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Mutant Information

Mutant NameFN4494-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4494-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 57
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr1936306A-THETNON_SYNONYMOUS_CODINGLOC_Os01g02730
SBSChr15344132G-THOMOINTERGENIC
SBSChr116331620T-GHETINTERGENIC
SBSChr117239993C-AHETINTERGENIC
SBSChr117332167C-THETNON_SYNONYMOUS_CODINGLOC_Os01g31660
SBSChr135551953A-GHETINTERGENIC
SBSChr139814402G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g68510
SBSChr220945880A-THOMOSPLICE_SITE_REGION
SBSChr31398269C-GHETNON_SYNONYMOUS_CODINGLOC_Os03g03260
SBSChr32330221A-GHETINTRON
SBSChr32475835T-AHETINTERGENIC
SBSChr38360325G-AHETINTERGENIC
SBSChr38378057G-AHETNON_SYNONYMOUS_CODINGLOC_Os03g15310
SBSChr313505158G-AHETINTERGENIC
SBSChr313796672G-THETINTRON
SBSChr325338358G-THETINTRON
SBSChr41882267G-CHETINTERGENIC
SBSChr48649572G-AHOMOINTERGENIC
SBSChr410448697C-THOMOINTERGENIC
SBSChr413068776A-THOMOINTRON
SBSChr415036164G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g25870
SBSChr421031056C-THETINTERGENIC
SBSChr427703127T-AHOMOINTERGENIC
SBSChr57663366G-AHOMOINTERGENIC
SBSChr512875203G-AHOMOINTERGENIC
SBSChr513972461G-THOMOINTRON
SBSChr521326587G-AHOMONON_SYNONYMOUS_CODINGLOC_Os05g36010
SBSChr529004962G-AHOMONON_SYNONYMOUS_CODINGLOC_Os05g50600
SBSChr6970501C-THOMOSYNONYMOUS_CODING
SBSChr610283412G-THETINTERGENIC
SBSChr612727849C-THETINTERGENIC
SBSChr74224279C-AHOMOINTERGENIC
SBSChr713609459C-THETINTERGENIC
SBSChr729452473G-THETINTRON
SBSChr813237109A-THOMOINTERGENIC
SBSChr821150618T-CHETINTERGENIC
SBSChr822485744G-CHETINTERGENIC
SBSChr91598324G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g03300
SBSChr97805010G-AHETNON_SYNONYMOUS_CODINGLOC_Os09g13480
SBSChr916216288C-AHETINTERGENIC
SBSChr107142970G-AHETINTERGENIC
SBSChr1010270504C-AHETINTERGENIC
SBSChr1011546284G-AHETINTERGENIC
SBSChr1012530143G-AHETINTRON
SBSChr113020685G-AHETUTR_5_PRIME
SBSChr114462760G-AHOMOINTERGENIC
SBSChr1113993416G-THETINTERGENIC
SBSChr1116925564T-CHOMOINTERGENIC
SBSChr1123497668G-AHETINTERGENIC
SBSChr128358042G-THETNON_SYNONYMOUS_CODINGLOC_Os12g14630
SBSChr128358113G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g14630
SBSChr129253128A-GHETINTERGENIC
SBSChr1214010947G-AHETINTERGENIC
SBSChr1214010949T-AHETINTERGENIC
SBSChr1216944042C-THETNON_SYNONYMOUS_CODINGLOC_Os12g28670
SBSChr1216989198C-THETINTRON
SBSChr1225446228G-AHETUTR_5_PRIME

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr11282021282042
DeletionChr8185468318546885
DeletionChr11224085622408582LOC_Os11g05110
DeletionChr12440760944076101
DeletionChr4513638051363811
DeletionChr5630926363092641
DeletionChr10631840563184061
DeletionChr8722234072223411
DeletionChr7764894776489547LOC_Os07g13340
DeletionChr58993028899304820
DeletionChr5923980092398077
DeletionChr89925883992595471
DeletionChr710768960107689633
DeletionChr611365564113655651
DeletionChr12148136781481370527
DeletionChr1215212693152126974
DeletionChr4152664741526648612
DeletionChr1216471312164713131
DeletionChr7181402211814028766
DeletionChr918207684182076851
DeletionChr1119416594194165984
DeletionChr2200712262007131791
DeletionChr921172505211725061
DeletionChr121713248217132491
DeletionChr425891275258912772
DeletionChr3267935222679353614
DeletionChr328918139289181412
DeletionChr729086688290866891
DeletionChr4290934162909343923
DeletionChr134927905349279061

Insertions: 11
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr2386398738639871
InsertionChr423086445230864451
InsertionChr176250076255657
InsertionChr2216506702165074273
InsertionChr228748696287486961
InsertionChr311279349112793568
InsertionChr7428019042801901
InsertionChr723661243236612464
InsertionChr10443703344370386
InsertionChr11723059172305911
InsertionChr1226967991269679922

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr51782206517822188

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr108111405Chr919170309
TranslocationChr621870113Chr1216522262