00000219271.3:p.Ala523Thr | 0.04575163 |
| P8-Tissue | TBC1D29 | 17 | 28890280 | C | T | Missense_Mutation | ENST00000584297.1:c.241C>T | ENSP00000463703.1:p.Arg81Cys | 0.07443365 |
| P8-Tissue | TTYH2 | 17 | 72227032 | C | T | Missense_Mutation | ENST00000529107.1:c.245C>T | ENSP00000433089.1:p.Ala82Val | 0.11627907 |
| P8-Tissue | MYO9B | 19 | 17317947 | C | A | Missense_Mutation | ENST00000595618.1:c.5518C>A | ENSP00000471457.1:p.Arg1840Ser | 0.09287925 |
| P8-Tissue | FKRP | 19 | 47259843 | G | A | Missense_Mutation | ENST00000391909.3:c.1136G>A | ENSP00000375776.2:p.Arg379Gln | 0.0625 |
| P8-Tissue | LILRA1 | 19 | 55106288 | A | C | Missense_Mutation | ENST00000453777.1:c.229A>C | ENSP00000413715.1:p.Ile77Leu | 0.15533980 |
| P8-Tissue | KRTAP13-3 | 21 | 31798010 | C | A | Missense_Mutation | ENST00000390690.2:c.221G>T | ENSP00000375109.2:p.Ser74Ile | 0.14285714 |
| P8-Tissue | CLDN5 | 22 | 19511457 | C | T | Missense_Mutation | ENST00000413119.2:c.577G>A | ENSP00000400612.2:p.Val193Met | 0.18279569 |
| P8-Tissue | COMT | 22 | 19950200 | A | C | Translation_Start_Site | ENST00000449653.1:c.1A>C | ENSP00000416778.1:p.Met1? | 0.00689655 |
| P8-Tissue | COMT | 22 | 19950202 | G | T | Translation_Start_Site | ENST00000449653.1:c.3G>T | ENSP00000416778.1:p.Met1? | 0.00680272 |
| P8-Tissue | RFPL1 | 22 | 29837827 | A | G | Missense_Mutation | ENST00000354373.2:c.670A>G | ENSP00000346342.2:p.Ser224Gly | 0.05698005 |
| P8-Tissue | ITIH6 | X | 54784573 | A | G | Missense_Mutation | ENST00000218436.6:c.1934T>C | ENSP00000218436.6:p.Val645Ala | 0.16470588 |
| P8-Tissue | ERCC6L | X | 71426903 | G | C | Missense_Mutation | ENST00000373657.1:c.1345C>G | ENSP00000362761.1:p.Arg449Gly | 0.07692307 |
| P8-Tissue | BRCC3 | X | 154305514 | C | T | Nonsense_Mutation | ENST00000399042.1:c.265C>T | ENSP00000381998.1:p.Arg89Ter | 0.09859154 |
Organoid
| ID | Gene | CHROM | POS | REF | ALT | Consequence | HGVSc | HGVSp | VAF |
| P8-Organoid | PER3 | 1 | 7887343 | C | A | Missense_Mutation | ENST00000377532.3:c.2354C>A | ENSP00000366755.3:NA | 0.05633802 |
| P8-Organoid | HECTD3 | 1 | 45472676 | C | T | Missense_Mutation | ENST00000372172.4:c.1568G>A | ENSP00000361245.4:p.Arg523His | 0.41032608 |
| P8-Organoid | NASP | 1 | 46073697 | C | A | Missense_Mutation | ENST00000537798.1:c.922C>A | ENSP00000438871.1:NA | 0.12574850 |
| P8-Organoid | FLG | 1 | 152281783 | C | A | Missense_Mutation | ENST00000368799.1:c.5579G>T | ENSP00000357789.1:NA | 0.40066225 |
| P8-Organoid | GBA | 1 | 155207287 | C | T | Missense_Mutation | ENST00000536770.1:c.505G>A | ENSP00000445560.1:p.Gly282Arg | 0.63448275 |
| P8-Organoid | CCDC181 | 1 | 169390821 | G | T | Nonsense_Mutation | ENST00000545005.1:c.848C>A | ENSP00000442297.1:p.Ser283Ter | 0.50241545 |
| P8-Organoid | HMCN1 | 1 | 186099193 | G | A | Missense_Mutation | ENST00000367492.2:c.13000G>A | ENSP00000356462.2:p.Val4334Ile | 0.50337837 |
| P8-Organoid | HEATR1 | 1 | 236746489 | G | T | Missense_Mutation | ENST00000366582.3:c.2249C>A | ENSP00000355541.3:p.Pro750His | 0.05 |
| P8-Organoid | GALNT14 | 2 | 31154986 | G | A | Missense_Mutation | ENST00000420311.2:c.901C>T | ENSP00000415514.2:p.Arg301Trp | 0.43157894 |
| P8-Organoid | TEKT4 | 2 | 95540690 | C | T | Missense_Mutation | ENST00000295201.4:c.883C>T | ENSP00000295201.4:p.Arg295Cys | 0.53418803 |
| P8-Organoid | KCNH7 | 2 | 163228461 | G | A | Missense_Mutation | ENST00000332142.5:c.3469C>T | ENSP00000331727.5:p.Arg1157Trp | 0.55905511 |
| P8-Organoid | GALNT3 | 2 | 166611543 | C | A | Nonsense_Mutation | ENST00000409882.1:c.637G>T | ENSP00000386955.1:p.Glu213Ter | 0.42105263 |
| P8-Organoid | TTN | 2 | 179396259 | G | A | Missense_Mutation | ENST00000591111.1:c.100160C>T | ENSP00000465570.1:p.Thr33387Met | 0.57281553 |
| P8-Organoid | CCDC141 | 2 | 179732758 | G | A | Missense_Mutation | ENST00000420890.2:c.2569C>T | ENSP00000395995.2:p.Arg857Trp | 0.47894736 |
| P8-Organoid | PTH1R | 3 | 46944904 | C | A | Missense_Mutation | ENST00000449590.1:c.1540C>A | ENSP00000402723.1:p.Leu514Ile | 0.36893203 |
| P8-Organoid | BSN | 3 | 49690629 | G | A | Missense_Mutation | ENST00000296452.4:c.3640G>A | ENSP00000296452.4:p.Gly1214Ser | 0.26436781 |
| P8-Organoid | HTR1F | 3 | 88040765 | G | A | Missense_Mutation | ENST00000319595.4:c.866G>A | ENSP00000322924.4:p.Arg289Gln | 0.33179723 |
| P8-Organoid | DLG1 | 3 | 196842906 | G | C | Missense_Mutation | ENST00000452595.1:c.1086C>G | ENSP00000398939.1:p.Phe362Leu | 0.48255814 |
| P8-Organoid | EPHA5 | 4 | 66535297 | G | T | Missense_Mutation | ENST00000511294.1:c.164C>A | ENSP00000427638.1:p.Ala55Asp | 0.49163879 |
| P8-Organoid | FGG | 4 | 155533284 | C | A | Missense_Mutation | ENST00000407946.1:c.193G>T | ENSP00000384552.1:p.Asp65Tyr | 0.43076923 |
| P8-Organoid | FRG1 | 4 | 190878562 | G | C | Missense_Mutation | ENST00000226798.4:c.442G>C | ENSP00000226798.4:p.Ala148Pro | 0.06785714 |
| P8-Organoid | DNAH5 | 5 | 13841872 | G | A | Missense_Mutation | ENST00000265104.4:c.5413C>T | ENSP00000265104.4:p.Arg1805Cys | 0.41637010 |
| P8-Organoid | PDZD2 | 5 | 31995725 | C | T | Missense_Mutation | ENST00000438447.1:c.1022C>T | ENSP00000402033.1:p.Ser341Leu | 0.58122743 |
| P8-Organoid | RASA1 | 5 | 86675600 | A | G | Missense_Mutation | ENST00000512763.1:c.2035A>G | ENSP00000422008.1:p.Thr679Ala | 0.01886792 |
| P8-Organoid | RASA1 | 5 | 86675613 | A | G | Missense_Mutation | ENST00000512763.1:c.2048A>G | ENSP00000422008.1:p.Asn683Ser | 0.01877934 |
| P8-Organoid | FBN2 | 5 | 127800456 | G | A | Missense_Mutation | ENST00000508989.1:c.688C>T | ENSP00000425596.1:p.Arg230Trp | 0.42950819 |
| P8-Organoid | CD14 | 5 | 140012123 | A | C | Missense_Mutation | ENST00000401743.2:c.446T>G | ENSP00000385519.2:p.Leu149Arg | 0.43298969 |
| P8-Organoid | FAT2 | 5 | 150945519 | G | A | Nonsense_Mutation | ENST00000261800.5:c.2974C>T | ENSP00000261800.5:p.Arg992Ter | 0.42971887 |
| P8-Organoid | GRK6 | 5 | 176863097 | C | T | Missense_Mutation | ENST00000528793.1:c.1081C>T | ENSP00000433511.1:p.Arg361Trp | 0.01302931 |
| P8-Organoid | TXNDC5 | 6 | 7889768 | C | A | Missense_Mutation | ENST00000539054.1:c.563G>T | ENSP00000442453.1:p.Arg188Leu | 0.052 |
| P8-Organoid | DEF6 | 6 | 35278368 | C | A | Missense_Mutation | ENST00000316637.5:c.370C>A | ENSP00000319831.5:p.Leu124Ile | 0.02439024 |
| P8-Organoid | DAAM2 | 6 | 39867880 | C | T | Missense_Mutation | ENST00000538976.1:c.2704C>T | ENSP00000437808.1:p.Arg902Trp | 0.47784810 |
| P8-Organoid | B3GAT2 | 6 | 71603915 | C | T | Missense_Mutation | ENST00000230053.6:c.652G>A | ENSP00000230053.6:p.Glu218Lys | 0.53125 |
| P8-Organoid | RIMS1 | 6 | 72809681 | G | A | Missense_Mutation | ENST00000522291.1:c.463G>A | ENSP00000430932.1:p.Asp155Asn | 0.43506493 |
| P8-Organoid | MTRF1L | 6 | 153323607 | TC | T | Frame_Shift_Del | ENST00000367233.5:c.213del | ENSP00000356202.5:p.Asn72ThrfsTer21 | 0.24 |
| P8-Organoid | MTRF1L | 6 | 153323609 | A | G | Missense_Mutation | ENST00000367233.5:c.212T>C | ENSP00000356202.5:p.Leu71Pro | 0.25630252 |
| P8-Organoid | INTS1 | 7 | 1539635 | C | T | Missense_Mutation | ENST00000404767.3:c.569G>A | ENSP00000385722.3:p.Arg190Gln | 0.55095541 |
| P8-Organoid | SAMD9 | 7 | 92734512 | GAT | G | Frame_Shift_Del | ENST00000379958.2:c.897_898del | ENSP00000369292.2:p.Ser300Ter | 0.27665706 |
| P8-Organoid | CCDC132 | 7 | 92935261 | A | C | Missense_Mutation | ENST00000544910.1:c.1484A>C | ENSP00000443104.1:p.Glu495Ala | 0.04246284 |
| P8-Organoid | SLC4A2 | 7 | 150773113 | G | A | Missense_Mutation | ENST00000485713.1:c.3485G>A | ENSP00000419412.1:p.Arg1162His | 0.68796068 |
| P8-Organoid | TNKS | 8 | 9627661 | G | T | Missense_Mutation | ENST00000518281.1:c.3075G>T | ENSP00000429890.1:p.Gln1025His | 0.41422594 |
| P8-Organoid | LOXL2 | 8 | 23198632 | C | T | Missense_Mutation | ENST00000389131.3:c.616G>A | ENSP00000373783.3:p.Val206Met | 0.50961538 |
| P8-Organoid | NRG1 | 8 | 31498025 | G | C | Missense_Mutation | ENST00000520407.1:c.525G>C | ENSP00000434640.1:p.Leu175Phe | 0.52586206 |
| P8-Organoid | SLCO5A1 | 8 | 70585409 | C | T | Missense_Mutation | ENST00000530307.1:c.2077G>A | ENSP00000431611.1:p.Val693Ile | 0.48155339 |
| P8-Organoid | RIMS2 | 8 | 105001597 | C | T | Nonsense_Mutation | ENST00000507740.1:c.2368C>T | ENSP00000423559.1:p.Arg790Ter | 0.46153846 |
| P8-Organoid | CSMD3 | 8 | 113303747 | T | G | Missense_Mutation | ENST00000455883.2:c.8459A>C | ENSP00000412263.2:p.Glu2820Ala | 0.50282485 |
| P8-Organoid | GLDC | 9 | 6645348 | C | T | Missense_Mutation | ENST00000321612.6:c.152G>A | ENSP00000370737.3:p.Arg51His | 0.52238806 |
| P8-Organoid | VPS13A | 9 | 79938064 | C | A | Missense_Mutation | ENST00000376636.3:c.5795C>A | ENSP00000365823.3:p.Ser1932Tyr | 0.01538461 |
| P8-Organoid | COL15A1 | 9 | 101767303 | G | A | Missense_Mutation | ENST00000375001.3:c.1324G>A | ENSP00000364140.3:p.Ala442Thr | 0.47852760 |
| P8-Organoid | SEC16A | 9 | 139370593 | AG | A | Frame_Shift_Del | ENST00000431893.2:c.940del | ENSP00000387583.2:p.Leu314PhefsTer80 | 0.33962264 |
| P8-Organoid | ABCA2 | 9 | 139902941 | C | A | Missense_Mutation | ENST00000371605.3:c.7199G>T | ENSP00000360666.3:p.Arg2400Leu | 0.43352601 |
| P8-Organoid | ZNF33A | 10 | 38343552 | C | A | Missense_Mutation | ENST00000458705.2:c.497C>A | ENSP00000387713.2:p.Ser166Tyr | 0.42056074 |
| P8-Organoid | COMTD1 | 10 | 76995486 | G | T | Missense_Mutation | ENST00000372538.3:c.110C>A | ENSP00000361616.3:p.Pro37Gln | 0.03053435 |
| P8-Organoid | IFITM3 | 11 | 320606 | G | T | Missense_Mutation | ENST00000602735.1:c.145C>A | ENSP00000473544.1:p.Pro49Thr | 0.17241379 |
| P8-Organoid | OR51E1 | 11 | 4674660 | C | T | Nonsense_Mutation | ENST00000396952.5:c.904C>T | ENSP00000380155.5:p.Arg302Ter | 0.22222222 |
| P8-Organoid | OR8K5 | 11 | 55927102 | G | A | Missense_Mutation | ENST00000313447.1:c.692C>T | ENSP00000323853.1:p.Ala231Val | 0.08888888 |
| P8-Organoid | CCDC87 | 11 | 66358943 | A | G | Missense_Mutation | ENST00000333861.3:c.1544T>C | ENSP00000328487.3:p.Val515Ala | 0.45323741 |
| P8-Organoid | CABP2 | 11 | 67290114 | C | A | Missense_Mutation | ENST00000294288.4:c.116G>T | ENSP00000294288.4:p.Gly39Val | 0.03067484 |
| P8-Organoid | POLD3 | 11 | 74345691 | C | T | Missense_Mutation | ENST00000532497.1:c.752C>T | ENSP00000436018.1:p.Pro251Leu | 0.4625 |
| P8-Organoid | FAM181B | 11 | 82443985 | CC | GA | Missense_Mutation | ENST00000329203.3:c.786_787delinsTC | ENSP00000365295.2:p.Glu263Gln | 0.07142857 |
| P8-Organoid | DLG2 | 11 | 83180399 | G | A | Nonsense_Mutation | ENST00000543673.1:c.2464C>T | ENSP00000441994.1:p.Arg822Ter | 0.37857142 |
| P8-Organoid | CACNA1C | 12 | 2676932 | C | T | Missense_Mutation | ENST00000480911.1:c.1867C>T | ENSP00000437936.1:p.Arg623Trp | 0.51470588 |
| P8-Organoid | KIAA1467 | 12 | 13208617 | C | T | Missense_Mutation | ENST00000197268.8:c.170C>T | ENSP00000197268.8:p.Ala57Val | 0.41578947 |
| P8-Organoid | KRAS | 12 | 25398284 | C | A | Missense_Mutation | ENST00000557334.1:c.35G>T | ENSP00000452512.1:p.Gly12Val | 0.41991342 |
| P8-Organoid | YARS2 | 12 | 32908360 | G | T | Missense_Mutation | ENST00000324868.8:c.449C>A | ENSP00000320658.8:p.Ala150Asp | 0.01185770 |
| P8-Organoid | NCKAP5L | 12 | 50189475 | C | A | Missense_Mutation | ENST00000335999.6:c.2168G>T | ENSP00000337998.6:p.Gly723Val | 0.04651162 |
| P8-Organoid | KRT18 | 12 | 53344140 | G | A | Missense_Mutation | ENST00000550600.1:c.446G>A | ENSP00000447278.1:p.Arg149His | 0.02702702 |
| P8-Organoid | TMEM132D | 12 | 130185148 | A | G | Missense_Mutation | ENST00000422113.2:c.175T>C | ENSP00000408581.2:p.Ser59Pro | 0.02013422 |
| P8-Organoid | MYH7 | 14 | 23887458 | G | A | Missense_Mutation | ENST00000355349.3:c.4130C>T | ENSP00000347507.3:p.Thr1377Met | 0.51555555 |
| P8-Organoid | DHRS4 | 14 | 24435037 | C | T | Nonsense_Mutation | ENST00000559632.1:c.373C>T | ENSP00000453983.1:p.Arg125Ter | 0.1796875 |
| P8-Organoid | REC8 | 14 | 24642136 | C | T | Nonsense_Mutation | ENST00000559919.1:c.154C>T | ENSP00000453242.1:p.Arg52Ter | 0.5 |
| P8-Organoid | NOVA1 | 14 | 27066585 | G | T | Missense_Mutation | ENST00000574031.1:c.58C>A | ENSP00000459545.1:p.Leu20Met | 0.48275862 |
| P8-Organoid | RP11-176H8.1 | 14 | 31926584 | G | A | Missense_Mutation | ENST00000547378.1:c.16C>T | ENSP00000447056.1:p.Arg6Trp | 0.16778523 |
| P8-Organoid | HERC2 | 15 | 28447727 | CAGCCAAGCACTGGCA | C | In_Frame_Del | ENST00000261609.7:c.7231_7245del | ENSP00000261609.7:p.Cys2411_Ala2415del | 0.00512820 |
| P8-Organoid | PARP6 | 15 | 72559151 | G | T | Missense_Mutation | ENST00000569795.1:c.16C>A | ENSP00000456348.1:p.Gln6Lys | 0.03731343 |
| P8-Organoid | SIN3A | 15 | 75715041 | G | A | Missense_Mutation | ENST00000567289.1:c.313C>T | ENSP00000455834.1:p.Pro105Ser | 0.46919431 |
| P8-Organoid | MSLNL | 16 | 825559 | GC | TT | Missense_Mutation | ENST00000293892.3:c.1201_1202delinsAA | ENSP00000293892.3:p.Ala401Lys | 0.09523809 |
| P8-Organoid | SALL1 | 16 | 51175481 | C | T | Missense_Mutation | ENST00000440970.1:c.361G>A | ENSP00000407914.1:p.Gly121Arg | 0.47651006 |
| P8-Organoid | MMP15 | 16 | 58077528 | G | A | Missense_Mutation | ENST00000219271.3:c.1567G>A | ENSP00000219271.3:p.Ala523Thr | 0.55140186 |
| P8-Organoid | TBC1D29 | 17 | 28890280 | C | T | Missense_Mutation | ENST00000584297.1:c.241C>T | ENSP00000463703.1:p.Arg81Cys | 0.42774566 |
| P8-Organoid | TTYH2 | 17 | 72227032 | C | T | Missense_Mutation | ENST00000529107.1:c.245C>T | ENSP00000433089.1:p.Ala82Val | 0.56666666 |
| P8-Organoid | SMAD4 | 18 | 48591855 | A | G | Missense_Mutation | ENST00000588745.1:c.730A>G | ENSP00000464901.1:p.Lys244Glu | 0.99074074 |
| P8-Organoid | FKRP | 19 | 47259843 | G | A | Missense_Mutation | ENST00000391909.3:c.1136G>A | ENSP00000375776.2:p.Arg379Gln | 0.63449692 |
| P8-Organoid | CACNG8 | 19 | 54485586 | G | T | Missense_Mutation | ENST00000270458.2:c.761G>T | ENSP00000270458.2:p.Gly254Val | 0.03680981 |
| P8-Organoid | KRTAP13-3 | 21 | 31798010 | C | A | Missense_Mutation | ENST00000390690.2:c.221G>T | ENSP00000375109.2:p.Ser74Ile | 0.66917293 |
| P8-Organoid | CLDN5 | 22 | 19511457 | C | T | Missense_Mutation | ENST00000413119.2:c.577G>A | ENSP00000400612.2:p.Val193Met | 1 |
| P8-Organoid | SMC1B | 22 | 45750900 | TG | T | Frame_Shift_Del | ENST00000404354.3:c.3056del | ENSP00000385902.3:p.Pro1019GlnfsTer9 | 0.94736842 |
| P8-Organoid | ITIH6 | X | 54784573 | A | G | Missense_Mutation | ENST00000218436.6:c.1934T>C | ENSP00000218436.6:p.Val645Ala | 1 |
| P8-Organoid | ERCC6L | X | 71426903 | G | C | Missense_Mutation | ENST00000373657.1:c.1345C>G | ENSP00000362761.1:p.Arg449Gly | 0.97938144 |
| P8-Organoid | ATRX | X | 76777835 | C | A | Missense_Mutation | ENST00000395603.3:c.6767G>T | ENSP00000378967.3:p.Gly2256Val | 0.02631578 |
| P8-Organoid | BRCC3 | X | 154305514 | C | T | Nonsense_Mutation | ENST00000399042.1:c.265C>T | ENSP00000381998.1:p.Arg89Ter | 1 |
Somatic Copy Number Alterations
Primary Tumor
Organoid
Concordance between Primary tumor and Organoid
VAF-VAF Plot
Number of Shared Mutations between Primary tumor and organoid (All mutations)
Number of Shared Mutations between Primary tumor and organoid (Functional mutations)
Drug Responses
| ID | Drug | IC50 |
| P8 | AZD2014 | ~ 45088820 |
| P8 | AZD3759 | ~ 2.073e-007 |
| P8 | AZD4547 | ~ 4996374013 |
| P8 | AZD5363 | 413.9 |
| P8 | AZD6738 | 2730 |
| P8 | AZD9291 | 2077 |
| P8 | I.BET.762 | 498.8 |
| P8 | Rapamycin..Sirolimus. | ~ 90915439 |
| P8 | AZD1775..MK.1775. | 299.3 |
| P8 | Triptolide..PG490. | 39.67 |
| P8 | Simvastatin | 96.09 |
| P8 | Temozolomide | 1.69E+56 |
| P8 | Imatinib.Mesylate..STI571. | ~ 2163137 |
| P8 | Pazopanib..GW786034. | ~ 587692 |
| P8 | Sunitinib.Malate | 2456 |
| P8 | Olaparib..AZD2281..KU0059436. | 14575 |
| P8 | Regorafenib..BAY.73.4506. | 2057 |
| P8 | Erlotinib | 1205 |
| P8 | Gefitinib | ~ 1.237e+031 |
| P8 | Afatinib | 1746 |
| P8 | OTX.015 | 190.6 |
| P8 | BKM120..NVP.BKM120. | 1484 |
| P8 | BYL719 | ~ 21020 |
| P8 | Cediranib..AZD2171. | 3268 |
| P8 | Ceritinib.LDK378. | 952.5 |
| P8 | Crizotinib...PF.02341066. | 4922 |
| P8 | Dabrafenib | 4902 |
| P8 | Dacomitinib | 305.5 |
| P8 | Everolimus..RAD001. | ~ 0.000 |
| P8 | Ibrutinib..PCI.32765. | 11003 |
| P8 | Lapatinib | ~ 5064 |
| P8 | LY2835219 | 438.6 |
| P8 | Brivanib..BMS.582664. | ~ 20683 |
| P8 | Panobinostat | 31.53 |
| P8 | Selumetinib..AZD6244. | 3100 |
| P8 | Sorafenib | ~ 5721 |
| P8 | Trametinib | 519.6 |
| P8 | Vandetanib..ZD6474. | ~ 1258 |
| P8 | Vemurafenib | 3.80455E+11 |
| P8 | AZD5153 | 32.48 |
| P8 | ABT.199..GDC.0199.. | ~ 46265439274194 |
| P8 | ABT.888..Veliparib..NSC.737664. | ~ 289484782983 |
| P8 | Avagacestat..BMS.708163. | 1.316E+42 |
| P8 | Axitinib...AG.013736. | 1081 |
| P8 | Bosutinib..SKI.606. | 3125 |
| P8 | Cabozantinib..XL184. | ~ 1.265e+031 |
| P8 | Dasatinib..BMS.354825. | 15884 |
| P8 | decitabine | ~ 2.967e+033 |
| P8 | defactinib | 1269 |
| P8 | Dovitinib..TKI258.CHIR258. | 807.7 |
| P8 | Fluorouracil..5.Fluoracil..5.FU. | 4561 |
| P8 | Foretinib..XL880. | ~ 47101787914 |
| P8 | Tivantinib..ARQ.197. | 183.9 |
| P8 | Abraxane | 97.19 |
| P8 | AZD2461.olaparib.analog. | 0.05244 |
| P8 | Olaparib. | ~ 299.8 |
| P8 | Idelalisib | ~ 186.1 |
| P8 | Irinotecan | 340.3 |
| P8 | Nilotinib..AMN.107. | ~ 1261 |
| P8 | NVP.AEW541 | ~ 2.319e+017 |
| P8 | Oxaliplatin | ~ 21.87 |
| P8 | PLX3397 | 4049 |
| P8 | Quizartinib..AC220. | 8876 |
| P8 | Saracatinib..AZD0530. | ~ 6069 |
| P8 | Semagacestat..LY450139. | ~ 26631 |
| P8 | TGX.221 | 8244 |
| P8 | tozasertib | 62.78 |
| P8 | Vorinostat..SAHA..MK0683. | 3893 |
| P8 | XAV939 | ~ 1.409e-006 |
| P8 | gemcitabine | 3845 |
| P8 | palbociclib | 12242 |
| P8 | Neratinib..HKI.272. | 24.51 |