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Mutant Information

Mutant NameFN1217-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1217-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 45
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr14518844A-THETNON_SYNONYMOUS_CODINGLOC_Os01g09000
SBSChr14637693T-CHETINTERGENIC
SBSChr111678409C-THETNON_SYNONYMOUS_CODINGLOC_Os01g20900
SBSChr114302883C-AHOMOSYNONYMOUS_CODING
SBSChr116279541T-CHOMOINTERGENIC
SBSChr131053666G-THETINTERGENIC
SBSChr139092256T-AHOMONON_SYNONYMOUS_CODINGLOC_Os01g67340
SBSChr24760785G-CHOMOINTERGENIC
SBSChr210489766G-CHETINTERGENIC
SBSChr226291702A-GHOMOINTERGENIC
SBSChr234293079T-CHOMOINTERGENIC
SBSChr234675256T-CHOMOINTRON
SBSChr37764911C-THETINTERGENIC
SBSChr38967717G-AHETINTERGENIC
SBSChr41453812G-AHOMOINTERGENIC
SBSChr414477892A-GHETINTERGENIC
SBSChr5314898T-AHOMOINTERGENIC
SBSChr510481035T-GHETINTERGENIC
SBSChr515435342C-THETINTERGENIC
SBSChr61706646G-AHETINTERGENIC
SBSChr63902442C-THETINTRON
SBSChr76543619C-GHETINTERGENIC
SBSChr78201247C-THOMOINTERGENIC
SBSChr83129017T-AHOMOUTR_3_PRIME
SBSChr87057034C-AHOMONON_SYNONYMOUS_CODINGLOC_Os08g12020
SBSChr813095815C-THETINTERGENIC
SBSChr816705853A-THETINTERGENIC
SBSChr99490704G-AHETINTRON
SBSChr99545857A-THETSYNONYMOUS_CODING
SBSChr1014158806G-THETNON_SYNONYMOUS_CODINGLOC_Os10g26920
SBSChr1014158807G-THETNON_SYNONYMOUS_CODINGLOC_Os10g26920
SBSChr118258990C-GHETINTRON
SBSChr1115828703G-AHETINTERGENIC
SBSChr1116466299G-THETINTERGENIC
SBSChr1118849139C-AHETINTRON
SBSChr1118876977A-THETUTR_3_PRIME
SBSChr1121421620C-THOMOINTRON
SBSChr1122477490T-CHOMOINTERGENIC
SBSChr121548998C-GHETINTERGENIC
SBSChr1213322949C-THETINTERGENIC
SBSChr1217174697G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g29020
SBSChr1217824523G-AHOMOINTERGENIC
SBSChr1221203347C-AHETINTERGENIC
SBSChr1221558308G-AHETINTRON
SBSChr1222938089C-AHETINTERGENIC

Deletions: 35
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr6121352212135231
DeletionChr1374848737484925
DeletionChr639022733925254229814
DeletionChr10405762240576231
DeletionChr6594733859473479
DeletionChr5683015268301542
DeletionChr994752529475438186
DeletionChr4987321498732173
DeletionChr4117259921172601119
DeletionChr711854117118541203
DeletionChr1115849242158492431
DeletionChr10164180671641808922
DeletionChr12176178411761785211
DeletionChr5179677721796778614
DeletionChr8183544881835454860
DeletionChr218465574184655795
DeletionChr118763504187635073LOC_Os01g34080
DeletionChr919231524192315295
DeletionChr1119625427196254369
DeletionChr1120007733200077429
DeletionChr720955688209556891
DeletionChr521254511212545176
DeletionChr321801110218011188
DeletionChr722026632220266408
DeletionChr922311274223112795
DeletionChr11242251502422516919
DeletionChr1224263056242630593
DeletionChr1124675781246817175936
DeletionChr627504568275045691
DeletionChr6277682792776829112
DeletionChr3298728732987295178
DeletionChr131232996312330004
DeletionChr3316912333169124613LOC_Os03g55660
DeletionChr131720975317209772
DeletionChr141112001411650005300010

Insertions: 6
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr914806864148068652
InsertionChr332637274326372741
InsertionChr820085411200854122
InsertionChr823611468236114692
InsertionChr827181136271811361
InsertionChr1122614828226148292

Inversions: 6
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr63385020110906202
InversionChr6370567511090625LOC_Os06g19470
InversionChr120383214219270412
InversionChr120383233219270432
InversionChr140238164418421562
InversionChr14111164441842146LOC_Os01g72130

Translocations: 9
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr122930092Chr668906422
TranslocationChr122930677Chr668906432
TranslocationChr1222729739Chr124726876
TranslocationChr1124681710Chr422088431LOC_Os04g36620
TranslocationChr1124681711Chr422088432LOC_Os04g36620
TranslocationChr1224883650Chr116038590LOC_Os12g40200
TranslocationChr825532905Chr63925293LOC_Os06g08090
TranslocationChr825532924Chr63902278LOC_Os06g08060
TranslocationChr1125635009Chr99475262LOC_Os11g42590