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Mutant Information

Mutant NameFN4529-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4529-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 106
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr11003187G-AHETLOC_Os01g02860
SBSChr112920229A-GHET
SBSChr121618032C-THET
SBSChr123232215G-AHOMO
SBSChr123232216T-CHOMO
SBSChr123232217G-THOMO
SBSChr124303197T-CHET
SBSChr126453056T-AHET
SBSChr129746244C-AHET
SBSChr131714076A-THET
SBSChr133901343T-AHET
SBSChr137634852T-CHET
SBSChr1015260002C-AHET
SBSChr102069652C-AHET
SBSChr1022287828C-THET
SBSChr1022868888G-THETLOC_Os10g42439
SBSChr1112993522A-GHET
SBSChr1115278725G-THETLOC_Os11g26670
SBSChr1123091428C-AHETLOC_Os11g38820
SBSChr11484957C-AHET
SBSChr117369897C-AHET
SBSChr118680663G-AHET
SBSChr1212375029T-CHET
SBSChr1212394335G-THETLOC_Os12g22030
SBSChr1213716881G-AHETLOC_Os12g24110
SBSChr1215359834G-CHET
SBSChr1215834728T-CHET
SBSChr1216653531A-THET
SBSChr1217103260T-CHET
SBSChr1222334512C-GHET
SBSChr1223100663C-AHETLOC_Os12g37620
SBSChr122511046G-AHETLOC_Os12g05490
SBSChr1225417186T-AHOMO
SBSChr1225417188G-AHOMO
SBSChr1226689069C-AHET
SBSChr124440277G-AHET
SBSChr126592268T-CHET
SBSChr212114032A-GHET
SBSChr215942022C-THET
SBSChr217840011G-THET
SBSChr219481002C-THET
SBSChr223028724T-CHOMO
SBSChr224911688G-CHETLOC_Os02g41540
SBSChr234884946A-GHETLOC_Os02g56910
SBSChr314840994T-AHET
SBSChr315620590T-CHET
SBSChr31701456G-AHET
SBSChr318818890C-GHOMO
SBSChr322518048G-AHET
SBSChr32593373C-AHOMO
SBSChr326058821G-AHETLOC_Os03g46080
SBSChr326954686G-THETLOC_Os03g47610
SBSChr332123475T-AHET
SBSChr34845032C-THOMO
SBSChr36920134T-AHET
SBSChr36920135T-AHET
SBSChr36920136G-AHET
SBSChr37969678A-GHET
SBSChr38806433C-AHET
SBSChr420002422G-AHOMO
SBSChr42288208G-AHET
SBSChr423826620C-AHET
SBSChr435034575T-CHET
SBSChr48485537C-AHETLOC_Os04g15600
SBSChr516827775A-GHET
SBSChr518180580T-AHETLOC_Os05g31254
SBSChr518180581G-AHETLOC_Os05g31254
SBSChr518788450G-AHET
SBSChr519151228A-CHET
SBSChr519295734G-AHETLOC_Os05g32940
SBSChr519361825A-THET
SBSChr523073199C-AHET
SBSChr526506731G-THET
SBSChr53689735T-CHET
SBSChr5702039C-THET
SBSChr611931589A-GHET
SBSChr612132365C-THET
SBSChr613629638G-THET
SBSChr617553015G-THETLOC_Os06g30380
SBSChr622192750T-AHET
SBSChr62387111T-GHET
SBSChr65597843G-AHET
SBSChr68223720G-AHETLOC_Os06g14610
SBSChr69819896G-AHET
SBSChr710594948G-THET
SBSChr712622262G-THOMO
SBSChr722282377A-THETLOC_Os07g37190
SBSChr72234828T-AHET
SBSChr723249433A-GHET
SBSChr724768843C-THETLOC_Os07g41350
SBSChr7382889A-GHET
SBSChr77296632C-THET
SBSChr79419866A-GHET
SBSChr812894398A-GHET
SBSChr814121747C-AHET
SBSChr815971212C-THET
SBSChr911059680A-THOMO
SBSChr912966780A-CHOMO
SBSChr913623692G-THOMO
SBSChr916527067A-GHET
SBSChr916707443C-THET
SBSChr92047937C-THET
SBSChr921324014C-AHET
SBSChr94410657C-THET
SBSChr95781687C-AHET
SBSChr98938422C-THET

Deletions: 27
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr11217875521787551
DeletionChr4333185133318511
DeletionChr6462201046220101
DeletionChr86648590664860516
DeletionChr1168430616843238178LOC_Os11g12250
DeletionChr127507217750722610LOC_Os12g13420
DeletionChr9783638178363811
DeletionChr6984028198402811
DeletionChr1210793249107932513
DeletionChr1012705045127050451
DeletionChr11372951513729619105
DeletionChr12151952401519530970
DeletionChr4152192851521937187
DeletionChr12169521231695218159LOC_Os12g28690
DeletionChr517756958177569581
DeletionChr51931300119337000240004
DeletionChr419821921198219211
DeletionChr10210584962105852934LOC_Os10g39460
DeletionChr1221920980219209812
DeletionChr12230243482302436922
DeletionChr123236305232363073
DeletionChr223617523236175231
DeletionChr1226811495268114951
DeletionChr5269720012712800015600027
DeletionChr628718710287187156LOC_Os06g47380
DeletionChr6290125172901261094
DeletionChr4296984432969845614

Insertions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr112538303125383031
InsertionChr119991226199912283
InsertionChr129661307296613071
InsertionChr10306197330619731
InsertionChr107867007867001
InsertionChr11216396821639681
InsertionChr11230319202303196142
InsertionChr1124993502249935021
InsertionChr114262535426255723
InsertionChr1211016854110168541
InsertionChr1212616516126165161
InsertionChr2326545773265459317
InsertionChr233662626336626261
InsertionChr2554215155421522
InsertionChr2745856274585665
InsertionChr315055195150551951
InsertionChr39150589150581
InsertionChr41163422911634350122
InsertionChr417209076172090761
InsertionChr4266487392664881274
InsertionChr512367664123676663LOC_Os05g21020image
InsertionChr6111444601114448425LOC_Os06g19570image
InsertionChr631125907311259071
InsertionChr6804566180456611
InsertionChr718061748180617481
InsertionChr722481083224810831
InsertionChr76862416862411
InsertionChr8958732895873281

Inversions: 7
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr967072376707500
InversionChr671027477102948LOC_Os06g12980
InversionChr781468258146991
InversionChr889817848981873
InversionChr1099262369926374
InversionChr41300854913008738
InversionChr71602023016020473

No Translocation