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Mutant Information

Mutant NameFN4402-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4402-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 42
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110828802A-THETINTERGENIC
SBSChr119800205C-THETNON_SYNONYMOUS_CODINGLOC_Os01g35740
SBSChr121710042C-THETINTERGENIC
SBSChr127137993A-THETINTERGENIC
SBSChr127539058C-GHETINTERGENIC
SBSChr1010262985C-THOMOINTERGENIC
SBSChr1012002323A-THOMOINTERGENIC
SBSChr1016919510C-THETNON_SYNONYMOUS_CODINGLOC_Os10g32210
SBSChr1018246793C-AHETSYNONYMOUS_CODING
SBSChr102290641A-THETINTRON
SBSChr10943477G-AHETINTERGENIC
SBSChr1113169618G-THETINTERGENIC
SBSChr1224302524C-AHETINTERGENIC
SBSChr12461388A-CHOMOINTERGENIC
SBSChr127556116C-THETINTERGENIC
SBSChr21238661G-AHETINTRON
SBSChr215724248C-THETNON_SYNONYMOUS_CODINGLOC_Os02g26780
SBSChr217601327C-THETSYNONYMOUS_CODING
SBSChr314247418G-AHOMOINTERGENIC
SBSChr319747713T-CHOMOINTRON
SBSChr328013903C-AHOMOINTERGENIC
SBSChr330231722C-AHETINTRON
SBSChr332312070G-AHETINTERGENIC
SBSChr41260008C-THETNON_SYNONYMOUS_CODINGLOC_Os04g03050
SBSChr42405249T-CHETINTERGENIC
SBSChr433349533C-THETINTERGENIC
SBSChr47378670T-CHETINTERGENIC
SBSChr48520812C-THOMOINTERGENIC
SBSChr528811426G-AHETINTERGENIC
SBSChr615363113A-THOMOINTRON
SBSChr617047962G-AHOMOINTERGENIC
SBSChr620085782C-THOMOSYNONYMOUS_CODING
SBSChr624660885C-THETINTERGENIC
SBSChr711481104T-CHETNON_SYNONYMOUS_CODINGLOC_Os07g19400
SBSChr717070887C-GHETNON_SYNONYMOUS_CODINGLOC_Os07g29160
SBSChr722368636A-THETINTERGENIC
SBSChr728128394G-AHETINTERGENIC
SBSChr74485686G-AHETINTRON
SBSChr77518758G-AHETINTRON
SBSChr810894552A-GHOMOINTRON
SBSChr824179869G-THETINTERGENIC
SBSChr88875671C-AHOMOINTRON

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr12956500295654343
DeletionChr2388433938843489
DeletionChr65390609539062011
DeletionChr6548568554856861
DeletionChr3574483757448425
DeletionChr8619637661963771
DeletionChr106257116625715236
DeletionChr59384304938432319
DeletionChr6948054894805557
DeletionChr7984742498474251
DeletionChr1210834771108347721
DeletionChr8116372011163726059
DeletionChr411800073118000741
DeletionChr1212046496120464971
DeletionChr2121850011241300022800030
DeletionChr111218768012187810130
DeletionChr713226920132269299LOC_Os07g23440
DeletionChr3155904011559042120
DeletionChr1015605986156059893
DeletionChr115634355156343594LOC_Os01g27960
DeletionChr815722555157225561
DeletionChr3171517441715179248
DeletionChr1017582361175823632
DeletionChr720355084203550851
DeletionChr1020611555206115561
DeletionChr1223057532230575353
DeletionChr823075918230759213
DeletionChr125823676258236771
DeletionChr232104545321045461
DeletionChr134886842348868431
DeletionChr137759437377594381

Insertions: 13
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr113695214136952141
InsertionChr117442466174424705
InsertionChr1751699375169931
InsertionChr11130952331309528149
InsertionChr1116724958167249669
InsertionChr114885318488539578
InsertionChr225797065257970651
InsertionChr325249297252492971
InsertionChr424944565249445651
InsertionChr510732526107325261
InsertionChr510776599107766024
InsertionChr525429885254298862
InsertionChr921649947216499482

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr968485676849145
InversionChr1284189678419191
InversionChr51570542115705683

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr125944357Chr718282706
TranslocationChr1113893260Chr210875028
TranslocationChr1113893261Chr210875028