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Mutant Information

Mutant NameFN4463-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4463-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 42
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr114636635T-CHETINTERGENIC
SBSChr123686248G-AHETINTERGENIC
SBSChr127793872T-CHETNON_SYNONYMOUS_CODINGLOC_Os01g48490
SBSChr128227895G-CHETINTERGENIC
SBSChr141271825T-AHETNON_SYNONYMOUS_CODINGLOC_Os01g71300
SBSChr215648437C-THETINTERGENIC
SBSChr222974337T-AHOMOSTOP_GAINEDLOC_Os02g38020
SBSChr222974339G-THOMONON_SYNONYMOUS_CODINGLOC_Os02g38020
SBSChr222974342T-GHOMONON_SYNONYMOUS_CODINGLOC_Os02g38020
SBSChr35776605T-CHETINTERGENIC
SBSChr35776613A-THOMOINTERGENIC
SBSChr39402730C-GHETSTART_GAINED
SBSChr39916943C-THETNON_SYNONYMOUS_CODINGLOC_Os03g17810
SBSChr317701094C-AHETINTERGENIC
SBSChr327348174C-THETINTRON
SBSChr328646840G-AHOMOINTERGENIC
SBSChr410529898G-AHETINTRON
SBSChr421129990G-AHETINTERGENIC
SBSChr426176385T-CHETINTERGENIC
SBSChr5398177T-AHETSYNONYMOUS_CODING
SBSChr5398178C-AHETNON_SYNONYMOUS_CODINGLOC_Os05g01670
SBSChr5398179C-AHETSTOP_GAINEDLOC_Os05g01670
SBSChr521634745A-CHETINTRON
SBSChr6883657T-CHETINTERGENIC
SBSChr623029823G-AHETINTERGENIC
SBSChr75960930A-THETNON_SYNONYMOUS_CODINGLOC_Os07g10900
SBSChr78682406C-THETINTRON
SBSChr78961431G-THETINTERGENIC
SBSChr79327097A-CHETINTERGENIC
SBSChr711166578C-THETINTERGENIC
SBSChr711962178T-CHETINTERGENIC
SBSChr718957108G-AHETINTRON
SBSChr726306351C-THETSYNONYMOUS_CODING
SBSChr728727472A-THETSTOP_GAINEDLOC_Os07g48100
SBSChr105924660A-GHETINTERGENIC
SBSChr107261599A-GHETNON_SYNONYMOUS_CODINGLOC_Os10g13430
SBSChr117080693G-AHETINTERGENIC
SBSChr117907136A-THETINTERGENIC
SBSChr119245966G-AHETINTRON
SBSChr1118745923T-AHETINTRON
SBSChr1123772745A-GHETSYNONYMOUS_CODING
SBSChr128250018A-GHETINTERGENIC

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr122186612186621
DeletionChr9243729024372911
DeletionChr4256419725641981
DeletionChr4308022630802282
DeletionChr11379582037958211
DeletionChr3493289349328941
DeletionChr8504607350460763
DeletionChr8578694557869461
DeletionChr9665881966588201
DeletionChr10822397882239813
DeletionChr4863517286351742
DeletionChr12868023986802423
DeletionChr5990429299042931
DeletionChr29964958996497921
DeletionChr810790743107907441
DeletionChr1211689740116897455
DeletionChr1112104528121045313
DeletionChr1112108413121084141
DeletionChr714259012142590142
DeletionChr4149762401497627131
DeletionChr515367859153678601
DeletionChr915670334156703351
DeletionChr717256421172564221
DeletionChr720797490207974911
DeletionChr520839914208399151LOC_Os05g35100
DeletionChr724794232247942331
DeletionChr126063515260635161LOC_Os01g45880
DeletionChr326131464261314706LOC_Os03g46220
DeletionChr2267223552672237621
DeletionChr3269000112690002716
DeletionChr629653116296531171

Insertions: 16
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr218494308184943081
InsertionChr321038827210388271
InsertionChr1223183714231837196
InsertionChr134070401340704011
InsertionChr218761118187611181
InsertionChr220474594204745941
InsertionChr223345060233450601
InsertionChr233348033333480331
InsertionChr3408762440876241
InsertionChr411483185114831862
InsertionChr414418783144187831
InsertionChr510591073105910731
InsertionChr612166880121668801
InsertionChr7995440599544051
InsertionChr10902367790236793
InsertionChr11120935711209359020

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr101822008518220275LOC_Os10g34140

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr93711240Chr274789662
TranslocationChr93712509Chr27478990LOC_Os09g07430