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Mutant Information

Mutant NameFN2760-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2760-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 44
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr124079900C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g42380
SBSChr133415770A-THETINTERGENIC
SBSChr138963367A-GHOMOINTRON
SBSChr142614682G-THOMOINTERGENIC
SBSChr222809468G-AHETINTERGENIC
SBSChr224119268G-AHETINTERGENIC
SBSChr35081935A-THETINTERGENIC
SBSChr315273771C-THETINTERGENIC
SBSChr324351741T-AHETUTR_3_PRIME
SBSChr41879352G-AHETSYNONYMOUS_CODING
SBSChr423624265G-THOMOINTERGENIC
SBSChr427189684G-AHETINTERGENIC
SBSChr57672215T-GHETINTERGENIC
SBSChr513167871C-AHETNON_SYNONYMOUS_CODINGLOC_Os05g23090
SBSChr519329526G-AHETINTRON
SBSChr520922188G-AHETINTERGENIC
SBSChr61931718A-CHETINTRON
SBSChr611656598G-THETINTERGENIC
SBSChr623279874C-AHETNON_SYNONYMOUS_CODINGLOC_Os06g39210
SBSChr77232423G-CHETINTERGENIC
SBSChr722021365T-CHOMOINTERGENIC
SBSChr81145855G-AHOMOINTERGENIC
SBSChr88346774C-GHETINTERGENIC
SBSChr88807498C-THOMOINTERGENIC
SBSChr89709994C-THETINTERGENIC
SBSChr810726780C-AHETINTERGENIC
SBSChr813592008G-AHETSYNONYMOUS_CODING
SBSChr814996931A-GHETINTERGENIC
SBSChr9927556C-GHOMOSYNONYMOUS_CODING
SBSChr91849659T-CHETINTERGENIC
SBSChr95815002A-GHOMOINTERGENIC
SBSChr915096594A-GHETNON_SYNONYMOUS_CODINGLOC_Os09g25200
SBSChr916064093A-CHETINTERGENIC
SBSChr916277900C-THETINTERGENIC
SBSChr104984701A-GHETSYNONYMOUS_CODING
SBSChr1014811180G-AHETINTRON
SBSChr1015468601C-GHOMOINTERGENIC
SBSChr1118750348G-THOMOINTERGENIC
SBSChr1118835617C-THOMOINTERGENIC
SBSChr1119514303A-GHETNON_SYNONYMOUS_CODINGLOC_Os11g33010
SBSChr124947647G-CHETINTERGENIC
SBSChr127476720G-THETINTRON
SBSChr128754309G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g15340
SBSChr1211156387T-GHETINTERGENIC

Deletions: 26
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr91544421544453
DeletionChr11041395104141116
DeletionChr8114621011462199
DeletionChr9376992037699222
DeletionChr3392663339266429
DeletionChr1475414247541508
DeletionChr28324181832426281LOC_Os02g14910
DeletionChr3833381883338191
DeletionChr1110493781104937821
DeletionChr610986253109862552
DeletionChr411697497116974981
DeletionChr111218355812183723165
DeletionChr12133771461337723185
DeletionChr10143749391437499859
DeletionChr12151968961519691216
DeletionChr6169070001690701111
DeletionChr11694454016945180640
DeletionChr1217193510171935133
DeletionChr5187062261870625125
DeletionChr1120261136202611382
DeletionChr122489499224895056
DeletionChr623897737238977436
DeletionChr825737633257376363
DeletionChr8276402292764024112
DeletionChr432458876324588771
DeletionChr136614284366142884

Insertions: 21
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr3163647816364792
InsertionChr5563747756374804
InsertionChr1010023519100235202
InsertionChr1133504281335044821
InsertionChr137224120372241201LOC_Os01g64080image
InsertionChr226741205267412051
InsertionChr227006153270061531
InsertionChr2315757833157582543
InsertionChr5268851926885202
InsertionChr5988470798847071
InsertionChr5233635112336360292
InsertionChr629567318295673181
InsertionChr79697229969724719
InsertionChr8773086077308634
InsertionChr8175849191758497052
InsertionChr985582855832
InsertionChr10677099967709991
InsertionChr11397478239747832
InsertionChr11121668841216696077
InsertionChr11177388031773885048
InsertionChr1121228138212281381

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1251621355369004
InversionChr1251621405369003

Translocations: 9
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr95167642Chr5113508172
TranslocationChr56369909Chr416080755
TranslocationChr106421368Chr44049220
TranslocationChr78883502Chr413157426
TranslocationChr78886936Chr413157416
TranslocationChr716449369Chr134373767
TranslocationChr420478531Chr326496410
TranslocationChr423352079Chr312730507
TranslocationChr1126258692Chr46930152