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Mutant Information

Mutant NameFN2102-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2102-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 42
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr140427164C-THomo
SBSChr141320465T-AHomo
SBSChr227358030G-AHomo
SBSChr227358031G-THomo
SBSChr227358048G-THomo
SBSChr235695842A-THETNON_SYNONYMOUS_CODINGLOC_Os02g58360
SBSChr31449810C-GHET
SBSChr310515348G-AHET
SBSChr310515349G-AHET
SBSChr312021924C-THET
SBSChr315621097T-AHomo
SBSChr315621098C-THomo
SBSChr315621099T-GHomo
SBSChr317960279G-AHET
SBSChr319837527A-CHomo
SBSChr323197331G-AHETSTOP_GAINEDLOC_Os03g41770
SBSChr335283737G-AHET
SBSChr335548945G-AHET
SBSChr47557454T-AHomo
SBSChr48253409C-THET
SBSChr53676021G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g07000
SBSChr58849718G-AHET
SBSChr515322913G-CHETNON_SYNONYMOUS_CODINGLOC_Os05g26340
SBSChr515363268C-GHET
SBSChr68778360G-AHETNON_SYNONYMOUS_CODINGLOC_Os06g15460
SBSChr68778361G-THET
SBSChr74424618G-THET
SBSChr717955361A-GHET
SBSChr81172123A-GHET
SBSChr89515721C-AHET
SBSChr810864980A-CHET
SBSChr810864981C-GHET
SBSChr818778790G-AHET
SBSChr823079824A-GHET
SBSChr93418634A-CHET
SBSChr911454353T-CHET
SBSChr916673813T-CHomo
SBSChr921649091G-AHET
SBSChr104770009G-THETNON_SYNONYMOUS_CODINGLOC_Os10g08820
SBSChr1015139057C-THETNON_SYNONYMOUS_CODINGLOC_Os10g29050
SBSChr1216851019C-THET
SBSChr1224485218T-CHET

Deletions: 15
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr677180771822
DeletionChr7421685442168584
DeletionChr2446367544636772
DeletionChr64721746472176418
DeletionChr1161329446133414470
DeletionChr474957187496067349
DeletionChr11755074675507471
DeletionChr21370239213702557165
DeletionChr21370283713702992155
DeletionChr215217157152171581LOC_Os02g25930
DeletionChr61548249615482960464
DeletionChr218431061184310621
DeletionChr619710245197102472
DeletionChr724085687240856892
DeletionChr230944039309440401LOC_Os02g50660

Insertions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr424662442246624454
InsertionChr6990804699080472
InsertionChr102871682871692
InsertionChr216496952164969521
InsertionChr314987577149875771
InsertionChr324566392245663921
InsertionChr529906816299068172
InsertionChr8913621591362162
InsertionChr96699620669965031
InsertionChr9705779770577982
InsertionChr1120495066204950672
InsertionChr12562849456284941

Inversions: 15
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr76852776855502
InversionChr667077036707911
InversionChr667077096707859
InversionChr1285408958541355LOC_Os12g14930
InversionChr696325959632866
InversionChr111247626120374662
InversionChr61409246514092811
InversionChr101912990519862020LOC_Os10g35770
InversionChr101912991319862038LOC_Os10g35770
InversionChr122055925420559511
InversionChr122055925920559445
InversionChr122055931620559471
InversionChr82492735424927461
InversionChr42909643429096843
InversionChr13912755039127878

Translocations: 13
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr43954889Chr313850482
TranslocationChr94699954Chr727254265
TranslocationChr117181431Chr1325194172
TranslocationChr47545633Chr132129091LOC_Os04g13530
TranslocationChr118406021Chr710616299
TranslocationChr1110924574Chr97407204
TranslocationChr1213510871Chr71293651
TranslocationChr1216084927Chr911363237
TranslocationChr1218690359Chr56215295
TranslocationChr1121138906Chr713468624LOC_Os11g35970
TranslocationChr1224680799Chr918280007
TranslocationChr329627043Chr12484851LOC_Os03g51710
TranslocationChr432040721Chr331809571