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Mutant Information

Mutant NameFN4353-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4353-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 71
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr117197523G-CHETUTR_3_PRIME
SBSChr135190692C-THETINTERGENIC
SBSChr135555868T-AHETINTERGENIC
SBSChr138342486C-THETINTERGENIC
SBSChr139886717T-CHETSPLICE_SITE_REGION
SBSChr142028501A-THETINTERGENIC
SBSChr1010740889C-THETINTERGENIC
SBSChr103284272G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g06390
SBSChr10659077T-GHETINTERGENIC
SBSChr117896117A-THETINTERGENIC
SBSChr118776407T-CHETINTERGENIC
SBSChr1220434190G-AHETINTERGENIC
SBSChr1223592551G-AHETINTRON
SBSChr125039362G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g09580
SBSChr215125323G-AHOMONON_SYNONYMOUS_CODINGLOC_Os02g25810
SBSChr220526845G-THETNON_SYNONYMOUS_CODINGLOC_Os02g34300
SBSChr228691744T-CHETINTRON
SBSChr231912908C-THOMOINTERGENIC
SBSChr231912909C-AHOMOINTERGENIC
SBSChr310113212C-THETINTERGENIC
SBSChr313239227T-CHETNON_SYNONYMOUS_CODINGLOC_Os03g22900
SBSChr31708817G-THETINTERGENIC
SBSChr322001597G-THETUTR_3_PRIME
SBSChr326734498C-AHETINTRON
SBSChr329362221G-AHETSPLICE_SITE_REGION
SBSChr412142165C-THOMOINTERGENIC
SBSChr412919458C-THETINTERGENIC
SBSChr421173096G-AHETINTERGENIC
SBSChr42361885C-AHETSYNONYMOUS_CODING
SBSChr423773601A-THOMOINTERGENIC
SBSChr425685472C-THETINTRON
SBSChr426070235G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g43980
SBSChr430611881C-AHETINTERGENIC
SBSChr433515887A-CHETINTERGENIC
SBSChr43363888C-GHETINTERGENIC
SBSChr433838209C-GHETINTERGENIC
SBSChr45702070T-CHETINTERGENIC
SBSChr47279312G-AHOMOINTRON
SBSChr48032388A-GHOMOINTERGENIC
SBSChr515415732A-THOMOINTRON
SBSChr515655138A-GHOMOINTERGENIC
SBSChr529342508A-GHOMOSYNONYMOUS_CODING
SBSChr614741277A-GHETNON_SYNONYMOUS_CODINGLOC_Os06g25200
SBSChr615626606G-AHETINTERGENIC
SBSChr616369018A-CHETINTERGENIC
SBSChr65274614G-AHETINTERGENIC
SBSChr68938825G-THETNON_SYNONYMOUS_CODINGLOC_Os06g15750
SBSChr710563398T-GHETINTERGENIC
SBSChr715156479T-CHETSYNONYMOUS_CODING
SBSChr718620776C-THETINTERGENIC
SBSChr721940266T-CHETNON_SYNONYMOUS_CODINGLOC_Os07g36660
SBSChr77825997A-GHETINTRON
SBSChr78145874G-AHETUTR_5_PRIME
SBSChr816027131T-AHETNON_SYNONYMOUS_CODINGLOC_Os08g26290
SBSChr816638133T-AHETINTERGENIC
SBSChr817718592C-AHETINTERGENIC
SBSChr817719299G-THETINTERGENIC
SBSChr817980502A-THETINTERGENIC
SBSChr820550625C-THETINTERGENIC
SBSChr825162438A-GHETINTERGENIC
SBSChr825732827A-THETINTRON
SBSChr827752008A-GHETINTERGENIC
SBSChr827865223C-THETNON_SYNONYMOUS_CODINGLOC_Os08g44260
SBSChr85219977G-AHETINTERGENIC
SBSChr91952426C-AHETINTERGENIC
SBSChr920101828T-GHETINTERGENIC
SBSChr921117381G-AHETINTERGENIC
SBSChr922420447C-THETINTERGENIC
SBSChr94105020T-CHETINTRON
SBSChr94826850G-AHETINTRON
SBSChr94827813T-CHETINTRON

Deletions: 35
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr11755248175526820
DeletionChr52963867296388518
DeletionChr3370282737028281LOC_Os03g07250
DeletionChr5383383938338401
DeletionChr1414645041464544
DeletionChr115098744509881773
DeletionChr12535100353510052
DeletionChr16428083642809815
DeletionChr97335141733523998
DeletionChr97946021794603110
DeletionChr7909757990975867
DeletionChr5975074797507481
DeletionChr1210241841102418421
DeletionChr510658557106585603
DeletionChr310795276107952771
DeletionChr11113364251133643611
DeletionChr7116237661162377711
DeletionChr1212280278122802879
DeletionChr10127975381279760062
DeletionChr1013384828133848291
DeletionChr1137707081377076355
DeletionChr116323546163235471
DeletionChr1017526473175264741
DeletionChr518371837183718381
DeletionChr1218402478184024791
DeletionChr2194190671941914477
DeletionChr72115300121174000210005
DeletionChr1121457696214577015
DeletionChr11214624372146244912
DeletionChr921618822216188242
DeletionChr1123677171236771721LOC_Os11g39730
DeletionChr1224016480240164822
DeletionChr4259709612597097110
DeletionChr129476577294765803
DeletionChr140211374402113751LOC_Os01g69190

Insertions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1263587332635877139
InsertionChr136991263369912631
InsertionChr1119082831190828366
InsertionChr1125120249251202491
InsertionChr12190266851902671935
InsertionChr314315783143157831
InsertionChr419254836192548361
InsertionChr426501103265011042
InsertionChr515369435153694351
InsertionChr617372725173727262
InsertionChr813486000134860012
InsertionChr9208436920843702

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr316869161687082
InversionChr1029045512904685
InversionChr22033470420862010
InversionChr22033470820862029
InversionChr32865322628653481

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1217927239Chr116605896
TranslocationChr624203346Chr418789587
TranslocationChr624203577Chr418789577LOC_Os06g40590