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Mutant Information

Mutant NameFN1481-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1481-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • TO:0000346 (Tiller number) = Normal (Between 75% and 125%)
  • TO:0000430 (Germination Rate) = Low (Between 25% and 75%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 43
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr120713841G-AHETINTERGENIC
SBSChr121499131G-AHETINTERGENIC
SBSChr122722794C-AHETINTRON
SBSChr133227212G-AHETINTERGENIC
SBSChr10166536T-CHETINTERGENIC
SBSChr1021831391C-THETSPLICE_SITE_DONORLOC_Os10g40700
SBSChr1115098597T-CHETINTERGENIC
SBSChr1115274259G-THETNON_SYNONYMOUS_CODINGLOC_Os11g26670
SBSChr1115567450G-THETINTERGENIC
SBSChr1121549837C-AHETNON_SYNONYMOUS_CODINGLOC_Os11g36520
SBSChr117197352G-AHETINTRON
SBSChr1214984577C-THETNON_SYNONYMOUS_CODINGLOC_Os12g25830
SBSChr1216744886A-GHETINTERGENIC
SBSChr1217264304G-CHETINTRON
SBSChr1220106504C-THETUTR_5_PRIME
SBSChr1223860292C-THETINTERGENIC
SBSChr128600903G-AHomoINTRON
SBSChr129901788G-AHETSTOP_GAINEDLOC_Os12g17300
SBSChr216919823C-AHETINTERGENIC
SBSChr25901867A-THETINTERGENIC
SBSChr25901868A-THETINTERGENIC
SBSChr31703159T-AHETINTERGENIC
SBSChr327078647G-THETINTERGENIC
SBSChr36713200T-CHETINTERGENIC
SBSChr412890685A-THomoINTERGENIC
SBSChr42848303T-CHETINTERGENIC
SBSChr433549670G-AHETINTERGENIC
SBSChr45930085C-GHomoINTERGENIC
SBSChr510229119T-CHomoINTERGENIC
SBSChr523479082A-THETINTERGENIC
SBSChr55169339C-THETINTERGENIC
SBSChr5848215T-AHETINTERGENIC
SBSChr619339850T-CHETINTRON
SBSChr620965721G-AHETINTERGENIC
SBSChr625622927A-THETINTERGENIC
SBSChr62719636C-AHETNON_SYNONYMOUS_CODINGLOC_Os06g05940
SBSChr63717452G-AHETINTERGENIC
SBSChr716801055C-THETINTERGENIC
SBSChr725639784A-GHETUTR_3_PRIME
SBSChr915572200G-AHETINTERGENIC
SBSChr916275736G-CHETINTERGENIC
SBSChr92629915C-THomoINTERGENIC
SBSChr93209899T-AHETINTERGENIC

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr8209425820942591
DeletionChr6221629522162972
DeletionChr45072751507276817LOC_Os04g09470
DeletionChr10540810154081043
DeletionChr2576359557636016LOC_Os02g10860
DeletionChr2576359757636036LOC_Os02g10860
DeletionChr6825619482561973
DeletionChr6977177197717732
DeletionChr1110359413103594152LOC_Os11g18366
DeletionChr811177016111840016985LOC_Os08g18730
DeletionChr311891353118913541
DeletionChr613667352136673531
DeletionChr514664663146646685LOC_Os05g25260
DeletionChr3148263251482633914
DeletionChr314973909149739101
DeletionChr916612833166128396
DeletionChr4179120011801400010200016
DeletionChr519247374192473762
DeletionChr419460945194609461
DeletionChr1198124991981255152LOC_Os01g35770
DeletionChr820754458207544591
DeletionChr22124300121299000560004
DeletionChr822508696225087015
DeletionChr1233796602337970040
DeletionChr424008097240080981
DeletionChr324939390249393944LOC_Os03g44360
DeletionChr1226240954262409551
DeletionChr327078619270786278
DeletionChr528810990288109944
DeletionChr139427416394274171

Insertions: 22
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr115100693151006942
InsertionChr128254758282547581
InsertionChr1332868333286831LOC_Os01g07080image
InsertionChr10150187481501876316
InsertionChr11154206071542061913LOC_Os11g26850image
InsertionChr1121356093213560942
InsertionChr11371038837103892
InsertionChr1222116317221163226
InsertionChr1226703691267036933
InsertionChr230643102306431032
InsertionChr2713767971376802
InsertionChr3182647951826483339
InsertionChr3208621162086215742
InsertionChr612426940124269401
InsertionChr618645796186458049
InsertionChr6383074138307411
InsertionChr6495484749548482
InsertionChr6754626475462652LOC_Os06g13630image
InsertionChr717087951170879566
InsertionChr72159302159312
InsertionChr8857043985704391
InsertionChr9546029454602941

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr3946803012373226
InversionChr101104359211141352

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr48612022Chr325690362LOC_Os03g45519
TranslocationChr712663529Chr518333720
TranslocationChr712663536Chr39468039
TranslocationChr1126646875Chr1011141355