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Mutant Information

Mutant NameFN2161-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2161-S Alignment File
Seed AvailabilityYes [Order Seeds]
Phenotype
  • TO:0000430 (Germination Rate) = Normal (Between 75% and 125%)
For more information, please see this phenotype file
Mapping
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Variant Information

Single base substitutions: 31
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr111744249C-THET
SBSChr12482963A-CHET
SBSChr136408575C-THET
SBSChr1011060663C-THET
SBSChr106406642G-CHomo
SBSChr111195730G-AHET
SBSChr111549188A-GHET
SBSChr1118755744C-AHET
SBSChr118679484A-GHomo
SBSChr121600648C-THomo
SBSChr1225989445A-THET
SBSChr210913190T-CHETNON_SYNONYMOUS_CODINGLOC_Os02g18700
SBSChr21525918T-CHETNON_SYNONYMOUS_CODINGLOC_Os02g03660
SBSChr313454491G-CHET
SBSChr31625011G-THomo
SBSChr330059259T-CHET
SBSChr38225247T-CHET
SBSChr419022365T-AHET
SBSChr433727319T-CHET
SBSChr518558427G-AHET
SBSChr521486229G-THET
SBSChr59003952C-THET
SBSChr614652885G-AHomo
SBSChr623074349G-THomoNON_SYNONYMOUS_CODINGLOC_Os06g38890
SBSChr65733028G-THETNON_SYNONYMOUS_CODINGLOC_Os06g10970
SBSChr714861586C-THomo
SBSChr724689586C-THET
SBSChr74810883G-AHomo
SBSChr912674683G-AHET
SBSChr912986443T-AHET
SBSChr99766932C-THET

Deletions: 11
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr6367268936726923
DeletionChr6561057456105751LOC_Os06g10740
DeletionChr112400394124003984
DeletionChr1213289451132894521
DeletionChr82212800122167000389997
DeletionChr8221710012232200015099924
DeletionChr12245871782458719315
DeletionChr126939874269398762
DeletionChr134848700348487088
DeletionChr335839871358398721
DeletionChr136907333369073352

Insertions: 11
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1012434813124348142
InsertionChr1121581488215814881
InsertionChr2357473935747391
InsertionChr2360105536010562
InsertionChr316565733165657342
InsertionChr39570690957072738
InsertionChr7876671887667181LOC_Os07g15210image
InsertionChr8726936672693661
InsertionChr8809250780925071
InsertionChr913258549132585491
InsertionChr9216945221694554

Inversions: 28
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr4198590199012
InversionChr8544118544603
InversionChr614562881456556LOC_Os06g03690
InversionChr639701853970462
InversionChr845533194553502LOC_Os08g08030
InversionChr1048768884877175
InversionChr452549165255105LOC_Os04g09800
InversionChr1154009945401296LOC_Os11g10060
InversionChr568217046822002
InversionChr571406427140844LOC_Os05g12420
InversionChr586077228607838LOC_Os05g15160
InversionChr591812629181367
InversionChr41381418313814400
InversionChr61613397316134093LOC_Os06g28370
InversionChr121779400717794399
InversionChr31793144117931563LOC_Os03g31460
InversionChr101881987218820018
InversionChr92139736221397479LOC_Os09g37100
InversionChr102152574121525930
InversionChr112227530322275465LOC_Os11g37700
InversionChr52325212023252276LOC_Os05g39600
InversionChr623956102239562972
InversionChr62395667423957138LOC_Os06g40220
InversionChr52630368926304012LOC_Os05g45340
InversionChr42757195627572173LOC_Os04g46480
InversionChr62938442929384730LOC_Os06g48570
InversionChr12987775829877919
InversionChr13575274335752916LOC_Os01g61800

Translocations: 4
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr38255468Chr214361985LOC_Os03g15120
TranslocationChr214983934Chr120917486
TranslocationChr918095053Chr4349041952
TranslocationChr827530336Chr331848814LOC_Os08g43530