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Mutant Information

Mutant NameFN-278 [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN-278 Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 46
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr11448524A-GHETSPLICE_SITE_REGION
SBSChr118254458C-THETINTRON
SBSChr126418162G-THOMOINTERGENIC
SBSChr17106171T-AHETINTRON
SBSChr17106173T-AHETINTRON
SBSChr10499474C-AHETINTERGENIC
SBSChr111173029C-THETINTERGENIC
SBSChr111267401A-THETNON_SYNONYMOUS_CODINGLOC_Os11g03360
SBSChr111267402A-THETNON_SYNONYMOUS_CODINGLOC_Os11g03360
SBSChr1113143512T-GHETNON_SYNONYMOUS_CODINGLOC_Os11g22850
SBSChr1113527008G-AHETINTERGENIC
SBSChr1116347208T-AHETNON_SYNONYMOUS_CODINGLOC_Os11g28400
SBSChr1120494484T-AHETINTERGENIC
SBSChr113455944C-THETSYNONYMOUS_CODING
SBSChr1217333924C-THETINTERGENIC
SBSChr1219808219A-GHOMOUTR_3_PRIME
SBSChr1219808277C-THOMOUTR_3_PRIME
SBSChr1225170572G-AHETINTRON
SBSChr213945668G-CHETINTERGENIC
SBSChr24203124C-THETINTERGENIC
SBSChr27608222G-AHOMOINTERGENIC
SBSChr28047764C-THETINTRON
SBSChr317954274G-THOMOINTERGENIC
SBSChr325296654C-AHETINTERGENIC
SBSChr333686502G-AHOMOINTRON
SBSChr412169523T-AHETINTERGENIC
SBSChr47357479T-CHETINTRON
SBSChr49617658T-GHETINTERGENIC
SBSChr519521954T-GHETINTERGENIC
SBSChr520228414T-AHETINTRON
SBSChr5241623G-AHETSTOP_GAINEDLOC_Os05g01410
SBSChr57292286G-THETINTERGENIC
SBSChr59823778C-THETINTRON
SBSChr611320121C-THOMOINTERGENIC
SBSChr617364850G-AHETINTERGENIC
SBSChr620136991G-AHETINTERGENIC
SBSChr627584608G-AHETNON_SYNONYMOUS_CODINGLOC_Os06g45560
SBSChr629380150G-THETINTERGENIC
SBSChr63737863A-GHETSPLICE_SITE_REGION
SBSChr72164815G-AHETSYNONYMOUS_CODING
SBSChr818182441A-GHOMOINTERGENIC
SBSChr821650572T-CHOMOINTERGENIC
SBSChr827746761C-THOMOINTERGENIC
SBSChr85787131C-THETINTERGENIC
SBSChr86083102G-AHETINTERGENIC
SBSChr92208603T-CHOMOINTRON

Deletions: 26
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1049952749956942
DeletionChr9156611815661191
DeletionChr9185268518526938
DeletionChr9238226123822621LOC_Os09g04470
DeletionChr5537130053713088
DeletionChr5659967765996803
DeletionChr11759104675929561910
DeletionChr27608197760821518
DeletionChr611198889111988956
DeletionChr12134066451340667025
DeletionChr713898461138984632
DeletionChr616413237164132425LOC_Os06g28820
DeletionChr1117818688178186924
DeletionChr1018320925183209294
DeletionChr10189915951899161217
DeletionChr1219808560198085622
DeletionChr1120295803202958041
DeletionChr522547964225479684
DeletionChr3230611882306120214
DeletionChr12373095123731403452LOC_Os01g41870
DeletionChr524362226243622271
DeletionChr125800579258005801
DeletionChr729192113291921174
DeletionChr129851215298512161
DeletionChr129990673299906829
DeletionChr4349099823490999210LOC_Os04g58710

Insertions: 7
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1011743742117437454
InsertionChr1123208034232080363
InsertionChr11371038837103892
InsertionChr218298484182984896
InsertionChr229365387293653893LOC_Os02g47980image
InsertionChr329291431292914322
InsertionChr8565755756575604

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1022124987221614832
InversionChr1022125001221614862

Translocations: 5
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr77356401Chr139678865
TranslocationChr119031430Chr723098259
TranslocationChr119031545Chr723098251
TranslocationChr1210171784Chr217608408
TranslocationChr624301539Chr225044490