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Mutant Information

Mutant NameFN4434-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4434-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 37
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr113022362C-THETINTERGENIC
SBSChr13327788A-THETUTR_3_PRIME
SBSChr135543820C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g61460
SBSChr1010699091G-AHETINTERGENIC
SBSChr1015932681G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g30610
SBSChr103901766G-AHETINTERGENIC
SBSChr105838816A-GHETINTERGENIC
SBSChr106256527G-AHETINTERGENIC
SBSChr109070801C-THETINTERGENIC
SBSChr1114480752G-AHOMOINTRON
SBSChr1117327854A-THOMOINTERGENIC
SBSChr1218225025G-THETSYNONYMOUS_CODING
SBSChr1225840229T-AHETNON_SYNONYMOUS_CODINGLOC_Os12g41720
SBSChr124156527G-AHETINTERGENIC
SBSChr210199560T-AHOMOINTRON
SBSChr224737607A-GHETINTRON
SBSChr232108903C-THETINTERGENIC
SBSChr316667089C-AHETINTERGENIC
SBSChr31838424C-AHETNON_SYNONYMOUS_CODINGLOC_Os03g04030
SBSChr415325223C-AHOMOSTOP_GAINEDLOC_Os04g26290
SBSChr419045630C-THETINTRON
SBSChr421132366G-AHETINTRON
SBSChr428232076T-CHETINTRON
SBSChr611601996A-GHETINTERGENIC
SBSChr620211010G-AHETINTERGENIC
SBSChr622692693C-AHETINTERGENIC
SBSChr625778143G-AHOMOINTERGENIC
SBSChr66465980T-GHOMOINTRON
SBSChr718462803T-CHETINTERGENIC
SBSChr718745419G-THOMOINTERGENIC
SBSChr726040275T-GHETNON_SYNONYMOUS_CODINGLOC_Os07g43530
SBSChr729033493G-AHOMOINTERGENIC
SBSChr729033494A-THOMOINTERGENIC
SBSChr813339704A-GHETINTERGENIC
SBSChr81950348T-CHOMOINTERGENIC
SBSChr922595468T-CHETINTRON
SBSChr92504686A-GHOMOINTERGENIC

Deletions: 38
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr112608001261800010000LOC_Os11g05700
DeletionChr1126230012633000100003
DeletionChr8269985026998511
DeletionChr5335012233501231
DeletionChr9344316834431691LOC_Os09g07090
DeletionChr5441956944195701
DeletionChr12462409946241012
DeletionChr34729866472992155
DeletionChr2488315648831571
DeletionChr8504595550459627
DeletionChr1714649571464961
DeletionChr47538302753831311
DeletionChr7797400180140004000010
DeletionChr68644940864496121
DeletionChr79728974972899319
DeletionChr10998343399834341
DeletionChr910376785103767872
DeletionChr411009132110091331
DeletionChr712176321121763221
DeletionChr8150643101506434939LOC_Os08g24880
DeletionChr7170168511701687726
DeletionChr917787968177879724
DeletionChr719132261191322621
DeletionChr220156928201569291
DeletionChr220972656209726582
DeletionChr121619219216192289
DeletionChr1222891456228914571
DeletionChr824766119247661201
DeletionChr125807251258072521
DeletionChr826704437267044392
DeletionChr428235348282353491
DeletionChr129686007296860081LOC_Os01g51650
DeletionChr1308140013118700037300055
DeletionChr1311950013136500017000032
DeletionChr131247855312478572
DeletionChr1313670013164200027500048
DeletionChr334069996340699971
DeletionChr134925376349253793LOC_Os01g60380

Insertions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr120981964209819641
InsertionChr125044988250449881
InsertionChr12956577295661943
InsertionChr1895928789592926
InsertionChr1021689157216891582
InsertionChr10227198322271984716
InsertionChr104059034405904714
InsertionChr1120630907206309071
InsertionChr1122812508228125103
InsertionChr1227324111273241111
InsertionChr211546562115465654
InsertionChr315789344157893452
InsertionChr319759561197595611
InsertionChr334698635346986362
InsertionChr429986072299860732
InsertionChr4646810964681091
InsertionChr524126885241268851
InsertionChr528175193281751942
InsertionChr5566144956614491
InsertionChr613932392139323921
InsertionChr6151688621516887211
InsertionChr7204427920442802
InsertionChr726578145265781473
InsertionChr74208194208191
InsertionChr813012161130121611LOC_Os08g21710image
InsertionChr816832934168329352
InsertionChr827575386275753894
InsertionChr8621952262195221
InsertionChr913367940133679412

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr931724243172526
InversionChr11068757410687778
InversionChr121891294918913111LOC_Os12g31440
InversionChr12608277726083061
InversionChr13074889530775583LOC_Os01g53550

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr524310583Chr130813677LOC_Os05g41510
TranslocationChr524310599Chr130775591LOC_Os05g41510
TranslocationChr233210455Chr115782035
TranslocationChr233210461Chr115781607