Search Nipponbare


Mutant Information

Mutant NameFN1572-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1572-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000346 (Tiller number) = Normal (Between 75% and 125%)
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 39
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr117317010C-GHETINTRON
SBSChr122023748T-GHETNON_SYNONYMOUS_CODINGLOC_Os01g39134
SBSChr123876354C-THETINTERGENIC
SBSChr134057660G-AHETSYNONYMOUS_CODING
SBSChr138220280C-THETNON_SYNONYMOUS_CODINGLOC_Os01g65810
SBSChr1015131277A-CHomoINTERGENIC
SBSChr108966168C-AHETINTERGENIC
SBSChr10965356C-THETSYNONYMOUS_CODING
SBSChr1110378174G-AHomoINTERGENIC
SBSChr1123038297C-THETINTERGENIC
SBSChr11316664C-THomoINTERGENIC
SBSChr117584810C-GHomoUTR_3_PRIME
SBSChr118201250T-AHomoINTRON
SBSChr1214030721G-CHomoNON_SYNONYMOUS_CODINGLOC_Os12g24550
SBSChr1215304766G-AHomoINTERGENIC
SBSChr1225858661C-THETINTERGENIC
SBSChr220530797C-THETSYNONYMOUS_CODING
SBSChr221450013T-CHETNON_SYNONYMOUS_CODINGLOC_Os02g35690
SBSChr223844830G-AHomoINTERGENIC
SBSChr23756077C-GHETINTERGENIC
SBSChr28384036C-THomoINTERGENIC
SBSChr28402922G-AHomoSTOP_GAINEDLOC_Os02g15070
SBSChr314735242G-AHETINTRON
SBSChr314735244G-AHETINTRON
SBSChr325218515A-THomoINTERGENIC
SBSChr32702327A-GHETINTERGENIC
SBSChr410376462A-GHETINTERGENIC
SBSChr410635111G-AHETINTERGENIC
SBSChr413856772A-THETNON_SYNONYMOUS_CODINGLOC_Os04g24210
SBSChr415051148G-THETINTERGENIC
SBSChr42327588G-CHETINTRON
SBSChr529652448C-THETINTERGENIC
SBSChr54602640G-THETINTRON
SBSChr5482251A-THomoINTERGENIC
SBSChr5929372T-GHomoINTRON
SBSChr75689086T-GHETINTERGENIC
SBSChr816567981A-CHETNON_SYNONYMOUS_CODINGLOC_Os08g27110
SBSChr914737212T-CHomoINTERGENIC
SBSChr918228192C-THETINTRON

Deletions: 32
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr33395643395651
DeletionChr11105267410526751
DeletionChr7140593314059341LOC_Os07g03520
DeletionChr3245929324593007
DeletionChr3262922926292356
DeletionChr6390374039037411LOC_Os06g08070
DeletionChr11394917239491731
DeletionChr10401132440113284
DeletionChr108419283841930320
DeletionChr210344164103441739
DeletionChr211781594117815962LOC_Os02g20010
DeletionChr911963444119634451
DeletionChr815056860150568622
DeletionChr1115445916154459182LOC_Os11g26880
DeletionChr315930731159307354
DeletionChr115980148159801491
DeletionChr1116278872162788742
DeletionChr417509994175099973LOC_Os04g29450
DeletionChr118103534181035384
DeletionChr51826100118301000400007
DeletionChr1220308012203082019
DeletionChr422444168224441779
DeletionChr1242478042424782319
DeletionChr426280502262805119
DeletionChr626324330263243322
DeletionChr326651621266516232LOC_Os03g47120
DeletionChr1126802247268022481LOC_Os11g44340
DeletionChr527640846276408471
DeletionChr527640847276408481
DeletionChr3280592352805924510
DeletionChr231095427310954292
DeletionChr335435131354362731142

Insertions: 22
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr126424691264246911
InsertionChr1576370357637042
InsertionChr1120878014208780152
InsertionChr11952167095216734
InsertionChr1221983154219831563
InsertionChr12767053176705311
InsertionChr2184601581846020346
InsertionChr316351803163518031
InsertionChr318983750189837523
InsertionChr321887146218871472
InsertionChr325164238251642392
InsertionChr4206104922061056675LOC_Os04g34030image
InsertionChr422587228225872281LOC_Os04g37960image
InsertionChr424275655242756562
InsertionChr426317313263173131
InsertionChr519846466198464661
InsertionChr5272269102722698071
InsertionChr618938673189386731
InsertionChr64484914484911
InsertionChr712237763122377631
InsertionChr723315021233150211
InsertionChr914737227147372271

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr22037342220528420
InversionChr32666844426909289
InversionChr32666845626909293

No Translocation