Search Nipponbare


Mutant Information

Mutant NameFN2895-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2895-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 27
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111483523T-CHETINTERGENIC
SBSChr1223779575G-AHETSYNONYMOUS_CODING
SBSChr235023462A-GHETINTERGENIC
SBSChr24183787G-THETINTERGENIC
SBSChr322671107C-THOMONON_SYNONYMOUS_CODINGLOC_Os03g40780
SBSChr323783851G-AHETINTERGENIC
SBSChr35271418C-AHETNON_SYNONYMOUS_CODINGLOC_Os03g10334
SBSChr38260727G-THETNON_SYNONYMOUS_CODINGLOC_Os03g15120
SBSChr425226347G-AHETINTRON
SBSChr432781000C-AHETINTERGENIC
SBSChr434109512G-THETINTERGENIC
SBSChr520647444T-GHETINTRON
SBSChr611334885C-THETINTERGENIC
SBSChr611334886A-THETINTERGENIC
SBSChr628201553A-THETINTERGENIC
SBSChr64052973C-AHETINTERGENIC
SBSChr64667803C-GHETINTRON
SBSChr712378092C-THETSYNONYMOUS_CODING
SBSChr71586084G-AHETINTERGENIC
SBSChr717511197A-THETINTERGENIC
SBSChr717610008T-CHETINTERGENIC
SBSChr718752262C-THETINTERGENIC
SBSChr721086638G-THETINTERGENIC
SBSChr77031246T-AHETINTERGENIC
SBSChr821750557C-THOMOINTERGENIC
SBSChr914752688G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g24760
SBSChr95711829G-CHETNON_SYNONYMOUS_CODINGLOC_Os09g10450

Deletions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr4178894717889481
DeletionChr102722884272290925
DeletionChr104808960480897010
DeletionChr67088001728500019699931
DeletionChr67894842789486624LOC_Os06g14150
DeletionChr2943910394391052
DeletionChr211930204119302051LOC_Os02g20260
DeletionChr212455477124554803
DeletionChr213787625137876261
DeletionChr1218996140189961411
DeletionChr1019821945198219461
DeletionChr921429585214295861
DeletionChr6219677352196775924
DeletionChr1225326355253263627
DeletionChr526013397260133981
DeletionChr528439124284391317
DeletionChr134270916342709171

Insertions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr113763923137639231
InsertionChr1213368121336811
InsertionChr137492112374921154LOC_Os01g64600image
InsertionChr10708094370809431
InsertionChr1116006926160069272
InsertionChr1116714835167148362
InsertionChr1213935481139354811
InsertionChr1215920631159206311
InsertionChr211922011119220133
InsertionChr29609950960996516
InsertionChr5111030061110301611
InsertionChr630585089305850891
InsertionChr822800889228008891
InsertionChr8275460427546041
InsertionChr91115311115322
InsertionChr921429693214296931
InsertionChr92157388621574005120

Inversions: 9
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr11147509272435
InversionChr510108851684505LOC_Os05g02810
InversionChr513988411684504
InversionChr121518264715321947
InversionChr72307036723244728
InversionChr72307038623244780
InversionChr62372089123930688LOC_Os06g40190
InversionChr14232565242624478LOC_Os01g73570
InversionChr14232565742624490LOC_Os01g73570

Translocations: 10
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr944561Chr47742301
TranslocationChr944594Chr47547059
TranslocationChr11147514Chr127841319LOC_Os01g48540
TranslocationChr11272437Chr127852507LOC_Os01g48570
TranslocationChr71583570Chr623720914
TranslocationChr71589713Chr623930701LOC_Os06g40190
TranslocationChr71969104Chr220513513
TranslocationChr116602818Chr24170016
TranslocationChr1126738186Chr218311741LOC_Os02g30730
TranslocationChr827374378Chr62829531