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Mutant Information

Mutant NameFN4752-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4752-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 46
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111469748C-THETINTERGENIC
SBSChr114535461G-THETINTERGENIC
SBSChr142469810G-CHETINTERGENIC
SBSChr1111087720C-THETINTERGENIC
SBSChr1124871543G-AHOMOSYNONYMOUS_CODING
SBSChr1125268784C-AHETINTERGENIC
SBSChr1214317427G-THOMOINTERGENIC
SBSChr122000252G-AHETINTERGENIC
SBSChr1225762110T-CHETINTERGENIC
SBSChr128600992C-GHETINTRON
SBSChr129864108C-AHETINTERGENIC
SBSChr23439387A-GHETINTERGENIC
SBSChr235105666C-AHETINTERGENIC
SBSChr28249448C-AHETINTERGENIC
SBSChr31373090C-AHETSYNONYMOUS_CODING
SBSChr318858162T-GHETINTERGENIC
SBSChr325577455C-THOMOSYNONYMOUS_CODING
SBSChr335408195C-GHETSYNONYMOUS_CODING
SBSChr335408197A-THETNON_SYNONYMOUS_CODINGLOC_Os03g62530
SBSChr39586779C-THETINTERGENIC
SBSChr515902665G-AHETINTERGENIC
SBSChr516607199A-THETINTERGENIC
SBSChr522727572A-CHETINTRON
SBSChr523359971G-THETSYNONYMOUS_CODING
SBSChr523936365C-THETINTRON
SBSChr524084797C-AHETSPLICE_SITE_REGION
SBSChr56382614T-AHETINTERGENIC
SBSChr58000642T-AHETUTR_5_PRIME
SBSChr612569033C-AHOMOINTERGENIC
SBSChr628364582G-AHOMOINTRON
SBSChr630792945T-AHOMOINTERGENIC
SBSChr63905306T-AHETNON_SYNONYMOUS_CODINGLOC_Os06g08070
SBSChr63905307G-AHETSYNONYMOUS_CODING
SBSChr64006809A-THETINTERGENIC
SBSChr74419218G-AHETINTERGENIC
SBSChr74902370T-CHETINTERGENIC
SBSChr77907112A-THETINTERGENIC
SBSChr815263070G-AHETINTRON
SBSChr819403044G-CHOMOINTERGENIC
SBSChr82316747C-THOMOINTERGENIC
SBSChr823560918C-GHETINTERGENIC
SBSChr826025794C-THOMOINTRON
SBSChr914013217G-AHETINTERGENIC
SBSChr98962253G-THETINTERGENIC
SBSChr99742124G-THETNON_SYNONYMOUS_CODINGLOC_Os09g15940
SBSChr99854998G-AHETINTERGENIC

Deletions: 22
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr124492844492851
DeletionChr99459609459611
DeletionChr99688189688235
DeletionChr2170733917073412
DeletionChr4262179726217992
DeletionChr10535521053552111
DeletionChr95425176542522044
DeletionChr7792678679267871
DeletionChr99132033913211178
DeletionChr10949777994977801
DeletionChr311654230116542399
DeletionChr514482993144829941
DeletionChr715072965150729661
DeletionChr415938609159386123
DeletionChr417481747174817536
DeletionChr1017562449175624501
DeletionChr1019648219196482201
DeletionChr620801571208015721
DeletionChr1020843824208438317
DeletionChr421486830214868366LOC_Os04g35330
DeletionChr822070538220705402
DeletionChr1224546733245467363

Insertions: 20
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1277116022771165453
InsertionChr132519431325194311
InsertionChr1123375812233758143
InsertionChr11277257112772575444LOC_Os11g45820image
InsertionChr2210650421065052
InsertionChr2637329563732951
InsertionChr313200871132008711
InsertionChr361102611032
InsertionChr4129017401290178243
InsertionChr416136278161362781
InsertionChr417193021171930211
InsertionChr421404855214048551
InsertionChr431709213317092142
InsertionChr519288873192888731
InsertionChr523890190238901901
InsertionChr527453926274539261
InsertionChr813805227138052271
InsertionChr8520752352075242
InsertionChr9296097029609712
InsertionChr9828000382800031

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr72334516023345244LOC_Os07g38930

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr514541374Chr225966150
TranslocationChr1117693016Chr25950580
TranslocationChr625881613Chr210193788