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Mutant Information

Mutant NameFN1031-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1031-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 49
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110524216T-AHETINTERGENIC
SBSChr110567945C-THETINTERGENIC
SBSChr110660038C-THETUTR_5_PRIME
SBSChr115793169T-GHOMOINTRON
SBSChr134919998G-CHETINTERGENIC
SBSChr26579241T-CHETINTRON
SBSChr229970496C-THETINTERGENIC
SBSChr3688287C-THETINTERGENIC
SBSChr37731848C-AHETINTERGENIC
SBSChr39839413C-THETINTERGENIC
SBSChr322811533C-THOMOINTERGENIC
SBSChr328501288G-AHETINTRON
SBSChr329805508T-CHETINTERGENIC
SBSChr332893619G-CHETINTERGENIC
SBSChr41032517G-AHETSYNONYMOUS_CODING
SBSChr421321545A-GHETINTERGENIC
SBSChr427091154A-GHETINTERGENIC
SBSChr435496158T-AHETINTERGENIC
SBSChr53579783C-THOMOINTERGENIC
SBSChr59758195T-GHETINTERGENIC
SBSChr526876380T-CHETINTERGENIC
SBSChr61428342T-AHETINTERGENIC
SBSChr610384740C-GHETINTERGENIC
SBSChr622467073G-AHETNON_SYNONYMOUS_CODINGLOC_Os06g37990
SBSChr718735941G-AHETINTERGENIC
SBSChr837969A-THOMOINTRON
SBSChr81031828G-AHOMOINTERGENIC
SBSChr86307654C-AHOMOINTRON
SBSChr819319727G-AHETINTERGENIC
SBSChr827061567T-CHETINTERGENIC
SBSChr94107808C-GHOMOINTERGENIC
SBSChr96207036T-CHETNON_SYNONYMOUS_CODINGLOC_Os09g11190
SBSChr98720776G-THOMOINTRON
SBSChr914092171T-CHETINTERGENIC
SBSChr103169012C-THETINTERGENIC
SBSChr104200105C-THETINTERGENIC
SBSChr106649590T-AHETINTERGENIC
SBSChr109036224G-AHETSPLICE_SITE_REGION
SBSChr1010778331T-AHETINTERGENIC
SBSChr111171411G-AHETINTERGENIC
SBSChr1110562486C-THETINTERGENIC
SBSChr1112905866C-AHETINTERGENIC
SBSChr1113507536A-GHETINTERGENIC
SBSChr1118058099C-THETINTERGENIC
SBSChr121236506T-CHETSPLICE_SITE_REGION
SBSChr129389702A-GHOMOINTERGENIC
SBSChr1211668465G-AHETINTRON
SBSChr1216969469T-CHETINTRON
SBSChr1221963112C-THETINTERGENIC

Deletions: 23
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr36902226902231
DeletionChr27198427198431
DeletionChr6112305011230544
DeletionChr11351941935194234LOC_Os11g07060
DeletionChr11415337141533765
DeletionChr64315919431594021LOC_Os06g08660
DeletionChr65166579516660728
DeletionChr6756218475621851
DeletionChr6894346389445951132
DeletionChr10990068299006842
DeletionChr11102826851028269813LOC_Os11g18240
DeletionChr610840338108403479
DeletionChr212838851128388521
DeletionChr1113966353139663607
DeletionChr3150154131501542815
DeletionChr416041983160419874
DeletionChr718574577185745792LOC_Os07g31350
DeletionChr520223139202231401
DeletionChr122229880222299492690LOC_Os12g36440
DeletionChr1125984742259847475
DeletionChr827625588276255902
DeletionChr23038200130394000120003
DeletionChr1342089093420892819

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr717069001170690022
InsertionChr719025978190259792
InsertionChr4314432423144325615LOC_Os04g52810image
InsertionChr1121961800219618078
InsertionChr233737920337379201
InsertionChr628897523288975231
InsertionChr820535210205352101LOC_Os08g33050image
InsertionChr823241390232413901

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr71890020318902916LOC_Os07g31800
InversionChr230045958303817872

Translocations: 7
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr92717447Chr724948333LOC_Os07g41610
TranslocationChr817546062Chr49601802
TranslocationChr1222298838Chr21271885LOC_Os12g36440
TranslocationChr1222299474Chr21271880LOC_Os12g36440
TranslocationChr1127840964Chr721053039
TranslocationChr629699152Chr2303934482
TranslocationChr629699894Chr230361792LOC_Os06g49000