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Mutant Information

Mutant NameFN429-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN429-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 40
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr12662527G-AHOMOINTERGENIC
SBSChr13905569T-AHOMOSYNONYMOUS_CODING
SBSChr139340831C-AHETSYNONYMOUS_CODING
SBSChr1021816941G-AHOMOINTERGENIC
SBSChr107752556A-GHETNON_SYNONYMOUS_CODINGLOC_Os10g14795
SBSChr1118877542G-AHETINTERGENIC
SBSChr1121272719C-THETINTERGENIC
SBSChr1122038668T-GHETNON_SYNONYMOUS_CODINGLOC_Os11g37320
SBSChr1123881667G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g40050
SBSChr1212636112T-GHETINTRON
SBSChr1213078840G-THETINTERGENIC
SBSChr1214283473T-AHETINTERGENIC
SBSChr1217457285C-THETNON_SYNONYMOUS_CODINGLOC_Os12g29380
SBSChr1222908954A-THETINTERGENIC
SBSChr124928108C-THETINTRON
SBSChr219744260G-AHETSYNONYMOUS_CODING
SBSChr223630707T-AHOMOINTERGENIC
SBSChr232081505C-THETNON_SYNONYMOUS_CODINGLOC_Os02g52420
SBSChr321611196T-CHETINTERGENIC
SBSChr322717C-THETSYNONYMOUS_CODING
SBSChr330694461G-CHOMOUTR_3_PRIME
SBSChr417407611C-THETNON_SYNONYMOUS_CODINGLOC_Os04g29330
SBSChr41926561C-THETINTERGENIC
SBSChr44381115G-AHOMOINTERGENIC
SBSChr517177457C-THETINTERGENIC
SBSChr522099348T-GHOMOINTERGENIC
SBSChr55295969G-CHETSYNONYMOUS_CODING
SBSChr613847285T-CHOMOINTERGENIC
SBSChr614857884C-THOMOSYNONYMOUS_CODING
SBSChr714259863C-THETINTERGENIC
SBSChr718011209G-THETINTERGENIC
SBSChr728247783C-AHETNON_SYNONYMOUS_CODINGLOC_Os07g47260
SBSChr729249124A-GHETSPLICE_SITE_REGION
SBSChr810982403T-CHOMONON_SYNONYMOUS_CODINGLOC_Os08g17890
SBSChr816087853G-THOMOINTERGENIC
SBSChr816087856A-GHOMOINTERGENIC
SBSChr82546531T-AHETSYNONYMOUS_CODING
SBSChr912042302A-GHETINTERGENIC
SBSChr912908568T-CHETINTERGENIC
SBSChr96474717C-THETINTERGENIC

Deletions: 35
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr121720881720924
DeletionChr270845170849544
DeletionChr8153704215370464LOC_Os08g03310
DeletionChr3325000132500032
DeletionChr123574320357433010LOC_Os12g07270
DeletionChr3390978639097882
DeletionChr6479347647934771
DeletionChr4534879653487971
DeletionChr6616163061616311LOC_Os06g11630
DeletionChr6667886166788654LOC_Os06g12320
DeletionChr8813005481300562
DeletionChr12100504201005045131LOC_Os12g17530
DeletionChr1119092491190926213LOC_Os01g21320
DeletionChr1112898408128984124
DeletionChr1212963530129635399
DeletionChr3153584221535843210
DeletionChr4158957111589579786
DeletionChr816084549160845501LOC_Os08g26400
DeletionChr416603423166034296LOC_Os04g28120
DeletionChr2188802761888028812
DeletionChr719995303199953129
DeletionChr720360120203601211
DeletionChr11212427542124277016
DeletionChr421526224215262295
DeletionChr122195170221951755LOC_Os01g39385
DeletionChr222382683223826863LOC_Os02g37050
DeletionChr322831793228318007
DeletionChr6245880592458806910
DeletionChr825179440251794466LOC_Os08g39760
DeletionChr627589008275890157LOC_Os06g45560
DeletionChr3313496683134968113LOC_Os03g55100
DeletionChr232081490320814966LOC_Os02g52420
DeletionChr232216566322165715
DeletionChr434490206344902126LOC_Os04g57880
DeletionChr139135892391359019

Insertions: 5
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr11162314516231462
InsertionChr1223551114235511152
InsertionChr2307356830735681
InsertionChr6399941139994122
InsertionChr824487704244877041

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr72471962824939848

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1110453751Chr212969273
TranslocationChr1118280684Chr329622228
TranslocationChr1218702617Chr1123936814
TranslocationChr1220138349Chr513277467LOC_Os12g33280