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Mutant Information

Mutant NameFN2753-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2753-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 113
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr115824176G-AHETNON_SYNONYMOUS_CODINGLOC_Os01g28244
SBSChr117905812G-AHET
SBSChr118241368A-GHETNON_SYNONYMOUS_CODINGLOC_Os01g33136
SBSChr119869737C-THET
SBSChr122126670T-AHETNON_SYNONYMOUS_CODINGLOC_Os01g39310
SBSChr22138606G-AHET
SBSChr213981702G-CHET
SBSChr221978201G-AHomo
SBSChr222166422C-THET
SBSChr228020379A-THET
SBSChr37682798A-THET
SBSChr311016643G-AHomo
SBSChr319807278C-THomo
SBSChr328881227C-AHET
SBSChr330058467G-AHET
SBSChr331281611C-THET
SBSChr334375481G-CHET
SBSChr42844729G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g05590
SBSChr49449393C-GHET
SBSChr411957221C-THET
SBSChr413261573G-AHomo
SBSChr414794999T-GHomo
SBSChr418127627G-AHET
SBSChr418883696C-AHomo
SBSChr418883697T-CHomo
SBSChr419214358T-CHomo
SBSChr421204477C-AHomo
SBSChr56736152T-AHomo
SBSChr512140692C-THomoNON_SYNONYMOUS_CODINGLOC_Os05g20710
SBSChr513966379A-GHomo
SBSChr522972903C-THET
SBSChr526333603T-CHomo
SBSChr63336626G-AHomo
SBSChr613295840T-AHomo
SBSChr626588652A-GHET
SBSChr629084919G-AHET
SBSChr629479680T-CHET
SBSChr78724830G-AHET
SBSChr714862611C-THomo
SBSChr717135547G-AHET
SBSChr729425169C-AHET
SBSChr8446736G-AHET
SBSChr83384582A-GHET
SBSChr87049914G-AHomo
SBSChr88276829C-THETNON_SYNONYMOUS_CODINGLOC_Os08g13860
SBSChr89151688A-GHETNON_SYNONYMOUS_CODINGLOC_Os08g15100
SBSChr813660220C-THET
SBSChr919362809A-GHET
SBSChr919400857C-THET
SBSChr102692699A-GHET
SBSChr106468134T-AHET
SBSChr106488320G-AHET
SBSChr113124308G-THomo
SBSChr115149599G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g09630
SBSChr1118980858T-AHET
SBSChr1122125403G-THET
SBSChr1125338030C-THET
SBSChr128373141C-GHET
SBSChr129883563G-AHET
SBSChr1211973232G-THET
SBSChr1213719698G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g24110
SBSChr1220945927T-AHomo
SBSChr112999526C-THETSYNONYMOUS_CODING
SBSChr116657453G-THETNON_SYNONYMOUS_CODINGLOC_Os01g29730
SBSChr117714943G-CHETINTERGENIC
SBSChr137745648A-THETUTR_3_PRIME
SBSChr221073994C-THETSYNONYMOUS_CODING
SBSChr229695555C-THETINTRON
SBSChr233047059C-THETNON_SYNONYMOUS_CODINGLOC_Os02g53970
SBSChr233078448C-GHETSTART_GAINED
SBSChr233078452G-THETUTR_5_PRIME
SBSChr233674453A-THETINTRON
SBSChr317224578C-GHOMONON_SYNONYMOUS_CODINGLOC_Os03g30180
SBSChr320500872G-THETINTERGENIC
SBSChr328800928G-THETINTERGENIC
SBSChr329509764G-AHETINTERGENIC
SBSChr332175826G-AHETINTRON
SBSChr410403966C-THETNON_SYNONYMOUS_CODINGLOC_Os04g18750
SBSChr59070881G-AHETINTERGENIC
SBSChr59070882A-THETINTERGENIC
SBSChr511762075T-CHETINTERGENIC
SBSChr523531970T-AHOMOINTERGENIC
SBSChr525534120C-THETINTERGENIC
SBSChr527546792G-AHETINTERGENIC
SBSChr528633800G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g49920
SBSChr611963168T-AHOMOINTERGENIC
SBSChr627984388C-THETINTERGENIC
SBSChr7399401C-THETINTERGENIC
SBSChr727503070T-CHETINTRON
SBSChr81157317T-CHETINTERGENIC
SBSChr82199926A-GHETINTERGENIC
SBSChr812461122G-AHETINTRON
SBSChr819597116G-AHETINTERGENIC
SBSChr820721027G-AHETINTRON
SBSChr95992744G-THETINTRON
SBSChr97499894G-CHETINTERGENIC
SBSChr911207196T-CHETINTERGENIC
SBSChr912047368G-AHETINTERGENIC
SBSChr912306681G-AHETINTRON
SBSChr920518934T-AHETINTERGENIC
SBSChr920825910C-AHETINTERGENIC
SBSChr115794257C-THETINTERGENIC
SBSChr118638112A-CHETINTRON
SBSChr1113463650C-AHOMOINTRON
SBSChr1115050766C-THETINTERGENIC
SBSChr125291350C-THETSYNONYMOUS_CODING
SBSChr1210670185C-THETUTR_5_PRIME
SBSChr1210957923G-THETINTERGENIC
SBSChr1211441647C-THETSYNONYMOUS_CODING
SBSChr1213064266C-THETNON_SYNONYMOUS_CODINGLOC_Os12g23100
SBSChr1219341322C-GHETINTERGENIC
SBSChr1219343331A-THETINTERGENIC
SBSChr1221276986G-AHETSYNONYMOUS_CODING

Deletions: 41
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr48335068335071LOC_Os04g02350
DeletionChr51327551132759140
DeletionChr12152459015245966LOC_Os12g03750
DeletionChr7191583419158373
DeletionChr92225531222560170
DeletionChr82543625254368863
DeletionChr4351004435100451
DeletionChr45349104534913026
DeletionChr5641138164113821
DeletionChr12682638168263821
DeletionChr6724017472401795
DeletionChr128797140879714222
DeletionChr78851707885175144
DeletionChr610037983100379874
DeletionChr710968349109683501
DeletionChr6114854761148548711
DeletionChr712767245127672472
DeletionChr413010166130101704
DeletionChr5135417351354176934
DeletionChr713579697135796981
DeletionChr414753982147539897
DeletionChr81655600116576000199993
DeletionChr81657900116611000319997
DeletionChr1118956067189560681
DeletionChr920666289206662901
DeletionChr1220910937209109381
DeletionChr3214397072143972215
DeletionChr821734592217345942
DeletionChr221926504219265073
DeletionChr422303876223038782
DeletionChr824724154247241562
DeletionChr127205030272050333
DeletionChr1227205500272055055
DeletionChr5276656482766566416
DeletionChr4280957142809574228
DeletionChr6293347642933477410
DeletionChr4303241903032420212
DeletionChr331121859311218634
DeletionChr336045962360459642
DeletionChr139835952398359553
DeletionChr142653212426532186

Insertions: 14
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1125148081251480811
InsertionChr414896425148964251
InsertionChr1394789339478942
InsertionChr335274616352746194
InsertionChr913367940133679412
InsertionChr3539559853956036
InsertionChr315266466152664661
InsertionChr330834296308343016
InsertionChr52925037292505014
InsertionChr5702296170229666
InsertionChr612551051125510511
InsertionChr9490040649004061
InsertionChr11690068669006872
InsertionChr11251130402511305314

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1213733741402214
InversionChr1213733781402219
InversionChr111166055011660943
InversionChr21858276518583272
InversionChr41961221819612385LOC_Os04g32580

Translocations: 19
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr123766431Chr1117795284
TranslocationChr124788930Chr316568136
TranslocationChr115733929Chr110234167
TranslocationChr108110736Chr116916018
TranslocationChr128582249Chr119169551LOC_Os01g34760
TranslocationChr1110659256Chr615618050
TranslocationChr812890399Chr526582797
TranslocationChr812890406Chr120080061
TranslocationChr1213923178Chr219373260
TranslocationChr1214379827Chr1111845209LOC_Os11g20460
TranslocationChr1215191193Chr418885976
TranslocationChr819371940Chr720951359LOC_Os08g31320
TranslocationChr819372459Chr720951362
TranslocationChr820584384Chr61072417
TranslocationChr620931162Chr122551268LOC_Os06g35870
TranslocationChr921260004Chr824138969
TranslocationChr1122608900Chr911816282
TranslocationChr526005965Chr1338543322
TranslocationChr1127758202Chr43130962