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Mutant Information

Mutant NameFN4464-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4464-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
SBSChr115885269T-CHETINTRON
SBSChr12703580A-GHETINTRON
SBSChr128838412A-THOMOINTERGENIC
SBSChr135179297T-CHETUTR_5_PRIME
SBSChr139757200C-THETINTERGENIC
SBSChr19230724A-THETNON_SYNONYMOUS_CODINGLOC_Os01g16290
SBSChr1115624942T-CHETINTRON
SBSChr1115624946G-AHETINTRON
SBSChr112162385G-AHETINTERGENIC
SBSChr1122072229T-CHETINTERGENIC
SBSChr1126064770C-THETNON_SYNONYMOUS_CODINGLOC_Os11g43210
SBSChr1126064771G-AHETSYNONYMOUS_CODING
SBSChr1211094392T-AHOMOINTERGENIC
SBSChr1213168326T-CHOMOINTERGENIC
SBSChr1214308027T-GHOMOINTERGENIC
SBSChr128220535A-THETNON_SYNONYMOUS_CODINGLOC_Os12g14420
SBSChr212290743T-GHOMOINTERGENIC
SBSChr217634568C-THETINTERGENIC
SBSChr230849232C-GHETINTRON
SBSChr231080549A-GHETSYNONYMOUS_CODING
SBSChr26542914C-AHETINTRON
SBSChr312965937C-THETSYNONYMOUS_CODING
SBSChr314582834G-THOMONON_SYNONYMOUS_CODINGLOC_Os03g25540
SBSChr32922841A-CHETUTR_3_PRIME
SBSChr329525945C-AHETINTERGENIC
SBSChr39844722T-AHETINTRON
SBSChr410244501C-AHETINTERGENIC
SBSChr419718114T-CHETINTERGENIC
SBSChr430397086C-GHETUTR_3_PRIME
SBSChr511800535A-CHETSYNONYMOUS_CODING
SBSChr526751655C-AHETINTERGENIC
SBSChr58022354G-AHETINTERGENIC
SBSChr612318935G-THOMONON_SYNONYMOUS_CODINGLOC_Os06g21330
SBSChr619956643G-THETNON_SYNONYMOUS_CODINGLOC_Os06g34300
SBSChr628303600A-GHETINTERGENIC
SBSChr66181480G-AHOMOUTR_5_PRIME
SBSChr68638924T-CHETINTERGENIC
SBSChr68829610A-THETNON_SYNONYMOUS_CODINGLOC_Os06g15570
SBSChr69050742G-AHETINTERGENIC
SBSChr69050771G-AHETINTERGENIC
SBSChr69050774G-AHETINTERGENIC
SBSChr715681395G-AHETINTERGENIC
SBSChr718984209A-THOMOINTERGENIC
SBSChr82186787A-CHETINTERGENIC
SBSChr85797888T-AHETINTERGENIC
SBSChr86093481C-THETINTERGENIC
SBSChr916893125C-THETNON_SYNONYMOUS_CODINGLOC_Os09g27760
SBSChr9697163C-THOMOINTRON

Deletions: 26
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr631147831148911
DeletionChr7116589211658986
DeletionChr91938415193846651
DeletionChr42766996276705963
DeletionChr12412642141264232
DeletionChr9546497354649741LOC_Os09g10030
DeletionChr12607053360705341
DeletionChr9813221581322172
DeletionChr8832734983273501
DeletionChr2854565185456521
DeletionChr6857990285799031
DeletionChr11971696697169671LOC_Os11g17430
DeletionChr5976098897609902
DeletionChr1999358799935881
DeletionChr110772824107728284
DeletionChr12119199471191995710
DeletionChr413412658134126635
DeletionChr914215712142157131
DeletionChr1014451755144517561
DeletionChr1217524861175248632
DeletionChr920766578207665791
DeletionChr1021496209214962101LOC_Os10g40150
DeletionChr823189608231896091
DeletionChr429870570298705722
DeletionChr529955720299557211
DeletionChr137081565370815661

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1832506383250631
InsertionChr1019776481197764811
InsertionChr113471233471231
InsertionChr215998946159989461
InsertionChr29482919482911
InsertionChr2955565195556566LOC_Os02g16740image
InsertionChr3395095339509531
InsertionChr414218688142186936
InsertionChr421127348211273492
InsertionChr523249049232490491
InsertionChr5269840026984001
InsertionChr715281672152816721
InsertionChr723461536234615361
InsertionChr7445062744506271
InsertionChr76360097636013135
InsertionChr818856274188562741
InsertionChr8370484637048472
InsertionChr915658671156586711
InsertionChr9536523853652381

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr101620930716294994

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr96045067Chr332293355
TranslocationChr1211098438Chr1015600768
TranslocationChr1211098500Chr114758994LOC_Os01g19580
TranslocationChr1211099690Chr1015600767
TranslocationChr1211099694Chr1015601283
TranslocationChr1015600283Chr114758991LOC_Os01g27910
TranslocationChr419121525Chr332292359
TranslocationChr625956566Chr332274782