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Mutant Information

Mutant NameFN4455-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4455-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 51
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr114371180C-THETSTOP_GAINEDLOC_Os01g25402
SBSChr116373511T-CHETINTERGENIC
SBSChr137228803C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g64080
SBSChr138766484C-THETINTERGENIC
SBSChr142957774G-THOMOINTERGENIC
SBSChr1589355T-CHETINTRON
SBSChr15931762A-GHETINTRON
SBSChr18117322T-AHETINTRON
SBSChr1021828800A-CHETINTERGENIC
SBSChr108109301T-AHETINTERGENIC
SBSChr108109308A-THETINTERGENIC
SBSChr1110628099C-THETINTERGENIC
SBSChr111145132C-THOMOINTERGENIC
SBSChr1113576720G-CHOMOINTERGENIC
SBSChr1125650243T-GHOMOSPLICE_SITE_REGION
SBSChr119812976G-AHOMOINTERGENIC
SBSChr1213998496C-AHETSYNONYMOUS_CODING
SBSChr1219319945C-THETINTRON
SBSChr213457129T-GHETNON_SYNONYMOUS_CODINGLOC_Os02g22570
SBSChr217500435A-CHETINTRON
SBSChr226260275C-GHETINTERGENIC
SBSChr232407558T-AHETSYNONYMOUS_CODING
SBSChr232407559C-AHETNON_SYNONYMOUS_CODINGLOC_Os02g52970
SBSChr232674295G-AHETINTERGENIC
SBSChr29875409A-GHETINTERGENIC
SBSChr310637413T-AHOMOINTERGENIC
SBSChr317334041G-CHETINTERGENIC
SBSChr319063180G-CHETINTRON
SBSChr330412608T-CHETINTERGENIC
SBSChr412871873G-AHOMOINTERGENIC
SBSChr414369411A-GHOMOINTERGENIC
SBSChr418857907T-AHETINTERGENIC
SBSChr429892861G-AHETINTERGENIC
SBSChr432542191A-GHETINTERGENIC
SBSChr433840511T-CHETINTRON
SBSChr514737874A-GHOMOINTERGENIC
SBSChr519448616C-AHOMOINTERGENIC
SBSChr522647990G-AHOMOINTERGENIC
SBSChr522647991C-AHOMOINTERGENIC
SBSChr528696161C-THOMOINTRON
SBSChr54001220G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g07490
SBSChr59715068T-CHETINTERGENIC
SBSChr68739357A-THOMOINTERGENIC
SBSChr721422251G-AHETINTERGENIC
SBSChr76396602T-GHETINTERGENIC
SBSChr812962956A-GHOMOINTRON
SBSChr822515831G-AHETSYNONYMOUS_CODING
SBSChr83808339T-CHETINTRON
SBSChr917198216A-GHETNON_SYNONYMOUS_CODINGLOC_Os09g28330
SBSChr94011057G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g07890
SBSChr9713017T-CHETINTERGENIC

Deletions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr9197505819750624
DeletionChr2446846344684641
DeletionChr14666001468500019000LOC_Os01g09246
DeletionChr5473705247370608
DeletionChr6539157753915825
DeletionChr86176925617695833
DeletionChr1654065165406543
DeletionChr6943674694367559
DeletionChr6988182498818295LOC_Os06g17040
DeletionChr710738885107388861
DeletionChr612151612121516131LOC_Os06g21030
DeletionChr212155378121553791
DeletionChr2134142901341430111
DeletionChr913652558136525591
DeletionChr8140865761408666286
DeletionChr414495633144956341
DeletionChr1216307086163070871
DeletionChr1116655243166552485
DeletionChr1117164162171641653
DeletionChr517496967174969681
DeletionChr318917965189179661
DeletionChr119534277195342781
DeletionChr4252203792522044162
DeletionChr1226151260261512611
DeletionChr628495207284952092
DeletionChr629723571297235732
DeletionChr329966319299663201
DeletionChr332937915329379161
DeletionChr142158212421582131

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1110655611065561
InsertionChr10715975471597552LOC_Os10g12808image
InsertionChr1218990627189906282
InsertionChr12807540480754052
InsertionChr231408220314082201
InsertionChr2924422092442234
InsertionChr323561629235616291
InsertionChr330434909304349102
InsertionChr335435881354358811
InsertionChr417209076172090761
InsertionChr4284314428431452
InsertionChr514653158146531581
InsertionChr622905987229059871
InsertionChr6385019738501971
InsertionChr7646054564605451LOC_Os07g11680image
InsertionChr815859020158590201
InsertionChr823437205234372051
InsertionChr8726609672660972
InsertionChr918576995185769962

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr386453348645518
InversionChr51075453710820282
InversionChr51075454210820279
InversionChr31472608014726278
InversionChr13490237734902549LOC_Os01g60340

No Translocation