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Mutant Information

Mutant NameFN4491-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4491-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 40
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr117535829C-THOMOINTRON
SBSChr122511530G-AHETINTERGENIC
SBSChr124144971A-GHETINTERGENIC
SBSChr131328083A-THETNON_SYNONYMOUS_CODINGLOC_Os01g54460
SBSChr133956433C-GHETINTERGENIC
SBSChr142107512C-THETINTERGENIC
SBSChr29511257C-AHETNON_SYNONYMOUS_CODINGLOC_Os02g16650
SBSChr210639058C-AHOMOINTRON
SBSChr230470771C-THETINTERGENIC
SBSChr230817327A-THETINTERGENIC
SBSChr232636911A-THETINTERGENIC
SBSChr3956380C-THETSYNONYMOUS_CODING
SBSChr31634416T-CHOMOINTRON
SBSChr31653532C-GHOMONON_SYNONYMOUS_CODINGLOC_Os03g03710
SBSChr39455034C-GHOMOUTR_3_PRIME
SBSChr313787145G-AHETUTR_3_PRIME
SBSChr316142843C-THOMOINTERGENIC
SBSChr318962227G-AHOMOINTERGENIC
SBSChr319813059A-GHETINTERGENIC
SBSChr319961631C-AHETINTERGENIC
SBSChr335293321C-THETINTRON
SBSChr53038282T-CHETINTERGENIC
SBSChr53817892T-AHETINTRON
SBSChr510197746G-AHETINTERGENIC
SBSChr516075576G-AHOMOSYNONYMOUS_CODING
SBSChr525080659G-THOMOINTERGENIC
SBSChr610867562C-THETSYNONYMOUS_CODING
SBSChr612469871C-THETNON_SYNONYMOUS_CODINGLOC_Os06g21610
SBSChr616037593G-AHETINTERGENIC
SBSChr616332207G-AHETINTERGENIC
SBSChr710967038G-AHOMOINTRON
SBSChr721111650C-THOMOINTERGENIC
SBSChr89318713G-AHETINTERGENIC
SBSChr816486642T-CHETINTERGENIC
SBSChr911379268C-THETINTERGENIC
SBSChr1015566200C-THETSYNONYMOUS_CODING
SBSChr1121852097T-CHETINTERGENIC
SBSChr1213074504G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g23120
SBSChr1221792834G-CHETINTERGENIC
SBSChr1225879052A-CHOMOINTERGENIC

Deletions: 30
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr75311045311051
DeletionChr10157276415727651
DeletionChr1174961417496162
DeletionChr3305909230591019
DeletionChr73462309346232314
DeletionChr839760013991000150002
DeletionChr840030014024000210006
DeletionChr840280014050000220003
DeletionChr5408146140814621
DeletionChr8416315941631612
DeletionChr7424297242429742
DeletionChr49854056985413377LOC_Os04g17920
DeletionChr213894634138946362
DeletionChr2140325411403256322
DeletionChr115415060154150611
DeletionChr415537147155371481
DeletionChr216341287163412892
DeletionChr416605497166054981
DeletionChr717111742171117431
DeletionChr111719300117208000150003
DeletionChr10173926051739262823
DeletionChr819997767199977692
DeletionChr420059535200595361
DeletionChr321574734215747351
DeletionChr121933089219330945
DeletionChr122593585225935861
DeletionChr1225060020250600211
DeletionChr427274503272745052
DeletionChr232437292324372964
DeletionChr234694784346947906

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr136481165364811651
InsertionChr4634936163493611
InsertionChr512760956127609561
InsertionChr513988934139889341
InsertionChr621389882213898821
InsertionChr723435269234352713
InsertionChr8168997751689980935
InsertionChr9335301833530181

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1012708061318610LOC_Os10g03120
InversionChr1022761422276247
InversionChr82156382421563950

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr821275227Chr139382861
TranslocationChr1225890388Chr6353816