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Mutant Information

Mutant NameFN1022-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1022-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 61
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr114968033A-GHETUTR_3_PRIME
SBSChr118326070G-CHETINTRON
SBSChr119204175A-THETINTERGENIC
SBSChr125737710C-THOMOINTERGENIC
SBSChr19715775T-AHETINTERGENIC
SBSChr1011180781G-CHETUTR_3_PRIME
SBSChr1018925645G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g35400
SBSChr1112896705G-CHETINTERGENIC
SBSChr1119086600G-AHETINTRON
SBSChr1127741462T-GHETINTERGENIC
SBSChr114323098A-THETNON_SYNONYMOUS_CODINGLOC_Os11g08230
SBSChr11588385G-AHETINTERGENIC
SBSChr117365467A-THETSTOP_GAINEDLOC_Os11g13440
SBSChr1211472904G-THETNON_SYNONYMOUS_CODINGLOC_Os12g19700
SBSChr1212529197G-AHETSYNONYMOUS_CODING
SBSChr1212979241T-AHETINTERGENIC
SBSChr211648432T-GHETINTERGENIC
SBSChr230218480C-THETINTERGENIC
SBSChr233177614C-GHETINTERGENIC
SBSChr234487095G-AHETINTERGENIC
SBSChr23579220G-AHETINTERGENIC
SBSChr27108361G-AHETINTERGENIC
SBSChr313600720G-AHOMOINTERGENIC
SBSChr319507494G-AHETSYNONYMOUS_CODING
SBSChr32423051G-THETINTRON
SBSChr326929899T-CHETINTERGENIC
SBSChr413350602A-CHETNON_SYNONYMOUS_CODINGLOC_Os04g23360
SBSChr416051970T-AHETINTERGENIC
SBSChr420794452T-AHETINTERGENIC
SBSChr421149156C-THETINTERGENIC
SBSChr422440294T-AHETINTERGENIC
SBSChr423923986G-AHETSYNONYMOUS_CODING
SBSChr433511067G-AHOMOINTERGENIC
SBSChr434869379C-GHETUTR_5_PRIME
SBSChr49009536G-CHETNON_SYNONYMOUS_CODINGLOC_Os04g16570
SBSChr49408180A-GHETINTERGENIC
SBSChr514245994T-AHETUTR_3_PRIME
SBSChr518602499C-THETINTERGENIC
SBSChr521012802A-THETINTERGENIC
SBSChr521506239C-THETINTERGENIC
SBSChr528115451C-THETINTERGENIC
SBSChr56609905A-CHETINTERGENIC
SBSChr59547274T-CHETINTRON
SBSChr613641156A-THETINTERGENIC
SBSChr68021096G-AHETINTERGENIC
SBSChr718276752T-CHETINTERGENIC
SBSChr720140549C-THETSYNONYMOUS_CODING
SBSChr720374811T-AHETSYNONYMOUS_CODING
SBSChr723382720G-CHETINTERGENIC
SBSChr74217096A-THETINTERGENIC
SBSChr810370881T-AHETINTERGENIC
SBSChr810774490G-THETINTERGENIC
SBSChr813937646G-CHETUTR_3_PRIME
SBSChr81798990C-THETUTR_3_PRIME
SBSChr823629541C-AHETINTERGENIC
SBSChr826323932T-CHETINTERGENIC
SBSChr826602117T-CHETINTRON
SBSChr84115814T-CHETINTERGENIC
SBSChr84356173A-THETINTRON
SBSChr920309907G-AHETINTERGENIC
SBSChr93528595G-AHETINTERGENIC

Deletions: 24
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr106729496729523
DeletionChr9191580519158094
DeletionChr8246900125520008300010
DeletionChr8297675729767636
DeletionChr7493532049353211
DeletionChr1868782086878244
DeletionChr78766011876602312LOC_Os07g15210
DeletionChr1105663391056635011
DeletionChr110669338106693435
DeletionChr810963959109639656
DeletionChr912110114121101151LOC_Os09g20200
DeletionChr2124832821248329412
DeletionChr10139100011429300038300044
DeletionChr12145711971457121013
DeletionChr517246853172468618
DeletionChr518028804180288051
DeletionChr320242793202427996LOC_Os03g36530
DeletionChr22095207320973774217015
DeletionChr128846182288461831
DeletionChr429884952298849531LOC_Os04g50100
DeletionChr230176113301761141
DeletionChr231187972311879742
DeletionChr1315969993159701415LOC_Os01g54930
DeletionChr331599808315998102LOC_Os03g55530

Insertions: 4
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1225174117251741182
InsertionChr218667295186672951LOC_Os02g31170image
InsertionChr322313537223135393
InsertionChr43516653516662

Inversions: 7
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr820842742112217
InversionChr820842862468705
InversionChr821006613004339
InversionChr825519843004346
InversionChr101389813214763341LOC_Os10g26630
InversionChr22095259121164650
InversionChr22097321421163980LOC_Os02g34970

Translocations: 9
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr82084270Chr124677418
TranslocationChr412914757Chr220952485
TranslocationChr412914771Chr220952075
TranslocationChr1013898135Chr217673926LOC_Os10g26630
TranslocationChr1013910161Chr220973219LOC_Os02g34970
TranslocationChr1014292556Chr221163983
TranslocationChr1014763351Chr221164684
TranslocationChr522411100Chr128240038LOC_Os05g38219
TranslocationChr522411102Chr128241032LOC_Os05g38219