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Mutant Information

Mutant NameFN2647-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2647-S Alignment File
Seed AvailabilityNo
Mapping
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Variant Information

Single base substitutions: 106
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr13958249A-GHETUTR_5_PRIME
SBSChr17507478G-CHETNON_SYNONYMOUS_CODINGLOC_Os01g13470
SBSChr18342436T-CHETINTERGENIC
SBSChr114627508G-AHETINTRON
SBSChr115768827G-AHETINTERGENIC
SBSChr126325877T-CHETINTERGENIC
SBSChr135732817G-AHETUTR_5_PRIME
SBSChr139768623C-GHETNON_SYNONYMOUS_CODINGLOC_Os01g68430
SBSChr29970951C-THETINTERGENIC
SBSChr219272436G-THETSYNONYMOUS_CODING
SBSChr229797546C-THETINTERGENIC
SBSChr233123730G-THETINTERGENIC
SBSChr3891335T-CHETINTERGENIC
SBSChr39910661G-AHOMOINTERGENIC
SBSChr319682371C-THETINTERGENIC
SBSChr321198438C-AHETNON_SYNONYMOUS_CODINGLOC_Os03g38170
SBSChr322569038A-THETINTERGENIC
SBSChr323449384C-THETINTERGENIC
SBSChr326017064C-THETINTERGENIC
SBSChr328182656G-THETNON_SYNONYMOUS_CODINGLOC_Os03g49510
SBSChr330329537C-THETINTERGENIC
SBSChr330951131T-CHETINTERGENIC
SBSChr336376904C-THETSYNONYMOUS_CODING
SBSChr41413254C-AHETINTERGENIC
SBSChr41746738G-THETINTERGENIC
SBSChr45770799G-AHOMOINTERGENIC
SBSChr46606840C-THOMOSYNONYMOUS_CODING
SBSChr47868226A-GHETINTERGENIC
SBSChr413572941A-THOMONON_SYNONYMOUS_CODINGLOC_Os04g23739
SBSChr413572942A-THOMOSYNONYMOUS_CODING
SBSChr416122930C-THETINTERGENIC
SBSChr416318392A-THOMOINTERGENIC
SBSChr432713299C-AHETNON_SYNONYMOUS_CODINGLOC_Os04g55020
SBSChr433536468G-THETINTERGENIC
SBSChr433765070G-AHETUTR_3_PRIME
SBSChr435331886T-CHETINTRON
SBSChr52183723C-THETINTRON
SBSChr57616070T-AHETNON_SYNONYMOUS_CODINGLOC_Os05g13740
SBSChr59954684G-AHOMOINTERGENIC
SBSChr513623931A-GHETINTRON
SBSChr517005326G-AHETINTERGENIC
SBSChr518324433G-AHETINTERGENIC
SBSChr521034196T-CHOMONON_SYNONYMOUS_CODINGLOC_Os05g35400
SBSChr521990369G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g37580
SBSChr525474599T-AHETINTERGENIC
SBSChr66547923G-AHETINTERGENIC
SBSChr67176349C-AHETINTERGENIC
SBSChr610742687T-CHETINTERGENIC
SBSChr611716334C-AHETNON_SYNONYMOUS_CODINGLOC_Os06g20390
SBSChr612869957G-AHETSYNONYMOUS_CODING
SBSChr613269268T-CHETINTERGENIC
SBSChr617532837C-AHETINTERGENIC
SBSChr620394192G-CHETNON_SYNONYMOUS_CODINGLOC_Os06g35040
SBSChr621653431G-THETINTERGENIC
SBSChr623881583A-THETINTERGENIC
SBSChr7646692G-THOMOINTRON
SBSChr7837814T-AHETINTERGENIC
SBSChr710913939C-THETSYNONYMOUS_CODING
SBSChr711449826G-AHETINTERGENIC
SBSChr717435436C-THETINTERGENIC
SBSChr718357799C-GHETINTERGENIC
SBSChr720357082A-THETINTERGENIC
SBSChr726867327G-AHETNON_SYNONYMOUS_CODINGLOC_Os07g45020
SBSChr82202130A-THETINTERGENIC
SBSChr85470003C-AHETINTERGENIC
SBSChr811910550C-AHETSTOP_GAINEDLOC_Os08g19880
SBSChr812852078C-THETINTERGENIC
SBSChr815584835C-GHETINTERGENIC
SBSChr817059792C-GHETINTERGENIC
SBSChr818080379G-THETINTERGENIC
SBSChr819048950A-GHETSYNONYMOUS_CODING
SBSChr821865655C-GHETINTERGENIC
SBSChr823148918T-AHETSTOP_GAINEDLOC_Os08g36680
SBSChr823825145C-THETINTERGENIC
SBSChr98007969G-AHETSYNONYMOUS_CODING
SBSChr911624397G-AHOMOSYNONYMOUS_CODING
SBSChr913941064A-GHETINTERGENIC
SBSChr915668747T-CHETINTERGENIC
SBSChr915668751T-AHETINTERGENIC
SBSChr915668755G-THETINTERGENIC
SBSChr921976012A-THOMOINTERGENIC
SBSChr922067407G-AHOMOINTRON
SBSChr922211832C-GHOMOINTERGENIC
SBSChr10305090A-THETINTRON
SBSChr101181898G-THETINTERGENIC
SBSChr105756868T-AHOMOINTERGENIC
SBSChr105893123G-AHETINTERGENIC
SBSChr1012115634C-AHETINTRON
SBSChr1012814949A-GHOMOINTERGENIC
SBSChr1018335018G-AHETINTRON
SBSChr1019950463C-THETINTERGENIC
SBSChr1020981198A-GHETINTERGENIC
SBSChr111005502A-GHETINTERGENIC
SBSChr113357703G-AHETNON_SYNONYMOUS_CODINGLOC_Os11g06840
SBSChr1113954011G-THETINTERGENIC
SBSChr1115389280C-THETINTERGENIC
SBSChr1121477980T-CHETINTRON
SBSChr1121531714C-AHETINTERGENIC
SBSChr127736618G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g13720
SBSChr129534073T-CHETNON_SYNONYMOUS_CODINGLOC_Os12g16650
SBSChr1212386869G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g22020
SBSChr1214358316A-CHOMOINTERGENIC
SBSChr1215053756T-CHETINTERGENIC
SBSChr1221631046C-GHOMOINTERGENIC
SBSChr1224866285G-AHETINTERGENIC
SBSChr1224885607T-CHETINTERGENIC

Deletions: 29
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr109213499213501
DeletionChr11469764346976441
DeletionChr106227446622746216
DeletionChr96621135662115116
DeletionChr9784852678485337
DeletionChr9837746483774684
DeletionChr8996420899642102
DeletionChr610272186102721948
DeletionChr1110543036105430382
DeletionChr610723124107231251
DeletionChr1012291178122911791LOC_Os10g23990
DeletionChr1113249491132494943
DeletionChr613798969137989701
DeletionChr2152232411522325413
DeletionChr1017070057170700658
DeletionChr417370205173702094
DeletionChr6176980011779900010099912
DeletionChr8190092811900929312
DeletionChr4190807741908078410
DeletionChr619917114199171206
DeletionChr5206039822060399816
DeletionChr322273445222734472
DeletionChr1022953981229539821
DeletionChr525134414251344162LOC_Os05g43220
DeletionChr626367669263676778
DeletionChr827670187276701958LOC_Os08g43870
DeletionChr528022850280228555
DeletionChr429077100290771055
DeletionChr2301588693015889526

Insertions: 13
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr136846411368464122
InsertionChr140421947404219504
InsertionChr235076734350767352
InsertionChr3230773423077352
InsertionChr1110882934108829341
InsertionChr19490977949098610
InsertionChr29442938944295619
InsertionChr37708653770867826
InsertionChr3242317682423177710
InsertionChr52925037292505014
InsertionChr5140071301400714516
InsertionChr11251130402511304910
InsertionChr1225059687250596882

Inversions: 6
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr174318088272763
InversionChr981554938172110
InversionChr981555098172109
InversionChr82726534527766499
InversionChr33637380736402433
InversionChr33637382036374198

Translocations: 5
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1014363390Chr827766504
TranslocationChr1014363404Chr827768594
TranslocationChr916540012Chr617497729
TranslocationChr822680582Chr723002853LOC_Os08g35970
TranslocationChr827265369Chr118068368