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Mutant Information

Mutant NameFN2897-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2897-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 33
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr110404460A-GHETSPLICE_SITE_DONORLOC_Os01g18500
SBSChr126394294T-CHETNON_SYNONYMOUS_CODINGLOC_Os01g46380
SBSChr128962461C-THETINTERGENIC
SBSChr1011348269G-THETNON_SYNONYMOUS_CODINGLOC_Os10g21980
SBSChr1011348270C-GHETNON_SYNONYMOUS_CODINGLOC_Os10g21980
SBSChr1012914598A-GHETINTERGENIC
SBSChr107854407C-THETINTERGENIC
SBSChr1115196680G-AHETSYNONYMOUS_CODING
SBSChr1117827027T-CHETINTERGENIC
SBSChr1124648405A-THETINTRON
SBSChr1211877891C-THETINTRON
SBSChr1215260540G-THETINTERGENIC
SBSChr310970346A-GHETINTERGENIC
SBSChr321249331G-AHOMOSYNONYMOUS_CODING
SBSChr34063767A-GHOMOINTERGENIC
SBSChr414547660G-AHOMOINTERGENIC
SBSChr41998944G-AHETINTERGENIC
SBSChr427644425C-AHETINTERGENIC
SBSChr434452790A-THETINTRON
SBSChr526223390A-GHETINTERGENIC
SBSChr526668448A-THETINTERGENIC
SBSChr53579783C-THOMOINTERGENIC
SBSChr622841878G-CHETINTERGENIC
SBSChr65481990A-GHETINTERGENIC
SBSChr721715954C-THETINTERGENIC
SBSChr77188318G-AHETINTERGENIC
SBSChr77758335T-CHETINTERGENIC
SBSChr78015051C-THETINTRON
SBSChr815307845G-AHOMOINTRON
SBSChr86762455G-THETINTRON
SBSChr86762456G-THETINTRON
SBSChr916723758A-THETINTERGENIC
SBSChr93987949C-THETINTRON

Deletions: 38
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr4195910019591022
DeletionChr53345001345700011199917
DeletionChr5357155735715603
DeletionChr33707691370775160LOC_Os03g07270
DeletionChr5393692739369292
DeletionChr8591582959158323
DeletionChr86240565624058419
DeletionChr106695189669527384
DeletionChr116844094684410511
DeletionChr11695015069501533LOC_Os11g12440
DeletionChr9695348269534853
DeletionChr3730011273001131
DeletionChr2846817284681764
DeletionChr4906167890616791
DeletionChr10950300196010009799915
DeletionChr8110026111100262918
DeletionChr511598476115984793
DeletionChr412787751127877521
DeletionChr512901257129012647
DeletionChr8137922191379227960
DeletionChr116404901164049109
DeletionChr10167541431675415411
DeletionChr4187269261872693812
DeletionChr418884108188841124
DeletionChr7189686541896871056LOC_Os07g31900
DeletionChr519696785196967861
DeletionChr220287278202872824
DeletionChr1208990332089906128
DeletionChr32178000121825000449997
DeletionChr1121849129218491301
DeletionChr122572221225722221
DeletionChr724756502247565031LOC_Os07g41320
DeletionChr426050638260506391
DeletionChr827625588276255902
DeletionChr52984919129849899708
DeletionChr235253305352533116LOC_Os02g57530
DeletionChr1372096653720968621
DeletionChr137209759372097623

Insertions: 25
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr110348131103481333
InsertionChr1011844458118444581
InsertionChr1014002198140021981
InsertionChr10324488932448891
InsertionChr106722414672243724
InsertionChr10902367790236804
InsertionChr11145832721458329423
InsertionChr11529212552921262
InsertionChr1216798949167989524
InsertionChr1222991616229916205LOC_Os12g37460image
InsertionChr12299873029987301
InsertionChr24467456446751156
InsertionChr327940344279403441
InsertionChr328982499289825002
InsertionChr428820146288201461
InsertionChr431890704318907041
InsertionChr511574713115747131
InsertionChr520416205204162051
InsertionChr699760699769691
InsertionChr711302752113027521
InsertionChr812820254128202541
InsertionChr820767372207673721
InsertionChr8251236922512374251
InsertionChr8529183752918371
InsertionChr914772197147721971

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1095024419678858
InversionChr1095970039679168
InversionChr91672579316733745LOC_Os09g27540
InversionChr91672579716733753LOC_Os09g27540
InversionChr32124104421820094

Translocations: 11
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr101076403Chr130658065
TranslocationChr63024365Chr216275481
TranslocationChr74773878Chr44289191
TranslocationChr74774280Chr44289185LOC_Os07g09140
TranslocationChr105409188Chr42632481
TranslocationChr85495784Chr210021553
TranslocationChr109678868Chr138974461LOC_Os01g67134
TranslocationChr109679152Chr138974461LOC_Os01g67134
TranslocationChr419009544Chr217021801
TranslocationChr819389187Chr418052947
TranslocationChr1122529379Chr9902063LOC_Os11g37990