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Mutant Information

Mutant NameFN4522-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4522-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 66
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr120505642C-AHET
SBSChr122078583C-AHET
SBSChr126915073A-GHET
SBSChr129788411G-THET
SBSChr135731286C-THOMO
SBSChr1012300840C-THOMO
SBSChr1016062726A-THET
SBSChr1018087356C-THETLOC_Os10g33960
SBSChr1018641729G-AHOMOLOC_Os10g34930
SBSChr1018700050C-AHETLOC_Os10g35040
SBSChr1021516177G-CHET
SBSChr109493803C-THET
SBSChr1113233608G-AHETLOC_Os11g23010
SBSChr1121055368C-THET
SBSChr1125515968C-THET
SBSChr1125516005A-THET
SBSChr1212644223C-AHET
SBSChr1213698515C-AHETLOC_Os12g24080
SBSChr1258493G-THET
SBSChr219876440G-THET
SBSChr224176236G-AHET
SBSChr225023842C-THET
SBSChr230894087A-GHET
SBSChr24574308C-AHOMO
SBSChr24574309T-AHOMO
SBSChr265470C-THET
SBSChr310124759G-AHET
SBSChr317648050C-THOMO
SBSChr328008677C-THET
SBSChr330869229C-THET
SBSChr334533001T-CHET
SBSChr41700315A-GHET
SBSChr422498587C-THETLOC_Os04g37840
SBSChr43180251G-AHET
SBSChr45984193G-CHET
SBSChr510263828C-THET
SBSChr515709518C-THETLOC_Os05g27010
SBSChr518878050G-THET
SBSChr519616334A-THET
SBSChr519616337G-THET
SBSChr524601964G-AHET
SBSChr57029727T-CHET
SBSChr58936415A-GHET
SBSChr613451574C-THOMO
SBSChr616509770T-CHET
SBSChr617677132T-AHET
SBSChr621359061G-AHOMO
SBSChr63656005G-THET
SBSChr69806169T-AHET
SBSChr710534262A-THOMO
SBSChr710534263A-THOMO
SBSChr724005781C-AHOMO
SBSChr72936236T-AHOMO
SBSChr75639640C-AHOMO
SBSChr75990290G-THET
SBSChr77930300C-THOMOLOC_Os07g13850
SBSChr77930301G-AHOMO
SBSChr811386885A-THET
SBSChr823645612T-GHET
SBSChr825592103C-THETLOC_Os08g40440
SBSChr85312869G-AHET
SBSChr86950254C-THOMOLOC_Os08g11850
SBSChr922074791G-AHET
SBSChr93513362G-AHET
SBSChr9492647T-AHET
SBSChr96464308C-THETLOC_Os09g11580

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr7198976619897661
DeletionChr9219611921961191
DeletionChr8272464327246431
DeletionChr1383333138333388
DeletionChr2453952945395291
DeletionChr4620559162055911
DeletionChr1621587962158791
DeletionChr11646910264691032
DeletionChr3669291566929151
DeletionChr4707148070714801
DeletionChr10788822678882261
DeletionChr7793035379303531LOC_Os07g13850
DeletionChr108140190814021122
DeletionChr128515215851522814
DeletionChr11984670598467051
DeletionChr12123021081230212114
DeletionChr2148227501482276112
DeletionChr9154542881545430013
DeletionChr516935363169353664
DeletionChr1169415121694152110
DeletionChr517536534175365341
DeletionChr1218143944181439463
DeletionChr721199611211996111
DeletionChr121568325215683262
DeletionChr121800927218009315
DeletionChr2224879802248802142
DeletionChr522850177228501771
DeletionChr6264904972649051620LOC_Os06g43980
DeletionChr630409545304095495
DeletionChr136337403363374031
DeletionChr1427651314276514818

Insertions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1364346013643462929
InsertionChr138787938387879381
InsertionChr1014002198140021981
InsertionChr1020304360203043656
InsertionChr10880262988026291
InsertionChr1115578811155788166
InsertionChr12118363741183641946
InsertionChr1212666970126669701
InsertionChr220440560204405612
InsertionChr221913119219131191LOC_Os02g36290image
InsertionChr429369797293697982
InsertionChr431598752315987532
InsertionChr518570978185709781
InsertionChr621519232215192321
InsertionChr8175077831750782543
InsertionChr8206744252067446844
InsertionChr918633431186334322

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr117544602102853LOC_Os01g04030
InversionChr117544612102867LOC_Os01g04030
InversionChr988491558849418
InversionChr61271877812719076LOC_Os06g21990

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr815765284Chr3152480542
TranslocationChr516732072Chr421907968LOC_Os04g35930
TranslocationChr516787806Chr421909499