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Mutant Information

Mutant NameFN598-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN598-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 39
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr113649638T-CHETNON_SYNONYMOUS_CODINGLOC_Os01g24220
SBSChr128852334G-CHOMOINTERGENIC
SBSChr15982728C-THETINTERGENIC
SBSChr18530731A-GHETINTERGENIC
SBSChr1011080900T-AHOMOINTERGENIC
SBSChr108953453G-AHETINTERGENIC
SBSChr1110244604T-CHETINTRON
SBSChr1120210229C-GHOMONON_SYNONYMOUS_CODINGLOC_Os11g34500
SBSChr113696819C-THOMOINTERGENIC
SBSChr116132354G-AHOMOINTERGENIC
SBSChr1213311519T-AHETSPLICE_SITE_REGION
SBSChr1214185483C-GHETINTERGENIC
SBSChr1225802821G-AHETINTRON
SBSChr212048932C-GHOMOINTRON
SBSChr2222955A-GHOMOINTERGENIC
SBSChr22426465A-CHETINTERGENIC
SBSChr225041584A-THETINTERGENIC
SBSChr316057005A-THETNON_SYNONYMOUS_CODINGLOC_Os03g27950
SBSChr317664451A-CHETINTRON
SBSChr318817533G-AHETINTERGENIC
SBSChr327228055A-GHETINTERGENIC
SBSChr329434408T-CHOMOINTERGENIC
SBSChr41462452C-THOMONON_SYNONYMOUS_CODINGLOC_Os04g03410
SBSChr48963555G-AHOMOINTERGENIC
SBSChr49291028T-CHOMOINTERGENIC
SBSChr49537826C-THOMOSYNONYMOUS_CODING
SBSChr516873906C-THETINTERGENIC
SBSChr611103255C-THOMOINTRON
SBSChr616463973G-AHOMOINTERGENIC
SBSChr65314768C-GHETINTERGENIC
SBSChr68577919A-GHETINTERGENIC
SBSChr710305221C-THETINTERGENIC
SBSChr721277335T-AHETINTERGENIC
SBSChr729522502G-CHOMONON_SYNONYMOUS_CODINGLOC_Os07g49300
SBSChr75490354C-THOMOINTERGENIC
SBSChr813122882A-THETINTERGENIC
SBSChr814395283C-GHETINTERGENIC
SBSChr819636259G-AHETNON_SYNONYMOUS_CODINGLOC_Os08g31680
SBSChr82596687C-THOMOINTERGENIC

Deletions: 25
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr2376239237675725180LOC_Os02g07320
DeletionChr94012982401299210LOC_Os09g07890
DeletionChr12592971859297202
DeletionChr3618518761851925
DeletionChr11641185464118628LOC_Os11g11530
DeletionChr76794976679500125LOC_Os07g12140
DeletionChr28251682825169210
DeletionChr6917445291744531
DeletionChr4929325992932601
DeletionChr710226938102269391
DeletionChr310253028102530368
DeletionChr211864123118641307
DeletionChr12127780011278629682952
DeletionChr512860963128609641LOC_Os05g22660
DeletionChr413167725131677283
DeletionChr1137321531373217421LOC_Os01g24360
DeletionChr1018755055187550561
DeletionChr1119069264190692662LOC_Os11g32270
DeletionChr2218910472189105912
DeletionChr225036297250362992
DeletionChr4250537722505381745LOC_Os04g42330
DeletionChr1291630602916307010
DeletionChr329434458294344591
DeletionChr7295221112952212615LOC_Os07g49290
DeletionChr434611621346116221

Insertions: 5
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1117744204177442052
InsertionChr216048993160489942
InsertionChr4165643111656433222
InsertionChr615715161157151611
InsertionChr6188987718898782

Inversions: 7
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr625886422938739LOC_Os06g05730
InversionChr710649232118367112
InversionChr71064939511836714LOC_Os07g20500
InversionChr511613287117235072
InversionChr121418527516314354
InversionChr62822458629521101LOC_Os06g48770
InversionChr62822460629521099LOC_Os06g48770

Translocations: 6
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr36959011Chr237627552
TranslocationChr36959021Chr237623972
TranslocationChr710649232Chr5114796492
TranslocationChr710649393Chr511613401LOC_Os05g19910
TranslocationChr1111303517Chr63063650LOC_Os11g19610
TranslocationChr1111303525Chr63065976LOC_Os11g19610