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Mutant Information

Mutant NameFN4561-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4561-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 59
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr112278825G-AHET
SBSChr120197677G-THOMO
SBSChr128461367C-THET
SBSChr130301345T-AHET
SBSChr133679758C-THET
SBSChr136810276G-AHET
SBSChr140394875C-THOMO
SBSChr1013655424G-AHET
SBSChr1015748238C-THET
SBSChr105503953C-THET
SBSChr107098066T-AHETLOC_Os10g12720
SBSChr1113180002G-AHET
SBSChr1113267805G-AHET
SBSChr1114509577T-AHET
SBSChr1115669780G-THET
SBSChr1116772261G-AHET
SBSChr1121593029G-AHET
SBSChr1123507976G-AHET
SBSChr1123695072G-AHET
SBSChr1123846733A-THOMOLOC_Os11g39990
SBSChr1210663189T-AHET
SBSChr1210663190G-AHET
SBSChr1211529170G-THETLOC_Os12g19780
SBSChr1213421411T-CHETLOC_Os12g23640
SBSChr1217775761C-THET
SBSChr1226410627C-THOMO
SBSChr122857450G-AHET
SBSChr129638029C-GHET
SBSChr212209738G-AHET
SBSChr26115033C-THETLOC_Os02g11820
SBSChr26297736C-THOMO
SBSChr27056312G-AHOMO
SBSChr27497432T-AHET
SBSChr316338644C-THET
SBSChr320831124G-AHET
SBSChr333744877T-CHET
SBSChr335953042A-THET
SBSChr424429411C-THET
SBSChr46050111C-THET
SBSChr521003379C-THET
SBSChr522668657G-AHET
SBSChr55845925G-AHET
SBSChr58707964G-AHET
SBSChr611350405G-AHET
SBSChr617364850G-AHET
SBSChr621741964C-THETLOC_Os06g36900
SBSChr624377401G-AHET
SBSChr625037904G-AHET
SBSChr625037905C-AHET
SBSChr625446216C-THET
SBSChr77606536T-CHET
SBSChr77805061A-THET
SBSChr82203512T-GHOMOLOC_Os08g04480
SBSChr827746761C-THOMO
SBSChr86574115C-THET
SBSChr88402236G-AHET
SBSChr916652660A-THET
SBSChr92208603T-CHOMO
SBSChr94818674C-THET

Deletions: 35
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr91064981064981
DeletionChr65257975257971
DeletionChr463773163775121
DeletionChr613880861388379294LOC_Os06g03590
DeletionChr1233868823386881
DeletionChr6390692639069283
DeletionChr5392157139215711
DeletionChr124133019413303012LOC_Os12g08110
DeletionChr46015909601592820
DeletionChr77016089701613244LOC_Os07g12360
DeletionChr1081585428158703162
DeletionChr8818386281838621
DeletionChr58712003871201210
DeletionChr8931394293139454LOC_Os08g15320
DeletionChr310761809107618091
DeletionChr311019141110191411
DeletionChr111184213111842164LOC_Os01g19720
DeletionChr8124827921248285463
DeletionChr1213147524131475241
DeletionChr514255321142553244
DeletionChr814903787149037871
DeletionChr616127602161276021LOC_Os06g28350
DeletionChr616243537162435371
DeletionChr1016813487168134926
DeletionChr718316285183162851
DeletionChr41859900118614000150002
DeletionChr219604251196042566
DeletionChr1019652952196529521
DeletionChr12204978032049784442
DeletionChr920822442208224421
DeletionChr722838582228385821
DeletionChr1223652369236523691
DeletionChr126061891260618911
DeletionChr430649682306496821LOC_Os04g51720
DeletionChr1422380514223806717

Insertions: 21
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr125512358255123592
InsertionChr10136835031368355553
InsertionChr1015054067150540671
InsertionChr102935572935582
InsertionChr10726220772622104
InsertionChr1126859396268593961
InsertionChr213426659134266591
InsertionChr227283855272838562
InsertionChr234454055344540562
InsertionChr413639790136397923
InsertionChr414998882149988832
InsertionChr4150317871503187084
InsertionChr4191934819193481
InsertionChr4857618385761853
InsertionChr51699041699063
InsertionChr5260133092601339991
InsertionChr5982589798258971
InsertionChr659238485923971124
InsertionChr716402940164029412
InsertionChr723610120236101212
InsertionChr815302351153023511

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr41150414811504332
InversionChr122318989923190072

No Translocation