Search Results


Mutant Information

Mutant NameFN2976-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2976-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000430 (Germination Rate) = Low (Between 25% and 75%)
For more information, please see this phenotype file
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 57
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr125119541G-AHETINTERGENIC
SBSChr125601181T-AHOMOINTERGENIC
SBSChr129501608G-THETINTRON
SBSChr130547773A-THETINTERGENIC
SBSChr139162934G-AHETINTRON
SBSChr140234506T-AHETINTERGENIC
SBSChr25434862C-THETNON_SYNONYMOUS_CODINGLOC_Os02g10340
SBSChr211342559T-CHETINTRON
SBSChr211617149C-THETSYNONYMOUS_CODING
SBSChr214074470C-THETSTOP_GAINEDLOC_Os02g24270
SBSChr215369919C-THETINTRON
SBSChr225054956C-THETSYNONYMOUS_CODING
SBSChr225544498A-THETINTRON
SBSChr226900677C-THETSYNONYMOUS_CODING
SBSChr229564291A-GHETINTERGENIC
SBSChr231963575G-AHETINTERGENIC
SBSChr235073305C-AHETINTERGENIC
SBSChr314769442T-CHETINTERGENIC
SBSChr333512119T-CHOMOINTERGENIC
SBSChr41671003G-AHETINTERGENIC
SBSChr425641322G-THETINTRON
SBSChr5271877T-AHETSTOP_GAINEDLOC_Os05g01470
SBSChr53367296C-THETINTERGENIC
SBSChr59381874A-GHETINTERGENIC
SBSChr516972535C-GHOMOINTERGENIC
SBSChr624864633C-AHOMOINTERGENIC
SBSChr625423317G-AHETINTERGENIC
SBSChr627084456T-CHETINTERGENIC
SBSChr629630642G-AHETNON_SYNONYMOUS_CODINGLOC_Os06g48940
SBSChr7305429G-AHETINTERGENIC
SBSChr79186663G-CHETINTERGENIC
SBSChr716643195A-CHETINTERGENIC
SBSChr812101224G-AHETINTERGENIC
SBSChr815465978A-GHETINTERGENIC
SBSChr816455893C-THETINTERGENIC
SBSChr818748615G-AHETINTERGENIC
SBSChr826023826T-CHETINTERGENIC
SBSChr827061008C-THETINTERGENIC
SBSChr828038340G-AHETINTERGENIC
SBSChr99271631G-AHETINTERGENIC
SBSChr911069339T-GHETINTERGENIC
SBSChr916935263A-THETINTRON
SBSChr103667063C-THETINTERGENIC
SBSChr104110545C-THETINTERGENIC
SBSChr108413658G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g16880
SBSChr108933068T-GHETINTERGENIC
SBSChr1021685716G-AHETINTERGENIC
SBSChr115693388G-CHETINTERGENIC
SBSChr118340887A-GHETINTERGENIC
SBSChr1111533296C-THETINTERGENIC
SBSChr1114907398C-THETINTERGENIC
SBSChr1120441738G-CHOMOINTERGENIC
SBSChr127520493G-AHOMOINTERGENIC
SBSChr1219755833T-CHETNON_SYNONYMOUS_CODINGLOC_Os12g32710
SBSChr1222794594C-THETINTERGENIC
SBSChr1223556428C-THETNON_SYNONYMOUS_CODINGLOC_Os12g38400
SBSChr1225306611C-THETINTRON

Deletions: 32
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr5385200538520072
DeletionChr8593523259352331
DeletionChr86324712632472311
DeletionChr4801809380180952LOC_Os04g14304
DeletionChr38081706808173428
DeletionChr10931828793182892
DeletionChr311475167114751681
DeletionChr1012476285124762905LOC_Os10g24350
DeletionChr813398109133981112
DeletionChr10161806351618064813
DeletionChr216434103164341041LOC_Os02g27750
DeletionChr716665498166655013LOC_Os07g28470
DeletionChr318125984181259884
DeletionChr1219312845193128494
DeletionChr219514001196050009099912
DeletionChr219610001196800006999912
DeletionChr2196820011990300022099935
DeletionChr2199120012020500029299940
DeletionChr22021300120289000759998
DeletionChr2202940012050500021099923
DeletionChr222420096224200982
DeletionChr724005581240055821
DeletionChr1248240012503300020899929
DeletionChr125036001251020006599910
DeletionChr1252030012569000048699969
DeletionChr425287148252871491
DeletionChr1226523896265239048
DeletionChr627349317273493181
DeletionChr232086053320860552
DeletionChr133786001338460005999912
DeletionChr134073213340732152
DeletionChr1343169823431699412

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr210468250104682501
InsertionChr219518604195186041
InsertionChr4145386714538726
InsertionChr618041867180418671
InsertionChr107000089700017385
InsertionChr1212054206120542061
InsertionChr1218255869182558691
InsertionChr1219099706190997061

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr91692019616933278LOC_Os09g27810
InversionChr916920221169346332
InversionChr12482531025125728
InversionChr42868877728688915
InversionChr13378193033926453

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr916933291Chr133926482
TranslocationChr916934620Chr133878053LOC_Os09g27830
TranslocationChr419146627Chr317621955
TranslocationChr430287006Chr3744330LOC_Os03g02230