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Mutant Information

Mutant NameFN1327-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1327-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000014 (Panicle Weight) = Low (Between 25% and 74%)
  • TO:0000207 (Plant height) = Normal (Between 75% and 125%)
  • TO:0000445 (Seed Number) = Low (Between 25% and 74%)
  • TO:0000639 (Seed fertility) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 32
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr139049603G-CHOMOINTERGENIC
SBSChr102039964A-CHOMOINTRON
SBSChr1114212929G-AHETINTERGENIC
SBSChr1116112098C-THETINTERGENIC
SBSChr124906677A-GHETINTRON
SBSChr128599564A-GHETINTRON
SBSChr129699801C-THETINTERGENIC
SBSChr232359566C-GHETNON_SYNONYMOUS_CODINGLOC_Os02g52930
SBSChr25318590C-AHETINTERGENIC
SBSChr29820279G-AHETNON_SYNONYMOUS_CODINGLOC_Os02g17140
SBSChr410122523G-AHETINTERGENIC
SBSChr414564992C-THETINTERGENIC
SBSChr521445796C-THETNON_SYNONYMOUS_CODINGLOC_Os05g36180
SBSChr526805522A-THETINTERGENIC
SBSChr55163619C-THETINTERGENIC
SBSChr62386149G-THETNON_SYNONYMOUS_CODINGLOC_Os06g05300
SBSChr630530507A-GHETSYNONYMOUS_CODING
SBSChr719708422G-AHOMOINTERGENIC
SBSChr74917037T-AHETINTRON
SBSChr75700379C-THETINTERGENIC
SBSChr812687840C-AHETINTRON
SBSChr812687841A-THETINTRON
SBSChr818482938T-AHETINTRON
SBSChr85537140G-AHETINTRON
SBSChr910013582A-GHETINTRON
SBSChr910019867C-THETINTRON
SBSChr910475684A-GHETINTERGENIC
SBSChr910827665C-THETINTERGENIC
SBSChr91787702A-CHETINTERGENIC
SBSChr918722414A-THOMOINTERGENIC
SBSChr95621156C-THETNON_SYNONYMOUS_CODINGLOC_Os09g10310
SBSChr96237020T-CHETINTRON

Deletions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr9131272613127271
DeletionChr6242800125220009400021
DeletionChr9289676328967718LOC_Os09g06180
DeletionChr7488554648855471
DeletionChr1249504054950625220
DeletionChr75674830567488454
DeletionChr105733338573340567
DeletionChr117746358774639234LOC_Os11g13970
DeletionChr1878194387819474
DeletionChr999578119970810129993
DeletionChr9100134991001352223LOC_Os09g16380
DeletionChr611319133113191341
DeletionChr411552039115520489
DeletionChr1114295487142954892
DeletionChr414632936146329371
DeletionChr515021356150213648
DeletionChr615720001157910007100011
DeletionChr61663800116690000520009
DeletionChr816639419166394256
DeletionChr1191298901912990414
DeletionChr8196963261969636236
DeletionChr920323231203232321LOC_Os09g34870
DeletionChr9203872752059136220408731
DeletionChr820539291205392998
DeletionChr523207468232074702
DeletionChr325160343251603518
DeletionChr11254303102543032515
DeletionChr327009891270098921

Insertions: 4
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr132044669320446691
InsertionChr138794092387940921
InsertionChr6896572689657261
InsertionChr920595580205955823

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr6252215637647092
InversionChr744257025673842LOC_Os07g08570
InversionChr7442571756830752
InversionChr32378997123886516LOC_Os03g42730
InversionChr32381027623886505

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr75673858Chr138301839LOC_Os01g65986
TranslocationChr75683052Chr1383018172
TranslocationChr711991485Chr615790652LOC_Os07g20730