Search Nipponbare


Mutant Information

Mutant NameFN1076-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1076-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000014 (Panicle Weight) = Normal (Between 75% and 125%)
  • 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
Phenotype Changes
(Hover to Zoom-In)
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 32
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110381556C-THETINTRON
SBSChr112130833T-AHETNON_SYNONYMOUS_CODINGLOC_Os01g21650
SBSChr123771061G-THETNON_SYNONYMOUS_CODINGLOC_Os01g41910
SBSChr125369840C-THOMOINTRON
SBSChr140502152C-THETINTRON
SBSChr1010638516A-GHETINTRON
SBSChr1016370041G-AHETINTERGENIC
SBSChr1220981599G-THETINTERGENIC
SBSChr127446959A-THETINTERGENIC
SBSChr231226574G-AHETNON_SYNONYMOUS_CODINGLOC_Os02g51050
SBSChr317146514C-GHOMOINTERGENIC
SBSChr325225033G-AHETINTERGENIC
SBSChr327067163C-THETINTERGENIC
SBSChr330904379G-AHETINTRON
SBSChr330904725A-THETINTRON
SBSChr33120045C-THOMOUTR_3_PRIME
SBSChr417086786C-THOMOINTERGENIC
SBSChr420735769C-GHOMOINTRON
SBSChr43090101G-THETNON_SYNONYMOUS_CODINGLOC_Os04g05970
SBSChr51094161C-THETNON_SYNONYMOUS_CODINGLOC_Os05g02950
SBSChr513933874A-GHOMOINTERGENIC
SBSChr518410515T-CHOMOINTERGENIC
SBSChr526215187C-THETINTERGENIC
SBSChr53801182A-GHETINTRON
SBSChr613986799C-THOMOINTERGENIC
SBSChr61681340C-THETINTERGENIC
SBSChr622418075G-THOMOINTRON
SBSChr62474429A-GHETINTERGENIC
SBSChr813068842C-AHOMOINTERGENIC
SBSChr91941112A-GHOMONON_SYNONYMOUS_CODINGLOC_Os09g03830
SBSChr920871298C-AHETINTERGENIC
SBSChr921074352C-THETSYNONYMOUS_CODING

Deletions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr2371145437114573LOC_Os02g07220
DeletionChr4427318542731883
DeletionChr7580631558063172
DeletionChr107816362781637311
DeletionChr27925107792513730
DeletionChr1210471781104717821
DeletionChr7132176341321764915
DeletionChr1113613698136137002
DeletionChr1146357741465678621012LOC_Os01g25839
DeletionChr114912452149124531
DeletionChr715064389150643901
DeletionChr10181715011817152019
DeletionChr3187150011906800035300061
DeletionChr518745726187457348
DeletionChr719576627195766281
DeletionChr322663565226635661LOC_Os03g40725
DeletionChr323568476235684826LOC_Os03g42370
DeletionChr11239743422397436018
DeletionChr625156304251563084

Insertions: 9
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr112149114121491152
InsertionChr133477026334770316
InsertionChr1225463863254638664
InsertionChr332775225327752273
InsertionChr5212834221283421
InsertionChr5631657663165816
InsertionChr722426877224268804
InsertionChr825824153258241542
InsertionChr9751438675143861

No Inversion

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr41697763Chr122958758LOC_Os01g40630
TranslocationChr411225765Chr113093223LOC_Os01g23310
TranslocationChr717250533Chr45000289LOC_Os04g09380