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Mutant Information

Mutant NameFN2729-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2729-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 115
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr121632839G-AHET
SBSChr124636194T-CHomo
SBSChr124636194T-CHOMOINTRON
SBSChr128962461C-THomo
SBSChr1011323703T-CHET
SBSChr1011323703T-CHETINTERGENIC
SBSChr1011551343G-AHET
SBSChr1011551343G-AHETINTERGENIC
SBSChr1015077092C-AHETNON_SYNONYMOUS_CODINGLOC_Os10g28930
SBSChr1020949319C-GHET
SBSChr104712092C-GHET
SBSChr104712092C-GHETINTRON
SBSChr106161604A-GHET
SBSChr107470337G-AHET
SBSChr107470337G-AHETINTERGENIC
SBSChr107485821C-THET
SBSChr1115677527T-AHomo
SBSChr1115677527T-AHOMOINTRON
SBSChr1119443309C-THET
SBSChr1125706488T-AHET
SBSChr1125706488T-AHETINTERGENIC
SBSChr116458726T-CHET
SBSChr11969648A-THET
SBSChr11969648A-THETINTERGENIC
SBSChr119861882G-AHETINTERGENIC
SBSChr1211356787G-AHET
SBSChr1211356787G-AHETUTR_3_PRIME
SBSChr1211488441G-CHETNON_SYNONYMOUS_CODINGLOC_Os12g19720
SBSChr1217178116G-AHET
SBSChr128096864G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g14240
SBSChr128324054G-AHET
SBSChr129855012T-AHET
SBSChr210062556A-THETINTERGENIC
SBSChr214012277G-THET
SBSChr214012277G-THETINTRON
SBSChr216294762C-AHETNON_SYNONYMOUS_CODINGLOC_Os02g27520
SBSChr23167463T-AHETNON_SYNONYMOUS_CODINGLOC_Os02g06340
SBSChr232058510T-AHET
SBSChr311675304A-CHomo
SBSChr311675304A-CHOMOINTRON
SBSChr311675305C-AHomo
SBSChr311675305C-AHOMOINTRON
SBSChr319789352G-THET
SBSChr325761735C-THomo
SBSChr325761735C-THOMOINTERGENIC
SBSChr334027507G-AHET
SBSChr334027507G-AHETINTERGENIC
SBSChr335288532C-AHET
SBSChr414547660G-AHomo
SBSChr415468028C-THET
SBSChr419406370C-THET
SBSChr419406370C-THETINTERGENIC
SBSChr422772961C-AHET
SBSChr422772961C-AHETINTERGENIC
SBSChr423040975T-GHET
SBSChr423040975T-GHETINTRON
SBSChr425729965A-THET
SBSChr425729965A-THETINTRON
SBSChr429933990T-AHETNON_SYNONYMOUS_CODINGLOC_Os04g50172
SBSChr429933991C-AHETNON_SYNONYMOUS_CODINGLOC_Os04g50172
SBSChr510823678C-THETNON_SYNONYMOUS_CODINGLOC_Os05g18680
SBSChr526344327A-CHET
SBSChr526344327A-CHETINTERGENIC
SBSChr53579783C-THomo
SBSChr55317001A-THET
SBSChr55317001A-THETINTERGENIC
SBSChr56141914T-AHET
SBSChr56141914T-AHETINTERGENIC
SBSChr56141915C-AHET
SBSChr56141915C-AHETINTERGENIC
SBSChr59301646C-AHETNON_SYNONYMOUS_CODINGLOC_Os05g16400
SBSChr59989085G-THET
SBSChr615044528C-THET
SBSChr622386679T-CHET
SBSChr627733178A-THET
SBSChr627733178A-THETINTRON
SBSChr67782657T-AHomo
SBSChr67782657T-AHOMOINTRON
SBSChr716525832T-CHomo
SBSChr716525832T-CHOMOINTERGENIC
SBSChr718921814G-THomo
SBSChr718921814G-THOMOINTERGENIC
SBSChr719766393C-THomo
SBSChr719766393C-THOMOSYNONYMOUS_CODING
SBSChr720321499G-AHET
SBSChr726122265G-AHomo
SBSChr726122265G-AHOMOINTERGENIC
SBSChr77937477T-AHET
SBSChr77937477T-AHETINTRON
SBSChr77937478G-AHET
SBSChr77937478G-AHETINTRON
SBSChr77937479G-AHETINTRON
SBSChr77938125C-AHET
SBSChr77938125C-AHETINTERGENIC
SBSChr77938126T-AHET
SBSChr77938126T-AHETINTERGENIC
SBSChr811943277G-AHET
SBSChr811972147G-CHETNON_SYNONYMOUS_CODINGLOC_Os08g19990
SBSChr817063860G-THET
SBSChr817063860G-THETINTRON
SBSChr917758474C-THET
SBSChr920207254G-AHomo
SBSChr920207254G-AHOMOINTERGENIC
SBSChr94076048C-THET
SBSChr94214406T-AHET
SBSChr94214406T-AHETINTERGENIC
SBSChr95175425T-CHET
SBSChr95175425T-CHETINTERGENIC
SBSChr95640990C-THET
SBSChr97068746G-THET
SBSChr98371633G-AHomo
SBSChr98371633G-AHOMOINTERGENIC
SBSChr98908129C-THET
SBSChr99711270T-CHomo
SBSChr99711270T-CHOMOINTRON

Deletions: 43
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr102760001294700018699950
DeletionChr1029600012978000179994
DeletionChr1029610012978000169993
DeletionChr10298100130620008099912
DeletionChr10298200130590007699911
DeletionChr64329483432958198
DeletionChr65627001589300026599945
DeletionChr65631001588200025099943
DeletionChr1572603457260362
DeletionChr95770956577096610
DeletionChr6589500159650006999941
DeletionChr65970001610900013899917
DeletionChr76021662602167311
DeletionChr106235035623504712
DeletionChr8729731472973151
DeletionChr8790186379018674
DeletionChr98170450817045552
DeletionChr119517333951733962
DeletionChr110347968103479702
DeletionChr9117396921173969642
DeletionChr612545870125458711LOC_Os06g21700
DeletionChr1012635969126359789LOC_Os10g24620
DeletionChr3128582261285823152
DeletionChr21349100113504000129994
DeletionChr8141896201418962442
DeletionChr116975172169751731
DeletionChr418468602184686031
DeletionChr119679082196790886
DeletionChr12234171672341717142
DeletionChr624395001243950098
DeletionChr12248161252481613382
DeletionChr7261235442612361268
DeletionChr1126982412269824131
DeletionChr827625588276255902
DeletionChr128209328282093302
DeletionChr429349180293491822LOC_Os04g49220
DeletionChr1340450013436900032399948
DeletionChr1340530013433800028499944
DeletionChr134270916342709171
DeletionChr13434700134368000209993
DeletionChr135296180352961844
DeletionChr13676500136780000149994
DeletionChr137879178378791791

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1107799521077996110
InsertionChr114045450140454578
InsertionChr1367932883679329710
InsertionChr1220273415202734162
InsertionChr321326837213268371
InsertionChr3289824992898250022image
InsertionChr3289824992898250022image
InsertionChr411052243110522442
InsertionChr416977819169778224
InsertionChr4227714012277141212
InsertionChr5132996113299611LOC_Os05g03280image
InsertionChr5825641682564161
InsertionChr611000810110008101
InsertionChr622472065224720651
InsertionChr7257204825720481
InsertionChr7442707144270722
InsertionChr7573183657318361
InsertionChr822509329225093291
InsertionChr998722298723110

Inversions: 6
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1027614042762165LOC_Os10g05560
InversionChr1027616482762158LOC_Os10g05560
InversionChr1030589484031510
InversionChr1055220565522323LOC_Os10g10110
InversionChr661106016713679
InversionChr13292419032924346LOC_Os01g56980

Translocations: 12
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr9604732Chr43063060
TranslocationChr116135697Chr135969205
TranslocationChr117846350Chr6160784862
TranslocationChr57917874Chr384122072
TranslocationChr98226708Chr211631204
TranslocationChr1219144011Chr518325140
TranslocationChr1119748567Chr65893166
TranslocationChr622189392Chr424563559
TranslocationChr1123368404Chr513251372
TranslocationChr1125694182Chr109261636
TranslocationChr1125694526Chr104031488
TranslocationChr331068314Chr116252169