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Mutant Information

Mutant NameFN4600-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4600-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 48
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr1010611060T-GHETNON_SYNONYMOUS_CODINGLOC_Os10g20960
SBSChr1017115972C-THETINTERGENIC
SBSChr1018257483G-AHETINTERGENIC
SBSChr10598003A-THETINTERGENIC
SBSChr107122116C-AHETINTRON
SBSChr107122120G-THETINTRON
SBSChr1113359487A-THOMOINTERGENIC
SBSChr1113359490T-CHOMOINTERGENIC
SBSChr1117637534C-THOMOINTRON
SBSChr1117637535C-THOMOINTRON
SBSChr113775626A-CHETINTERGENIC
SBSChr117275302C-GHETINTERGENIC
SBSChr118592273C-GHETINTERGENIC
SBSChr1212261625T-CHETUTR_5_PRIME
SBSChr1221502884A-CHOMOINTERGENIC
SBSChr215115336G-AHETINTRON
SBSChr217241130G-AHETINTERGENIC
SBSChr224651038G-THOMOUTR_5_PRIME
SBSChr22970759C-THETINTERGENIC
SBSChr229993519G-CHOMONON_SYNONYMOUS_CODINGLOC_Os02g49060
SBSChr313790945C-AHOMOINTERGENIC
SBSChr314287441T-GHETINTERGENIC
SBSChr315605938T-CHETINTRON
SBSChr316732669T-CHETINTERGENIC
SBSChr41404137G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g03300
SBSChr417457755G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g29380
SBSChr424653280C-THETINTERGENIC
SBSChr429110346G-AHETUTR_5_PRIME
SBSChr435084353G-THETUTR_3_PRIME
SBSChr435084354G-THETUTR_3_PRIME
SBSChr48660649C-GHETSYNONYMOUS_CODING
SBSChr510351688C-THETINTRON
SBSChr511984416G-AHETINTRON
SBSChr514569724C-THETNON_SYNONYMOUS_CODINGLOC_Os05g25140
SBSChr518777601T-GHETINTERGENIC
SBSChr520699125G-AHETINTERGENIC
SBSChr626611732A-GHETINTERGENIC
SBSChr63677536G-CHETSTOP_GAINEDLOC_Os06g07600
SBSChr716059324G-AHOMOINTERGENIC
SBSChr717684590G-AHETINTERGENIC
SBSChr719998301C-THETINTERGENIC
SBSChr76708231G-THETINTERGENIC
SBSChr810006035C-THETINTERGENIC
SBSChr919803932T-CHETINTERGENIC
SBSChr94399174G-THETINTERGENIC
SBSChr94399176C-THETINTERGENIC
SBSChr95971678C-THETINTERGENIC
SBSChr99462925C-THETNON_SYNONYMOUS_CODINGLOC_Os09g15460

Deletions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr91303791303801
DeletionChr12098683209870522LOC_Os01g04660
DeletionChr2215282921528301
DeletionChr2498634049863411
DeletionChr6512043751204403
DeletionChr6708864470886451
DeletionChr7746806774680681
DeletionChr78914710891472111
DeletionChr7943176494317651
DeletionChr99507596950762832
DeletionChr4979975797997603LOC_Os04g17850
DeletionChr9107372341073731783
DeletionChr610962525109625261
DeletionChr811100928111009313
DeletionChr101168700111716000290003
DeletionChr212092138120921391
DeletionChr1012301280123012866
DeletionChr712638812126388208
DeletionChr718701297187012981
DeletionChr1119165562191655631
DeletionChr5198612431986126219
DeletionChr10203790042037902622LOC_Os10g38050
DeletionChr1021954813219548141
DeletionChr322171598221716002
DeletionChr627006897270068992
DeletionChr431607629316076301
DeletionChr433095076330950771
DeletionChr433604045336040461
DeletionChr43430200134331000290004

Insertions: 18
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1237483022374834342
InsertionChr123960258239602603LOC_Os01g42270image
InsertionChr10207063542070636916
InsertionChr10651445865144581
InsertionChr3179160951791612430LOC_Os03g31440image
InsertionChr3265698782656990629
InsertionChr3467533946753391
InsertionChr410884121108841222
InsertionChr41325801325801
InsertionChr419845739198457391
InsertionChr4261050626105061
InsertionChr525545469255454691
InsertionChr6548785054878534
InsertionChr721626882216268821
InsertionChr7792739779273971
InsertionChr816650559166505591
InsertionChr912615143126151431
InsertionChr9315936931593691

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr12383428324014164
InversionChr52764268927642992LOC_Os05g48220

Translocations: 6
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr111003499Chr92744631
TranslocationChr817619660Chr125416522
TranslocationChr1118098130Chr121510416LOC_Os11g31100
TranslocationChr722979905Chr433023288LOC_Os04g38680
TranslocationChr722980737Chr433023286
TranslocationChr333862419Chr142565419