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Mutant Information

Mutant NameFN3934-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN3934-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 34
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr115988766G-THomo
SBSChr119762410G-AHET
SBSChr120335370C-THomo
SBSChr136329983T-AHomo
SBSChr1010589943C-THET
SBSChr1021536790C-THET
SBSChr104734131G-AHET
SBSChr1115647289C-THomo
SBSChr1120736445G-AHET
SBSChr1120736446G-AHET
SBSChr1120736451G-AHET
SBSChr1221604348A-GHomo
SBSChr315433205T-AHomo
SBSChr317075963C-THET
SBSChr321991024T-AHomoNON_SYNONYMOUS_CODINGLOC_Os03g39598
SBSChr331989547C-THomo
SBSChr332672322T-GHomoNON_SYNONYMOUS_CODINGLOC_Os03g57290
SBSChr39690927T-AHomo
SBSChr426491554T-CHET
SBSChr429018538T-CHET
SBSChr43040379G-AHET
SBSChr4385518C-AHomo
SBSChr48974324C-AHomo
SBSChr618131802T-CHETNON_SYNONYMOUS_CODINGLOC_Os06g31200
SBSChr620047106C-THET
SBSChr620666886C-THET
SBSChr712692966G-THETNON_SYNONYMOUS_CODINGLOC_Os07g22550
SBSChr715083449C-AHET
SBSChr721044007C-THomo
SBSChr721044010G-AHomo
SBSChr812662139T-CHETNON_SYNONYMOUS_CODINGLOC_Os08g21210
SBSChr815569403C-THET
SBSChr86372384C-THomo
SBSChr913454119G-THET

Deletions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr8564823756482425
DeletionChr5108651151086513621
DeletionChr1012796974127969784
DeletionChr1113238546132385471LOC_Os11g23020
DeletionChr3139360531393608128
DeletionChr1215120034151200439
DeletionChr1215691330156913311
DeletionChr816567784165677917LOC_Os08g27110
DeletionChr1119416594194165984
DeletionChr319927975199279838
DeletionChr521911299219113012
DeletionChr1022677246226772471LOC_Os10g42160
DeletionChr423570261235702621
DeletionChr424760600247606066
DeletionChr1125527122255271242
DeletionChr526009564260095651
DeletionChr631229558312295591

Insertions: 4
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr10509144650914461LOC_Os10g09440image
InsertionChr21805833818058477140
InsertionChr7792704479270441
InsertionChr915529192155291932

No Inversion

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr89803838Chr69802277