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Mutant Information

Mutant NameFN1652-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1652-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 28
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr125304244G-AHomoNON_SYNONYMOUS_CODINGLOC_Os01g44150
SBSChr23370070G-CHETINTERGENIC
SBSChr212664173C-THETINTRON
SBSChr230277452G-THomoINTRON
SBSChr322753326C-THETINTERGENIC
SBSChr330372171T-CHomoINTRON
SBSChr415937864G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g26940
SBSChr419950274G-THomoINTERGENIC
SBSChr421424412C-THomoNON_SYNONYMOUS_CODINGLOC_Os04g35250
SBSChr428032461G-AHETINTERGENIC
SBSChr52675978T-CHETINTRON
SBSChr58299214A-THETINTERGENIC
SBSChr518474461G-CHomoINTERGENIC
SBSChr529404554T-CHomoINTERGENIC
SBSChr64421190G-AHETINTERGENIC
SBSChr625999647T-GHETINTERGENIC
SBSChr627383114G-THETINTERGENIC
SBSChr74169474A-GHETINTERGENIC
SBSChr74761142C-THETINTERGENIC
SBSChr76894587C-THETINTERGENIC
SBSChr710682045A-THETINTRON
SBSChr720989486T-CHomoINTERGENIC
SBSChr81466079T-AHETINTERGENIC
SBSChr1018189744G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g34078
SBSChr122340456A-GHomoINTERGENIC
SBSChr1218073290G-CHETINTERGENIC
SBSChr1219634794C-AHETUTR_5_PRIME
SBSChr1220840590C-GHETINTRON

Deletions: 32
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr43037333037341LOC_Os04g01439
DeletionChr6111847111184721
DeletionChr9171874717187514
DeletionChr72522472252248614
DeletionChr9295520729552169
DeletionChr3421373942137401
DeletionChr2485571848557191
DeletionChr3508717650871771
DeletionChr8532285053228511LOC_Os08g09190
DeletionChr10797192279719242
DeletionChr1186537218668151144302
DeletionChr1110577806105802032397
DeletionChr110582536105825382
DeletionChr911136700111367055
DeletionChr7119394831193949411
DeletionChr1112913022129130242
DeletionChr10134612371346128043
DeletionChr91503000115065000350003
DeletionChr12152421971524225962
DeletionChr515646261156462709
DeletionChr615931508159315179LOC_Os06g28060
DeletionChr417930001180140008400014
DeletionChr521000213210002152
DeletionChr1124108468241084702
DeletionChr524595778245957791LOC_Os05g42020
DeletionChr825066926250669315
DeletionChr1125335051253350543LOC_Os11g42080
DeletionChr825358546253585482
DeletionChr626941202269412031
DeletionChr42942993429430712778
DeletionChr6294888172948882912
DeletionChr4299643452996435611

Insertions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr127134019271340202LOC_Os01g47470image
InsertionChr135770112357701132
InsertionChr140137248401372481
InsertionChr1946464794646526
InsertionChr211491965114919662
InsertionChr2165025271650257448
InsertionChr2167689011676897373
InsertionChr4108398210839821
InsertionChr516128616161286172
InsertionChr826736967267369726
InsertionChr1015723646157236472
InsertionChr10207063532070636816
InsertionChr1116655549166555491
InsertionChr11221262112212628878
InsertionChr12602550460255041
InsertionChr1223064310230643101
InsertionChr1223213440232134412

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr42644219828074921
InversionChr42694722028074936

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1227049947Chr66604590LOC_Os06g12270