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Mutant Information

Mutant NameFN2687-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2687-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 82
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr118713288C-THETINTERGENIC
SBSChr133628472G-AHETINTERGENIC
SBSChr134890123A-THETINTRON
SBSChr16098068C-THomo
SBSChr16969175C-THETINTRON
SBSChr1741849A-GHET
SBSChr108411033G-THET
SBSChr109539218C-AHET
SBSChr1116493950C-AHET
SBSChr1116493950C-AHETINTERGENIC
SBSChr1116493951G-AHET
SBSChr1116493951G-AHETINTERGENIC
SBSChr1125247462A-GHET
SBSChr1129001206G-THET
SBSChr1129001206G-THETINTERGENIC
SBSChr116477110A-THomo
SBSChr116477110A-THOMOINTRON
SBSChr117414075T-CHET
SBSChr1213031360A-THET
SBSChr1213031360A-THETINTERGENIC
SBSChr1223541166C-AHET
SBSChr1224449715G-AHomo
SBSChr1224449715G-AHOMOINTERGENIC
SBSChr129893018G-AHETSTOP_GAINEDLOC_Os12g17290
SBSChr218092046G-THETNON_SYNONYMOUS_CODINGLOC_Os02g30380
SBSChr230212386T-CHET
SBSChr230212386T-CHETINTERGENIC
SBSChr230782225C-THET
SBSChr312170095C-THomo
SBSChr312170095C-THOMOINTERGENIC
SBSChr36473224T-CHET
SBSChr36473224T-CHETSYNONYMOUS_CODING
SBSChr412343611A-CHETNON_SYNONYMOUS_CODINGLOC_Os04g21790
SBSChr413834097T-CHET
SBSChr416551540C-THET
SBSChr416551540C-THETINTERGENIC
SBSChr420033703A-GHET
SBSChr420033703A-GHETINTERGENIC
SBSChr420033712G-AHET
SBSChr420033712G-AHETINTERGENIC
SBSChr427923067G-THET
SBSChr427923067G-THETINTRON
SBSChr45790280C-THET
SBSChr514297594G-THET
SBSChr514980319T-CHETNON_SYNONYMOUS_CODINGLOC_Os05g25750
SBSChr520768500G-AHET
SBSChr521101966G-THETINTERGENIC
SBSChr527889063T-GHomo
SBSChr527889063T-GHOMOSPLICE_SITE_REGION
SBSChr53735695T-AHET
SBSChr53735695T-AHETINTERGENIC
SBSChr64154261A-THET
SBSChr64154261A-THETINTERGENIC
SBSChr64876222G-THETINTRON
SBSChr65888138C-THETINTERGENIC
SBSChr711293103C-THET
SBSChr718095552C-AHETNON_SYNONYMOUS_CODINGLOC_Os07g30580
SBSChr718095553A-CHETNON_SYNONYMOUS_CODINGLOC_Os07g30580
SBSChr718963511G-CHET
SBSChr718963511G-CHETINTERGENIC
SBSChr719153135C-THET
SBSChr724198867C-THET
SBSChr725003273A-THET
SBSChr727925150C-AHET
SBSChr727925150C-AHETINTERGENIC
SBSChr76069413A-GHET
SBSChr76069413A-GHETINTERGENIC
SBSChr813976246C-THETINTERGENIC
SBSChr81399006A-THET
SBSChr826169272G-CHomo
SBSChr826169272G-CHOMOINTERGENIC
SBSChr87272318G-AHETINTERGENIC
SBSChr911748998G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g19650
SBSChr913833451G-AHomo
SBSChr913833451G-AHOMOUTR_3_PRIME
SBSChr916824334G-THomo
SBSChr916824334G-THOMOSYNONYMOUS_CODING
SBSChr917058830G-AHET
SBSChr919130043G-THET
SBSChr97333416T-GHET
SBSChr97333416T-GHETINTERGENIC
SBSChr98276632C-THET

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr36142946142962
DeletionChr310282151028227122
DeletionChr2240369624037037
DeletionChr32648685264870621
DeletionChr3370727237072731
DeletionChr10510199351019996LOC_Os10g09460
DeletionChr75395845539586116LOC_Os07g10080
DeletionChr125633839563386526
DeletionChr910443317104433181
DeletionChr711816198118161991
DeletionChr212259160122591611
DeletionChr9126808481268084912
DeletionChr12129165431291658441
DeletionChr9134619281346192912
DeletionChr415182299151823001
DeletionChr1115722872157228731
DeletionChr10159233791592338562
DeletionChr617764103177641041
DeletionChr1217996187179961881LOC_Os12g30050
DeletionChr3213915612139156872
DeletionChr5229415572294156142
DeletionChr1223748961237489621
DeletionChr5265877392658774012
DeletionChr5266933022669330312
DeletionChr11279748022797482624LOC_Os11g46190
DeletionChr728176929281769301
DeletionChr729086688290866891
DeletionChr230173658301736591
DeletionChr333842319338423267
DeletionChr138688619386886289LOC_Os01g66610
DeletionChr139713093397130952

Insertions: 9
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr10980797998079791
InsertionChr1113356703133567031LOC_Os11g23200image
InsertionChr214810340148103401
InsertionChr223808168238081681
InsertionChr315780243157802442
InsertionChr5228960322896108
InsertionChr714901434149014341
InsertionChr8267164852671648622image
InsertionChr8267164852671648622image

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr32043555883272
InversionChr32043575883292
InversionChr139665163966644
InversionChr111186773611867927

Translocations: 23
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr11898529Chr417915299
TranslocationChr91269806Chr318058077
TranslocationChr103120137Chr123590110
TranslocationChr54292257Chr4134152702
TranslocationChr126248354Chr84190745
TranslocationChr1014333309Chr910527948LOC_Os10g27200
TranslocationChr1115401580Chr418466158
TranslocationChr1016401320Chr2199645292
TranslocationChr616817203Chr129886717
TranslocationChr618884707Chr55645992LOC_Os05g10340
TranslocationChr719416460Chr134821287
TranslocationChr420478519Chr326496416
TranslocationChr1220535474Chr134375468
TranslocationChr1221737271Chr678624782
TranslocationChr622827900Chr515579833
TranslocationChr223723930Chr114275920LOC_Os02g39280
TranslocationChr1224393553Chr619207692
TranslocationChr824683903Chr139127474
TranslocationChr1124994225Chr417874176
TranslocationChr725285592Chr213402391
TranslocationChr826906514Chr325348842LOC_Os08g42570
TranslocationChr1127570450Chr516490148
TranslocationChr1127761200Chr726193088LOC_Os11g45890