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Mutant Information

Mutant NameFN4466-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4466-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 48
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr119284483G-AHETINTERGENIC
SBSChr123755260A-GHETINTERGENIC
SBSChr127014758C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g47270
SBSChr128805962G-AHETINTERGENIC
SBSChr132516251T-CHETINTRON
SBSChr133922001T-CHETNON_SYNONYMOUS_CODINGLOC_Os01g58680
SBSChr106756997G-AHOMOINTERGENIC
SBSChr112519055C-GHETINTRON
SBSChr1211648761G-AHETINTRON
SBSChr1221694593C-GHETINTRON
SBSChr122856680A-THETINTERGENIC
SBSChr124281938C-THETINTERGENIC
SBSChr12683877G-CHETINTERGENIC
SBSChr21118779G-AHETINTERGENIC
SBSChr211845502G-AHOMOSYNONYMOUS_CODING
SBSChr212985169T-GHOMOINTERGENIC
SBSChr212985170G-THOMOINTERGENIC
SBSChr228933418G-AHETINTERGENIC
SBSChr321553602C-THETINTERGENIC
SBSChr324920867A-THETINTERGENIC
SBSChr331618995G-CHETSYNONYMOUS_CODING
SBSChr332268990A-GHETSYNONYMOUS_CODING
SBSChr34773395A-GHETINTERGENIC
SBSChr410275426A-THETNON_SYNONYMOUS_CODINGLOC_Os04g18600
SBSChr418876328C-THOMOSTOP_GAINEDLOC_Os04g31570
SBSChr429282402T-CHETINTERGENIC
SBSChr431990410A-THETSTOP_GAINEDLOC_Os04g53670
SBSChr510138637T-CHETINTERGENIC
SBSChr510432801G-AHETINTERGENIC
SBSChr513274141C-THOMOINTRON
SBSChr522202970T-CHETINTERGENIC
SBSChr523168241G-AHETSYNONYMOUS_CODING
SBSChr523612939A-THETINTERGENIC
SBSChr529237157C-THETSYNONYMOUS_CODING
SBSChr53903176G-AHETSYNONYMOUS_CODING
SBSChr55453462C-GHETINTERGENIC
SBSChr615751423C-THOMOINTERGENIC
SBSChr622462902T-CHETINTERGENIC
SBSChr624734489G-AHOMOINTRON
SBSChr627489317C-THETINTERGENIC
SBSChr631177988C-THOMOINTERGENIC
SBSChr65766826G-THETINTERGENIC
SBSChr711192707C-AHETNON_SYNONYMOUS_CODINGLOC_Os07g18890
SBSChr77639276T-AHETINTRON
SBSChr79317960C-THETINTERGENIC
SBSChr811599518G-AHETNON_SYNONYMOUS_CODINGLOC_Os08g19400
SBSChr826591842G-AHETINTERGENIC
SBSChr85782034A-THETINTERGENIC

Deletions: 49
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr42062562062571
DeletionChr170690870692517
DeletionChr77337337337341
DeletionChr10125509212550931
DeletionChr6152050915205101
DeletionChr11825272182535179
DeletionChr12217795821779591
DeletionChr43350476335049923
DeletionChr1340170934017178LOC_Os01g07212
DeletionChr9668764966876501
DeletionChr37263065726307611
DeletionChr3898910889891091
DeletionChr110150633101506341
DeletionChr510649957106499603
DeletionChr710968349109683501
DeletionChr811181878111818791LOC_Os08g18730
DeletionChr3112334651123347813
DeletionChr711606100116061055
DeletionChr1211952720119527222
DeletionChr312295487122954881
DeletionChr512879547128795525
DeletionChr212915939129159434LOC_Os02g21730
DeletionChr613224438132244391
DeletionChr8132920011346200017000021
DeletionChr213455038134550391LOC_Os02g22570
DeletionChr813583682135836853
DeletionChr11379400113832000380007
DeletionChr11383800113861000230005
DeletionChr814952447149524481
DeletionChr8166504011665041211
DeletionChr216757935167579372
DeletionChr1216841767168417703
DeletionChr416981874169818773
DeletionChr619687794196877995LOC_Os06g33840
DeletionChr5204520372045204811
DeletionChr7204868542048693884
DeletionChr1021079344210793484
DeletionChr521198001212640006600014
DeletionChr122177300121789000160002
DeletionChr4232576182325763820
DeletionChr125174506251745082LOC_Os01g43930
DeletionChr6259874242598746238
DeletionChr426059208260592091
DeletionChr1126982412269824131
DeletionChr127939720279397222
DeletionChr1291759982917604042LOC_Os01g50790
DeletionChr129640472296404731
DeletionChr130126646301266471LOC_Os01g52430
DeletionChr1391204983912051618

Insertions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr119330590193305901
InsertionChr120441901204419011
InsertionChr128814598288146003
InsertionChr130699386306993861
InsertionChr10216562421656252
InsertionChr1127968595279685951
InsertionChr11758013475801352
InsertionChr11792071679207172
InsertionChr12237606712376074272
InsertionChr3267668842676689916
InsertionChr410372738103727403
InsertionChr4137048113704811
InsertionChr413775750137757501
InsertionChr423681155236811551
InsertionChr511102261111022622
InsertionChr512204265122042651
InsertionChr521823814218238152
InsertionChr5383140838314081
InsertionChr610988216109882161
InsertionChr611827213118272131
InsertionChr621474906214749061
InsertionChr6302115843021159411
InsertionChr722434571224345722
InsertionChr7242401082424018679
InsertionChr7247849412478499050
InsertionChr813399250133992512
InsertionChr814837365148373651
InsertionChr913846489138464902
InsertionChr917452420174524201
InsertionChr9874394287439421LOC_Os09g14720image

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr122169258221773080LOC_Os12g35670

Translocations: 10
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr77638010Chr23798617
TranslocationChr79561138Chr512027106LOC_Os05g16790
TranslocationChr1111305409Chr38275495LOC_Os11g19610
TranslocationChr1015151887Chr714732032
TranslocationChr917923005Chr330851529LOC_Os09g29470
TranslocationChr917923171Chr330851494
TranslocationChr1118144085Chr235610329
TranslocationChr722380316Chr318876768
TranslocationChr722380317Chr318877003
TranslocationChr529707326Chr218202509LOC_Os05g51770