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Mutant Information

Mutant NameFN2752-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2752-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 86
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111085472G-AHETINTERGENIC
SBSChr138329087T-AHETINTERGENIC
SBSChr15734781T-CHET
SBSChr1013322043G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g25720
SBSChr1014198418G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g26960
SBSChr1016923342G-AHomo
SBSChr1016936883C-AHET
SBSChr1019310054C-THomo
SBSChr10268031T-AHETINTERGENIC
SBSChr108924128T-CHET
SBSChr1113595362C-THETINTERGENIC
SBSChr1113595363C-THETINTERGENIC
SBSChr1114463859T-CHETINTERGENIC
SBSChr1116839493G-AHomo
SBSChr1119312246C-GHET
SBSChr1120621523A-GHETINTERGENIC
SBSChr1121862430C-AHETNON_SYNONYMOUS_CODINGLOC_Os11g37040
SBSChr114450055G-AHETINTRON
SBSChr118964784C-AHETINTERGENIC
SBSChr1211613192C-THETNON_SYNONYMOUS_CODINGLOC_Os12g19930
SBSChr1212126480T-AHET
SBSChr1220325124A-THET
SBSChr122507640A-GHET
SBSChr1225807949G-CHETUTR_3_PRIME
SBSChr122684496C-THET
SBSChr123358586G-THETNON_SYNONYMOUS_CODINGLOC_Os12g06900
SBSChr129791407G-AHET
SBSChr214556979G-CHET
SBSChr220017290G-THETSYNONYMOUS_CODING
SBSChr222254500C-GHET
SBSChr235011523A-GHOMOUTR_3_PRIME
SBSChr315157907G-CHomo
SBSChr321198057T-AHET
SBSChr322836943G-AHET
SBSChr323123639G-AHomo
SBSChr324991745A-GHETINTERGENIC
SBSChr326074698A-CHOMOINTRON
SBSChr32779069A-CHomo
SBSChr335816617A-CHET
SBSChr34658856A-CHomo
SBSChr37067518T-CHET
SBSChr37533718C-AHET
SBSChr3758046T-AHomo
SBSChr39693514C-THOMOINTERGENIC
SBSChr410549755C-THomo
SBSChr410571919G-AHET
SBSChr411850838C-THET
SBSChr413282736A-GHETINTERGENIC
SBSChr414328301A-GHET
SBSChr414555339C-THomo
SBSChr434110384G-THomo
SBSChr43439632G-AHETINTERGENIC
SBSChr44394064A-GHomo
SBSChr48402055G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g14940
SBSChr49411765G-AHomo
SBSChr519981449A-GHET
SBSChr52183428C-THET
SBSChr524686172T-AHET
SBSChr524878722C-AHET
SBSChr525335409G-AHOMONON_SYNONYMOUS_CODINGLOC_Os05g43570
SBSChr5524062G-CHETINTERGENIC
SBSChr616543925C-THETINTERGENIC
SBSChr616586458G-AHET
SBSChr61854729T-CHETINTERGENIC
SBSChr620182219C-AHETINTERGENIC
SBSChr622165436C-THETSYNONYMOUS_CODING
SBSChr622281600G-AHET
SBSChr631238421C-THomo
SBSChr711741318C-THET
SBSChr711741319C-THET
SBSChr717845212T-CHET
SBSChr721742057G-AHETINTRON
SBSChr723972237T-AHomo
SBSChr7485240G-AHETINTERGENIC
SBSChr812324413C-THomo
SBSChr814123077A-CHET
SBSChr821195051G-AHOMOINTRON
SBSChr821195053G-AHOMOINTRON
SBSChr821257219T-AHOMONON_SYNONYMOUS_CODINGLOC_Os08g33950
SBSChr825452213C-THET
SBSChr84288197G-AHomo
SBSChr84419035T-CHETINTERGENIC
SBSChr84419036G-AHETINTERGENIC
SBSChr913755872T-GHET
SBSChr921254558T-CHETNON_SYNONYMOUS_CODINGLOC_Os09g36860
SBSChr921254559G-AHETSYNONYMOUS_CODING

Deletions: 44
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr72290342290384
DeletionChr28138648138651
DeletionChr6173292317329241
DeletionChr11241641424164195
DeletionChr63089458308947214
DeletionChr7371327837132791
DeletionChr12405598640559926
DeletionChr4461676546167661
DeletionChr11559616055961611
DeletionChr76082689608278192
DeletionChr8676051567605161
DeletionChr4711636171163632
DeletionChr27509736750976125LOC_Os02g13850
DeletionChr79612033961204916
DeletionChr710071021100710309LOC_Os07g17140
DeletionChr410543478105434791LOC_Os04g18980
DeletionChr610869131108691398LOC_Os06g19100
DeletionChr12115576211155763817
DeletionChr411939996119399982
DeletionChr4121699921217004856
DeletionChr912626465126264672
DeletionChr712938685129386872LOC_Os07g22960
DeletionChr6132284571322848326LOC_Os06g22740
DeletionChr214327914143279151
DeletionChr914670798146707991
DeletionChr414967133149671374
DeletionChr1215540968155409691
DeletionChr4160739101607395646
DeletionChr116534207165342081
DeletionChr1179412121794122210
DeletionChr118915877189158792
DeletionChr121918800119234000459996
DeletionChr121923800119287000489995
DeletionChr219685614196856173
DeletionChr622178018221780202
DeletionChr7226866752268674368
DeletionChr422740769227407701
DeletionChr222902795229027961
DeletionChr126192332261923331
DeletionChr430479024304790273
DeletionChr131498875314988783
DeletionChr133853177338531781
DeletionChr234463476344634837LOC_Os02g56300
DeletionChr335708142357081464

Insertions: 14
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr121772474217724763
InsertionChr107497547497541LOC_Os10g02180image
InsertionChr112607245026072459102image
InsertionChr11260724502607245122image
InsertionChr1221997879219978802
InsertionChr2220095692200958416
InsertionChr313380250133802501
InsertionChr314831618148316236
InsertionChr314987577149875771
InsertionChr4754647075464701LOC_Os04g13530image
InsertionChr529103569291035702
InsertionChr8891868089186856
InsertionChr9136631401366315920
InsertionChr9189709461897096116

Inversions: 9
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1122233072223408
InversionChr531909473969039
InversionChr531909543969053
InversionChr31803236718073228LOC_Os03g31650
InversionChr82185518622366710LOC_Os08g34760
InversionChr82185520022366711LOC_Os08g34760
InversionChr82413843424138581
InversionChr12596286126492157
InversionChr12596286426492159

Translocations: 13
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr112785627Chr316685673
TranslocationChr94040357Chr68105987
TranslocationChr114272848Chr93387619LOC_Os09g06990
TranslocationChr34835539Chr231043205
TranslocationChr45588399Chr125576624
TranslocationChr311066394Chr229255718
TranslocationChr1211794917Chr114847551LOC_Os12g20220
TranslocationChr1112942262Chr47792432
TranslocationChr313539829Chr230014446LOC_Os03g23860
TranslocationChr916882224Chr2347425872
TranslocationChr1017232345Chr17861565
TranslocationChr517883172Chr331648212
TranslocationChr227133113Chr125821321