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Mutant Information

Mutant NameFN4498-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4498-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 69
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr119021600C-THET
SBSChr12973036T-CHET
SBSChr17084677G-THETLOC_Os01g12790
SBSChr17094440C-GHETLOC_Os01g12810
SBSChr17301673T-AHET
SBSChr1012386668C-THET
SBSChr1014915385C-THET
SBSChr1015008763T-CHET
SBSChr1017276395T-AHET
SBSChr1017536680C-GHET
SBSChr1019459676T-CHOMO
SBSChr104424910A-THETLOC_Os10g08180
SBSChr1114988391G-THET
SBSChr111674935C-AHET
SBSChr1121153201C-THET
SBSChr1126055311G-THOMO
SBSChr1127372646G-THOMOLOC_Os11g45230
SBSChr119354780C-AHET
SBSChr119354781C-AHETLOC_Os11g16850
SBSChr1213431970C-THETLOC_Os12g23670
SBSChr1217127385G-THOMO
SBSChr1222246935A-GHET
SBSChr1223347860C-THET
SBSChr1226093368G-THET
SBSChr1226093369T-GHET
SBSChr21111580G-AHET
SBSChr212901312C-AHET
SBSChr217658240G-CHETLOC_Os02g29660
SBSChr218769683G-THOMO
SBSChr219726600G-AHET
SBSChr22696339T-GHETLOC_Os02g05560
SBSChr229740751A-THET
SBSChr235867711C-THOMOLOC_Os02g58710
SBSChr312788125C-AHOMO
SBSChr314024124C-THOMO
SBSChr319035129G-AHETLOC_Os03g33280
SBSChr325044447G-AHET
SBSChr327465629G-AHET
SBSChr327731676A-THET
SBSChr346039G-THET
SBSChr416302299A-THOMO
SBSChr41946912C-THOMO
SBSChr426455122A-THET
SBSChr429820569G-THETLOC_Os04g50000
SBSChr43833704C-AHET
SBSChr46546355G-THOMO
SBSChr510369529C-THET
SBSChr510705460C-THET
SBSChr515639445G-THET
SBSChr516122988G-AHET
SBSChr520587555G-THET
SBSChr520587557A-THET
SBSChr525729610C-AHET
SBSChr611682423T-CHETLOC_Os06g20330
SBSChr615758825A-GHET
SBSChr622357251T-CHETLOC_Os06g37760
SBSChr67381769G-AHET
SBSChr68329705C-THET
SBSChr68559674C-THETLOC_Os06g15100
SBSChr713991998T-CHETLOC_Os07g24590
SBSChr714110879C-AHET
SBSChr719603596A-THET
SBSChr75493733T-CHET
SBSChr7927310T-AHET
SBSChr811520003G-CHET
SBSChr813510509C-THET
SBSChr911058825C-GHET
SBSChr919740806C-THOMO
SBSChr920104239G-AHOMO

Deletions: 48
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr8227285422728541
DeletionChr2304522630452338
DeletionChr7348959534895951
DeletionChr9459061045906101
DeletionChr10487152148715222
DeletionChr8570406957040702
DeletionChr8616589061658901
DeletionChr8668855066885501
DeletionChr7883336088333601
DeletionChr4940014094001478LOC_Os04g17140
DeletionChr1978686597868662
DeletionChr711451447114514548
DeletionChr1111733691117336911
DeletionChr6124342001243421112
DeletionChr513239780132397801
DeletionChr8133616521336166615
DeletionChr313468456134684594
DeletionChr113625198136251981
DeletionChr1142540431425407331
DeletionChr7149313321493134817
DeletionChr12155252891552529810LOC_Os12g26560
DeletionChr815539798155398014
DeletionChr11160994911609950212
DeletionChr3164748171647483216LOC_Os03g29020
DeletionChr116628611166286111
DeletionChr116894380168943801
DeletionChr317945406179454061
DeletionChr118277564182775696
DeletionChr218769670187696712
DeletionChr1119790504197905041
DeletionChr620323142203231498
DeletionChr520603497206034971
DeletionChr520625487206254871LOC_Os05g34760
DeletionChr522113896221138972
DeletionChr222293367222933671
DeletionChr1022405187224051882LOC_Os10g41610
DeletionChr5225675792256758911
DeletionChr722798753227987608
DeletionChr2242533902425347384
DeletionChr724335366243353694LOC_Os07g40610
DeletionChr624531108245311092
DeletionChr1225735822257358221
DeletionChr1125994498259944981
DeletionChr226003675260036762
DeletionChr7267741832677420018
DeletionChr2286670872866709610
DeletionChr328983778289837781
DeletionChr331593514315935141

Insertions: 34
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr115788693157886931
InsertionChr130326319303263191
InsertionChr132157225321572251
InsertionChr134123379341233791
InsertionChr1018442930184429301
InsertionChr10705492270549221
InsertionChr11121103891211043648
InsertionChr11121727421217281978
InsertionChr1219334771193347711
InsertionChr1225527266255272672
InsertionChr12696256769625737
InsertionChr129054349054352
InsertionChr12982919998291991
InsertionChr2121188271211891387
InsertionChr218198963181989653
InsertionChr2227718922277191423
InsertionChr314795103147951031
InsertionChr4279720622797207514
InsertionChr43977257397727923
InsertionChr4903580890358081
InsertionChr5169604216960421
InsertionChr6377953837795381
InsertionChr6854651685465161
InsertionChr7141480631414811250
InsertionChr718184723181847231
InsertionChr7241738424173841
InsertionChr726765375267653751
InsertionChr8110441471104419044
InsertionChr819945355199453617
InsertionChr82016425420164359106
InsertionChr9141349951413500511
InsertionChr9317823031782312
InsertionChr9551762455176241LOC_Os09g10140image
InsertionChr9738540773854082

Inversions: 6
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr7423871592511
InversionChr7423876592521
InversionChr153140375314211
InversionChr112085798620885593
InversionChr112085801720885605
InversionChr22415612024156277

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr716998603Chr621004596
TranslocationChr1118846692Chr416025045
TranslocationChr220476679Chr123511189LOC_Os01g41530
TranslocationChr220476688Chr124042911