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Mutant Information

Mutant NameFN1278-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1278-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000014 (Panicle Weight) = Low (Between 25% and 74%)
  • TO:0000207 (Plant height) = Normal (Between 75% and 125%)
  • TO:0000445 (Seed Number) = Low (Between 25% and 74%)
  • TO:0000639 (Seed fertility) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 50
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111608707C-AHETINTERGENIC
SBSChr113236707A-THETINTERGENIC
SBSChr118502084G-AHOMOINTERGENIC
SBSChr119626536G-AHOMONON_SYNONYMOUS_CODINGLOC_Os01g35470
SBSChr12958775T-AHOMOINTERGENIC
SBSChr134209005T-AHETINTRON
SBSChr134209006T-AHETINTRON
SBSChr141043808G-AHETINTERGENIC
SBSChr15431653A-THOMOINTERGENIC
SBSChr15995170C-THOMOSYNONYMOUS_CODING
SBSChr1023053497A-THETSPLICE_SITE_REGION
SBSChr1023053498C-AHETSPLICE_SITE_REGION
SBSChr109048183G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g17900
SBSChr116250398A-CHETNON_SYNONYMOUS_CODINGLOC_Os11g11290
SBSChr119316026G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g16790
SBSChr119728930G-AHETINTERGENIC
SBSChr119728932G-AHETINTERGENIC
SBSChr119728935T-AHETINTERGENIC
SBSChr1211207680T-CHETINTERGENIC
SBSChr1217846224G-THETINTERGENIC
SBSChr1223011274T-CHOMOINTRON
SBSChr1226875728T-CHOMOINTRON
SBSChr128168331G-THETINTERGENIC
SBSChr129030948A-CHETINTRON
SBSChr217213996A-GHOMOINTRON
SBSChr217214370A-GHOMOINTRON
SBSChr223561874G-AHETINTERGENIC
SBSChr230190365C-GHETSPLICE_SITE_REGION
SBSChr26575279A-THOMOINTRON
SBSChr316792857C-AHETINTERGENIC
SBSChr321145250C-GHETINTERGENIC
SBSChr325078048T-CHETINTERGENIC
SBSChr34839864T-CHETINTERGENIC
SBSChr412999371G-THOMOSYNONYMOUS_CODING
SBSChr414875767T-AHOMOINTERGENIC
SBSChr426293214C-THOMOINTERGENIC
SBSChr510714491T-CHOMOINTERGENIC
SBSChr51141702C-THETINTERGENIC
SBSChr513594042T-CHOMOINTRON
SBSChr55108442A-GHOMOINTERGENIC
SBSChr612988236G-THETNON_SYNONYMOUS_CODINGLOC_Os06g22370
SBSChr613176802C-AHETINTERGENIC
SBSChr613827410G-AHOMOINTERGENIC
SBSChr617185842C-GHETINTERGENIC
SBSChr627669943A-GHOMOSYNONYMOUS_CODING
SBSChr716695555G-AHETSYNONYMOUS_CODING
SBSChr815340786C-THOMOINTERGENIC
SBSChr94886230A-GHOMOINTRON
SBSChr95257029T-CHOMOSYNONYMOUS_CODING
SBSChr98218304C-GHOMOINTERGENIC

Deletions: 33
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr102191252191283
DeletionChr929788929789910
DeletionChr66211736211785
DeletionChr7650247165024765
DeletionChr86788458678848123
DeletionChr3745464274546431
DeletionChr7752240175224065
DeletionChr48174288817429911
DeletionChr10101329661013297711LOC_Os10g20180
DeletionChr910162636101626371
DeletionChr810954773109547763
DeletionChr711687148116871513LOC_Os07g20270
DeletionChr1111699922116999231
DeletionChr11118037471180376417
DeletionChr12127583541275836814
DeletionChr1140629341423693517400125
DeletionChr8175519011755194140
DeletionChr217911281179112909LOC_Os02g30150
DeletionChr419128716191287248
DeletionChr821270224212702262
DeletionChr821947344219473506
DeletionChr323523199235232067
DeletionChr624088460240884644
DeletionChr324160296241602971
DeletionChr124358226243582271
DeletionChr6245215632452157310
DeletionChr727249307272493125
DeletionChr231168691311686943
DeletionChr232453196324532048
DeletionChr232901213329012218
DeletionChr3349413153494132510LOC_Os03g61630
DeletionChr235327026353301343108LOC_Os02g57690
DeletionChr138914084389140939

Insertions: 5
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr111768578117685792
InsertionChr10196064719606471
InsertionChr1125763332257633354
InsertionChr719471453194714531
InsertionChr719981738199817381

No Inversion

Translocations: 6
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr82324484Chr210167366
TranslocationChr614778297Chr35107995
TranslocationChr614779253Chr35107974
TranslocationChr1122349561Chr35107950
TranslocationChr329049448Chr235330132LOC_Os02g57690
TranslocationChr329049459Chr235327035LOC_Os02g57690