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Mutant Information

Mutant NameFN4367-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4367-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 45
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr13039648G-THOMOSYNONYMOUS_CODING
SBSChr13039649A-THOMONON_SYNONYMOUS_CODINGLOC_Os01g06450
SBSChr13039650G-THOMONON_SYNONYMOUS_CODINGLOC_Os01g06450
SBSChr123576207T-GHOMOUTR_3_PRIME
SBSChr137445938C-THOMOINTERGENIC
SBSChr140707749A-THOMONON_SYNONYMOUS_CODINGLOC_Os01g70290
SBSChr23579220G-AHOMOINTERGENIC
SBSChr217353438C-THETINTERGENIC
SBSChr224550782T-AHETINTERGENIC
SBSChr226492785T-AHETINTERGENIC
SBSChr228344731A-THETINTERGENIC
SBSChr228344732G-THETINTERGENIC
SBSChr228344738G-AHETINTERGENIC
SBSChr231370721G-AHETINTERGENIC
SBSChr232216610C-THOMOINTRON
SBSChr312081427G-AHETNON_SYNONYMOUS_CODINGLOC_Os03g21180
SBSChr312387011C-THETINTERGENIC
SBSChr322438265C-AHOMOINTERGENIC
SBSChr322439497G-AHOMOINTERGENIC
SBSChr322439500T-CHOMOINTERGENIC
SBSChr43233141G-THETSYNONYMOUS_CODING
SBSChr48991137G-AHOMOINTERGENIC
SBSChr421418064C-THETINTRON
SBSChr54078587G-CHETINTERGENIC
SBSChr55840586G-AHETINTERGENIC
SBSChr526381899A-THETSPLICE_SITE_REGION
SBSChr685756G-AHETINTERGENIC
SBSChr69884879G-AHETSYNONYMOUS_CODING
SBSChr621176543T-CHOMOINTERGENIC
SBSChr712474125C-GHETINTERGENIC
SBSChr714277244A-GHETINTRON
SBSChr726218083G-AHOMOINTRON
SBSChr726218084T-GHOMOINTRON
SBSChr727170024G-AHETINTERGENIC
SBSChr84115814T-CHOMOINTERGENIC
SBSChr818388396G-AHOMONON_SYNONYMOUS_CODINGLOC_Os08g29930
SBSChr92198992G-AHOMOINTERGENIC
SBSChr95559972C-THETINTERGENIC
SBSChr912838371T-AHETINTRON
SBSChr917544289G-AHETINTERGENIC
SBSChr918593909C-THETINTERGENIC
SBSChr1112896705G-CHETINTERGENIC
SBSChr1115131953C-GHETINTRON
SBSChr1212689944G-CHETINTERGENIC
SBSChr1223879459C-THETINTERGENIC

Deletions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr104610594610612
DeletionChr2139584213958431LOC_Os02g03420
DeletionChr122670404267043127
DeletionChr131190013132000130003
DeletionChr3761796576179672
DeletionChr6843154084315466
DeletionChr2888914788891481
DeletionChr4983024898302491LOC_Os04g17890
DeletionChr211294629112946301LOC_Os02g19330
DeletionChr713062332130623331
DeletionChr1114223087142230903
DeletionChr114355208143552102
DeletionChr4146704401467047333
DeletionChr215073924150739251
DeletionChr8216771152167714328
DeletionChr325684184256841851
DeletionChr1226458989264589912
DeletionChr826847326268473282
DeletionChr132461689324616901

Insertions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr136285096362850961
InsertionChr312144087121440871
InsertionChr727980078279800792
InsertionChr1225174117251741182
InsertionChr116890996168909961
InsertionChr2551880355188031
InsertionChr425375317253753182
InsertionChr622348467223484671
InsertionChr7130831613083249
InsertionChr7745661874566181
InsertionChr8245513724551404
InsertionChr814654201146542011LOC_Os08g24280image
InsertionChr910199407101994071
InsertionChr1111187246111872461
InsertionChr1211264955112649562
InsertionChr1211531678115316781
InsertionChr1223702161237021611

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr220962692096503LOC_Os02g04670
InversionChr91227152712351042
InversionChr13807666338076800

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr618104032Chr41508888LOC_Os06g31160