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Mutant Information

Mutant NameFN4234-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4234-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 61
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr115219485G-AHET
SBSChr122762439G-CHET
SBSChr124582620T-AHET
SBSChr124734267C-THET
SBSChr127795284C-THomo
SBSChr132646318T-AHomo
SBSChr132772105A-GHETNON_SYNONYMOUS_CODINGLOC_Os01g56790
SBSChr17346312T-AHETNON_SYNONYMOUS_CODINGLOC_Os01g13180
SBSChr19234106C-THET
SBSChr102940067A-GHomo
SBSChr105384461G-AHET
SBSChr1116054912G-AHET
SBSChr1118086187A-GHET
SBSChr1121060465T-AHET
SBSChr1125892805A-GHomo
SBSChr1126645837G-AHomo
SBSChr115341922G-AHomo
SBSChr1212504911T-AHET
SBSChr1214638366G-AHET
SBSChr1226404868T-CHET
SBSChr125650994G-AHET
SBSChr128181674C-THETNON_SYNONYMOUS_CODINGLOC_Os12g14360
SBSChr210533999G-AHET
SBSChr215056048C-THET
SBSChr217266880C-THET
SBSChr21889435A-GHET
SBSChr224891965G-AHET
SBSChr230539923A-GHET
SBSChr233182473G-CHET
SBSChr235921719G-CHET
SBSChr315174038C-THomo
SBSChr32776482A-THET
SBSChr331778911A-CHomo
SBSChr331994016G-THET
SBSChr33753631A-GHET
SBSChr39529766T-CHET
SBSChr410815079A-GHETNON_SYNONYMOUS_CODINGLOC_Os04g19410
SBSChr411368023T-AHET
SBSChr412418383A-CHET
SBSChr419711691T-CHET
SBSChr419841436G-AHET
SBSChr434433053G-AHET
SBSChr521438407C-GHET
SBSChr529418044G-AHET
SBSChr58405741C-THET
SBSChr614658488C-GHETNON_SYNONYMOUS_CODINGLOC_Os06g25050
SBSChr616121662G-AHET
SBSChr616685113G-AHET
SBSChr64912842G-THET
SBSChr718998620C-THomo
SBSChr725312166A-THomo
SBSChr7313913C-GHET
SBSChr812851362G-AHET
SBSChr816960354T-CHET
SBSChr822537506A-THET
SBSChr823136925G-AHET
SBSChr823796922T-CHET
SBSChr84295588G-CHET
SBSChr914780712G-AHET
SBSChr91708093C-THomo
SBSChr93417586G-AHET

Deletions: 20
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr128559338559352
DeletionChr5169182116918232
DeletionChr11797537179755518
DeletionChr73554709355472617
DeletionChr10548220854822091
DeletionChr29119265911929530
DeletionChr11127925001279251717LOC_Os11g22310
DeletionChr10195204671952048013
DeletionChr7200990012023100013199915
DeletionChr1121916012219160186
DeletionChr12220408162204083317
DeletionChr1122901036229010426LOC_Os11g38630
DeletionChr1123192682231926831
DeletionChr323504897235049036
DeletionChr325036357250363614
DeletionChr126222812262228142LOC_Os01g46120
DeletionChr126501474265014762
DeletionChr1126759330267593322
DeletionChr726828542268285431
DeletionChr1421310014242000028899947

Insertions: 7
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr27458562745858019
InsertionChr428350242283502432
InsertionChr4953014395301431
InsertionChr528997540289975412
InsertionChr5545702554570251
InsertionChr7793097479309774
InsertionChr9282673428267341

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr981797298180140
InversionChr120497701214289222
InversionChr120497706214289602

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr12229431Chr11204190LOC_Os12g01370
TranslocationChr105457160Chr214657860
TranslocationChr38825037Chr217955708LOC_Os02g30200
TranslocationChr914951257Chr137409863
TranslocationChr1218630149Chr76891519
TranslocationChr720101660Chr122096382
TranslocationChr720230651Chr122096367
TranslocationChr1125027911Chr827374348