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Mutant Information

Mutant NameFN508-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN508-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 30
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr120275474C-THETINTERGENIC
SBSChr120987456A-GHETINTERGENIC
SBSChr120987457A-THETINTERGENIC
SBSChr126681081C-THETINTERGENIC
SBSChr142258110G-AHETINTERGENIC
SBSChr1016372939G-AHETSYNONYMOUS_CODING
SBSChr1016607758C-AHOMOINTERGENIC
SBSChr1020785914T-AHETINTERGENIC
SBSChr1111912521A-THETINTRON
SBSChr1118365634C-THETINTERGENIC
SBSChr1124814762T-CHETINTERGENIC
SBSChr1125295409T-AHETINTERGENIC
SBSChr127189973C-THETINTERGENIC
SBSChr127811027C-THETINTERGENIC
SBSChr229100753T-GHETSYNONYMOUS_CODING
SBSChr31189726C-GHETINTERGENIC
SBSChr324739053C-THOMOINTERGENIC
SBSChr334352986G-AHETINTERGENIC
SBSChr35257569C-THETINTRON
SBSChr416732583A-THETINTRON
SBSChr515470498A-GHETINTERGENIC
SBSChr518718382G-THETINTERGENIC
SBSChr612672722C-THOMOINTERGENIC
SBSChr617652576T-AHOMOINTERGENIC
SBSChr628604747C-GHOMONON_SYNONYMOUS_CODINGLOC_Os06g47170
SBSChr65687717C-THETINTERGENIC
SBSChr77213071G-THOMOINTERGENIC
SBSChr78437178G-THOMOSYNONYMOUS_CODING
SBSChr913805119C-GHOMOINTRON
SBSChr99083723T-AHETINTERGENIC

Deletions: 16
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr112098722098742
DeletionChr4653535065353511LOC_Os04g11910
DeletionChr7673031767303258
DeletionChr614007687140076925
DeletionChr1114719947147199525
DeletionChr21767499017675202212LOC_Os02g29710
DeletionChr419680785196807949LOC_Os04g32650
DeletionChr5210144942101450511
DeletionChr121531203215312074
DeletionChr821805141218051421
DeletionChr1122526410225264111
DeletionChr824764198247642013
DeletionChr224965671249656743
DeletionChr125519002255190075
DeletionChr4271641002716411717
DeletionChr137299528372995302

Insertions: 4
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr114632859146328624
InsertionChr1126129615261296162
InsertionChr6664510066451001
InsertionChr7322355832235614

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr452607627091682

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1212101157Chr117417177