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Mutant Information

Mutant NameFN2657-S-1 [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2657-S-1 Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 67
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr112075898A-THETINTERGENIC
SBSChr112129599A-GHETUTR_3_PRIME
SBSChr120150662T-CHETINTERGENIC
SBSChr124115542G-CHETINTERGENIC
SBSChr124377951G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g42830
SBSChr13131828G-THETINTERGENIC
SBSChr140423792C-THOMOINTERGENIC
SBSChr140793911A-GHETINTERGENIC
SBSChr17031170C-THETINTERGENIC
SBSChr19560623C-GHETINTERGENIC
SBSChr19856877G-AHETINTERGENIC
SBSChr10122153G-AHETINTRON
SBSChr1022751246G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g42240
SBSChr104453900C-THETINTERGENIC
SBSChr1117841574G-AHETINTERGENIC
SBSChr1214045077C-THETINTERGENIC
SBSChr1216117761C-THOMOINTERGENIC
SBSChr1216184264G-AHETSYNONYMOUS_CODING
SBSChr1220260198C-THOMONON_SYNONYMOUS_CODINGLOC_Os12g33530
SBSChr1222705168C-AHETNON_SYNONYMOUS_CODINGLOC_Os12g37050
SBSChr124407270C-AHETINTERGENIC
SBSChr127817618G-CHETINTERGENIC
SBSChr211652177G-AHETINTERGENIC
SBSChr219517941C-THOMOINTERGENIC
SBSChr235931594C-GHOMO#VALUE!
SBSChr24752019C-THETINTERGENIC
SBSChr316652106G-AHETINTERGENIC
SBSChr320569314C-AHETUTR_5_PRIME
SBSChr324784694A-GHETINTERGENIC
SBSChr329855228G-AHOMOSYNONYMOUS_CODING
SBSChr333628028T-AHETNON_SYNONYMOUS_CODINGLOC_Os03g59070
SBSChr336344507T-CHOMOINTRON
SBSChr36581337G-THETNON_SYNONYMOUS_CODINGLOC_Os03g12460
SBSChr36879711G-AHETINTERGENIC
SBSChr39517651A-THOMOINTRON
SBSChr412044000A-GHETINTERGENIC
SBSChr413091793T-CHOMOINTRON
SBSChr414201602T-AHOMOINTERGENIC
SBSChr417698948T-AHETINTERGENIC
SBSChr419462099C-THETINTERGENIC
SBSChr422697891C-AHETINTERGENIC
SBSChr433507551G-THETINTERGENIC
SBSChr517833199C-THETINTERGENIC
SBSChr55139023G-AHETINTERGENIC
SBSChr614072701C-AHETINTERGENIC
SBSChr622424098T-GHETINTERGENIC
SBSChr630713687G-THETINTERGENIC
SBSChr630713688C-THETINTERGENIC
SBSChr630713689C-THETINTERGENIC
SBSChr66824316C-THETNON_SYNONYMOUS_CODINGLOC_Os06g12590
SBSChr66824319C-THETNON_SYNONYMOUS_CODINGLOC_Os06g12590
SBSChr67316597C-AHETINTERGENIC
SBSChr67316598T-GHETINTERGENIC
SBSChr67316599A-THETINTERGENIC
SBSChr67429697G-AHETINTERGENIC
SBSChr727547363C-AHOMOINTRON
SBSChr74283338G-AHETINTERGENIC
SBSChr75554353T-CHETINTRON
SBSChr815471670C-GHETINTERGENIC
SBSChr816929054G-AHETSYNONYMOUS_CODING
SBSChr81806451C-THETINTERGENIC
SBSChr826303279C-THETINTERGENIC
SBSChr85057293T-AHETINTERGENIC
SBSChr912265040T-AHETINTRON
SBSChr913507587G-CHOMONON_SYNONYMOUS_CODINGLOC_Os09g22350
SBSChr913551576C-AHETINTERGENIC
SBSChr917580736T-AHETINTERGENIC

Deletions: 23
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr11235435323543541
DeletionChr11300199830019991
DeletionChr3414156841415691
DeletionChr9522365852236591
DeletionChr10702829370282941
DeletionChr9850163885016402
DeletionChr10877312287731264LOC_Os10g17400
DeletionChr11102808071028081710
DeletionChr3112376371123765720
DeletionChr12123021081230212214
DeletionChr914494966144949671
DeletionChr718561182185611831LOC_Os07g31340
DeletionChr222735043227350463
DeletionChr1122812858228128679
DeletionChr1248911122489115038
DeletionChr126513559265135601
DeletionChr6265848632658488320
DeletionChr726757310267573111
DeletionChr827970626279706282
DeletionChr7284380012844500069992
DeletionChr431250853312508552LOC_Os04g52560
DeletionChr334484716344847215
DeletionChr235809575358095805

Insertions: 6
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1015054067150540671
InsertionChr1214518922145189221
InsertionChr1221760065217600662
InsertionChr2293933942939341926
InsertionChr312881950128819512
InsertionChr811049434110494341

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1081068638685880
InversionChr111637670717008514

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr711781006Chr120049378
TranslocationChr1115778951Chr911329510
TranslocationChr1215976550Chr711781189
TranslocationChr1215977128Chr711780997