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Mutant Information

Mutant NameFN1264-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1264-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Albino and Normal (20% Albino)
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • TO:0000346 (Tiller number) = High (Between 126% and 175%)
  • 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: 34
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr129892130A-THETINTERGENIC
SBSChr138435424G-THOMOINTERGENIC
SBSChr138726659G-AHETINTERGENIC
SBSChr143306A-GHETINTERGENIC
SBSChr1012926467G-THETNON_SYNONYMOUS_CODINGLOC_Os10g25090
SBSChr103470004G-THETINTERGENIC
SBSChr1115690487A-CHETINTRON
SBSChr115969174C-THOMONON_SYNONYMOUS_CODINGLOC_Os11g10820
SBSChr1222858418G-AHETINTRON
SBSChr1224420049C-THOMOINTERGENIC
SBSChr222604160C-THETINTRON
SBSChr226254385C-THETINTERGENIC
SBSChr228954704G-AHETINTRON
SBSChr231900357C-THETINTRON
SBSChr317085702G-AHOMOSYNONYMOUS_CODING
SBSChr324739053C-THETINTERGENIC
SBSChr334352986G-AHETINTERGENIC
SBSChr334832667T-AHETINTERGENIC
SBSChr336311996G-THETINTERGENIC
SBSChr41159321C-THOMOINTERGENIC
SBSChr46527339G-AHETINTERGENIC
SBSChr481924C-THOMOINTERGENIC
SBSChr59458535C-THOMOINTERGENIC
SBSChr59458536T-AHOMOINTERGENIC
SBSChr610587606A-CHOMOINTERGENIC
SBSChr612672722C-THOMOINTERGENIC
SBSChr617652576T-AHOMOINTERGENIC
SBSChr619953420T-AHETINTRON
SBSChr626770456A-GHETINTERGENIC
SBSChr712464078C-THOMOINTERGENIC
SBSChr74718229C-THOMOINTERGENIC
SBSChr78437178G-THOMOSYNONYMOUS_CODING
SBSChr83643535C-THETINTERGENIC
SBSChr913805119C-GHOMOINTRON

Deletions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1196191719619225
DeletionChr11531130053113022LOC_Os11g09919
DeletionChr8624044362404463LOC_Os08g10600
DeletionChr106988363698837714
DeletionChr6123497201234973818LOC_Os06g21380
DeletionChr8156750571567506912
DeletionChr918032629180326323
DeletionChr121426733214267352
DeletionChr322141082221410919
DeletionChr222180439221804445LOC_Os02g36780
DeletionChr1224454232244553721140LOC_Os12g39620
DeletionChr1124647169246471767
DeletionChr425924551259245532
DeletionChr112668900126704000150003
DeletionChr426907442269074464
DeletionChr1226960994269610028LOC_Os12g43450
DeletionChr827332903273329096LOC_Os08g43240
DeletionChr5280036252800364015LOC_Os05g48850
DeletionChr138386150383861511

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1222882991228829911
InsertionChr228502866285028661
InsertionChr3961599596159951
InsertionChr520783822207838221
InsertionChr718898804188988041
InsertionChr8168711251687113612
InsertionChr9150247471502476418
InsertionChr9606531060653101

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1013494081138846072
InversionChr522210360229775442
InversionChr52487061224992151

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr118483266Chr230163186LOC_Os11g15070
TranslocationChr89573477Chr522210385LOC_Os05g37900
TranslocationChr710476836Chr11512463LOC_Os01g03660
TranslocationChr810991580Chr3152457422
TranslocationChr514705823Chr212182619
TranslocationChr315238126Chr23401782LOC_Os03g26690
TranslocationChr1126265710Chr7133894292
TranslocationChr1126492320Chr230163179LOC_Os11g43860