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Mutant Information

SOS indicates the sequenced line is sterile and seeds from siblings are available.
Mutant NameFN1310-S [Download]
GenerationM2-SOS
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1310-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 29
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr13403977A-CHETINTRON
SBSChr113764401C-AHETINTERGENIC
SBSChr117603730G-AHETINTERGENIC
SBSChr118737099G-AHETINTRON
SBSChr120432286G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g36780
SBSChr127200105C-THOMOSPLICE_SITE_REGION
SBSChr127200107C-THOMOSPLICE_SITE_REGION
SBSChr128090290C-THETINTERGENIC
SBSChr134392738C-THETINTERGENIC
SBSChr223264090T-CHETINTERGENIC
SBSChr32737967A-GHETINTERGENIC
SBSChr33144879G-AHETINTRON
SBSChr315080629C-THOMOSYNONYMOUS_CODING
SBSChr328572816A-THOMOUTR_3_PRIME
SBSChr328572817C-THOMOUTR_3_PRIME
SBSChr427380156G-AHOMOINTERGENIC
SBSChr54932824T-CHETINTERGENIC
SBSChr54932828G-AHETINTERGENIC
SBSChr6782244G-AHETUTR_3_PRIME
SBSChr627249377C-THETINTERGENIC
SBSChr77036282C-AHOMOINTRON
SBSChr712459896C-THOMOINTERGENIC
SBSChr82418827G-THETINTERGENIC
SBSChr96717190C-THETINTERGENIC
SBSChr1015620005T-AHETINTERGENIC
SBSChr1110879266G-AHETINTERGENIC
SBSChr1113776860A-GHETINTRON
SBSChr1126959816C-THOMOINTERGENIC
SBSChr127894609C-AHETINTERGENIC

Deletions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr5921543092154344
DeletionChr3966919296691964
DeletionChr1110829557108295658
DeletionChr413454350134543555
DeletionChr113960054139600551
DeletionChr2164433571644340245
DeletionChr10216856272168564720
DeletionChr621962018219620191
DeletionChr523102103231021107LOC_Os05g39380
DeletionChr6291910012929600010500018
DeletionChr629340001294220008200015
DeletionChr136206204362062062

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr233113264331132641
InsertionChr1579918557991851
InsertionChr314983403149834042
InsertionChr325480101254801022
InsertionChr5642466164246622
InsertionChr521765747217657504
InsertionChr8163962331639625826
InsertionChr1021520601215206022

No Inversion

Translocations: 1
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr415030937Chr2105224582