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Mutant Information

Mutant NameFN2682-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2682-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 65
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111153921T-CHET
SBSChr111153921T-CHETINTERGENIC
SBSChr117788143C-THET
SBSChr117788143C-THETINTERGENIC
SBSChr120149490T-CHETINTERGENIC
SBSChr121588752G-AHET
SBSChr121588752G-AHETINTRON
SBSChr131065292A-GHETNON_SYNONYMOUS_CODINGLOC_Os01g54010
SBSChr132479365A-GHET
SBSChr132479365A-GHETINTERGENIC
SBSChr137206277C-THETINTERGENIC
SBSChr141546204C-GHETINTERGENIC
SBSChr19857319C-THET
SBSChr1015840902G-AHETINTERGENIC
SBSChr1114664421C-THET
SBSChr1114664421C-THETINTRON
SBSChr1119974998T-CHomo
SBSChr1119974998T-CHOMOINTRON
SBSChr1127275450G-CHET
SBSChr1127275450G-CHETINTERGENIC
SBSChr1215173894A-GHET
SBSChr1223989381G-CHET
SBSChr1223989381G-CHETINTERGENIC
SBSChr125152579T-CHET
SBSChr125152579T-CHETINTERGENIC
SBSChr210154136T-AHET
SBSChr210154136T-AHETINTRON
SBSChr214649463A-THETSTOP_GAINEDLOC_Os02g25180
SBSChr25240006G-AHET
SBSChr25240006G-AHETINTRON
SBSChr27665574A-THET
SBSChr27665574A-THETINTERGENIC
SBSChr320277937G-AHETINTRON
SBSChr3902142A-THET
SBSChr3902142A-THETINTERGENIC
SBSChr3956984G-AHETNON_SYNONYMOUS_CODINGLOC_Os03g02580
SBSChr419950274G-THETINTERGENIC
SBSChr426360681G-THETINTERGENIC
SBSChr426360682C-THETINTERGENIC
SBSChr426613156C-AHETNON_SYNONYMOUS_CODINGLOC_Os04g44980
SBSChr426916884C-THETINTERGENIC
SBSChr429972042T-CHETSTART_GAINED
SBSChr46334994C-AHomo
SBSChr46334994C-AHOMOINTERGENIC
SBSChr49947091C-THETINTRON
SBSChr525256675C-THomo
SBSChr525256675C-THOMOINTRON
SBSChr58456202C-THET
SBSChr59618704C-THETNON_SYNONYMOUS_CODINGLOC_Os05g16880
SBSChr628483092G-AHET
SBSChr628483092G-AHETINTERGENIC
SBSChr630186036A-CHET
SBSChr67076495A-GHET
SBSChr715016641C-THETINTERGENIC
SBSChr72315390T-AHETNON_SYNONYMOUS_CODINGLOC_Os07g05190
SBSChr78233552C-THET
SBSChr79154157A-THET
SBSChr79154157A-THETINTRON
SBSChr812220572T-CHETNON_SYNONYMOUS_CODINGLOC_Os08g20350
SBSChr828263394C-AHomo
SBSChr828263394C-AHOMOINTERGENIC
SBSChr83365193A-GHomo
SBSChr83365193A-GHOMOINTERGENIC
SBSChr84331177T-CHomo
SBSChr84331177T-CHOMOINTERGENIC

Deletions: 26
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr2150497915049801
DeletionChr8179079617907993
DeletionChr94753131475320473
DeletionChr9526029952603001LOC_Os09g09720
DeletionChr8803229780323014LOC_Os08g13500
DeletionChr9892624489262451
DeletionChr2903720390372041
DeletionChr49331681933169716
DeletionChr29353291935331423
DeletionChr9970665997066601LOC_Os09g15880
DeletionChr99735385973539510
DeletionChr610671820106718222
DeletionChr8116372011163726059
DeletionChr1111937328119373291
DeletionChr712229807122298081
DeletionChr11141811341418115218
DeletionChr1156959921569599312
DeletionChr12190273281902735426
DeletionChr619294439192944401
DeletionChr322381645223816494
DeletionChr325017619250176223
DeletionChr826700653267006552
DeletionChr7268847062688473024
DeletionChr330699164306991684
DeletionChr23244102132441167146
DeletionChr234104776341047837

Insertions: 22
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr113763923137639231
InsertionChr119729900197299001
InsertionChr135770112357701132
InsertionChr1903197290319721
InsertionChr10392386339238631
InsertionChr11208783092087833022
InsertionChr1211475623114756231
InsertionChr1211484604114846041
InsertionChr219521372195213721
InsertionChr227283855272838551
InsertionChr3309242803092431536
InsertionChr333993649339936491
InsertionChr3730075973007591
InsertionChr413737263137372631
InsertionChr425995558259955581
InsertionChr529114308291143092
InsertionChr5811638781163871LOC_Os05g14400image
InsertionChr629254786292547872
InsertionChr712164891121648911
InsertionChr719805571198055711
InsertionChr726828512268285121
InsertionChr912792840127928401

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1159590936671257
InversionChr1213377758134062562

Translocations: 17
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr9339199Chr511351917LOC_Os05g19530
TranslocationChr122399395Chr132064842LOC_Os12g05334
TranslocationChr55022236Chr2253418972
TranslocationChr106900321Chr52479642
TranslocationChr126993479Chr1576210
TranslocationChr88928502Chr6174977292
TranslocationChr98941257Chr130237136
TranslocationChr1213547459Chr11229737972
TranslocationChr1115779026Chr911329565LOC_Os11g27420
TranslocationChr816263154Chr6158829102
TranslocationChr919929206Chr4266487472
TranslocationChr619955775Chr431332668
TranslocationChr1122608894Chr911816277
TranslocationChr1122773586Chr318629691
TranslocationChr1224883607Chr1110658313
TranslocationChr825143113Chr224605943
TranslocationChr1127827270Chr625897960