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Mutant Information

Mutant NameFN4559-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4559-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 39
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr12600344G-CHETINTRON
SBSChr17722633T-GHETINTERGENIC
SBSChr119857876G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g35860
SBSChr128962461C-THOMOINTERGENIC
SBSChr23161237G-AHETINTERGENIC
SBSChr23161238C-AHETINTERGENIC
SBSChr24555036T-AHETINTERGENIC
SBSChr215935660T-AHETNON_SYNONYMOUS_CODINGLOC_Os02g27110
SBSChr218371424G-AHETINTERGENIC
SBSChr227350930T-AHETINTERGENIC
SBSChr227350931G-AHETINTERGENIC
SBSChr235286640T-GHETINTERGENIC
SBSChr36927330G-THETINTERGENIC
SBSChr324488907G-THETSYNONYMOUS_CODING
SBSChr325251888A-THETSTOP_GAINEDLOC_Os03g44780
SBSChr328984926A-GHOMOINTERGENIC
SBSChr334527297T-AHETINTRON
SBSChr334527298C-AHETINTRON
SBSChr49082998C-THOMOINTERGENIC
SBSChr49925561A-GHOMOINTERGENIC
SBSChr417881431G-THOMOINTERGENIC
SBSChr427476143C-GHETINTERGENIC
SBSChr430276368G-THETINTERGENIC
SBSChr515772829T-AHOMOINTRON
SBSChr518522639T-AHOMOINTERGENIC
SBSChr69388789G-AHETINTERGENIC
SBSChr74194003A-CHOMOINTRON
SBSChr714637525C-THOMOINTERGENIC
SBSChr89156339C-GHETNON_SYNONYMOUS_CODINGLOC_Os08g15120
SBSChr99549556T-CHETINTERGENIC
SBSChr919405645C-THETINTERGENIC
SBSChr921053815C-GHETUTR_3_PRIME
SBSChr104351344G-AHETINTERGENIC
SBSChr108506780A-GHETUTR_3_PRIME
SBSChr114783224A-THOMOINTERGENIC
SBSChr119582746T-AHOMONON_SYNONYMOUS_CODINGLOC_Os11g17200
SBSChr1111685467T-AHOMOUTR_3_PRIME
SBSChr1116225391A-GHETINTERGENIC
SBSChr1124763424G-AHOMOINTERGENIC

Deletions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr6123422512342261
DeletionChr12226935522693649
DeletionChr1233868823386891
DeletionChr3239198423919851
DeletionChr10456599745660014
DeletionChr12668556466855662LOC_Os12g12180
DeletionChr9676020367602096LOC_Os09g12000
DeletionChr4993517999351834
DeletionChr1111501358115013591
DeletionChr113229786132297937LOC_Os01g23560
DeletionChr413435277134352858
DeletionChr614215155142151561
DeletionChr71436600114383000170002
DeletionChr6146704131467043724
DeletionChr12149208381492085012
DeletionChr614964001150610009700022
DeletionChr61508100115109000280005
DeletionChr715083234150832373
DeletionChr716657740166577411
DeletionChr1119049862190498653
DeletionChr419122096191221026
DeletionChr119937879199378812
DeletionChr1120624971206249721LOC_Os11g35160
DeletionChr222550444225504451
DeletionChr223351549233515534
DeletionChr827625588276255902
DeletionChr529664552296645531
DeletionChr430654714306547151

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr112153934121539341
InsertionChr223044425230444251
InsertionChr63827733827742
InsertionChr621044257210442571
InsertionChr728875945288759451
InsertionChr12301779030177912
InsertionChr130751617307516171
InsertionChr132653945326539451
InsertionChr212008374120083741
InsertionChr3531355553135551
InsertionChr331883446318834461
InsertionChr411977217119772171
InsertionChr4199965981999666265
InsertionChr566615866619942
InsertionChr611000810110008101
InsertionChr8669992566999251
InsertionChr9116288741162894471
InsertionChr10596123959612391
InsertionChr12483516248351632

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr629535991305209692
InversionChr33107390131169887

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr89045833Chr215080072LOC_Os02g15950
TranslocationChr1012017585Chr613843614LOC_Os10g23050
TranslocationChr1012017733Chr615108779LOC_Os10g23050
TranslocationChr1220230683Chr224154289