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Mutant Information

Mutant NameFN2696-S-1 [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2696-S-1 Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 56
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr113907033C-AHETINTERGENIC
SBSChr120113792C-THOMOINTRON
SBSChr142111458G-THOMOINTERGENIC
SBSChr15778802C-THETINTERGENIC
SBSChr1012101135G-AHETINTERGENIC
SBSChr1013147824A-GHETINTERGENIC
SBSChr1016465959A-THETINTERGENIC
SBSChr105184816C-THETINTERGENIC
SBSChr107352155C-THETINTERGENIC
SBSChr1110923621C-GHETINTERGENIC
SBSChr1111151639T-CHETNON_SYNONYMOUS_CODINGLOC_Os11g19380
SBSChr1118635179T-CHETINTRON
SBSChr1121516732A-GHETINTERGENIC
SBSChr1122839130C-THOMOINTERGENIC
SBSChr1123523805T-AHETSYNONYMOUS_CODING
SBSChr1126760605G-AHETINTERGENIC
SBSChr119043345T-AHETINTERGENIC
SBSChr121057562T-CHOMOINTERGENIC
SBSChr1219323116C-AHETINTERGENIC
SBSChr1223779575G-AHETSYNONYMOUS_CODING
SBSChr1223980895C-GHETNON_SYNONYMOUS_CODINGLOC_Os12g38990
SBSChr226441635C-THOMOINTERGENIC
SBSChr231325573C-THOMOINTERGENIC
SBSChr233395675C-THETINTERGENIC
SBSChr27852059G-THETNON_SYNONYMOUS_CODINGLOC_Os02g14300
SBSChr319403080C-THETINTERGENIC
SBSChr319673080G-AHETINTERGENIC
SBSChr332726847C-THETINTRON
SBSChr335894073C-AHETUTR_3_PRIME
SBSChr36573004C-THETINTERGENIC
SBSChr417311686C-THETSYNONYMOUS_CODING
SBSChr420980275T-GHETINTERGENIC
SBSChr421174321T-CHETINTERGENIC
SBSChr424208331A-GHETINTRON
SBSChr42701471C-THETINTERGENIC
SBSChr433123656T-CHOMOUTR_3_PRIME
SBSChr47184219C-THETNON_SYNONYMOUS_CODINGLOC_Os04g13030
SBSChr49402747T-AHETINTERGENIC
SBSChr526173739C-GHETINTERGENIC
SBSChr617232918C-AHETNON_SYNONYMOUS_CODINGLOC_Os06g29920
SBSChr65146983G-AHETINTERGENIC
SBSChr66250718C-THETSTART_GAINED
SBSChr66382052A-THETINTERGENIC
SBSChr67315505C-THETINTERGENIC
SBSChr717999662G-AHETINTERGENIC
SBSChr719574853C-AHETINTRON
SBSChr719822489T-CHETINTERGENIC
SBSChr723019879G-CHETNON_SYNONYMOUS_CODINGLOC_Os07g38320
SBSChr724781804C-AHETINTERGENIC
SBSChr727542539A-GHETINTERGENIC
SBSChr728111842A-THETINTERGENIC
SBSChr812053810A-GHOMOSYNONYMOUS_CODING
SBSChr85847688T-AHETINTRON
SBSChr911044317T-AHETINTERGENIC
SBSChr914289727G-THETSYNONYMOUS_CODING
SBSChr9397612A-GHETNON_SYNONYMOUS_CODINGLOC_Os09g01560

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr661640616422
DeletionChr31254303125439592
DeletionChr52512260251227717
DeletionChr11375977937597867LOC_Os11g07460
DeletionChr2624336162433632
DeletionChr67122001722500010299919
DeletionChr674200017470000499998
DeletionChr77460001773700027699944
DeletionChr10990108599010872
DeletionChr111076900110795000259992
DeletionChr210926504109265084LOC_Os02g18730
DeletionChr12134385721343858917
DeletionChr1015261004152610073
DeletionChr1116486271164862743
DeletionChr416753460167534611
DeletionChr217543920175439222
DeletionChr11183716581837167416
DeletionChr118899152188991531
DeletionChr1219083255190832561
DeletionChr1021394825213948283LOC_Os10g39950
DeletionChr421834372218343731
DeletionChr3224686732246871441
DeletionChr122507806225078071
DeletionChr423197288231972902
DeletionChr827497074274970762
DeletionChr428350242283502442
DeletionChr128378131283781332
DeletionChr628718710287187166LOC_Os06g47380
DeletionChr134049175340491761
DeletionChr1380396063803962014

Insertions: 12
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr115948543159485508
InsertionChr1213152117131521215
InsertionChr12222290582222906912
InsertionChr12261890362618904914
InsertionChr2153972531539728634
InsertionChr219065392190653921
InsertionChr232487529324875302
InsertionChr234141028341410292
InsertionChr312881950128819523
InsertionChr711895796118958038
InsertionChr726517098265170992
InsertionChr797793597794612

Inversions: 6
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1159590936671300
InversionChr694027209403593
InversionChr694028549403593
InversionChr1299153039954710LOC_Os12g17320
InversionChr1299153049954712LOC_Os12g17320
InversionChr71039256910656378

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr8392592Chr69402844
TranslocationChr8392593Chr69402735