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Mutant Information

Mutant NameFN3235-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN3235-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 46
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr13392624C-THETNON_SYNONYMOUS_CODINGLOC_Os01g07180
SBSChr130188600T-CHOMOSYNONYMOUS_CODING
SBSChr130847632C-AHOMOINTERGENIC
SBSChr133415855T-AHOMOINTERGENIC
SBSChr211090563G-AHOMOINTRON
SBSChr217595424C-AHETINTERGENIC
SBSChr224934526A-CHETINTERGENIC
SBSChr315500283A-GHETINTERGENIC
SBSChr323901899T-CHETNON_SYNONYMOUS_CODINGLOC_Os03g42870
SBSChr333284117T-CHETINTERGENIC
SBSChr335942243G-AHETINTERGENIC
SBSChr49475924C-AHETNON_SYNONYMOUS_CODINGLOC_Os04g17280
SBSChr431281608G-AHETINTRON
SBSChr432081869T-AHETUTR_3_PRIME
SBSChr55141062T-GHETINTRON
SBSChr57280007G-AHETINTRON
SBSChr59660416T-GHETINTERGENIC
SBSChr524246940G-AHOMONON_SYNONYMOUS_CODINGLOC_Os05g41410
SBSChr62421030C-THOMOUTR_3_PRIME
SBSChr62940483A-GHETINTRON
SBSChr65380110G-AHETINTERGENIC
SBSChr76543809A-GHOMOINTERGENIC
SBSChr723258848A-GHETSYNONYMOUS_CODING
SBSChr726185772G-THETINTERGENIC
SBSChr83346528A-GHETINTERGENIC
SBSChr84436752C-THETINTERGENIC
SBSChr86466393G-AHETINTERGENIC
SBSChr86797149C-AHETSTOP_GAINEDLOC_Os08g11590
SBSChr820653778T-CHOMOINTERGENIC
SBSChr9355205A-GHETNON_SYNONYMOUS_CODINGLOC_Os09g01480
SBSChr915748883A-GHETINTERGENIC
SBSChr101227152G-THETINTERGENIC
SBSChr105028681C-THETINTRON
SBSChr105616093C-THOMOSYNONYMOUS_CODING
SBSChr1015670232C-AHOMOINTERGENIC
SBSChr1022012756A-GHETUTR_3_PRIME
SBSChr1115180057G-AHOMOINTERGENIC
SBSChr1115532912T-GHETNON_SYNONYMOUS_CODINGLOC_Os11g26990
SBSChr1115997905G-AHETINTERGENIC
SBSChr1118742957T-GHETNON_SYNONYMOUS_CODINGLOC_Os11g31890
SBSChr1121347402C-THETSYNONYMOUS_CODING
SBSChr1124762378C-AHOMOINTERGENIC
SBSChr122290420C-THETNON_SYNONYMOUS_CODINGLOC_Os12g05180
SBSChr127490000T-GHETINTERGENIC
SBSChr1211148699G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g19200
SBSChr1220567780T-CHOMOINTERGENIC

Deletions: 23
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr67920679559353
DeletionChr4231618623161871
DeletionChr10257914725791481
DeletionChr833050013343000379994
DeletionChr7518722251872231LOC_Os07g09730
DeletionChr7592664359266441
DeletionChr1845265684526582
DeletionChr12911733791173392LOC_Os12g16000
DeletionChr10114562981145635961
DeletionChr512974311129743132
DeletionChr514803613148036163
DeletionChr3169577371695776427
DeletionChr1217059018170590268
DeletionChr217793853177938541LOC_Os02g29920
DeletionChr418161760181617611
DeletionChr319362931193629376
DeletionChr3197589221975898765LOC_Os03g35670
DeletionChr1219883127198831292
DeletionChr52052600120563000369996
DeletionChr420749713207497141
DeletionChr322311001223210009999LOC_Os03g40160
DeletionChr1223259866232598671
DeletionChr225639394256394017LOC_Os02g42620

Insertions: 20
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr816212030162120312
InsertionChr29034220903423718
InsertionChr313381615133816151
InsertionChr324138400241384001LOC_Os03g43290image
InsertionChr4155270015527001
InsertionChr4791431679143194
InsertionChr4288837022888373635
InsertionChr4335211243352120683
InsertionChr5612713461271341
InsertionChr5143644721436454372
InsertionChr5170362821703629312
InsertionChr529179565291795651
InsertionChr6930832093083201
InsertionChr7905751090575134LOC_Os07g15620image
InsertionChr8165999491660002072
InsertionChr817293658172936614
InsertionChr102445796244585964
InsertionChr11865755286575521
InsertionChr11134351961343523742
InsertionChr1212038230120382301

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr41003303610042982LOC_Os04g18150
InversionChr41003303810042980LOC_Os04g18150
InversionChr52052617820753238
InversionChr52056237620753247
InversionChr14072223840722345

Translocations: 9
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr12262349Chr614440085
TranslocationChr126029211Chr315242979LOC_Os12g11190
TranslocationChr57361082Chr131164154
TranslocationChr88928502Chr617497732
TranslocationChr48961811Chr18614310
TranslocationChr1012388005Chr118490988
TranslocationChr712634256Chr134701303
TranslocationChr712634260Chr134701297
TranslocationChr1121580976Chr98955214