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Mutant Information

Mutant NameFN1506-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1506-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • TO:0000346 (Tiller number) = Normal (Between 75% and 125%)
  • TO:0000430 (Germination Rate) = Low (Between 25% and 75%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 52
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110531805T-GHETINTERGENIC
SBSChr1301642G-THETINTERGENIC
SBSChr135910261G-AHETINTERGENIC
SBSChr137940785G-THETINTERGENIC
SBSChr140358435A-GHETINTRON
SBSChr140753029A-THETINTERGENIC
SBSChr1116118085A-GHETINTERGENIC
SBSChr1118780010A-GHETINTRON
SBSChr112189572T-AHETINTERGENIC
SBSChr113159601G-THETINTERGENIC
SBSChr113601472C-THETINTERGENIC
SBSChr115969174C-THETNON_SYNONYMOUS_CODINGLOC_Os11g10820
SBSChr118660674C-AHETINTERGENIC
SBSChr1217881374G-AHETINTERGENIC
SBSChr1222997301C-THETSTOP_GAINEDLOC_Os12g37470
SBSChr1225676880G-AHETINTERGENIC
SBSChr127490368G-AHETINTERGENIC
SBSChr128824483T-CHETUTR_3_PRIME
SBSChr212119369G-AHETINTERGENIC
SBSChr214147567C-AHETINTERGENIC
SBSChr226882862A-GHETINTERGENIC
SBSChr317668128C-AHETINTERGENIC
SBSChr321356150T-CHomoINTRON
SBSChr324080178G-AHomoNON_SYNONYMOUS_CODINGLOC_Os03g43160
SBSChr329780382C-THETINTERGENIC
SBSChr330938442T-CHETINTRON
SBSChr331578634A-THETINTERGENIC
SBSChr334832667T-AHETINTERGENIC
SBSChr37841719C-THETINTRON
SBSChr421055497G-THETINTERGENIC
SBSChr47579217G-THETINTRON
SBSChr510704413A-THETINTERGENIC
SBSChr611882240G-AHETINTERGENIC
SBSChr617652576T-AHomoINTERGENIC
SBSChr628532765G-AHETINTRON
SBSChr628565191C-THETINTERGENIC
SBSChr628604747C-GHomoNON_SYNONYMOUS_CODINGLOC_Os06g47170
SBSChr64329662G-THETINTERGENIC
SBSChr716991746C-AHETINTERGENIC
SBSChr728682892C-THETINTERGENIC
SBSChr77644064C-THETINTERGENIC
SBSChr7786271A-THomoINTERGENIC
SBSChr814728141C-THETNON_SYNONYMOUS_CODINGLOC_Os08g24390
SBSChr822902793G-THETINTERGENIC
SBSChr825137412T-AHETINTERGENIC
SBSChr825137416G-THETINTERGENIC
SBSChr915927592G-THETINTRON
SBSChr915927594G-THETINTRON
SBSChr916508344G-AHETSYNONYMOUS_CODING
SBSChr97410020C-AHETINTERGENIC
SBSChr97783969G-THETINTERGENIC
SBSChr97847293C-THomoINTERGENIC

Deletions: 24
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1126871912687201
DeletionChr13663176366318711
DeletionChr7402815540281572
DeletionChr12444262944426301
DeletionChr9912232991223334
DeletionChr69563001976400020100021
DeletionChr11993096299309686
DeletionChr1121658051216581510
DeletionChr112661856126618571
DeletionChr313152831131528321
DeletionChr313876671138766721
DeletionChr716244771162447721
DeletionChr9165080571650807013
DeletionChr9168352271683525124LOC_Os09g27660
DeletionChr1117624532176245375
DeletionChr520982187209821881
DeletionChr1121760683217606841
DeletionChr1021903152219031531
DeletionChr2219572392195725415
DeletionChr822592262225922675
DeletionChr1222595978225959791
DeletionChr2237999232379993310
DeletionChr1247420462474209145LOC_Os01g43290
DeletionChr227427059274270612

Insertions: 14
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1496749149674966
InsertionChr10132841413284141
InsertionChr1124526983245269842
InsertionChr1216822894168228952
InsertionChr220036593200365986
InsertionChr226377565263775684
InsertionChr4121439231214396442
InsertionChr4195044319504431
InsertionChr514255770142557701
InsertionChr618644092186440921
InsertionChr712374112123741154
InsertionChr814632082146320832
InsertionChr8184334121843342312LOC_Os08g30010image
InsertionChr8288466528846651

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr11161139913232394LOC_Os01g20830
InversionChr111611819123353882
InversionChr41320177414870565LOC_Os04g25660
InversionChr716240815163456202

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr65549235Chr528600192LOC_Os05g49840
TranslocationChr65558136Chr5286001792