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Mutant Information

Mutant NameFN4448-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4448-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 32
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr13136810G-AHETSYNONYMOUS_CODING
SBSChr121160539G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g37825
SBSChr135045078C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g60620
SBSChr217026277C-THETSYNONYMOUS_CODING
SBSChr217559029C-THETINTERGENIC
SBSChr219595861G-AHOMOINTERGENIC
SBSChr224633814G-AHOMOINTERGENIC
SBSChr38957525A-THOMOINTERGENIC
SBSChr322697242C-THETINTERGENIC
SBSChr333657222C-THETINTERGENIC
SBSChr335849607A-CHETINTRON
SBSChr45998762C-THETINTERGENIC
SBSChr46772989A-GHOMONON_SYNONYMOUS_CODINGLOC_Os04g12260
SBSChr47540165G-AHOMOSYNONYMOUS_CODING
SBSChr424653297G-AHETINTERGENIC
SBSChr430535965C-THETSYNONYMOUS_CODING
SBSChr55498490C-THETINTERGENIC
SBSChr516448270G-AHETSTOP_GAINEDLOC_Os05g28120
SBSChr520713290G-THETINTERGENIC
SBSChr528219369G-THETINTERGENIC
SBSChr64888989C-THETSYNONYMOUS_CODING
SBSChr611080609T-AHOMOINTERGENIC
SBSChr615908368C-AHOMOINTERGENIC
SBSChr76485608T-GHETINTERGENIC
SBSChr79516043G-AHOMOINTERGENIC
SBSChr719351877G-THETINTERGENIC
SBSChr922833103G-AHETINTRON
SBSChr103198927A-GHETINTERGENIC
SBSChr105104504G-THETINTERGENIC
SBSChr1114816189T-CHOMOINTRON
SBSChr1122278435C-THETNON_SYNONYMOUS_CODINGLOC_Os11g37700
SBSChr129229162T-CHOMOINTERGENIC

Deletions: 46
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1013150011334000190005
DeletionChr11147632214763231
DeletionChr101493001159500010200016
DeletionChr2150497915049801
DeletionChr11265417926541801
DeletionChr12279254627925471
DeletionChr10330395533039561LOC_Os10g06430
DeletionChr5407867440786751
DeletionChr6456807345680774
DeletionChr9464022346402241
DeletionChr5509888150988865
DeletionChr115830276583028812
DeletionChr6613936061393611
DeletionChr10691685469168562
DeletionChr77250670725069121
DeletionChr2787371378737141
DeletionChr12851253485125351
DeletionChr5951445695144571
DeletionChr911674405116744061
DeletionChr711986830119868333LOC_Os07g20720
DeletionChr1112093572120935753
DeletionChr71224843012248590160
DeletionChr414391659143916601
DeletionChr717385492173854931
DeletionChr10178480011818300033500032
DeletionChr10180628461806287428
DeletionChr10182010011830200010100018
DeletionChr1118214172182141731
DeletionChr1218795655187956561
DeletionChr1021173471211734765
DeletionChr521509511215095121
DeletionChr2227972592279728223
DeletionChr824526936245269371LOC_Os08g38800
DeletionChr124826560248265633
DeletionChr524917968249179691
DeletionChr1225678009256780156LOC_Os12g41450
DeletionChr525899944258999462
DeletionChr526451369264513701
DeletionChr427002727270027281
DeletionChr1127075273270752741
DeletionChr1273528782735288911
DeletionChr3273643572736437417
DeletionChr428567804285678051
DeletionChr629273253292732541
DeletionChr3316406563164067721
DeletionChr134011951340119609

Insertions: 44
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr123701485237014862
InsertionChr123978506239785094
InsertionChr140326882403268843
InsertionChr3787904678790461
InsertionChr4613815161381511
InsertionChr919488586194885872
InsertionChr12555981355598175
InsertionChr1903197290319721
InsertionChr112346137123461371
InsertionChr132723184327231841
InsertionChr3376459437645941
InsertionChr3414349741434971
InsertionChr317521048175210481
InsertionChr332241562322415621
InsertionChr4233204523320451
InsertionChr4655273265527321
InsertionChr410471975104719751
InsertionChr422704544227045441
InsertionChr423166864231668641
InsertionChr431847295318472951
InsertionChr5163429916342991
InsertionChr56363883636393856
InsertionChr5818352881835281
InsertionChr511217752112177521
InsertionChr511681775116817751
InsertionChr5157260911572611929
InsertionChr517598412175984121
InsertionChr529179565291795651
InsertionChr612548252125482521
InsertionChr7980325398032531
InsertionChr8132330913233091
InsertionChr8731727273172743
InsertionChr814469275144692751
InsertionChr95763555763562
InsertionChr10693147469314741
InsertionChr10835786883578681
InsertionChr1020234735202347362
InsertionChr1158165058166112
InsertionChr11103249810324981
InsertionChr1116183446161834461
InsertionChr12845389584538962
InsertionChr12985248098524812
InsertionChr12152284421522845514LOC_Os12g26140image
InsertionChr1222682846226828461

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr62468460824730205

Translocations: 7
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr101315288Chr4209104702
TranslocationChr101315401Chr4209104692
TranslocationChr98711177Chr815782154
TranslocationChr1010355522Chr815782149LOC_Os08g16910
TranslocationChr916416495Chr22673873
TranslocationChr419119507Chr222665665
TranslocationChr431826025Chr24174006LOC_Os04g53450