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Mutant Information

Mutant NameFN2719-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2719-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 85
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr14726833C-THET
SBSChr19376583G-AHETSYNONYMOUS_CODING
SBSChr19853058G-AHomo
SBSChr19853058G-AHOMOINTERGENIC
SBSChr1013690425C-AHET
SBSChr1014039808G-THET
SBSChr1019148426T-AHET
SBSChr1019148426T-AHETUTR_3_PRIME
SBSChr1021500310C-AHETSTOP_LOSTLOC_Os10g40160
SBSChr106351727G-AHETINTERGENIC
SBSChr106352729T-AHETINTERGENIC
SBSChr109962926C-AHET
SBSChr1110770342T-CHET
SBSChr1110770342T-CHETINTERGENIC
SBSChr1114705596C-THETNON_SYNONYMOUS_CODINGLOC_Os11g25780
SBSChr1115342906A-GHET
SBSChr1115342906A-GHETUTR_3_PRIME
SBSChr11191158C-THET
SBSChr1121661551A-GHET
SBSChr1121661551A-GHETINTERGENIC
SBSChr1126487239G-AHomo
SBSChr1126487239G-AHOMOINTERGENIC
SBSChr1126709113C-THETINTERGENIC
SBSChr118785743T-CHETNON_SYNONYMOUS_CODINGLOC_Os11g15510
SBSChr1210886791C-THOMONON_SYNONYMOUS_CODINGLOC_Os12g18800
SBSChr1210886791C-THomoNON_SYNONYMOUS_CODINGLOC_Os12g18800
SBSChr1212528080T-CHETINTERGENIC
SBSChr1215187143G-THETINTERGENIC
SBSChr1216401920A-CHET
SBSChr1222073437A-THET
SBSChr1222153317T-GHETNON_SYNONYMOUS_CODINGLOC_Os12g36140
SBSChr124584095T-AHETINTERGENIC
SBSChr127218020G-AHOMONON_SYNONYMOUS_CODINGLOC_Os12g13020
SBSChr127218020G-AHomoNON_SYNONYMOUS_CODINGLOC_Os12g13020
SBSChr127675754C-THETINTRON
SBSChr127931834G-AHETINTERGENIC
SBSChr210921848T-CHET
SBSChr210921848T-CHETINTERGENIC
SBSChr214038746C-GHET
SBSChr235552139T-CHETINTRON
SBSChr25668969A-GHET
SBSChr3151486G-CHET
SBSChr321778063T-AHET
SBSChr322981035G-THET
SBSChr322981035G-THETINTERGENIC
SBSChr328243792A-GHET
SBSChr328243792A-GHETINTRON
SBSChr330215260T-CHomo
SBSChr335495343T-CHET
SBSChr413854963A-GHET
SBSChr416368897A-GHET
SBSChr419918787T-AHETINTERGENIC
SBSChr427366290A-GHET
SBSChr427706483T-AHET
SBSChr428627310C-THET
SBSChr428627310C-THOMOINTRON
SBSChr430937156C-AHETINTERGENIC
SBSChr48926661G-AHETSTOP_GAINEDLOC_Os04g16420
SBSChr48959179C-THET
SBSChr48959179C-THETINTERGENIC
SBSChr516545878A-GHETINTRON
SBSChr516925178T-AHET
SBSChr516925178T-AHETINTERGENIC
SBSChr517844918C-AHET
SBSChr517844918C-AHETINTERGENIC
SBSChr520169241C-AHETINTERGENIC
SBSChr528116333T-CHomo
SBSChr528116333T-CHOMOINTERGENIC
SBSChr611010698T-CHETNON_SYNONYMOUS_CODINGLOC_Os06g19350
SBSChr613553381G-AHETINTERGENIC
SBSChr623731550C-AHET
SBSChr711598160T-AHomoNON_SYNONYMOUS_CODINGLOC_Os07g19570
SBSChr71288868G-AHETINTERGENIC
SBSChr724531915C-AHOMOINTERGENIC
SBSChr725481770T-AHomo
SBSChr725481770T-AHOMOINTERGENIC
SBSChr76408002G-AHETNON_SYNONYMOUS_CODINGLOC_Os07g11610
SBSChr78660769T-CHET
SBSChr818170009T-CHET
SBSChr818170009T-CHETINTRON
SBSChr819247926C-THETINTERGENIC
SBSChr819910688G-AHET
SBSChr8253466G-AHETNON_SYNONYMOUS_CODINGLOC_Os08g01390
SBSChr921061546C-THET
SBSChr921061546C-THETSYNONYMOUS_CODING

Deletions: 28
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr95041261504126212
DeletionChr3638949063894911
DeletionChr57065001707000049992
DeletionChr11714070071407011
DeletionChr4752617775261781
DeletionChr11804502780450281
DeletionChr3823151782315181
DeletionChr2827365482736551
DeletionChr3898910889891091
DeletionChr11969384296938442
DeletionChr4109439431094394852
DeletionChr411446264114462662
DeletionChr712145719121457201
DeletionChr712156938121569391
DeletionChr4145261011452610322
DeletionChr214760085147600861
DeletionChr4197280701972809222
DeletionChr120619004206190062
DeletionChr222184920221849211
DeletionChr12272916422729181172
DeletionChr825576472255764731
DeletionChr1226843549268435523
DeletionChr127426830274268311
DeletionChr4308254913082557887
DeletionChr431160547311605481
DeletionChr2343187623431877614
DeletionChr335081682350816842
DeletionChr139977473399774807

Insertions: 21
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1144821091448212214
InsertionChr1813139481313952
InsertionChr10227111462271114722image
InsertionChr10227111462271114832image
InsertionChr10714575371457531
InsertionChr1218990627189906282
InsertionChr122939560293957516
InsertionChr211590335115903384
InsertionChr230639797306397971
InsertionChr314316094143160952
InsertionChr328037278280372792
InsertionChr4280150592801506022image
InsertionChr4280150592801506022image
InsertionChr4794789179478911
InsertionChr529931151299311511
InsertionChr69464981946498772image
InsertionChr69464981946498772image
InsertionChr811049434110494341
InsertionChr816867262168672621
InsertionChr819211524192115252
InsertionChr914315063143150664

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr233313073331548
InversionChr8612030767354112
InversionChr8612032167370002
InversionChr121334486713377641
InversionChr62248312422521349

Translocations: 14
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr102265231Chr95503275
TranslocationChr36780070Chr212010625
TranslocationChr66823006Chr427350794LOC_Os06g12590
TranslocationChr117720116Chr64358327
TranslocationChr28310769Chr131296068
TranslocationChr108620598Chr112472002
TranslocationChr911816226Chr26533224
TranslocationChr1212883131Chr104481271
TranslocationChr913448269Chr871458532
TranslocationChr1113708396Chr611097876LOC_Os11g24120
TranslocationChr915005716Chr81594438
TranslocationChr916564127Chr124311693
TranslocationChr1119693914Chr25291366
TranslocationChr826906514Chr325348841LOC_Os08g42570