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Mutant Information

Mutant NameFN2735-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2735-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 60
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr127387925C-AHOMONON_SYNONYMOUS_CODINGLOC_Os01g47840
SBSChr127387925C-AHomoNON_SYNONYMOUS_CODINGLOC_Os01g47840
SBSChr1616894C-THET
SBSChr18272420T-GHET
SBSChr18272420T-GHETUTR_3_PRIME
SBSChr19168536G-AHomo
SBSChr19168536G-AHOMOINTRON
SBSChr101280514C-THETNON_SYNONYMOUS_CODINGLOC_Os10g03070
SBSChr104415597C-THET
SBSChr106931317A-THET
SBSChr106931317A-THETINTERGENIC
SBSChr115592997C-THomo
SBSChr115592997C-THOMOUTR_3_PRIME
SBSChr1217047000C-GHET
SBSChr1217047000C-GHETINTRON
SBSChr129201439G-THET
SBSChr232872840G-AHET
SBSChr232872840G-AHETINTERGENIC
SBSChr235082389C-THET
SBSChr235082389C-THETINTRON
SBSChr24780196C-AHETNON_SYNONYMOUS_CODINGLOC_Os02g09280
SBSChr311934805G-CHomo
SBSChr311934805G-CHOMOINTERGENIC
SBSChr321049440G-AHET
SBSChr321049440G-AHETINTERGENIC
SBSChr321049441C-AHET
SBSChr321049441C-AHETINTERGENIC
SBSChr322719043C-AHET
SBSChr322719043C-AHETINTERGENIC
SBSChr322719044T-AHET
SBSChr322719044T-AHETINTERGENIC
SBSChr328326449T-CHETINTERGENIC
SBSChr35625085T-CHomo
SBSChr35625085T-CHOMOINTERGENIC
SBSChr38739209C-AHETSYNONYMOUS_CODING
SBSChr411967C-THET
SBSChr419611566C-THETNON_SYNONYMOUS_CODINGLOC_Os04g32580
SBSChr428193306C-AHomo
SBSChr428193306C-AHOMOINTRON
SBSChr519407161G-THET
SBSChr519407161G-THETINTERGENIC
SBSChr611976900T-CHET
SBSChr611976900T-CHETINTERGENIC
SBSChr611976901A-THET
SBSChr611976901A-THETINTERGENIC
SBSChr611976902C-THET
SBSChr611976902C-THETINTERGENIC
SBSChr612769637C-THETINTERGENIC
SBSChr616715294G-AHETNON_SYNONYMOUS_CODINGLOC_Os06g29260
SBSChr631190382T-GHomo
SBSChr631190382T-GHOMOINTERGENIC
SBSChr68735655G-THomo
SBSChr68735655G-THOMOINTERGENIC
SBSChr69699199C-AHET
SBSChr812265008G-CHET
SBSChr812265008G-CHETINTERGENIC
SBSChr826986863A-CHET
SBSChr826986863A-CHETINTERGENIC
SBSChr87779656C-THET
SBSChr916501564C-THETNON_SYNONYMOUS_CODINGLOC_Os09g27135

Deletions: 51
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr31334571334581
DeletionChr105186045186051
DeletionChr199225099229545
DeletionChr8191141919114212
DeletionChr4193779719377981
DeletionChr5240520024052011
DeletionChr1290620629062071
DeletionChr63287783328778962
DeletionChr2381990338199041
DeletionChr84252392425245765
DeletionChr9475910147591065
DeletionChr4530610753061169
DeletionChr10585732658573271
DeletionChr8728305872830591
DeletionChr10872811487281151
DeletionChr12889588088958822
DeletionChr5956537395653741
DeletionChr5990824899082491
DeletionChr8104569131045694128
DeletionChr110884004108840062
DeletionChr9110159741101598062
DeletionChr711447635114476361
DeletionChr121203514412035309165
DeletionChr712166680121666811
DeletionChr712169778121697791
DeletionChr312206509122065101
DeletionChr312206713122067141
DeletionChr812584371125843721
DeletionChr412686839126868401
DeletionChr213051627130516292
DeletionChr614040088140400891
DeletionChr4146198681461988517
DeletionChr815304149153041501LOC_Os08g25190
DeletionChr10155344671553448922
DeletionChr717305022173050231
DeletionChr1117738876177388771
DeletionChr619641970196419711
DeletionChr220070677200706836
DeletionChr522014692220146931
DeletionChr1022621280226212822
DeletionChr123494088234940935
DeletionChr326061955260619561LOC_Os03g46080
DeletionChr826672356266723571
DeletionChr826736967267369736
DeletionChr1126895145268951461
DeletionChr2283844252838444621
DeletionChr42955123229551348116
DeletionChr334199001342620006299910
DeletionChr334201001342610005999910
DeletionChr136921033369210341
DeletionChr1372064113720642918

Insertions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr111281091112810911
InsertionChr116220855162208551
InsertionChr119621410196214101
InsertionChr123401001234010066
InsertionChr126678442266784421
InsertionChr133860431338604311
InsertionChr1576318357631886
InsertionChr10188770631887707412
InsertionChr1020977113209771131
InsertionChr1218817390188173901
InsertionChr221223671212236711
InsertionChr223353062233530621
InsertionChr2569921356992186
InsertionChr2913926491392641LOC_Os02g16060image
InsertionChr426597673265976731
InsertionChr428033918280339181
InsertionChr513212615132126151
InsertionChr517503644175036496
InsertionChr529750609297506168
InsertionChr611110065111100651
InsertionChr619967524199675263
InsertionChr726050686260506861
InsertionChr810714504107145052
InsertionChr817547260175472601
InsertionChr824481451244814533
InsertionChr8493261449326141LOC_Os08g08550image
InsertionChr85192175519217732image
InsertionChr85192175519218172image
InsertionChr910011417100114171

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr11959677963747

Translocations: 35
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr11728649Chr2132255522
TranslocationChr71503924Chr43249683
TranslocationChr82694146Chr116146323
TranslocationChr73694378Chr43213554
TranslocationChr75440325Chr67372684
TranslocationChr106538384Chr49746190
TranslocationChr97218440Chr24247059
TranslocationChr97228101Chr67358335
TranslocationChr87820676Chr18343013
TranslocationChr1211058664Chr815320629
TranslocationChr1211861800Chr111474966
TranslocationChr1212547956Chr1018187587LOC_Os12g22260
TranslocationChr614459837Chr48661879
TranslocationChr1116827494Chr102906715LOC_Os10g05770
TranslocationChr818074316Chr118737722LOC_Os01g34040
TranslocationChr1118177016Chr817758093
TranslocationChr218249663Chr115324159
TranslocationChr518271745Chr428907054
TranslocationChr718715623Chr12892092LOC_Os07g31530
TranslocationChr419146715Chr317621955
TranslocationChr619268947Chr115459835
TranslocationChr819690453Chr613904217
TranslocationChr1220096544Chr623395012
TranslocationChr820135621Chr12999829
TranslocationChr1020165813Chr431852132
TranslocationChr620520242Chr1878755
TranslocationChr1221494618Chr1117511549
TranslocationChr1222003598Chr233566140
TranslocationChr922299529Chr221647280
TranslocationChr1122502094Chr103012238LOC_Os11g37950
TranslocationChr623802805Chr34986014
TranslocationChr1226916650Chr217337443
TranslocationChr1227085284Chr1118154422
TranslocationChr330999477Chr1199807572
TranslocationChr335300731Chr2164815272