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Mutant Information

Mutant NameFN2725-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2725-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 132
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr11251589A-GHomo
SBSChr14177322C-AHET
SBSChr111756568C-THET
SBSChr115572817C-THomo
SBSChr117010469A-GHomo
SBSChr117135189T-GHomo
SBSChr133073022C-THET
SBSChr133162737C-GHET
SBSChr133942994G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g58710
SBSChr134392738C-THET
SBSChr140884064C-THET
SBSChr27171336A-GHomo
SBSChr27502431G-CHomo
SBSChr223658613A-THomo
SBSChr225670941A-CHomo
SBSChr233274863C-THET
SBSChr32537993G-AHET
SBSChr38710033C-THomo
SBSChr315080629C-THET
SBSChr320556672A-THET
SBSChr327409767A-CHET
SBSChr330974030T-CHET
SBSChr333399366G-AHETNON_SYNONYMOUS_CODINGLOC_Os03g58640
SBSChr335587572G-AHET
SBSChr44896678A-THET
SBSChr48985558A-CHET
SBSChr424486051G-THET
SBSChr430138716C-AHET
SBSChr55064534C-GHET
SBSChr514260461G-AHET
SBSChr518225851C-THomo
SBSChr519150799T-CHET
SBSChr64002638G-AHET
SBSChr69936920G-THET
SBSChr615568844A-THET
SBSChr615568845T-AHET
SBSChr617740750C-THET
SBSChr620088079C-AHET
SBSChr77162950T-CHET
SBSChr718754915G-AHomo
SBSChr723496658C-THET
SBSChr723571070G-AHomo
SBSChr726750819A-GHomo
SBSChr727956711T-AHETNON_SYNONYMOUS_CODINGLOC_Os07g46780
SBSChr88503200T-CHET
SBSChr817128570T-CHET
SBSChr820892264C-THET
SBSChr823436547A-THomo
SBSChr91926523G-AHET
SBSChr91969887C-THET
SBSChr95008652C-AHET
SBSChr917483253T-CHomo
SBSChr922374907T-CHET
SBSChr103322159C-THET
SBSChr103328261G-CHomo
SBSChr106707478A-GHomo
SBSChr109049350C-THomo
SBSChr1010179376A-GHomo
SBSChr1012051403T-AHomo
SBSChr1020563734C-AHomo
SBSChr1022054887G-THomo
SBSChr112366329G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g05340
SBSChr1114531401G-THET
SBSChr1117331039C-THETNON_SYNONYMOUS_CODINGLOC_Os11g29850
SBSChr1123639822C-THET
SBSChr123472955C-THET
SBSChr126225119G-AHET
SBSChr1212262962G-CHET
SBSChr1222115824C-THET
SBSChr111756568C-THETINTERGENIC
SBSChr115572817C-THOMOINTRON
SBSChr117010469A-GHOMOINTERGENIC
SBSChr117135189T-GHOMOINTERGENIC
SBSChr133073022C-THETINTERGENIC
SBSChr133162737C-GHETINTERGENIC
SBSChr134392738C-THETINTERGENIC
SBSChr140884064C-THETINTERGENIC
SBSChr27171336A-GHOMOINTERGENIC
SBSChr27502431G-CHOMOINTRON
SBSChr215920171G-AHETINTERGENIC
SBSChr223658613A-THOMOINTRON
SBSChr225670941A-CHOMOINTRON
SBSChr233274863C-THETINTERGENIC
SBSChr32537993G-AHETINTERGENIC
SBSChr38710033C-THOMOINTERGENIC
SBSChr315080629C-THETSYNONYMOUS_CODING
SBSChr320556672A-THETINTRON
SBSChr326893589C-AHETINTRON
SBSChr327409767A-CHETINTRON
SBSChr330974030T-CHETSYNONYMOUS_CODING
SBSChr48985558A-CHETINTRON
SBSChr413106144A-THETINTERGENIC
SBSChr422576125T-CHETINTERGENIC
SBSChr423800692C-THETINTERGENIC
SBSChr424486051G-THETINTRON
SBSChr430138716C-AHETINTERGENIC
SBSChr434736713T-CHETINTERGENIC
SBSChr514260461G-AHETINTERGENIC
SBSChr518225851C-THOMOINTERGENIC
SBSChr528348596T-CHETINTERGENIC
SBSChr6448797C-THETINTERGENIC
SBSChr615568844A-THETINTRON
SBSChr615568845T-AHETINTRON
SBSChr620088079C-AHETUTR_3_PRIME
SBSChr77162950T-CHETINTERGENIC
SBSChr78544040C-THETSYNONYMOUS_STOP
SBSChr718754915G-AHOMOINTERGENIC
SBSChr723571070G-AHOMOINTERGENIC
SBSChr726750819A-GHOMOINTERGENIC
SBSChr88503200T-CHETINTERGENIC
SBSChr817128570T-CHETINTRON
SBSChr823436547A-THOMOINTERGENIC
SBSChr91969887C-THETINTRON
SBSChr92715111G-THETINTERGENIC
SBSChr94530675T-CHETNON_SYNONYMOUS_CODINGLOC_Os09g08650
SBSChr915965745C-THETINTERGENIC
SBSChr917483253T-CHOMOINTERGENIC
SBSChr922374907T-CHETINTERGENIC
SBSChr103328261G-CHOMOINTERGENIC
SBSChr106707478A-GHOMOINTERGENIC
SBSChr109049350C-THOMOINTRON
SBSChr1010179376A-GHOMOINTERGENIC
SBSChr1012051403T-AHOMOINTRON
SBSChr1016967570T-CHOMOINTERGENIC
SBSChr1020563734C-AHOMOINTERGENIC
SBSChr1022054887G-THOMOINTERGENIC
SBSChr1114531401G-THETINTERGENIC
SBSChr1123639822C-THETINTERGENIC
SBSChr126225119G-AHETSYNONYMOUS_CODING
SBSChr1212262962G-CHETINTERGENIC
SBSChr1218061438T-CHETINTERGENIC
SBSChr1222115824C-THETINTERGENIC

Deletions: 41
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr23688423688431
DeletionChr79728919728921
DeletionChr121590810159081662
DeletionChr5227483022748311
DeletionChr102549515254951942
DeletionChr22656475265647832
DeletionChr1033360413336054132
DeletionChr23394477339448252
DeletionChr34172910417291112
DeletionChr44849085484915671
DeletionChr75301251530127019
DeletionChr86341654634173379
DeletionChr97335141733523998
DeletionChr28058748805874912
DeletionChr28177575817757612
DeletionChr3828537082853711LOC_Os03g15160
DeletionChr184811308481145152
DeletionChr6971129897113024
DeletionChr510198056101980571
DeletionChr3103931921039319422
DeletionChr611800947118009525
DeletionChr912679376126793771LOC_Os09g21020
DeletionChr10133473571334735922
DeletionChr713347508133475091LOC_Os07g23610
DeletionChr713690648136906535
DeletionChr8149160321491603862
DeletionChr71549350415493516122
DeletionChr7161372251613723712
DeletionChr101695000116991000409995
DeletionChr101695200116991000389995
DeletionChr51726357917263592132
DeletionChr7174059431740594522
DeletionChr7186944571869446710
DeletionChr919936471199364743LOC_Os09g33750
DeletionChr1120235107202351081
DeletionChr22550335725503369122
DeletionChr6272446622724466422
DeletionChr327328619273286201
DeletionChr11284059222840601492
DeletionChr430859493308594952
DeletionChr140770942407709431

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr19866617986661822image
InsertionChr8258241532582415422image
InsertionChr230175401301754033
InsertionChr1114145230141452301
InsertionChr19866617986661822image
InsertionChr8258241532582415422image
InsertionChr11580161580161LOC_Os01g01320image
InsertionChr1706536870653736
InsertionChr234434078344340781
InsertionChr3957069095706978
InsertionChr4770679677067961
InsertionChr410182469101824691
InsertionChr611098499110984991
InsertionChr8169701216970154
InsertionChr10588374158837411
InsertionChr11998719999871991
InsertionChr1113254646132546461
InsertionChr1123155758231557636
InsertionChr1224906263249062631

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr129813482981541

Translocations: 14
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr102470738Chr4679517
TranslocationChr106618984Chr6134574042
TranslocationChr106928220Chr819394181
TranslocationChr109912215Chr2329087832
TranslocationChr119960409Chr822924000
TranslocationChr710706080Chr34570858LOC_Os03g08834
TranslocationChr1112631453Chr104408877
TranslocationChr1013030905Chr918669036
TranslocationChr1013030909Chr9186682092
TranslocationChr1213936898Chr416502356LOC_Os12g24420
TranslocationChr819194685Chr795654732
TranslocationChr819691030Chr79266819
TranslocationChr720402996Chr629925132
TranslocationChr725340100Chr331170074