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Mutant Information

Mutant NameFN2631-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2631-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 36
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr113669555T-CHETNON_SYNONYMOUS_CODINGLOC_Os01g24260
SBSChr1209766A-THomo
SBSChr128961743G-AHET
SBSChr19474257G-THomo
SBSChr1015378908G-AHET
SBSChr1015378909C-THET
SBSChr1016571153A-GHET
SBSChr1112911121C-THET
SBSChr111584522A-THET
SBSChr1118114580G-AHETSTOP_GAINEDLOC_Os11g31120
SBSChr1126315175A-GHomo
SBSChr1126981857C-GHET
SBSChr118977722C-THET
SBSChr1214339182G-AHET
SBSChr122108499C-THET
SBSChr1223524789G-CHET
SBSChr211110218G-CHET
SBSChr31013561C-THET
SBSChr32324308A-THETNON_SYNONYMOUS_CODINGLOC_Os03g04860
SBSChr324702744C-AHomo
SBSChr425852071C-AHET
SBSChr426214586G-AHET
SBSChr428727461C-GHET
SBSChr433804433G-AHET
SBSChr433804434C-THET
SBSChr48047015A-GHET
SBSChr516943255C-THET
SBSChr529902267C-GHET
SBSChr61285195A-THomo
SBSChr615370066G-AHET
SBSChr616184382C-AHET
SBSChr629891942G-AHETNON_SYNONYMOUS_CODINGLOC_Os06g49340
SBSChr73362328G-CHomo
SBSChr75980918G-AHET
SBSChr815945266G-CHET
SBSChr917591339C-THomo

Deletions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr3128426012842611
DeletionChr51752763175277310LOC_Os05g03920
DeletionChr12189649418965017LOC_Os12g04450
DeletionChr10275354127535487
DeletionChr2675778367577852
DeletionChr3895251689525182
DeletionChr6111991031119911916
DeletionChr811281730112817377
DeletionChr411679852116798608
DeletionChr215605188156051902
DeletionChr517605995176060049
DeletionChr1017922061179220632
DeletionChr81964000119653000129993
DeletionChr520357940203579411
DeletionChr10227075912270760110
DeletionChr625405552254055608LOC_Os06g42300
DeletionChr235353967353539692
DeletionChr235922631359226343
DeletionChr138129822381298253

Insertions: 2
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr326714535267145362
InsertionChr5659040165904099

No Inversion

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr68871821Chr118619628
TranslocationChr613698860Chr12504238
TranslocationChr1022550435Chr12473716
TranslocationChr430715907Chr128240039