Search Nipponbare


Mutant Information

Mutant NameFN897-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN897-S Alignment File
Seed AvailabilityNo
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 36
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr121655012G-AHOMOSYNONYMOUS_CODING
SBSChr1013397231C-AHETINTRON
SBSChr103866302C-THETINTERGENIC
SBSChr104245072G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g07966
SBSChr104539377A-GHETINTERGENIC
SBSChr1121454551C-AHOMOINTERGENIC
SBSChr1222147999G-THETINTERGENIC
SBSChr1222347169A-GHOMOINTERGENIC
SBSChr227589543A-GHETINTERGENIC
SBSChr27466577C-THETUTR_3_PRIME
SBSChr310988430G-AHETINTERGENIC
SBSChr315076670G-THETINTERGENIC
SBSChr316145161C-GHETINTERGENIC
SBSChr321196461T-AHETINTRON
SBSChr321550227C-AHETINTERGENIC
SBSChr331590530T-CHETINTERGENIC
SBSChr333454043C-GHETSYNONYMOUS_CODING
SBSChr334066233T-CHETINTERGENIC
SBSChr427331286G-AHOMOINTERGENIC
SBSChr429279097A-THETINTERGENIC
SBSChr44431993G-AHETINTERGENIC
SBSChr45912G-AHETINTRON
SBSChr47938684T-AHETINTERGENIC
SBSChr522344725A-GHETINTERGENIC
SBSChr57879630G-THETINTERGENIC
SBSChr611598457T-CHOMONON_SYNONYMOUS_CODINGLOC_Os06g20210
SBSChr623800533C-AHETINTERGENIC
SBSChr625822391G-CHETNON_SYNONYMOUS_CODINGLOC_Os06g42980
SBSChr726110332T-GHETINTERGENIC
SBSChr727228748T-GHOMOINTERGENIC
SBSChr78588492C-GHETINTERGENIC
SBSChr811098165G-AHETNON_SYNONYMOUS_CODINGLOC_Os08g18100
SBSChr817604534C-THETINTERGENIC
SBSChr81867446C-AHOMOINTERGENIC
SBSChr820389512T-GHOMOINTERGENIC
SBSChr917071614T-CHETINTERGENIC

Deletions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr8175250617525148
DeletionChr8178597717859781
DeletionChr8243401324340163LOC_Os08g04840
DeletionChr83399714339972713
DeletionChr103793461379347514
DeletionChr152429145262289193756
DeletionChr2622419562242027
DeletionChr106250799625082425LOC_Os10g11260
DeletionChr9992604599260538
DeletionChr4123838811238390827
DeletionChr1013296289132962923
DeletionChr414209298142093035
DeletionChr214352500143525066
DeletionChr416519435165194405
DeletionChr916897142168971431LOC_Os09g27770
DeletionChr9182594631826917097072
DeletionChr819276346192763471
DeletionChr320033468200334757
DeletionChr121409211214092176
DeletionChr1221872597218726003
DeletionChr123854567238545703
DeletionChr1226106422261064231LOC_Os12g42100
DeletionChr227020721270207265LOC_Os02g44590
DeletionChr127134421271344287
DeletionChr627215895272158994
DeletionChr72862034228620550208LOC_Os07g47920
DeletionChr332309854323098551
DeletionChr3334270803342709111

Insertions: 7
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr111739696117396994
InsertionChr133303789333037891LOC_Os01g57599image
InsertionChr1227134457271344604
InsertionChr332575446325754461
InsertionChr332950453329504542
InsertionChr521765747217657504
InsertionChr529627689296276924

Inversions: 7
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr43087541087425LOC_Os04g01439
InversionChr2303285417852685
InversionChr994345509578681LOC_Os09g15700
InversionChr9957868614526956LOC_Os09g15700
InversionChr51586605717096989LOC_Os05g29110
InversionChr51618334417096921LOC_Os05g29110
InversionChr112844020428440390

Translocations: 14
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr5449000Chr3109880752
TranslocationChr5449001Chr3109778062
TranslocationChr121286706Chr215353558LOC_Os02g26130
TranslocationChr102161990Chr15243200LOC_Os01g10040
TranslocationChr102166305Chr15262353LOC_Os01g10090
TranslocationChr515865971Chr15242913LOC_Os01g10040
TranslocationChr517096917Chr152431962
TranslocationChr918268281Chr727006693LOC_Os07g45260
TranslocationChr918269155Chr7270066922
TranslocationChr322942522Chr139679149
TranslocationChr1127827885Chr725412078LOC_Os07g42440
TranslocationChr728620355Chr33374800LOC_Os07g47920
TranslocationChr728620541Chr33374798LOC_Os07g47920
TranslocationChr334354293Chr218055340