Search Nipponbare


Mutant Information

Mutant NameFN1182-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1182-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 35
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr116265525G-AHETINTRON
SBSChr122798621C-THETSYNONYMOUS_CODING
SBSChr126407381C-AHETINTERGENIC
SBSChr19713005A-GHETINTERGENIC
SBSChr109701916C-THETINTRON
SBSChr1114164428C-THETNON_SYNONYMOUS_CODINGLOC_Os11g24840
SBSChr1114851168T-AHETINTERGENIC
SBSChr1211022263C-THETINTERGENIC
SBSChr1226325271G-AHETNON_SYNONYMOUS_CODINGLOC_Os12g42340
SBSChr1226806715A-GHETSTART_GAINEDLOC_Os12g43165
SBSChr124630026T-CHOMOINTERGENIC
SBSChr129298985G-AHETINTRON
SBSChr214737621A-THETINTERGENIC
SBSChr214743144T-AHETINTERGENIC
SBSChr214743146T-CHETINTERGENIC
SBSChr314593751C-THOMOINTERGENIC
SBSChr319924289C-THOMOINTERGENIC
SBSChr321563873G-THOMOINTERGENIC
SBSChr331495606A-GHOMOINTERGENIC
SBSChr334355514G-AHOMOINTERGENIC
SBSChr334479253T-AHETINTERGENIC
SBSChr37332449A-GHETINTRON
SBSChr414223349T-AHETINTERGENIC
SBSChr4293100C-THETINTERGENIC
SBSChr433511067G-AHOMOINTERGENIC
SBSChr522997167C-THETSYNONYMOUS_CODING
SBSChr53637393T-CHETINTERGENIC
SBSChr63292372G-AHOMOINTERGENIC
SBSChr814057839A-GHETNON_SYNONYMOUS_CODINGLOC_Os08g23290
SBSChr817331515C-GHETINTERGENIC
SBSChr827374355T-AHETINTERGENIC
SBSChr828083442T-GHETUTR_3_PRIME
SBSChr84704050A-GHETNON_SYNONYMOUS_CODINGLOC_Os08g08220
SBSChr84704051C-THETNON_SYNONYMOUS_CODINGLOC_Os08g08220
SBSChr8801625G-THETINTERGENIC

Deletions: 34
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr291233791235215
DeletionChr6145390114539076
DeletionChr3279214427921517
DeletionChr5429425642942571
DeletionChr11600495260049619
DeletionChr361868546187044190
DeletionChr4653420265342053
DeletionChr9655518965551945
DeletionChr37851413785142512
DeletionChr118334248833427931LOC_Os11g14810
DeletionChr9916429191642943
DeletionChr59210066921007610
DeletionChr5991179199117921LOC_Os05g17300
DeletionChr110327296103273004
DeletionChr911067871110678798
DeletionChr1011209388112093891
DeletionChr112120046121200559
DeletionChr1013150079131518941815LOC_Os10g25430
DeletionChr11152837881528380921LOC_Os11g26680
DeletionChr11153210341532105016
DeletionChr1015530878155308791
DeletionChr1017329253173292552
DeletionChr317489188174891902
DeletionChr11181828901818290515
DeletionChr418294655182946616LOC_Os04g30630
DeletionChr521247874212478828
DeletionChr521504463215044685
DeletionChr321518639215186412
DeletionChr222134810221348111
DeletionChr323209191232091921
DeletionChr523673720236737222LOC_Os05g40290
DeletionChr125511755255117605
DeletionChr2310532263105324216
DeletionChr4346068943460690814

Insertions: 8
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr112883923128839242
InsertionChr1232988023298812
InsertionChr139916646399166494
InsertionChr5183794718379482
InsertionChr6325593132559322
InsertionChr820282596202825972
InsertionChr820382113203821208
InsertionChr8600345960034602

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr179736268087350LOC_Os01g14220
InversionChr179736387976641LOC_Os01g14220
InversionChr112221176123045482
InversionChr112221187123045512
InversionChr31345808013459178LOC_Os03g23250

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr63234375Chr123346976
TranslocationChr56994875Chr36186858
TranslocationChr129390181Chr1013150088
TranslocationChr129390182Chr1013151935LOC_Os10g25430