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Mutant Information

Mutant NameFN1379-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1379-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • TO:0000346 (Tiller number) = Normal (Between 75% and 125%)
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 52
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr116831429C-AHETINTERGENIC
SBSChr123078274G-THETINTRON
SBSChr123696551C-THETINTERGENIC
SBSChr17987320C-THETINTERGENIC
SBSChr1013610698A-GHETINTERGENIC
SBSChr1018221691A-GHETINTERGENIC
SBSChr1113191982T-CHETINTERGENIC
SBSChr1210856436A-CHETINTERGENIC
SBSChr1213578179C-THETNON_SYNONYMOUS_CODINGLOC_Os12g23880
SBSChr1215378508T-CHETINTERGENIC
SBSChr12461388A-CHETINTERGENIC
SBSChr125109676T-AHETINTRON
SBSChr127591899C-THomoINTERGENIC
SBSChr219445033A-GHETINTRON
SBSChr312442289T-AHomoINTRON
SBSChr319747713T-CHomoINTRON
SBSChr322362433A-THomoINTERGENIC
SBSChr328013903C-AHETINTERGENIC
SBSChr331897807G-AHETINTERGENIC
SBSChr336148164A-GHETINTERGENIC
SBSChr418361909C-THETSPLICE_SITE_REGION
SBSChr422094978T-AHETINTERGENIC
SBSChr428483592C-THETINTERGENIC
SBSChr429712006G-AHETINTRON
SBSChr433221060T-CHETINTERGENIC
SBSChr45461058A-THETINTRON
SBSChr45461059C-THETINTRON
SBSChr48520812C-THomoINTERGENIC
SBSChr511831603C-GHETINTERGENIC
SBSChr519878929C-THETSYNONYMOUS_CODING
SBSChr57407708C-THomoINTERGENIC
SBSChr612194303G-AHETINTERGENIC
SBSChr612281400A-GHETUTR_3_PRIME
SBSChr616401373T-CHETINTRON
SBSChr625455641G-AHETINTERGENIC
SBSChr712497096T-CHETINTERGENIC
SBSChr714044458C-THETNON_SYNONYMOUS_CODINGLOC_Os07g24690
SBSChr717070887C-GHETNON_SYNONYMOUS_CODINGLOC_Os07g29160
SBSChr717228502T-CHETINTERGENIC
SBSChr727090740T-CHomoNON_SYNONYMOUS_CODINGLOC_Os07g45410
SBSChr74900664A-THETINTERGENIC
SBSChr76025689A-GHomoINTERGENIC
SBSChr77872830C-AHETINTERGENIC
SBSChr810696815C-THomoNON_SYNONYMOUS_CODINGLOC_Os08g17460
SBSChr810696816C-THomoNON_SYNONYMOUS_CODINGLOC_Os08g17460
SBSChr811022296C-AHETNON_SYNONYMOUS_CODINGLOC_Os08g17980
SBSChr811149381G-AHETINTRON
SBSChr811588974A-CHomoUTR_3_PRIME
SBSChr825211614G-THETINTRON
SBSChr825211625G-THETINTRON
SBSChr85627081C-THETINTERGENIC
SBSChr91254066C-THomoINTERGENIC

Deletions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr31143321143342
DeletionChr1252709825270991
DeletionChr6259867725986803
DeletionChr6275584327558452
DeletionChr3433651343365141
DeletionChr9541656754165681
DeletionChr4747747674774771
DeletionChr611197683111976841
DeletionChr11137716061377162014
DeletionChr1014849589148495901
DeletionChr516351030163510311
DeletionChr6182340011868800045400073
DeletionChr420012972200129731
DeletionChr920442720204427222
DeletionChr920511150205111577LOC_Os09g35660
DeletionChr1020611555206115561
DeletionChr6209569522095699341
DeletionChr820969080209690877
DeletionChr11213786822137870018
DeletionChr10213855052138552924
DeletionChr221803328218033291
DeletionChr621831021218310221
DeletionChr6219925302199255828LOC_Os06g37224
DeletionChr126822652268226608LOC_Os01g46984
DeletionChr2272899862729004256
DeletionChr727847003278470096LOC_Os07g46610
DeletionChr431881381318813832
DeletionChr333754256337542648
DeletionChr140685071406850743

Insertions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr119519264195192674
InsertionChr121115852211158521
InsertionChr18786968786972
InsertionChr10516794651679472
InsertionChr314103551141035522
InsertionChr4861925886192581
InsertionChr510776599107766024
InsertionChr511511193115111931
InsertionChr517464032174640332
InsertionChr723610120236101212
InsertionChr824344729243447291
InsertionChr8244640724464071LOC_Os08g04850image

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr2680620117449712LOC_Os02g29380
InversionChr2680705817449698LOC_Os02g29380
InversionChr112011911220178196
InversionChr82046074420767020LOC_Os08g32970
InversionChr820460755210279992

No Translocation