FN4492-S Chr1 18192317 C-A 0 0 Single Base Substitution 0 INTRON HOMO FN4492-S Chr1 18845021 C-T 0 0 Single Base Substitution 0 INTERGENIC HOMO FN4492-S Chr1 30349325 30349326 0 0 Deletion 1 HOMO FN4492-S Chr1 38860088 G-T 0 0 Single Base Substitution 0 NON_SYNONYMOUS_CODING HET LOC_Os01g66910 expressed protein FN4492-S Chr1 42275968 42275968 0 0 Insertion 1 HET FN4492-S Chr1 8224765 T-C 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr1 9414716 A-T 0 0 Single Base Substitution 0 NON_SYNONYMOUS_CODING HET LOC_Os01g16580 retrotransposon protein, putative, unclassified FN4492-S Chr10 14091886 14091886 0 0 Insertion 1 HET FN4492-S Chr10 257609 C-T 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr11 12727519 G-T 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr11 13131038 T-G 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr11 14542477 14542478 0 0 Deletion 1 HOMO FN4492-S Chr11 20665326 20665326 0 0 Insertion 1 HET FN4492-S Chr11 25200701 25200701 0 0 Insertion 1 HET FN4492-S Chr11 27170986 27170987 0 0 Deletion 1 HOMO FN4492-S Chr11 738113 738122 0 0 Deletion 9 HOMO FN4492-S Chr11 7947681 7947688 0 0 Deletion 7 HOMO FN4492-S Chr11 8152456 G-A 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr11 8578385 8578385 0 0 Insertion 22 HET FN4492-S Chr12 14259175 C-A 0 0 Single Base Substitution 0 NON_SYNONYMOUS_CODING HOMO LOC_Os12g24870 SWIM zinc finger family protein, putative, expressed FN4492-S Chr12 1616012 A-T 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr12 23090899 23090919 0 0 Deletion 20 HOMO FN4492-S Chr12 4233833 4233833 0 0 Insertion 2 HET FN4492-S Chr12 8980445 C-T 0 0 Single Base Substitution 0 INTERGENIC HOMO FN4492-S Chr12 9721026 9721026 0 0 Insertion 1 HET FN4492-S Chr2 111180 111181 0 0 Deletion 1 HOMO FN4492-S Chr2 1504810 1504810 0 0 Insertion 1 HET FN4492-S Chr2 23341540 23341540 0 0 Insertion 1 HET FN4492-S Chr2 336414 A-G 0 0 Single Base Substitution 0 INTERGENIC HOMO FN4492-S Chr2 7367001 7380000 0 0 Deletion 13000 HET FN4492-S Chr2 837741 T-A 0 0 Single Base Substitution 0 INTERGENIC HOMO FN4492-S Chr3 16145258 16145258 0 0 Insertion 2 HET FN4492-S Chr3 20230098 20230099 0 0 Deletion 1 HOMO FN4492-S Chr3 21570120 A-G 0 0 Single Base Substitution 0 NON_SYNONYMOUS_CODING HET LOC_Os03g38840 retrotransposon, putative, centromere-specific FN4492-S Chr3 21830678 C-T 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr3 22540594 22540595 0 0 Deletion 1 HOMO FN4492-S Chr3 25837312 T-C 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr3 26103093 G-A 0 0 Single Base Substitution 0 NON_SYNONYMOUS_CODING HET LOC_Os03g46170 retrotransposon protein, putative, Ty3-gypsy subclass, expressed FN4492-S Chr3 27564363 27564475 0 0 Inversion 113 HET FN4492-S Chr3 29154654 C-T 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr3 2922510 C-T 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr3 31571915 G-A 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr3 6037212 6037218 0 0 Deletion 6 HOMO FN4492-S Chr4 11889546 11889547 0 0 Deletion 1 HOMO FN4492-S Chr4 21221994 21221995 0 0 Deletion 1 HOMO FN4492-S Chr4 29815324 G-A 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr4 32893831 32893832 0 0 Deletion 1 HOMO FN4492-S Chr4 34462528 34462529 0 0 Deletion 1 HOMO FN4492-S Chr5 13597921 13597921 0 0 Insertion 1 HET FN4492-S Chr5 1431760 1431761 0 0 Deletion 1 HOMO FN4492-S Chr5 15218839 C-T 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr5 15218843 G-T 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr5 22790489 22790490 0 0 Deletion 1 HOMO LOC_Os05g38850 MCM8 - Putative minichromosome maintenance MCM family subunit 8, expressed FN4492-S Chr5 27979829 T-G 0 0 Single Base Substitution 0 NON_SYNONYMOUS_CODING HET LOC_Os05g48820 DDT, putative, expressed FN4492-S Chr5 29903555 G-A 0 0 Single Base Substitution 0 INTRON HET FN4492-S Chr5 5170589 A-T 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr6 20188829 T-C 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr6 20936045 A-G 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr6 2383059 G-A 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr6 28880844 Chr2 7385049 0 Translocation 0 HET FN4492-S Chr7 18385200 T-C 0 0 Single Base Substitution 0 SYNONYMOUS_CODING HOMO FN4492-S Chr7 184007 G-A 0 0 Single Base Substitution 0 INTERGENIC HET FN4492-S Chr7 20689103 A-G 0 0 Single Base Substitution 0 SPLICE_SITE_REGION HET FN4492-S Chr7 23871034 23871041 0 0 Deletion 7 HOMO FN4492-S Chr7 370539 370549 0 0 Deletion 10 HOMO FN4492-S Chr7 7601329 7601330 0 0 Deletion 1 HOMO FN4492-S Chr7 9727317 9727319 0 0 Deletion 2 HOMO FN4492-S Chr8 19039592 A-T 0 0 Single Base Substitution 0 INTERGENIC HOMO FN4492-S Chr8 27871057 27871058 0 0 Deletion 1 HOMO FN4492-S Chr8 8015595 8015809 0 0 Inversion 215 HET FN4492-S Chr8 9744461 Chr3 16641765 0 Translocation 0 HET LOC_Os03g17540 TBC domain containing protein, expressed FN4492-S Chr9 11273397 11273403 0 0 Deletion 6 HOMO FN4492-S Chr9 12398363 T-C 0 0 Single Base Substitution 0 UTR_5_PRIME HOMO FN4492-S Chr9 14005365 14005379 0 0 Deletion 14 HOMO FN4492-S Chr9 18014348 18014530 0 0 Inversion 183 HET FN4492-S Chr9 2055218 2055219 0 0 Deletion 1 HOMO FN4492-S Chr9 2307505 A-G 0 0 Single Base Substitution 0 INTERGENIC HOMO