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Mutant Information

Mutant NameFN2654-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2654-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 50
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111859923C-THETINTERGENIC
SBSChr113337197T-AHETINTERGENIC
SBSChr114230251A-THETINTRON
SBSChr117041475T-AHETINTRON
SBSChr122060509C-THETINTERGENIC
SBSChr13975927G-AHETUTR_5_PRIME
SBSChr15671382C-THETUTR_5_PRIME
SBSChr1016096311T-CHETINTRON
SBSChr1016647213C-THETINTERGENIC
SBSChr1017357182G-AHETINTERGENIC
SBSChr103176816C-THETINTERGENIC
SBSChr103869787T-GHETUTR_3_PRIME
SBSChr108683184C-THETINTRON
SBSChr109698715T-CHETINTERGENIC
SBSChr109698716A-GHETINTERGENIC
SBSChr111617203C-THETSYNONYMOUS_CODING
SBSChr1119655329C-GHETINTRON
SBSChr1120050670G-AHETINTERGENIC
SBSChr1210047192G-AHETINTERGENIC
SBSChr1216757674G-AHETINTRON
SBSChr121933607A-CHETNON_SYNONYMOUS_CODINGLOC_Os12g04550
SBSChr1223853668G-AHETINTERGENIC
SBSChr1226802803C-THETINTERGENIC
SBSChr213273669C-THETINTERGENIC
SBSChr22576372C-AHOMONON_SYNONYMOUS_CODINGLOC_Os02g05360
SBSChr25425094A-GHOMOINTERGENIC
SBSChr26770951A-THOMOINTERGENIC
SBSChr327245734C-THETINTRON
SBSChr411152782G-THETINTERGENIC
SBSChr416021497C-AHETINTERGENIC
SBSChr416906017G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g28550
SBSChr422323938C-GHOMOSYNONYMOUS_CODING
SBSChr46211041C-AHETINTERGENIC
SBSChr48251075C-THOMOINTERGENIC
SBSChr518951325A-GHETINTERGENIC
SBSChr52439330A-CHETINTERGENIC
SBSChr524914904A-GHETINTERGENIC
SBSChr527801535T-CHETINTRON
SBSChr55775765C-THETINTERGENIC
SBSChr611953211A-GHETINTRON
SBSChr628383275G-AHETINTERGENIC
SBSChr66297141T-CHETINTRON
SBSChr66297149G-AHETINTRON
SBSChr811868671G-AHETINTERGENIC
SBSChr912188597G-AHETINTERGENIC
SBSChr914471600C-THETINTERGENIC
SBSChr921876495A-THETINTRON
SBSChr921876498A-GHETINTRON
SBSChr99658128C-GHOMOINTRON
SBSChr99658135A-GHOMOINTRON

Deletions: 34
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr22139942139995
DeletionChr482115282122573LOC_Os04g02340
DeletionChr7148078614807871
DeletionChr6171056017105611
DeletionChr32766382276641634
DeletionChr1305998030599822
DeletionChr11397111839711224LOC_Os11g07790
DeletionChr6474570647457093
DeletionChr25326961532697211LOC_Os02g10160
DeletionChr35617505561751510
DeletionChr6575185857518602
DeletionChr6575218957521956
DeletionChr39339504933952824
DeletionChr810774837107748381
DeletionChr9113961161139612711
DeletionChr1011705248117052524
DeletionChr712872595128725961
DeletionChr51485300114909000559999
DeletionChr1014889519148895223LOC_Os10g28590
DeletionChr717002361170023698
DeletionChr1182771241827719672
DeletionChr219844275198442772LOC_Os02g33400
DeletionChr1019937088199370902
DeletionChr522987841229878443
DeletionChr523758506237585115LOC_Os05g40440
DeletionChr724474030244740355
DeletionChr624873024248730251
DeletionChr126253062262530686
DeletionChr327783836277838426
DeletionChr828150708281507102
DeletionChr529081508290815146
DeletionChr333314658333146657
DeletionChr233827389338273923LOC_Os02g55230
DeletionChr435285173352851741

Insertions: 10
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1176346331763471381
InsertionChr18483844848390966
InsertionChr11121216131212169078
InsertionChr11931132193113222
InsertionChr223151472231514732
InsertionChr223969407239694071
InsertionChr5969817696981761
InsertionChr7242401032424019694
InsertionChr815537211155372111
InsertionChr817293658172936614

No Inversion

Translocations: 6
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr532916Chr323639478
TranslocationChr97057099Chr131953042
TranslocationChr1117836748Chr1012209849
TranslocationChr1122532682Chr55767275LOC_Os05g10590
TranslocationChr324883120Chr28852240
TranslocationChr625585467Chr325151135LOC_Os03g44670