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Mutant Information

Mutant NameFN1630-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1630-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000137 (Days to heading) = Normal (Between 75% and 125%)
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 53
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr121792679G-AHomoINTERGENIC
SBSChr1016604583G-AHETINTERGENIC
SBSChr1020697641C-THETINTERGENIC
SBSChr1110111933C-GHETNON_SYNONYMOUS_CODINGLOC_Os11g17990
SBSChr1114100823T-CHETINTERGENIC
SBSChr1117716746G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g30470
SBSChr1120218222T-CHETINTERGENIC
SBSChr1120783228T-AHomoINTERGENIC
SBSChr119514556G-AHETINTERGENIC
SBSChr1217435778G-THETINTERGENIC
SBSChr1218712657G-THETINTERGENIC
SBSChr1220406476C-AHETINTERGENIC
SBSChr128264907T-CHETINTERGENIC
SBSChr211510302T-GHomoINTRON
SBSChr227517627G-CHomoINTERGENIC
SBSChr232212683C-AHETINTERGENIC
SBSChr314005514T-CHETINTERGENIC
SBSChr319830286T-CHETINTERGENIC
SBSChr326924224C-THETINTRON
SBSChr3470091G-THETINTERGENIC
SBSChr35117584A-GHETSYNONYMOUS_CODING
SBSChr413888214G-AHomoINTERGENIC
SBSChr416399900G-AHETINTERGENIC
SBSChr421810413T-AHomoINTERGENIC
SBSChr423979097C-THETNON_SYNONYMOUS_CODINGLOC_Os04g40330
SBSChr510617848G-AHETINTERGENIC
SBSChr518819226T-CHETINTERGENIC
SBSChr520860796C-THETINTERGENIC
SBSChr524059929C-THomoINTERGENIC
SBSChr524059933A-THomoINTERGENIC
SBSChr526290121A-CHomoINTRON
SBSChr527404796G-AHETINTERGENIC
SBSChr527633305C-THETINTRON
SBSChr56770482G-AHETINTERGENIC
SBSChr620921471G-AHETINTERGENIC
SBSChr67251190G-AHomoINTERGENIC
SBSChr712791736C-THETINTERGENIC
SBSChr717248992C-THETINTERGENIC
SBSChr718880290G-THETINTERGENIC
SBSChr718880291A-THETINTERGENIC
SBSChr718880296C-THETINTERGENIC
SBSChr726705339A-CHETINTERGENIC
SBSChr727439607T-GHETINTERGENIC
SBSChr79882076A-GHETSYNONYMOUS_CODING
SBSChr814412828G-AHETINTERGENIC
SBSChr816216144T-CHETINTERGENIC
SBSChr816244820G-AHETINTERGENIC
SBSChr824169735G-AHETINTERGENIC
SBSChr86481005G-THETSYNONYMOUS_CODING
SBSChr87618304C-THETINTRON
SBSChr88359394G-AHomoNON_SYNONYMOUS_CODINGLOC_Os08g13950
SBSChr93785355G-THETINTERGENIC
SBSChr94165307C-AHETINTERGENIC

Deletions: 43
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr115333435333518LOC_Os11g02000
DeletionChr108626508626511
DeletionChr109998509998511
DeletionChr2374324037432411
DeletionChr23869584386959612
DeletionChr2398047939804834
DeletionChr44789224478923915LOC_Os04g08780
DeletionChr55028003502802421
DeletionChr3671256267125686
DeletionChr5691697269169731
DeletionChr6704653070465388
DeletionChr10849672784967336
DeletionChr10864379786513297532LOC_Os10g17210
DeletionChr1879679787967992
DeletionChr810571500105715077
DeletionChr1111794048117940568
DeletionChr111227459112274708117
DeletionChr312952482129524853LOC_Os03g22540
DeletionChr113746962137469642
DeletionChr1015021465150214672
DeletionChr115073296150733048
DeletionChr1215551672155516786
DeletionChr121610580316105906103
DeletionChr516301721163017243
DeletionChr716329665163296661
DeletionChr1116720900167209011LOC_Os11g28890
DeletionChr717706686177066937LOC_Os07g30040
DeletionChr11184225291842254314
DeletionChr3193229851932299611
DeletionChr220313537203135381
DeletionChr620359975203612751300LOC_Os06g35010
DeletionChr72053000120570000400004
DeletionChr721181788211817891
DeletionChr9216405452164056621
DeletionChr8219064582190648022LOC_Os08g34820
DeletionChr723972585239725861
DeletionChr524202001242550005300010
DeletionChr725804528258045291LOC_Os07g43070
DeletionChr229344603293446129LOC_Os02g47970
DeletionChr1304216413042165413
DeletionChr131828417318284203LOC_Os01g55290
DeletionChr333609841336098443
DeletionChr334182184341821895

Insertions: 17
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr101465131465131
InsertionChr1222593966225939661
InsertionChr313822301138223011
InsertionChr3239835682398362356
InsertionChr415604028156040281
InsertionChr415766681157666811
InsertionChr4200748520074851
InsertionChr5150874715087471
InsertionChr5207046992070472022
InsertionChr5740706774070682
InsertionChr6149869751498698612
InsertionChr6967859396785942
InsertionChr7190564519056484
InsertionChr760973860975518
InsertionChr814434579144345813
InsertionChr8865382286538221
InsertionChr910441469104414691

No Inversion

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1011338822Chr6108501622
TranslocationChr612594675Chr132531298