Search Nipponbare


Mutant Information

Mutant NameFN1739-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN1739-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000326 (Leaf Color) = Normal
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
(Hover to Zoom-In)


Variant Information

Single base substitutions: 27
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111088201C-AHomo
SBSChr135150823G-AHET
SBSChr10534980G-AHET
SBSChr111008275T-CHET
SBSChr1116401321C-THET
SBSChr113901315T-CHET
SBSChr114272875C-THET
SBSChr114440000T-CHETNON_SYNONYMOUS_CODINGLOC_Os11g08420
SBSChr119658132G-THET
SBSChr126775202G-AHET
SBSChr228514415G-AHET
SBSChr33087048A-GHET
SBSChr410292766G-AHomoNON_SYNONYMOUS_CODINGLOC_Os04g18610
SBSChr433734701T-GHET
SBSChr512918775C-THETNON_SYNONYMOUS_CODINGLOC_Os05g22770
SBSChr59584201A-THET
SBSChr616716694G-AHomoSTOP_GAINEDLOC_Os06g29280
SBSChr626922513T-CHETNON_SYNONYMOUS_CODINGLOC_Os06g44590
SBSChr65918407G-CHET
SBSChr66172782T-AHET
SBSChr712542329T-AHET
SBSChr718986813G-CHomo
SBSChr77447494C-GHETNON_SYNONYMOUS_CODINGLOC_Os07g12980
SBSChr810779077G-AHET
SBSChr82110557C-THET
SBSChr88681189C-THET
SBSChr919950493C-GHomo

Deletions: 14
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr124710504710555LOC_Os12g01770
DeletionChr105838285838335LOC_Os10g01920
DeletionChr33801001396600016499930
DeletionChr124273678427369113LOC_Os12g08410
DeletionChr361076206107740120
DeletionChr10625764162576421
DeletionChr710071021100710309LOC_Os07g17140
DeletionChr110098199100982023
DeletionChr111081000110834000239993
DeletionChr41843800118452000139992
DeletionChr7206343742063439016
DeletionChr727635069276350701
DeletionChr529936290299362911
DeletionChr130076812300768208LOC_Os01g52330

Insertions: 11
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr113286266132862672
InsertionChr119234766192347661
InsertionChr102288239228830264
InsertionChr1222243474222434741
InsertionChr12516396751639759
InsertionChr310210956102109561
InsertionChr3227596062275962015
InsertionChr5452347645234761
InsertionChr6962223896222392
InsertionChr718888839188888391
InsertionChr8202863342028636734

Inversions: 12
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr520943852094497
InversionChr126030262603346LOC_Os01g05500
InversionChr101058875310589088LOC_Os10g20900
InversionChr51120801911208180
InversionChr51314197513142136LOC_Os05g23050
InversionChr21877293018773278LOC_Os02g31290
InversionChr82015674820157150LOC_Os08g32540
InversionChr122380812223808452LOC_Os12g38750
InversionChr112772463927792555LOC_Os11g45820
InversionChr62875703228757193LOC_Os06g47470
InversionChr22980882729809132
InversionChr13116978531170249

Translocations: 3
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr11916018Chr33015431LOC_Os11g02778
TranslocationChr97389228Chr213965460
TranslocationChr1218566076Chr5102666522