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Mutant Information

Mutant NameFN414-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN414-S Alignment File
Seed AvailabilityNo
Phenotype
  • TO:0000014 (Panicle Weight) = Low (Between 25% and 74%)
  • TO:0000207 (Plant height) = Normal (Between 75% and 125%)
  • TO:0000445 (Seed Number) = Low (Between 25% and 74%)
  • TO:0000639 (Seed fertility) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 34
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr127610781C-THETINTERGENIC
SBSChr1016876206G-AHOMOINTRON
SBSChr1110845900C-THETINTRON
SBSChr111239364T-CHOMOINTERGENIC
SBSChr127597021T-AHETINTERGENIC
SBSChr212569877T-AHOMOINTERGENIC
SBSChr212569880C-AHOMOUTR_5_PRIME
SBSChr219181468G-THETINTERGENIC
SBSChr229020687T-CHETUTR_5_PRIME
SBSChr231919040A-THOMOINTRON
SBSChr233687588A-CHETINTERGENIC
SBSChr234383037T-CHOMOSYNONYMOUS_CODING
SBSChr29425374T-CHOMOINTERGENIC
SBSChr311903888A-THETNON_SYNONYMOUS_CODINGLOC_Os03g20980
SBSChr3200010G-THETINTERGENIC
SBSChr335225100A-GHETNON_SYNONYMOUS_CODINGLOC_Os03g62190
SBSChr410606396G-AHETINTERGENIC
SBSChr425088817A-GHOMONON_SYNONYMOUS_CODINGLOC_Os04g42399
SBSChr426872782A-GHETINTERGENIC
SBSChr430846725C-THETINTERGENIC
SBSChr434563303T-AHOMOINTERGENIC
SBSChr45609214T-AHETNON_SYNONYMOUS_CODINGLOC_Os04g10380
SBSChr45609215C-AHETSTOP_GAINEDLOC_Os04g10380
SBSChr48298864C-THETINTERGENIC
SBSChr49612683G-AHETINTERGENIC
SBSChr511632087T-GHETINTRON
SBSChr514298692A-THETINTRON
SBSChr57275038T-AHETINTERGENIC
SBSChr58718539G-CHETINTERGENIC
SBSChr717673566C-THETSYNONYMOUS_CODING
SBSChr726169817G-AHOMOINTERGENIC
SBSChr727695418G-AHOMONON_SYNONYMOUS_CODINGLOC_Os07g46410
SBSChr810756048C-GHETINTERGENIC
SBSChr92059577A-GHETINTERGENIC

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr3100121000200005
DeletionChr4119600112900009400012
DeletionChr4149638914963901
DeletionChr7221022122102221LOC_Os07g05010
DeletionChr22683493268350613LOC_Os02g05550
DeletionChr6278649627864971
DeletionChr2293937629393804LOC_Os02g05920
DeletionChr11327774132777465
DeletionChr6641693664169371
DeletionChr8112877041128771612
DeletionChr2130858811308589110
DeletionChr214071226140712337
DeletionChr215201858152018591
DeletionChr416388804163888073LOC_Os04g27730
DeletionChr219060828190608346
DeletionChr820060886200608871LOC_Os08g32390
DeletionChr2207788962077890812
DeletionChr1021201920212019222LOC_Os10g39670
DeletionChr121626691216267009LOC_Os01g38480
DeletionChr52223948022254715152352
DeletionChr823230384232303873
DeletionChr12238298562382987014
DeletionChr123989302239893042
DeletionChr8243511082435112517
DeletionChr425364162253641642
DeletionChr129172241291722421
DeletionChr430999971310012201249LOC_Os04g52180
DeletionChr231932012319320131
DeletionChr134007914340079195
DeletionChr136444443364444518

Insertions: 1
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr218412677184126771

Inversions: 6
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr11772625579676202
InversionChr31200666312554849LOC_Os03g21080
InversionChr31200667912554855LOC_Os03g21080
InversionChr1121096575288506032
InversionChr23191532532371085
InversionChr23191534032371090

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr812049967Chr427823534
TranslocationChr1019158654Chr226014056
TranslocationChr1019158658Chr225512988LOC_Os02g42406
TranslocationChr522239490Chr312158520LOC_Os05g37930
TranslocationChr522254714Chr312158511
TranslocationChr1126099974Chr8174923132
TranslocationChr1226150506Chr223421992LOC_Os02g38760
TranslocationChr1128850604Chr1191545202