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Mutant Information

Mutant NameFN886-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN886-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 37
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr113414082C-THETINTERGENIC
SBSChr126767897C-THOMOUTR_3_PRIME
SBSChr127976326A-GHETINTERGENIC
SBSChr1020512195G-AHOMONON_SYNONYMOUS_CODINGLOC_Os10g38386
SBSChr1115706879A-GHETSYNONYMOUS_CODING
SBSChr1122999473C-THETINTERGENIC
SBSChr1123387748C-THETINTERGENIC
SBSChr119680728G-CHETNON_SYNONYMOUS_CODINGLOC_Os11g17370
SBSChr1219541031T-CHETINTRON
SBSChr1223593232G-AHETINTRON
SBSChr210399803T-GHETINTERGENIC
SBSChr214148541T-AHETINTERGENIC
SBSChr217533721C-GHETINTRON
SBSChr217865253A-GHETINTRON
SBSChr223691737C-THETSYNONYMOUS_CODING
SBSChr227043449C-THETINTERGENIC
SBSChr310429488C-THETINTRON
SBSChr314101827T-CHETINTERGENIC
SBSChr315756800C-THETINTERGENIC
SBSChr328490869G-AHOMOINTERGENIC
SBSChr333784090A-CHETNON_SYNONYMOUS_CODINGLOC_Os03g59340
SBSChr411609536G-AHOMOINTERGENIC
SBSChr433348689C-THETINTERGENIC
SBSChr48912519A-GHOMOSYNONYMOUS_CODING
SBSChr516929493G-AHETINTRON
SBSChr528797131T-AHETINTRON
SBSChr622973955A-GHETINTERGENIC
SBSChr624280416T-AHETSYNONYMOUS_CODING
SBSChr628976808C-THETINTERGENIC
SBSChr712456921A-THOMOINTERGENIC
SBSChr712456922A-THOMOINTERGENIC
SBSChr728553160G-AHOMOINTRON
SBSChr7693725A-CHOMONON_SYNONYMOUS_CODINGLOC_Os07g02180
SBSChr79154182G-AHOMOINTRON
SBSChr815423636A-GHOMOINTERGENIC
SBSChr828217997G-AHETINTERGENIC
SBSChr919209660G-AHOMOINTERGENIC

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1227156422715662
DeletionChr5268429726843058LOC_Os05g05400
DeletionChr529398752940701826LOC_Os05g05860
DeletionChr1354745435474562
DeletionChr2399974339997507
DeletionChr44291204429122117
DeletionChr5463301846330235
DeletionChr95294523529460885LOC_Os09g09770
DeletionChr8835019183501943
DeletionChr1210696206106962137LOC_Os12g18500
DeletionChr615540733155407396
DeletionChr615707867157078692
DeletionChr216288489162884967
DeletionChr5169307611693077110
DeletionChr1118736587187365881
DeletionChr1020509471205094721
DeletionChr921703884217038895LOC_Os09g37660
DeletionChr722982172229821808
DeletionChr3244036022440361412
DeletionChr125611857256118636
DeletionChr625766305257663061
DeletionChr8283539872835401124
DeletionChr828373668283736724
DeletionChr6285381252853813611
DeletionChr1128657916286579171
DeletionChr6288766812887669716LOC_Os06g47720
DeletionChr729529257295292592
DeletionChr2314367693143678112
DeletionChr133460154334601639
DeletionChr140694301406943021

Insertions: 2
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr325828609258286168
InsertionChr6785524278552432

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr2892619010872630LOC_Os02g18660

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr34141742Chr217320663LOC_Os03g08110