Search Nipponbare


Mutant Information

Mutant NameFN1156-XA21 [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1156-XA21 Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 49
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr114455487A-GHETINTERGENIC
SBSChr115665347A-THETINTERGENIC
SBSChr118210458T-CHETINTERGENIC
SBSChr118210460G-AHETINTERGENIC
SBSChr123268010G-AHETINTERGENIC
SBSChr135319726T-CHomoINTERGENIC
SBSChr140431153C-THomoINTERGENIC
SBSChr101201175C-THomoINTERGENIC
SBSChr103443342G-AHETINTERGENIC
SBSChr107819217G-AHETINTERGENIC
SBSChr107819219G-AHETINTERGENIC
SBSChr108053698A-GHETINTRON
SBSChr1115066705G-AHETSYNONYMOUS_CODING
SBSChr1119873061A-GHETINTERGENIC
SBSChr1124932309T-GHomoINTERGENIC
SBSChr1210086983G-AHETINTERGENIC
SBSChr1213542204G-CHETINTERGENIC
SBSChr127648535A-GHETINTERGENIC
SBSChr215887979T-AHETINTERGENIC
SBSChr220406918A-GHETINTERGENIC
SBSChr24390881A-THomoINTRON
SBSChr316446584C-THomoINTERGENIC
SBSChr32174826C-AHomoINTERGENIC
SBSChr323666559G-AHomoINTRON
SBSChr327822326T-CHomoINTRON
SBSChr328044625C-GHETSYNONYMOUS_CODING
SBSChr328441415T-CHomoINTERGENIC
SBSChr328976998C-THomoINTERGENIC
SBSChr330336354C-THomoINTRON
SBSChr412897839C-THomoINTERGENIC
SBSChr417482551A-GHomoINTERGENIC
SBSChr428314016T-CHETINTERGENIC
SBSChr43063018A-THETINTERGENIC
SBSChr43490289G-AHETINTERGENIC
SBSChr516281175A-CHETINTERGENIC
SBSChr52803488C-AHomoINTERGENIC
SBSChr52803489T-GHomoINTERGENIC
SBSChr528991326G-AHETUTR_5_PRIME
SBSChr616077139T-AHETSTOP_GAINEDLOC_Os06g28310
SBSChr624162688A-THETINTERGENIC
SBSChr625741927T-CHETUTR_3_PRIME
SBSChr628976397A-GHomoINTERGENIC
SBSChr68631280G-AHomoINTERGENIC
SBSChr68631282G-AHomoINTERGENIC
SBSChr726954216C-THomoINTRON
SBSChr816263448T-CHETINTERGENIC
SBSChr816263449G-AHETINTERGENIC
SBSChr88401764C-THETINTERGENIC
SBSChr912525868G-AHomoINTERGENIC

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr127539057539072
DeletionChr4100385910038645
DeletionChr1210454571045890433
DeletionChr12134859013485922
DeletionChr11140672214067242LOC_Os11g03620
DeletionChr9160642816064291
DeletionChr11223352722335336LOC_Os11g05090
DeletionChr2250461825046202
DeletionChr4306010330601041
DeletionChr7641400064190005001
DeletionChr7655200065540002001
DeletionChr77585187758522740
DeletionChr99137628913764416
DeletionChr10978593697859415
DeletionChr1010473000104730011
DeletionChr1111766187117661892
DeletionChr1112785992127859931
DeletionChr71285500012870000150012
DeletionChr21479500014815000200014
DeletionChr218080254180802551
DeletionChr220406942204069431
DeletionChr920764446207644471LOC_Os09g36060
DeletionChr721153679211536856
DeletionChr521764624217711156491
DeletionChr1123379666233796671
DeletionChr1223570559235705601
DeletionChr524777315247773183
DeletionChr7247849622478497816
DeletionChr427943809279438101
DeletionChr23000427830004751473
DeletionChr336060762360607719LOC_Os03g63830

Insertions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1258094125809444
InsertionChr1013628949136289502
InsertionChr1128757355287573584
InsertionChr1213355254133552541
InsertionChr1221737790217377912
InsertionChr127130107713011913
InsertionChr12853928585392851
InsertionChr12853945785394582
InsertionChr2454118445411852
InsertionChr314195189141951924
InsertionChr329240431292404322
InsertionChr614168614141686152

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr483591542302LOC_Os04g01860

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr524576050Chr76416891LOC_Os05g41960
TranslocationChr726640278Chr3215010942