Search Nipponbare


Mutant Information

Mutant NameFN1375-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1375-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) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 48
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr130545214T-CHETINTERGENIC
SBSChr139828384G-AHOMOSYNONYMOUS_CODING
SBSChr19934064A-THETNON_SYNONYMOUS_CODINGLOC_Os01g17260
SBSChr1016391620C-GHETINTRON
SBSChr107944190G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g15150
SBSChr1117807847C-THETINTERGENIC
SBSChr11662654C-AHOMOINTERGENIC
SBSChr1211949264G-THETINTERGENIC
SBSChr1215963108T-AHETINTRON
SBSChr121617649T-GHETINTRON
SBSChr1219170258G-THETINTERGENIC
SBSChr122476959C-THETINTERGENIC
SBSChr122558077C-AHETINTRON
SBSChr1226658657A-GHETNON_SYNONYMOUS_CODINGLOC_Os12g42884
SBSChr213758162C-AHETINTERGENIC
SBSChr219007678T-AHETINTERGENIC
SBSChr27974884T-CHETINTERGENIC
SBSChr37304193A-THOMOINTERGENIC
SBSChr414782207T-CHETINTERGENIC
SBSChr417356532G-THOMOINTERGENIC
SBSChr423944532G-THETSYNONYMOUS_CODING
SBSChr42519853C-GHETINTERGENIC
SBSChr433451752G-AHOMOINTERGENIC
SBSChr433451753C-AHOMOINTERGENIC
SBSChr512249940A-GHETINTERGENIC
SBSChr526971458A-GHOMOINTERGENIC
SBSChr527600147G-AHETINTERGENIC
SBSChr529197817T-GHOMOINTERGENIC
SBSChr529304999A-THOMOINTERGENIC
SBSChr529335102T-CHOMOINTERGENIC
SBSChr54074026T-AHOMOINTERGENIC
SBSChr614589792A-THETUTR_3_PRIME
SBSChr615797899G-AHETINTERGENIC
SBSChr622522070G-AHETINTERGENIC
SBSChr66430180G-AHETINTERGENIC
SBSChr72044935T-CHETINTERGENIC
SBSChr724587982G-THETINTERGENIC
SBSChr818053872C-THOMOINTERGENIC
SBSChr818909122C-THOMOSYNONYMOUS_CODING
SBSChr819865365T-AHOMONON_SYNONYMOUS_CODINGLOC_Os08g32020
SBSChr827177T-CHETINTRON
SBSChr910907914G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g17830
SBSChr920380044G-AHOMOINTRON
SBSChr920895511A-CHOMOSYNONYMOUS_CODING
SBSChr921950799T-AHETINTRON
SBSChr93533461G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g07220
SBSChr97851872C-AHETNON_SYNONYMOUS_CODINGLOC_Os09g13540
SBSChr99247880T-AHETINTERGENIC

Deletions: 23
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr8245992824599291
DeletionChr2307233230723375LOC_Os02g06150
DeletionChr10356703835670446LOC_Os10g06830
DeletionChr450500015098000480008
DeletionChr11565048356504852
DeletionChr178150017844000290005
DeletionChr2923712792371303LOC_Os02g16240
DeletionChr611542261115422643
DeletionChr212603619126036245
DeletionChr1214855491148554943
DeletionChr614883013148830141
DeletionChr5148897011488973635LOC_Os05g25610
DeletionChr1216764341167643421
DeletionChr317087486170874882
DeletionChr1017671260176712633
DeletionChr221043405210434116
DeletionChr821354304213543084LOC_Os08g34060
DeletionChr1222757825227578261
DeletionChr825027577250275792
DeletionChr626351432263514331
DeletionChr428031005280310094
DeletionChr333257244332572517
DeletionChr434452994344547451751LOC_Os04g57860

Insertions: 6
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1119576681195766833
InsertionChr1128862757288627593
InsertionChr2185880401858805011
InsertionChr631029553310295542
InsertionChr6632596663259716
InsertionChr912624213126242142

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr21164827011739624LOC_Os02g19950
InversionChr21429182014306525LOC_Os02g24660
InversionChr22112615421233038
InversionChr630866796310840382

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr114925773Chr519143982
TranslocationChr98410983Chr17845587
TranslocationChr98411259Chr17814831LOC_Os09g14220
TranslocationChr314481022Chr178445662
TranslocationChr314481023Chr17845535LOC_Os03g25340
TranslocationChr724229874Chr3255194132
TranslocationChr630866804Chr4344529962
TranslocationChr631084046Chr434454801LOC_Os06g51320