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Mutant Information

Mutant NameFN3211-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN3211-S 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
SBSChr112032286C-THETINTERGENIC
SBSChr113378877T-CHETINTERGENIC
SBSChr11814490T-GHETINTERGENIC
SBSChr119537963T-CHETSYNONYMOUS_CODING
SBSChr129542577G-AHETINTERGENIC
SBSChr134919998G-CHETINTERGENIC
SBSChr17545707A-GHETINTERGENIC
SBSChr19208525G-AHOMOINTRON
SBSChr1021226056G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g39710
SBSChr1022899129C-THOMONON_SYNONYMOUS_CODINGLOC_Os10g42470
SBSChr103230086C-THETSYNONYMOUS_CODING
SBSChr105085353C-THETINTRON
SBSChr111221348G-AHETINTERGENIC
SBSChr113150608C-THETINTRON
SBSChr1212303348A-GHETINTERGENIC
SBSChr1220787002T-CHOMOINTRON
SBSChr1220839151T-CHOMOINTRON
SBSChr1221080041G-AHOMOINTERGENIC
SBSChr1221120915G-THOMOINTERGENIC
SBSChr1221120923A-GHOMOINTERGENIC
SBSChr12343635A-GHOMOINTERGENIC
SBSChr123603510T-GHOMOINTRON
SBSChr210176695G-AHETINTERGENIC
SBSChr210827294T-CHETINTERGENIC
SBSChr212690831C-GHETINTERGENIC
SBSChr223513813G-AHETINTRON
SBSChr229470724C-THETINTERGENIC
SBSChr24140992C-THETINTERGENIC
SBSChr26579241T-CHETINTRON
SBSChr328501288G-AHOMOINTRON
SBSChr37331711A-THOMOINTRON
SBSChr421705714T-AHETINTERGENIC
SBSChr43036608C-AHOMOINTERGENIC
SBSChr435206730T-AHETINTERGENIC
SBSChr47909466A-CHETINTERGENIC
SBSChr47962905C-THOMOINTRON
SBSChr514281927G-THOMOINTRON
SBSChr519288487T-CHOMOINTRON
SBSChr54156021A-CHOMOINTERGENIC
SBSChr55679153G-AHETINTERGENIC
SBSChr68462G-AHETINTERGENIC
SBSChr82102491C-THETINTERGENIC
SBSChr85008414A-GHETINTERGENIC
SBSChr85612175A-THETUTR_3_PRIME
SBSChr913141541A-THETUTR_3_PRIME
SBSChr94107808C-GHOMOINTERGENIC

Deletions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr3111801611180182
DeletionChr3208784220878453
DeletionChr9428691542869194LOC_Os09g08290
DeletionChr125029953502998330
DeletionChr278320117832129118
DeletionChr12843717884371802
DeletionChr68600695860076267
DeletionChr10901366490136651
DeletionChr5101942621019427311
DeletionChr111184213111842174LOC_Os01g19720
DeletionChr611475343114753496
DeletionChr815395839153958412
DeletionChr317431215174312161
DeletionChr517609575176095772
DeletionChr1118909432189094342
DeletionChr1019136053191360541
DeletionChr520318970203189755
DeletionChr220395414203954162
DeletionChr222091028220910291
DeletionChr1224855745248557461
DeletionChr426231761262317632
DeletionChr1126299305262993061
DeletionChr1226475409264754101
DeletionChr626763371267633754
DeletionChr827625588276255902
DeletionChr6279722972797231114
DeletionChr428976013289760152
DeletionChr138090641380906421

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1117317441173174488
InsertionChr2771650877165081
InsertionChr312760317127603182
InsertionChr3888198888819881
InsertionChr420056184200561841
InsertionChr469043369045826
InsertionChr526651070266510712
InsertionChr826877346268773472

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr122078865321122323
InversionChr122078866521122332
InversionChr82125793021500741LOC_Os08g33950
InversionChr82125794621470779LOC_Os08g33950
InversionChr42764140327641618LOC_Os04g46620

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr99573937Chr16540105
TranslocationChr129917951Chr46963432