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Mutant Information

Mutant NameFN4445-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4445-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 41
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr117889747C-AHETNON_SYNONYMOUS_CODINGLOC_Os01g32630
SBSChr120948572C-AHETINTERGENIC
SBSChr122805242C-GHETNON_SYNONYMOUS_CODINGLOC_Os01g40390
SBSChr24807587G-AHETINTERGENIC
SBSChr26616334G-THETSYNONYMOUS_CODING
SBSChr26866756A-GHETINTERGENIC
SBSChr212254828A-THETINTERGENIC
SBSChr217635508A-THETINTERGENIC
SBSChr220096803G-THETINTERGENIC
SBSChr223192905C-AHETINTERGENIC
SBSChr225002916T-AHETINTERGENIC
SBSChr232802281C-THETINTERGENIC
SBSChr234601020G-AHETINTRON
SBSChr37730173C-THETINTERGENIC
SBSChr322843833C-AHETINTERGENIC
SBSChr333122697C-THOMOINTERGENIC
SBSChr333128847C-THETINTERGENIC
SBSChr333585921C-THETINTERGENIC
SBSChr412712150C-AHETINTERGENIC
SBSChr423347816C-THETINTERGENIC
SBSChr427442807G-AHOMOINTERGENIC
SBSChr55199520C-THETINTRON
SBSChr520433043C-AHETINTERGENIC
SBSChr524339431G-AHETNON_SYNONYMOUS_CODINGLOC_Os05g41560
SBSChr524995832A-GHETINTERGENIC
SBSChr525429082C-THETINTERGENIC
SBSChr64086876G-AHETINTERGENIC
SBSChr66740023G-THETINTERGENIC
SBSChr611887272T-AHETINTERGENIC
SBSChr615641448C-THOMOINTERGENIC
SBSChr71266981A-CHETINTERGENIC
SBSChr710608673C-THOMOINTERGENIC
SBSChr713694634C-THETINTERGENIC
SBSChr9533220C-AHETINTERGENIC
SBSChr94367332C-GHOMOINTERGENIC
SBSChr104826368G-AHETNON_SYNONYMOUS_CODINGLOC_Os10g08920
SBSChr1116343272C-THETINTERGENIC
SBSChr1117565779C-THOMOINTERGENIC
SBSChr1122017715T-CHETINTRON
SBSChr1210844427G-AHOMOINTERGENIC
SBSChr1225918087C-THETINTERGENIC

Deletions: 43
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr26889566889582
DeletionChr4173138517313872
DeletionChr10201006920100723
DeletionChr11314116431411673
DeletionChr10336559933656056LOC_Os10g06550
DeletionChr11340014334001441
DeletionChr2368336736833681
DeletionChr104386314438635238
DeletionChr7449440744944103
DeletionChr5450805445080551
DeletionChr1455519745551981
DeletionChr5655298865529979
DeletionChr5670836667083704
DeletionChr3899713189971321
DeletionChr692090019236000270006
DeletionChr12952777395277752
DeletionChr310009361100093621LOC_Os03g17980
DeletionChr11017837610178503127
DeletionChr910237461102374621
DeletionChr9102859641028601854
DeletionChr510291420102914211
DeletionChr11115268091152685748LOC_Os11g20030
DeletionChr1011924953119249541
DeletionChr412108102121081031
DeletionChr712181358121813591
DeletionChr10128014311280144514
DeletionChr714059437140594425
DeletionChr4146198681461988517
DeletionChr1215579584155795884
DeletionChr717443526174435271
DeletionChr1117717176177171771LOC_Os11g30470
DeletionChr7180944451809451671LOC_Os07g30580
DeletionChr818328973183289741
DeletionChr1018899571188995721
DeletionChr818925483189254874LOC_Os08g30680
DeletionChr821061846210618471
DeletionChr122804903228049041
DeletionChr522850177228501781
DeletionChr727669107276691169
DeletionChr628219651282196532
DeletionChr329485860294858611
DeletionChr234591765345917661
DeletionChr43549638535496500115

Insertions: 22
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr9373851537385162
InsertionChr1216557721655771
InsertionChr128379722283797221
InsertionChr2394115739411571
InsertionChr215752183157521831
InsertionChr2191562771915632246
InsertionChr332309380323093801
InsertionChr4393338939333891
InsertionChr4540787054078712
InsertionChr5403419040341901
InsertionChr512739782127397821
InsertionChr5189919411899197030
InsertionChr520540390205403901
InsertionChr630055415300554151
InsertionChr721916097219160982
InsertionChr722434379224343791
InsertionChr10551286555128651
InsertionChr1015383034153830341
InsertionChr11134351891343523042
InsertionChr1123637084236370841
InsertionChr125786691578670313
InsertionChr12682736668273661

Inversions: 2
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr43270074032753284LOC_Os04g54980
InversionChr43270074132753288LOC_Os04g54980

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr55375715Chr118178348
TranslocationChr55375720Chr118178200
TranslocationChr911245225Chr69250514LOC_Os06g19690
TranslocationChr911262745Chr69250522