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Mutant Information

Mutant NameFN2723-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2723-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 92
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr116851299C-THET
SBSChr117077485C-AHETINTERGENIC
SBSChr118255199G-AHETINTRON
SBSChr120247758G-AHET
SBSChr120247758G-AHETINTERGENIC
SBSChr130841359C-THET
SBSChr130841359C-THETINTRON
SBSChr132936458A-THETINTERGENIC
SBSChr134012468G-AHETINTERGENIC
SBSChr140279793T-AHETINTERGENIC
SBSChr1018791917A-THET
SBSChr1018791917A-THETINTERGENIC
SBSChr1018843404T-AHET
SBSChr1022149372C-THET
SBSChr10325354G-AHET
SBSChr104512937C-THETINTERGENIC
SBSChr1110175029C-THET
SBSChr1110175029C-THETINTERGENIC
SBSChr1112761990C-AHET
SBSChr1122081896C-AHET
SBSChr119943259G-THET
SBSChr121023814A-THomo
SBSChr121023814A-THOMOINTERGENIC
SBSChr1213606442A-CHETINTERGENIC
SBSChr1213924539T-CHET
SBSChr1214508232C-THET
SBSChr1214508232C-THETINTRON
SBSChr1215613360A-GHomo
SBSChr1215613360A-GHOMOSYNONYMOUS_CODING
SBSChr1216327320A-GHET
SBSChr1216518102G-AHETINTERGENIC
SBSChr123054935C-AHET
SBSChr123054935C-AHETINTERGENIC
SBSChr211876071C-THET
SBSChr2139166T-AHETINTERGENIC
SBSChr2139168C-GHETINTERGENIC
SBSChr215419543G-THETINTERGENIC
SBSChr216312423C-THET
SBSChr216312423C-THETSYNONYMOUS_CODING
SBSChr221751281G-AHET
SBSChr221751281G-AHETINTERGENIC
SBSChr223021799G-AHET
SBSChr22424846C-GHET
SBSChr22424846C-GHETINTERGENIC
SBSChr228971528C-AHETINTRON
SBSChr24287145G-AHomo
SBSChr24287145G-AHOMOUTR_3_PRIME
SBSChr31519129G-AHomo
SBSChr31519129G-AHOMOUTR_5_PRIME
SBSChr321988069G-THomo
SBSChr321988069G-THOMOINTERGENIC
SBSChr328809447T-GHET
SBSChr334421284G-THETINTERGENIC
SBSChr36340620G-AHETSTOP_GAINEDLOC_Os03g12080
SBSChr412521245G-AHomo
SBSChr412521245G-AHOMOINTERGENIC
SBSChr412521246G-AHomo
SBSChr412521246G-AHOMOINTERGENIC
SBSChr412859413C-THETNON_SYNONYMOUS_CODINGLOC_Os04g22690
SBSChr420382700C-THETINTRON
SBSChr42510417G-AHETINTERGENIC
SBSChr425590116G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g43250
SBSChr434025892G-AHETSTOP_GAINEDLOC_Os04g57100
SBSChr512230112C-AHETINTERGENIC
SBSChr518184354G-AHET
SBSChr518184354G-AHETSYNONYMOUS_CODING
SBSChr522889438C-AHETSYNONYMOUS_CODING
SBSChr524410027G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g41720
SBSChr52750587C-AHET
SBSChr529486665T-CHET
SBSChr613101046G-AHETINTERGENIC
SBSChr619682220A-GHETINTERGENIC
SBSChr714690442C-THET
SBSChr714690442C-THETINTERGENIC
SBSChr717093962A-GHET
SBSChr717093962A-GHETINTERGENIC
SBSChr721679367T-GHET
SBSChr721679367T-GHETINTERGENIC
SBSChr726081899A-GHETINTERGENIC
SBSChr7454764G-AHomo
SBSChr7454764G-AHOMOINTRON
SBSChr812449521T-CHET
SBSChr818559385C-AHETNON_SYNONYMOUS_CODINGLOC_Os08g30190
SBSChr85411434G-AHET
SBSChr86258402G-AHET
SBSChr87424333G-AHETINTRON
SBSChr914986632A-THET
SBSChr914986632A-THETINTERGENIC
SBSChr917876182A-CHET
SBSChr917876182A-CHETINTRON
SBSChr92902222G-THET
SBSChr98179897C-GHET

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr63571986357198712
DeletionChr12525981552598161LOC_Os12g09930
DeletionChr46059245605925272
DeletionChr4667080766708081
DeletionChr278320117832129118
DeletionChr7845272984527301LOC_Os07g14800
DeletionChr2900543890054402
DeletionChr1111722420117224211
DeletionChr3133486501334870252
DeletionChr315001483150014852LOC_Os03g26210
DeletionChr415002607150026081
DeletionChr815189784151897851LOC_Os08g25020
DeletionChr1215373681153736821
DeletionChr1216898154168981562
DeletionChr1117583001176190003599910
DeletionChr1117585001176180003299910
DeletionChr1218801751188017565
DeletionChr1019320924193209317
DeletionChr1019494605194946061LOC_Os10g36430
DeletionChr1201881172018820689LOC_Os01g36380
DeletionChr320391081203910821
DeletionChr122082780720827829222
DeletionChr9214353832143539916LOC_Os09g37160
DeletionChr122241353222413596
DeletionChr426161210261612188
DeletionChr5261875462618755812
DeletionChr628417945284179494
DeletionChr429806195298062016
DeletionChr133576556335765571
DeletionChr142997097429971047

Insertions: 19
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr131933798319337981
InsertionChr1120993894209938952
InsertionChr1217096932170969321LOC_Os12g28920image
InsertionChr225476436254764361
InsertionChr2671092767109348
InsertionChr319759561197595611
InsertionChr3229236922923702
InsertionChr410182469101824691
InsertionChr61026777102677822image
InsertionChr61026777102677822image
InsertionChr612551051125510511
InsertionChr6152564081525642316
InsertionChr6270945092709451022image
InsertionChr6270945092709451022image
InsertionChr813844239138442391
InsertionChr824362510243625101
InsertionChr8267369672673697610
InsertionChr8644807464480741
InsertionChr8956899595689951

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr2470011150297612
InversionChr2470012150297752
InversionChr650180835018183LOC_Os06g09860
InversionChr121192144411922062

Translocations: 20
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr12127738Chr111288972
TranslocationChr92592229Chr7271011632
TranslocationChr94920900Chr119588631
TranslocationChr105298646Chr814523301
TranslocationChr115743800Chr1012207983
TranslocationChr86538918Chr43094411LOC_Os08g11110
TranslocationChr108097551Chr116931745
TranslocationChr79387189Chr420072514
TranslocationChr610117993Chr521218472
TranslocationChr912438833Chr3173438672
TranslocationChr912438834Chr3173443542
TranslocationChr813038720Chr714407536
TranslocationChr614457838Chr48094447LOC_Os06g24620
TranslocationChr1115613259Chr9749691
TranslocationChr316812701Chr118860178
TranslocationChr1117509681Chr2944616LOC_Os11g30110
TranslocationChr1117510217Chr2944616
TranslocationChr1224881287Chr6157208802
TranslocationChr1224881292Chr5124228552
TranslocationChr1227114959Chr317206796