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Mutant Information

Mutant NameFN2667-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2667-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 108
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111334190G-CHomo
SBSChr111334190G-CHOMOINTRON
SBSChr112040921T-CHomo
SBSChr112040921T-CHOMOINTERGENIC
SBSChr121249906C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g37930
SBSChr122493925C-GHET
SBSChr129497419A-GHomo
SBSChr129497419A-GHOMOINTERGENIC
SBSChr130580943G-THET
SBSChr132363817A-THET
SBSChr136324589G-CHET
SBSChr1953179G-AHET
SBSChr1012845922G-AHET
SBSChr1012845922G-AHETSPLICE_SITE_REGION
SBSChr1015317901T-CHET
SBSChr1015317901T-CHETINTRON
SBSChr10272497G-AHOMONON_SYNONYMOUS_CODINGLOC_Os10g01450
SBSChr10272497G-AHomoNON_SYNONYMOUS_CODINGLOC_Os10g01450
SBSChr1115078255G-AHET
SBSChr1118180309G-THET
SBSChr1120945524G-AHETINTRON
SBSChr1127811016T-AHET
SBSChr1212101219G-AHET
SBSChr1212101219G-AHETINTERGENIC
SBSChr1218071896G-CHET
SBSChr1218071896G-CHETINTERGENIC
SBSChr124968337G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g09470
SBSChr125013862G-AHET
SBSChr125013862G-AHETUTR_3_PRIME
SBSChr220353988A-GHET
SBSChr220353988A-GHETSYNONYMOUS_CODING
SBSChr226720549C-THET
SBSChr226720549C-THETINTERGENIC
SBSChr230980440G-CHET
SBSChr231974692C-THET
SBSChr231974692C-THETINTERGENIC
SBSChr232063413T-CHET
SBSChr28443091G-THET
SBSChr311999278T-GHET
SBSChr311999278T-GHETINTERGENIC
SBSChr312451475T-AHET
SBSChr312451475T-AHETINTERGENIC
SBSChr313956805A-GHET
SBSChr313956805A-GHETSYNONYMOUS_CODING
SBSChr314454862T-GHETNON_SYNONYMOUS_CODINGLOC_Os03g25320
SBSChr316391822T-AHET
SBSChr316391822T-AHETINTERGENIC
SBSChr316962158G-AHET
SBSChr336195289G-AHET
SBSChr39184654A-GHET
SBSChr414851317G-AHomo
SBSChr414851317G-AHETINTERGENIC
SBSChr421776572G-AHomo
SBSChr421776572G-AHOMOINTERGENIC
SBSChr422957084A-GHET
SBSChr423874808G-AHETINTERGENIC
SBSChr426393515C-AHET
SBSChr426553387C-THETSYNONYMOUS_CODING
SBSChr427780665C-THETINTERGENIC
SBSChr428979118C-AHET
SBSChr429013810G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g48660
SBSChr44180235C-GHomo
SBSChr44180235C-GHOMOINTERGENIC
SBSChr44185433C-GHOMOUTR_3_PRIME
SBSChr46174427G-THET
SBSChr517394550T-CHOMONON_SYNONYMOUS_CODINGLOC_Os05g30070
SBSChr517394550T-CHomoNON_SYNONYMOUS_CODINGLOC_Os05g30070
SBSChr523414631A-CHomo
SBSChr523414631A-CHOMOINTERGENIC
SBSChr5310454C-AHET
SBSChr58159933T-CHomo
SBSChr58159933T-CHOMOINTERGENIC
SBSChr612977409C-AHET
SBSChr613062251C-THET
SBSChr614860784C-THOMONON_SYNONYMOUS_CODINGLOC_Os06g25370
SBSChr614860784C-THomoNON_SYNONYMOUS_CODINGLOC_Os06g25370
SBSChr62396521G-AHET
SBSChr62396521G-AHETUTR_3_PRIME
SBSChr625627351A-GHET
SBSChr631136604A-GHomo
SBSChr631136604A-GHOMOINTERGENIC
SBSChr66834121C-THomo
SBSChr66834121C-THOMOINTERGENIC
SBSChr68351093A-THomo
SBSChr68351093A-THOMOINTERGENIC
SBSChr710570155T-CHET
SBSChr712886092C-GHETINTERGENIC
SBSChr715372330G-AHET
SBSChr715372330G-AHETINTERGENIC
SBSChr7160671C-THETINTERGENIC
SBSChr72790773A-CHETINTERGENIC
SBSChr73592723T-CHET
SBSChr73592723T-CHETINTRON
SBSChr76676403G-AHET
SBSChr76676403G-AHETINTERGENIC
SBSChr79835937C-THET
SBSChr813697075T-AHET
SBSChr821596089T-AHET
SBSChr821596089T-AHETINTERGENIC
SBSChr824746569C-AHET
SBSChr913433001A-GHETINTERGENIC
SBSChr914978876G-THET
SBSChr92749621T-GHomo
SBSChr92749621T-GHOMOINTRON
SBSChr93016876T-CHET
SBSChr93016876T-CHETINTRON
SBSChr93164651G-THETNON_SYNONYMOUS_CODINGLOC_Os09g06660
SBSChr97075511T-CHET

Deletions: 26
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1247870147870322
DeletionChr12245001524500194
DeletionChr727580012773000149993
DeletionChr7279700128960009899916
DeletionChr7280000129000009999916
DeletionChr1134894643489482182
DeletionChr8591293459129428
DeletionChr7647785264778531
DeletionChr97139545713954722
DeletionChr12983418098341811
DeletionChr101077697910776990112
DeletionChr1211689743116897452
DeletionChr812161356121613571
DeletionChr1130123631301236632
DeletionChr1013029475130294816
DeletionChr1013534702135347031
DeletionChr1116829622168296231
DeletionChr1117702497177024992
DeletionChr4193654321936543642
DeletionChr6223599192235993112
DeletionChr42281137422811387132
DeletionChr11249651212496512762
DeletionChr726764960267649611
DeletionChr827808093278080963
DeletionChr2336064933360650182
DeletionChr136792087367920881

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr113679991136799911
InsertionChr1455508845550881
InsertionChr1016392350163923534
InsertionChr235077154350771563
InsertionChr323942107239421071
InsertionChr5811638781163871LOC_Os05g14400image
InsertionChr817916507179165071
InsertionChr911531490115314901

Inversions: 1
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr13941994939420120

Translocations: 16
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr10164478Chr514966498
TranslocationChr102694518Chr622683226
TranslocationChr107833402Chr923823862
TranslocationChr98289918Chr611646591
TranslocationChr315692309Chr218844091
TranslocationChr1218179682Chr1110218713
TranslocationChr1018190003Chr48855441LOC_Os10g34078
TranslocationChr1118371992Chr10879842LOC_Os11g31440
TranslocationChr518580910Chr17861353
TranslocationChr1019291321Chr216123058
TranslocationChr719416595Chr31603838
TranslocationChr1220175900Chr1113411844LOC_Os12g33360
TranslocationChr1122529369Chr810765832LOC_Os11g37990
TranslocationChr1226966677Chr64303675
TranslocationChr1227044721Chr1120669049
TranslocationChr1227530417Chr87729489