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Mutant Information

Mutant NameFN4758-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4758-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 74
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111752203C-AHOMO
SBSChr120409924A-GHOMO
SBSChr127199896C-THETLOC_Os01g47560
SBSChr131759789G-AHET
SBSChr13617099C-THETLOC_Os01g07550
SBSChr13905569T-AHOMO
SBSChr19493305C-THET
SBSChr1019493875C-THETLOC_Os10g36430
SBSChr1020431621A-THET
SBSChr103503992G-AHET
SBSChr103799063A-THET
SBSChr105628132C-THET
SBSChr1115220400C-THET
SBSChr1116760171G-AHET
SBSChr1125311462C-THOMO
SBSChr1125484041G-AHOMOLOC_Os11g42320
SBSChr113075001C-THET
SBSChr118823449C-THET
SBSChr119541791G-AHET
SBSChr1211842866G-AHET
SBSChr1213551380T-AHET
SBSChr1213551381T-AHET
SBSChr1214273485C-THET
SBSChr1214777503A-GHET
SBSChr1220686761G-AHET
SBSChr1226985804C-THET
SBSChr219478153T-AHET
SBSChr220493358A-THET
SBSChr230968402C-AHET
SBSChr231454235T-CHET
SBSChr311205504G-AHET
SBSChr313939450C-AHET
SBSChr319788113A-THET
SBSChr324490428G-AHET
SBSChr328019409A-GHET
SBSChr334004044C-AHET
SBSChr412521024C-AHETLOC_Os04g22100
SBSChr416161856C-THET
SBSChr416944905G-AHET
SBSChr417648547T-CHOMOLOC_Os04g29650
SBSChr417888899G-AHOMO
SBSChr41811410C-THET
SBSChr41811414G-THET
SBSChr421057798G-AHOMO
SBSChr421905692T-AHOMO
SBSChr423225055G-THOMO
SBSChr434964977T-CHET
SBSChr48328965C-AHET
SBSChr49873615C-AHET
SBSChr511687385C-THETLOC_Os05g19990
SBSChr521600189G-THET
SBSChr521621562C-THET
SBSChr524143510G-THET
SBSChr52681614G-AHET
SBSChr53302259T-AHET
SBSChr56202477T-AHET
SBSChr57365611G-THET
SBSChr59541120T-AHET
SBSChr614270898C-THOMO
SBSChr620822813A-GHET
SBSChr626674848G-THOMO
SBSChr65194423A-THET
SBSChr66702612A-GHET
SBSChr710314299G-AHET
SBSChr71064925C-THET
SBSChr712625680G-AHET
SBSChr716615279T-CHET
SBSChr74687855G-THET
SBSChr813300224C-AHET
SBSChr821260287G-AHETLOC_Os08g33950
SBSChr82476135T-CHET
SBSChr87333694G-AHET
SBSChr913204475C-THET
SBSChr913267087A-THET

Deletions: 37
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr31853981853981
DeletionChr107687887687881
DeletionChr6157139815714069
DeletionChr42987307298732216
DeletionChr54201001454600034500052
DeletionChr5450789145078911
DeletionChr9451339845133981LOC_Os09g08630
DeletionChr8652657165265744
DeletionChr11759600176820008600011
DeletionChr117692001784400015200019
DeletionChr117849001841400056500083
DeletionChr1184150018428000130002
DeletionChr11843500185110007600015
DeletionChr5970433797043371
DeletionChr5989468498946841
DeletionChr810350542103505421
DeletionChr810382955103829551
DeletionChr912954529129545324
DeletionChr513098204130982107
DeletionChr914313214143132141
DeletionChr215864435158644351
DeletionChr116367345163673462
DeletionChr217938541179385411
DeletionChr520844486208444861
DeletionChr1020975571209755744
DeletionChr521096927210969282
DeletionChr922681727226817271
DeletionChr5227430652274307410
DeletionChr423222958232229581
DeletionChr124736563247365653
DeletionChr125136150251361545LOC_Os01g43870
DeletionChr225530970255309745
DeletionChr728050984280509918
DeletionChr128376017283760204
DeletionChr7296967892969683244
DeletionChr230935224309352241
DeletionChr232216566322165705

Insertions: 13
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr111833671118336826116
InsertionChr11199832119983222
InsertionChr1120143255201432562
InsertionChr1125983201259832011
InsertionChr1213921592139215943
InsertionChr2293760629376061
InsertionChr235176583351765831
InsertionChr3279400652794007410
InsertionChr426511898265118992
InsertionChr427771554277715541
InsertionChr515490219154902224
InsertionChr720608444206084441
InsertionChr912711227127112271

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1266007287334164LOC_Os12g13170
InversionChr1187126279640238

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr127333622Chr722722333LOC_Os12g13170
TranslocationChr127334156Chr722722338LOC_Os12g13170
TranslocationChr118548490Chr32904210LOC_Os11g15170