Search Results


Mutant Information

Mutant NameFN4387-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4387-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 45
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr15386586T-CHETINTERGENIC
SBSChr120259582A-GHETNON_SYNONYMOUS_CODINGLOC_Os01g36500
SBSChr122974517G-AHOMOINTERGENIC
SBSChr124362495A-GHOMOINTERGENIC
SBSChr125943273C-THETNON_SYNONYMOUS_CODINGLOC_Os01g45690
SBSChr27092735T-CHOMOINTERGENIC
SBSChr212054792C-THETINTERGENIC
SBSChr214660365C-AHETINTERGENIC
SBSChr219355343C-THETINTERGENIC
SBSChr235867711C-THETSTOP_GAINEDLOC_Os02g58710
SBSChr314763819C-AHETINTRON
SBSChr329107467A-THOMOINTERGENIC
SBSChr329914889C-THOMONON_SYNONYMOUS_CODINGLOC_Os03g52100
SBSChr46184658G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g11330
SBSChr49700372C-THETINTRON
SBSChr410279765T-CHETSTOP_LOSTLOC_Os04g18600
SBSChr423438583A-GHETINTERGENIC
SBSChr429335956C-THETINTRON
SBSChr57685773G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g13830
SBSChr510162662C-THETINTERGENIC
SBSChr520195354G-AHETINTERGENIC
SBSChr521340022G-CHETINTRON
SBSChr526040563T-CHETINTRON
SBSChr528762454T-CHETINTRON
SBSChr6173772C-THETINTRON
SBSChr66074044G-AHETINTERGENIC
SBSChr67304589C-THETINTERGENIC
SBSChr617407980G-CHETINTERGENIC
SBSChr623754804G-AHETINTERGENIC
SBSChr75502373T-CHETINTRON
SBSChr718499260T-CHETINTRON
SBSChr728917145T-CHETINTERGENIC
SBSChr83545309C-THOMONON_SYNONYMOUS_CODINGLOC_Os08g06380
SBSChr87095143G-AHETNON_SYNONYMOUS_CODINGLOC_Os08g12050
SBSChr815977059A-GHETUTR_3_PRIME
SBSChr819328382T-AHETINTERGENIC
SBSChr822451583T-CHOMOINTERGENIC
SBSChr915727775C-AHOMOINTERGENIC
SBSChr920564720A-THOMOINTERGENIC
SBSChr103132179A-GHETINTERGENIC
SBSChr1012386668C-THETINTERGENIC
SBSChr1121440128A-THETINTERGENIC
SBSChr124003025C-GHETINTERGENIC
SBSChr1220392717A-GHETINTERGENIC
SBSChr1224943531T-CHETUTR_3_PRIME

Deletions: 27
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr217698517700217
DeletionChr3103758610375959
DeletionChr3225327122532754
DeletionChr3464532546453283
DeletionChr1567404156740421
DeletionChr312044835120448394
DeletionChr413306934133069351
DeletionChr913577000135770011
DeletionChr515240652152406542LOC_Os05g26190
DeletionChr617957574179575773
DeletionChr918175082181750831LOC_Os09g29890
DeletionChr918817214188172151
DeletionChr1219238706192387082
DeletionChr720498435204984361
DeletionChr220747531207475321
DeletionChr320852136208521371
DeletionChr1209369782093701032LOC_Os01g37460
DeletionChr1125899558258995591
DeletionChr425996161259961621
DeletionChr2265670352656711479
DeletionChr727412388274123891
DeletionChr529396274293962839LOC_Os05g51250
DeletionChr330299257302992581
DeletionChr330961268309612702LOC_Os03g54000
DeletionChr432308896323088971LOC_Os04g54260
DeletionChr138844018388440279
DeletionChr141710165417101672

Insertions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1751722475172252
InsertionChr522659608226596103
InsertionChr1923312792331271
InsertionChr2359057635905761
InsertionChr226333550263335512
InsertionChr415177145151771451
InsertionChr511112452111124521
InsertionChr7278920182789205942
InsertionChr8273257027325712
InsertionChr9172303601723038021
InsertionChr9214728412147285919
InsertionChr102477982247801837
InsertionChr11149103781491039922
InsertionChr1125056435250564351
InsertionChr1213964542139645421
InsertionChr1214962359149623591
InsertionChr1226155950261559501

Inversions: 8
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr327426273689578
InversionChr327426413689584
InversionChr41267401212674213
InversionChr91592172816263895LOC_Os09g26360
InversionChr915921731162640342
InversionChr91975906819759249
InversionChr62029846620298637
InversionChr52278143123204668LOC_Os05g39540

No Translocation