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Mutant Information

Mutant NameFN2572-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2572-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 114
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110353457A-GHETINTERGENIC
SBSChr111911810T-CHETINTERGENIC
SBSChr113000231G-AHET
SBSChr115748113C-THomo
SBSChr120438343C-THET
SBSChr121716978T-CHET
SBSChr128892527T-CHOMOINTERGENIC
SBSChr135960102A-GHET
SBSChr135960102A-GHETINTERGENIC
SBSChr137303883C-THETNON_SYNONYMOUS_CODINGLOC_Os01g64250
SBSChr139061965A-THOMOINTERGENIC
SBSChr142725701A-THETNON_SYNONYMOUS_CODINGLOC_Os01g73760
SBSChr142761246A-GHET
SBSChr15995170C-THomo
SBSChr15995170C-THOMOSYNONYMOUS_CODING
SBSChr1620805C-THOMOUTR_3_PRIME
SBSChr1676117G-THOMOINTERGENIC
SBSChr1010738902A-THET
SBSChr1010738902A-THETINTERGENIC
SBSChr1010739128C-THET
SBSChr1010739128C-THETINTERGENIC
SBSChr10137396G-CHET
SBSChr1014755863A-CHET
SBSChr1017351029C-GHOMOINTERGENIC
SBSChr1017399066G-AHET
SBSChr1017399066G-AHOMOINTERGENIC
SBSChr1019358309A-CHET
SBSChr1019358309A-CHOMOSPLICE_SITE_REGION
SBSChr103747862A-GHETINTERGENIC
SBSChr106190529G-AHET
SBSChr106871509C-AHET
SBSChr106871509C-AHETINTRON
SBSChr107379797G-AHETSTOP_GAINEDLOC_Os10g13610
SBSChr107553183T-CHETNON_SYNONYMOUS_CODINGLOC_Os10g13900
SBSChr109844900C-GHET
SBSChr1126451252G-AHET
SBSChr11574224A-THOMONON_SYNONYMOUS_CODINGLOC_Os11g02110
SBSChr119316026G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g16790
SBSChr1210592411T-GHET
SBSChr1221866797G-CHETINTERGENIC
SBSChr214223292C-AHET
SBSChr214223292C-AHOMOINTERGENIC
SBSChr217756497A-GHOMOINTERGENIC
SBSChr217994326A-GHET
SBSChr227004765C-THETINTERGENIC
SBSChr229461066C-THET
SBSChr230937608A-GHET
SBSChr230937608A-GHETINTERGENIC
SBSChr231964091T-GHET
SBSChr233114092A-THET
SBSChr233114092A-THETINTERGENIC
SBSChr27756276C-THET
SBSChr310144767T-AHOMOINTERGENIC
SBSChr315816794G-AHET
SBSChr320448565C-AHET
SBSChr326935301C-THETSYNONYMOUS_CODING
SBSChr333854442G-AHOMONON_SYNONYMOUS_CODINGLOC_Os03g59480
SBSChr335875684G-AHET
SBSChr38437723A-CHomo
SBSChr412714507C-THOMONON_SYNONYMOUS_CODINGLOC_Os04g22460
SBSChr418451218G-AHETSTOP_GAINEDLOC_Os04g30870
SBSChr421186906G-CHETINTERGENIC
SBSChr424221480G-THOMOINTERGENIC
SBSChr431631914T-CHET
SBSChr4864734C-AHET
SBSChr512162741G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g20730
SBSChr514472026A-CHET
SBSChr517506147G-THET
SBSChr517506147G-THOMOINTERGENIC
SBSChr518583619G-AHET
SBSChr518583619G-AHETINTERGENIC
SBSChr524626346T-AHET
SBSChr524626346T-AHOMOUTR_3_PRIME
SBSChr524827694C-AHETINTERGENIC
SBSChr526585827A-GHET
SBSChr527872646C-THETNON_SYNONYMOUS_CODINGLOC_Os05g48620
SBSChr52797305A-GHETNON_SYNONYMOUS_CODINGLOC_Os05g05620
SBSChr57857729T-GHET
SBSChr57857732T-GHET
SBSChr57930264T-CHET
SBSChr610398457A-THOMONON_SYNONYMOUS_CODINGLOC_Os06g17910
SBSChr610398457A-THomoNON_SYNONYMOUS_CODINGLOC_Os06g17910
SBSChr610604829C-THomo
SBSChr610604829C-THOMOINTERGENIC
SBSChr617423049T-CHomo
SBSChr617423049T-CHOMOINTRON
SBSChr625170058A-THOMOINTERGENIC
SBSChr65324569C-THET
SBSChr712520786C-AHET
SBSChr713968602C-THomo
SBSChr713968602C-THOMOINTERGENIC
SBSChr719779761G-AHET
SBSChr71981646C-GHET
SBSChr75291268G-AHETINTERGENIC
SBSChr78902460C-GHomo
SBSChr78902460C-GHOMOINTERGENIC
SBSChr79825007C-THOMONON_SYNONYMOUS_CODINGLOC_Os07g16750
SBSChr79825007C-THomoNON_SYNONYMOUS_CODINGLOC_Os07g16750
SBSChr821715424C-THETINTERGENIC
SBSChr85087161A-THETSTOP_GAINEDLOC_Os08g08770
SBSChr89136073G-AHETINTRON
SBSChr913351373C-THET
SBSChr913351373C-THOMOINTERGENIC
SBSChr91926886C-AHET
SBSChr91926886C-AHOMOINTRON
SBSChr91926892C-AHET
SBSChr91926892C-AHOMOINTRON
SBSChr942844C-THET
SBSChr942844C-THETINTERGENIC
SBSChr94886230A-GHET
SBSChr94886230A-GHOMOINTRON
SBSChr94916966T-CHET
SBSChr96361628A-CHET
SBSChr991617C-THET

Deletions: 41
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr114713094713101
DeletionChr119197179197236
DeletionChr79302339302429
DeletionChr198051898051912
DeletionChr12043608204362416
DeletionChr32582878258288911
DeletionChr7290681929068289
DeletionChr114470515447054429
DeletionChr55636798563680911
DeletionChr106634001674800011400013
DeletionChr7686345568634561
DeletionChr283629258362938132
DeletionChr2910188691018871
DeletionChr49225927922592812
DeletionChr10105760301057603112
DeletionChr2108422491084225910
DeletionChr810884010108840122
DeletionChr61134226611342281152
DeletionChr1011558704115587051
DeletionChr6135036781350368462
DeletionChr5136046611360466212
DeletionChr2142156091421561892
DeletionChr914423230144232311
DeletionChr12155223741552237842
DeletionChr1161260011623400010800019
DeletionChr2168401961684020482
DeletionChr9178095741781633367592
DeletionChr8198202541982025842
DeletionChr720781157207811581
DeletionChr10215624962156250610LOC_Os10g40250
DeletionChr1222604673226046774LOC_Os12g36890
DeletionChr5284460052844601510
DeletionChr528882749288827501
DeletionChr629657847296578481
DeletionChr130941777309417836
DeletionChr4312232243122322952
DeletionChr43127404331274078352
DeletionChr3351891023518911210
DeletionChr13565476135654779182
DeletionChr13612257436122588142
DeletionChr138813289388132901

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr115970530159705301LOC_Os01g28530image
InsertionChr139804019398040202
InsertionChr108176308176301
InsertionChr1212896716128967161
InsertionChr1224095494240954952
InsertionChr212801310128013101
InsertionChr221300284213002841
InsertionChr312850614128506141
InsertionChr5152512101525121012image
InsertionChr5152512101525121012image
InsertionChr522050941220509411
InsertionChr5258463062584630722image
InsertionChr5258463062584630722image
InsertionChr56179376617937722image
InsertionChr56179376617937722image
InsertionChr5913286391328631
InsertionChr715924046159240461
InsertionChr719981738199817381
InsertionChr819903555199035551

Inversions: 28
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr211921671192305LOC_Os02g03030
InversionChr317751601775665LOC_Os03g03890
InversionChr845845294584727
InversionChr751343665134578LOC_Os07g09675
InversionChr553639345364086
InversionChr1154275625438438
InversionChr758664285866539
InversionChr363439666344168
InversionChr1066336016910090
InversionChr1067480206910111
InversionChr1067480216910112
InversionChr31544186115442058
InversionChr51831892218319066
InversionChr71934811419348353
InversionChr111962883819628951LOC_Os11g33170
InversionChr81989589719896080
InversionChr122081761720817820LOC_Os12g34350
InversionChr42106586621066137
InversionChr121586694217149062
InversionChr121586705217149102
InversionChr112161144421611553LOC_Os11g36620
InversionChr62309753623097664
InversionChr12507040025070511
InversionChr72883595828836181
InversionChr52907138129071489LOC_Os05g50720
InversionChr42973555629735785
InversionChr13366822233668426LOC_Os01g58240
InversionChr13971833639718675

Translocations: 7
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr917809574Chr7252152172
TranslocationChr917809576Chr7252152172
TranslocationChr917816328Chr7252152092
TranslocationChr1218508134Chr212962842
TranslocationChr721347695Chr116125670
TranslocationChr721349906Chr116234001LOC_Os01g28989
TranslocationChr334394716Chr2316964502