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Mutant Information

Mutant NameFN978-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN978-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
SBSChr110567248C-THOMOINTERGENIC
SBSChr122256596T-AHETINTRON
SBSChr17191280T-CHOMOINTERGENIC
SBSChr101691227G-AHETSTART_GAINEDLOC_Os10g03740
SBSChr1018941317C-THOMOUTR_3_PRIME
SBSChr1117689817A-CHETINTERGENIC
SBSChr1124262431G-AHETINTERGENIC
SBSChr1218211695G-CHETINTERGENIC
SBSChr121898014C-THOMOINTRON
SBSChr12277670G-THETINTRON
SBSChr219101526A-THOMONON_SYNONYMOUS_CODINGLOC_Os02g32350
SBSChr230652947G-AHETNON_SYNONYMOUS_CODINGLOC_Os02g50174
SBSChr230654846A-THETINTERGENIC
SBSChr231696381C-AHETINTRON
SBSChr232227242T-GHETINTERGENIC
SBSChr234547853T-CHETINTRON
SBSChr24108019C-THOMOINTERGENIC
SBSChr27817220A-THOMOINTERGENIC
SBSChr316340082T-CHOMOINTERGENIC
SBSChr317233482T-CHOMOINTERGENIC
SBSChr319287231G-AHOMOINTERGENIC
SBSChr332364484C-THOMOINTERGENIC
SBSChr333349580A-THETUTR_3_PRIME
SBSChr333349581A-THETUTR_3_PRIME
SBSChr432540853G-AHETNON_SYNONYMOUS_CODINGLOC_Os04g54710
SBSChr48979393C-AHETINTERGENIC
SBSChr52022903A-GHOMOINTERGENIC
SBSChr611646889C-AHETINTERGENIC
SBSChr616172062C-THETINTERGENIC
SBSChr616172063C-THETINTERGENIC
SBSChr620411993T-AHETINTERGENIC
SBSChr624615311T-AHETINTERGENIC
SBSChr627955752C-THETINTRON
SBSChr64535826G-CHETINTERGENIC
SBSChr722588144G-AHETINTERGENIC
SBSChr725751570G-AHOMOINTERGENIC
SBSChr73740678C-THETINTERGENIC
SBSChr75951715C-THETINTRON
SBSChr77172121T-CHETINTERGENIC
SBSChr812508393C-THETNON_SYNONYMOUS_CODINGLOC_Os08g20849
SBSChr915510050A-GHOMOINTERGENIC

Deletions: 26
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr10175036917503778
DeletionChr4239083923908467
DeletionChr6456481045648155
DeletionChr15007522500753311
DeletionChr1510439451044017
DeletionChr12567251956746432124LOC_Os12g10630
DeletionChr4102209061022091711
DeletionChr710912926109129304LOC_Os07g18450
DeletionChr2122985491229857526
DeletionChr814907148149071568
DeletionChr915585045155850461
DeletionChr3162075211620753817
DeletionChr3164118941641190410
DeletionChr2190914121909143422LOC_Os02g32340
DeletionChr1119191736191917393
DeletionChr919593456195934571
DeletionChr5199780721997808311LOC_Os05g33860
DeletionChr102018532920185349202
DeletionChr1209072232090723310
DeletionChr523498148234981535
DeletionChr325195037251950381
DeletionChr5255113792551144162
DeletionChr526146170261461733LOC_Os05g44970
DeletionChr1226266653262666607
DeletionChr2325134683251348719
DeletionChr233758045337580483LOC_Os02g55110

Insertions: 6
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1232988023298812
InsertionChr1226909980269099823LOC_Os12g43370image
InsertionChr228012238280122392
InsertionChr43129933129942
InsertionChr614639836146398361
InsertionChr6747752974775291

Inversions: 9
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1722923433506545LOC_Os01g57960
InversionChr173755547804133
InversionChr173755677804156
InversionChr11056747111325213
InversionChr11716777417535659LOC_Os01g32030
InversionChr82078581921078843LOC_Os08g33740
InversionChr82078583021078856LOC_Os08g33740
InversionChr32892466529073843
InversionChr32894619229073843

Translocations: 7
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr91943435Chr6252734192
TranslocationChr53543877Chr313563773
TranslocationChr213467141Chr126060845LOC_Os01g45880
TranslocationChr1018628322Chr59638214
TranslocationChr1220909879Chr68520812
TranslocationChr422896294Chr213396941LOC_Os04g38530
TranslocationChr328946283Chr221947216