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Mutant Information

Mutant NameFN3165-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN3165-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
SBSChr114628700C-AHOMOINTERGENIC
SBSChr132519950A-THETSYNONYMOUS_CODING
SBSChr1016055731C-THETSYNONYMOUS_CODING
SBSChr1016795333C-THETINTRON
SBSChr1016795337G-THETINTRON
SBSChr1020516655C-THETSYNONYMOUS_CODING
SBSChr1020516656T-AHETNON_SYNONYMOUS_CODINGLOC_Os10g38402
SBSChr1110162797G-AHETINTERGENIC
SBSChr1112829976A-THETINTERGENIC
SBSChr1211937854C-THOMOINTERGENIC
SBSChr1218002467C-THOMOINTRON
SBSChr1222272617C-THOMOSTOP_GAINEDLOC_Os12g36380
SBSChr124311369G-AHOMOINTRON
SBSChr127473375A-THOMOINTERGENIC
SBSChr214378463C-AHOMOINTRON
SBSChr216911492G-THOMOINTRON
SBSChr219989165C-THETINTERGENIC
SBSChr228083502C-THETINTERGENIC
SBSChr228822167A-CHETINTRON
SBSChr314149567T-CHETSYNONYMOUS_CODING
SBSChr328200199G-AHETINTERGENIC
SBSChr329652658G-AHETINTERGENIC
SBSChr41605980G-AHOMOSYNONYMOUS_CODING
SBSChr42095308C-GHETNON_SYNONYMOUS_CODINGLOC_Os04g04400
SBSChr433889385G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g56850
SBSChr48916912T-AHETINTERGENIC
SBSChr516890867T-AHETINTRON
SBSChr56519464T-AHOMOINTERGENIC
SBSChr57855875G-CHETINTERGENIC
SBSChr612203578A-GHOMOINTERGENIC
SBSChr612318935G-THOMONON_SYNONYMOUS_CODINGLOC_Os06g21330
SBSChr619580338A-CHOMOINTERGENIC
SBSChr67345165G-CHOMOINTERGENIC
SBSChr67782338G-AHETINTRON
SBSChr71436141A-THOMOINTERGENIC
SBSChr718984209A-THOMOINTERGENIC
SBSChr726701797G-CHETINTRON
SBSChr727739298G-AHETINTERGENIC
SBSChr911216690C-THETSYNONYMOUS_CODING
SBSChr96569800C-THETSYNONYMOUS_CODING
SBSChr96622486T-AHETINTERGENIC
SBSChr99909398C-GHETNON_SYNONYMOUS_CODINGLOC_Os09g16230

Deletions: 32
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr57693497693589
DeletionChr11340295834029591LOC_Os11g06920
DeletionChr1476700147770009999LOC_Os01g09384
DeletionChr1478100148420006099911
DeletionChr973560497356916867
DeletionChr12745331474533184
DeletionChr7816567181656721
DeletionChr8838752583875261
DeletionChr109404388940441123
DeletionChr411666862116668664
DeletionChr211931805119318061
DeletionChr1112157466121574671
DeletionChr5138125451381258035
DeletionChr713903213139032152
DeletionChr9158488171584885841
DeletionChr616844212168442197
DeletionChr10201843212018437150
DeletionChr1020502589205025901
DeletionChr620738754207387562
DeletionChr721189500211895022
DeletionChr822128427221284314
DeletionChr724644201246442021
DeletionChr624982279249822867
DeletionChr625662382256623919
DeletionChr625988358259883591
DeletionChr8268039582680397012
DeletionChr828307514283075151
DeletionChr6285690012858600016999LOC_Os06g50960
DeletionChr428811609288116145
DeletionChr230406424304064262
DeletionChr432893831328938321
DeletionChr135896812358968131

Insertions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr120810863208108631
InsertionChr142907856429078594
InsertionChr1213076843130768431
InsertionChr1225976035259760362
InsertionChr525552582255525821
InsertionChr525867602258676021
InsertionChr712087805120878051
InsertionChr717965031179650311
InsertionChr724854156248541572
InsertionChr814868290148682901
InsertionChr8648306364830631
InsertionChr92253782253781

No Inversion

Translocations: 13
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr634037Chr316882320
TranslocationChr34463815Chr22674139LOC_Os02g05530
TranslocationChr95118424Chr126919364
TranslocationChr95118428Chr126927575
TranslocationChr117158246Chr106978185
TranslocationChr810343873Chr111602709
TranslocationChr810388279Chr111602708
TranslocationChr1113485820Chr218272186
TranslocationChr1215953891Chr91340903
TranslocationChr416579755Chr221668128
TranslocationChr722010603Chr38428627
TranslocationChr1122193654Chr45327082
TranslocationChr1123694688Chr125246388