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Mutant Information

Mutant NameFN4354-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4354-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
SBSChr111841335C-THETINTRON
SBSChr130252166A-THETINTRON
SBSChr138396289C-THOMOINTERGENIC
SBSChr102879960G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g05710
SBSChr1110421449A-CHOMOINTRON
SBSChr1112807232G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g22342
SBSChr1117209158A-GHETUTR_5_PRIME
SBSChr1218824882G-AHETINTERGENIC
SBSChr121885608A-GHETINTRON
SBSChr125286339C-THETINTERGENIC
SBSChr219433833G-AHETNON_SYNONYMOUS_CODINGLOC_Os02g32720
SBSChr227172839C-GHETINTERGENIC
SBSChr313395197G-CHETINTERGENIC
SBSChr36617486C-THETINTERGENIC
SBSChr412520241G-THETINTRON
SBSChr414913863C-THETSTOP_GAINEDLOC_Os04g25730
SBSChr414935725T-CHETINTERGENIC
SBSChr41704244T-AHETINTRON
SBSChr42985028G-AHOMONON_SYNONYMOUS_CODINGLOC_Os04g05810
SBSChr434211889A-GHETNON_SYNONYMOUS_CODINGLOC_Os04g57510
SBSChr510461996G-THOMOINTERGENIC
SBSChr510461997C-THOMOINTERGENIC
SBSChr526847138C-GHETNON_SYNONYMOUS_CODINGLOC_Os05g46320
SBSChr610677023G-THETINTERGENIC
SBSChr613536942C-THETINTERGENIC
SBSChr615073735G-AHETINTRON
SBSChr615397684C-THETINTERGENIC
SBSChr628786824C-THETINTERGENIC
SBSChr71181003G-AHETNON_SYNONYMOUS_CODINGLOC_Os07g03100
SBSChr74363727A-CHETINTERGENIC
SBSChr812972727T-AHETINTERGENIC
SBSChr816285428G-AHETINTERGENIC
SBSChr916343040T-CHETINTERGENIC
SBSChr921339566A-CHOMONON_SYNONYMOUS_CODINGLOC_Os09g37000
SBSChr94931640C-THETINTRON
SBSChr95758995C-THETINTERGENIC

Deletions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr33451463451526LOC_Os03g01540
DeletionChr81288043128805916LOC_Os08g02960
DeletionChr12423344042334411
DeletionChr65564113556415340
DeletionChr9638005863800591
DeletionChr8726771272677131
DeletionChr8854556185455621
DeletionChr10911142191114221
DeletionChr4957172395717241LOC_Os04g17500
DeletionChr611098983110989852
DeletionChr11121113361211139559
DeletionChr11144718441447185713
DeletionChr515442509154425112
DeletionChr10155197441551980763
DeletionChr111571500115770000550006
DeletionChr11157750011588100010600016
DeletionChr315835442158354431
DeletionChr816933189169331923LOC_Os08g27800
DeletionChr12169521231695218259LOC_Os12g28690
DeletionChr9171891921718926169
DeletionChr5196467481964676315LOC_Os05g33430
DeletionChr220418781204187832
DeletionChr9228703212287034524LOC_Os09g39890
DeletionChr11272891792728919314
DeletionChr429249506292495071
DeletionChr233133286331332871
DeletionChr135404500354045011LOC_Os01g61160
DeletionChr1424685404246861070

Insertions: 16
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1223693715236937173
InsertionChr1224073238240732392
InsertionChr1250432504321
InsertionChr310897436108974372
InsertionChr317060881170608811
InsertionChr410422845104228451
InsertionChr625488478254884781
InsertionChr7725210572521051LOC_Os07g12690image
InsertionChr7970420997042091
InsertionChr8110390121103902312
InsertionChr8133230413323041
InsertionChr813388316133883183
InsertionChr9180821311808215222
InsertionChr921898030218980301
InsertionChr922006664220066674
InsertionChr92232622232621LOC_Os09g01260image

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr630800063080391
InversionChr630800083080397
InversionChr1087808568780938
InversionChr52251765022517840
InversionChr62921751029217722LOC_Os06g48320

No Translocation