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Mutant Information

Mutant NameFN1625-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1625-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • 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: 43
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr117287349C-THETNON_SYNONYMOUS_CODINGLOC_Os01g31590
SBSChr120879771C-THETINTRON
SBSChr129472767T-CHETINTERGENIC
SBSChr142356389G-CHomoINTERGENIC
SBSChr143183354C-THETINTERGENIC
SBSChr16413835G-AHETINTRON
SBSChr101029287C-THETINTERGENIC
SBSChr1012212715C-THomoINTERGENIC
SBSChr1019691925A-CHomoSTOP_LOSTLOC_Os10g36780
SBSChr105543226A-CHETUTR_5_PRIME
SBSChr10972685A-GHETINTERGENIC
SBSChr111415562C-AHomoINTERGENIC
SBSChr111415563G-AHomoINTERGENIC
SBSChr119896751A-GHomoUTR_3_PRIME
SBSChr121093998A-THETUTR_3_PRIME
SBSChr125066445C-THETSPLICE_SITE_REGION
SBSChr127785851T-GHETINTERGENIC
SBSChr222804361C-AHETINTERGENIC
SBSChr231974734T-AHETINTERGENIC
SBSChr28150934C-AHETINTERGENIC
SBSChr36008766C-AHETNON_SYNONYMOUS_CODINGLOC_Os03g11580
SBSChr421765384G-AHomoINTERGENIC
SBSChr511346490G-THETINTRON
SBSChr514030327C-GHETINTERGENIC
SBSChr515109189C-THETINTERGENIC
SBSChr520636146C-THETINTERGENIC
SBSChr527786373C-GHETSYNONYMOUS_CODING
SBSChr623077422G-AHomoINTRON
SBSChr627404425A-CHETINTERGENIC
SBSChr627961286A-THETINTRON
SBSChr628248330T-CHETNON_SYNONYMOUS_CODINGLOC_Os06g46520
SBSChr64781945G-AHETINTERGENIC
SBSChr722124902G-AHomoINTERGENIC
SBSChr729454628C-THETINTERGENIC
SBSChr825105200C-THETNON_SYNONYMOUS_CODINGLOC_Os08g39640
SBSChr825153267C-THETINTERGENIC
SBSChr85215928A-GHETINTERGENIC
SBSChr913978047T-CHETINTERGENIC
SBSChr915568122C-AHETINTERGENIC
SBSChr918593617G-AHomoINTERGENIC
SBSChr918593618G-AHomoINTERGENIC
SBSChr9589319C-THETINTERGENIC
SBSChr96315964C-THETINTERGENIC

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr101576551576572
DeletionChr977392177398968
DeletionChr2180763618076371
DeletionChr6255472525547283
DeletionChr22867063286708017LOC_Os02g05810
DeletionChr1463151946315212
DeletionChr2469700147790008200013
DeletionChr3668467266895224850LOC_Os03g12600
DeletionChr9947997594799772
DeletionChr110088658100886657
DeletionChr91375600113823000670009
DeletionChr314715603147156041
DeletionChr3148263251482633914
DeletionChr1148870861488710418
DeletionChr915392087153920903
DeletionChr115722010157220166
DeletionChr815978684159786939
DeletionChr116290790162907911
DeletionChr816802771168027721
DeletionChr111749465917494779120
DeletionChr917678287176782881
DeletionChr918198710181987177
DeletionChr52006518020065283103LOC_Os05g33980
DeletionChr620444075204440794
DeletionChr625287126252871271
DeletionChr725348094253480962LOC_Os07g42370
DeletionChr827842126278421282
DeletionChr2321473193214733718
DeletionChr3347970863479709711
DeletionChr2348638393486385112
DeletionChr23570455235714599100472

Insertions: 15
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1107779411077795818LOC_Os01g19050image
InsertionChr111387051113870533
InsertionChr124524866245248694
InsertionChr126513763265137664
InsertionChr138401727384017271
InsertionChr123701937370197034
InsertionChr2129387791293878810
InsertionChr2935989893598992
InsertionChr318056814180568141
InsertionChr521036906210369061
InsertionChr521280846212808472
InsertionChr523445280234452812
InsertionChr6234086923408691
InsertionChr727544679275446791
InsertionChr87743957744006

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr127754491362370LOC_Os12g03470
InversionChr81881892819219172

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr61207606Chr4149571322
TranslocationChr111986111Chr140935919
TranslocationChr111986283Chr140935911
TranslocationChr124372113Chr621999589LOC_Os06g37250
TranslocationChr1113157035Chr36684690
TranslocationChr1113157045Chr36689547LOC_Os03g12600
TranslocationChr1121327648Chr325354092
TranslocationChr1127466140Chr511752869