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Mutant Information

Mutant NameFN786-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN786-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 33
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr18324780A-GHETINTERGENIC
SBSChr115862234G-AHOMOINTERGENIC
SBSChr119493616T-CHOMOINTERGENIC
SBSChr120456357C-THOMOINTERGENIC
SBSChr210867285A-GHETINTERGENIC
SBSChr211535329T-AHOMOINTERGENIC
SBSChr221064027A-GHETINTERGENIC
SBSChr223607059A-CHETUTR_5_PRIME
SBSChr234768141G-CHOMOINTERGENIC
SBSChr44761374C-AHOMOINTERGENIC
SBSChr46350233T-CHETINTERGENIC
SBSChr411830795C-THETINTERGENIC
SBSChr420299021A-THETINTERGENIC
SBSChr56336268G-THETINTERGENIC
SBSChr56784299T-CHETINTERGENIC
SBSChr58117495C-AHETINTRON
SBSChr510918245C-THETINTERGENIC
SBSChr516378789C-THETINTERGENIC
SBSChr529257552G-AHETINTERGENIC
SBSChr529257553T-AHETINTERGENIC
SBSChr617115600T-CHETINTERGENIC
SBSChr630435943C-THETINTRON
SBSChr712298513G-AHETINTERGENIC
SBSChr714901129C-THETUTR_5_PRIME
SBSChr722027589C-THOMOINTERGENIC
SBSChr818391490G-CHOMOINTERGENIC
SBSChr1017109527G-AHETINTERGENIC
SBSChr1018852446T-AHETNON_SYNONYMOUS_CODINGLOC_Os10g35280
SBSChr117392568C-THETINTRON
SBSChr1111308733T-CHOMOSYNONYMOUS_CODING
SBSChr1111974037C-THOMOINTRON
SBSChr1127304108G-AHOMOINTERGENIC
SBSChr1226423959A-GHETINTERGENIC

Deletions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr51961471961536LOC_Os05g01300
DeletionChr44634904634922
DeletionChr11788060804414163543
DeletionChr81664924166493612
DeletionChr23773161377319433
DeletionChr123947113394712310LOC_Os12g07810
DeletionChr124459637445964811LOC_Os12g08725
DeletionChr45661877566190831LOC_Os04g10420
DeletionChr563720016390000180003
DeletionChr11731571773157214
DeletionChr183520018362000100002
DeletionChr118966349896636011
DeletionChr9918682991868334
DeletionChr1011242403112424118
DeletionChr111366579114359336935413
DeletionChr61298062612996734161083
DeletionChr2135628221356285230
DeletionChr21461891214619492580
DeletionChr82002014820020265117
DeletionChr320880338208803468
DeletionChr122228300023141538858538130
DeletionChr222986771229867787
DeletionChr1126413963264139663
DeletionChr7278010522780109745
DeletionChr528776362287763664
DeletionChr529363164293631717
DeletionChr3297927252979273712
DeletionChr232613286326132871LOC_Os02g53280
DeletionChr1370268583702687921LOC_Os01g63820

Insertions: 7
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr330434909304349124
InsertionChr71455532145554312
InsertionChr11719266471926663
InsertionChr330434921304349233
InsertionChr114275371142753722
InsertionChr221772174217721752
InsertionChr9428955242895521

Inversions: 8
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr563712156407170
InversionChr563898286408146
InversionChr5640718512999895
InversionChr5640814212999882
InversionChr21207738617190738LOC_Os02g29030
InversionChr122228301523197212LOC_Os12g37780
InversionChr122314153623197080LOC_Os12g37780
InversionChr13029929330470106

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr329549601Chr214618916LOC_Os03g51620