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Mutant Information

Mutant NameFN673-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN673-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: 37
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr121079068C-AHOMOINTRON
SBSChr1010695854T-GHOMOINTERGENIC
SBSChr107209217G-CHETNON_SYNONYMOUS_CODINGLOC_Os10g13350
SBSChr107380444G-AHOMONON_SYNONYMOUS_CODINGLOC_Os10g13610
SBSChr10885369C-THOMONON_SYNONYMOUS_CODINGLOC_Os10g02420
SBSChr1111183588C-AHETSYNONYMOUS_CODING
SBSChr1120300916A-THOMOINTRON
SBSChr117391556G-THOMOINTERGENIC
SBSChr1210844427G-AHOMOINTERGENIC
SBSChr1219447421T-AHETINTERGENIC
SBSChr128199901A-THETINTRON
SBSChr214082178C-GHETNON_SYNONYMOUS_CODINGLOC_Os02g24280
SBSChr223962042C-THOMOINTERGENIC
SBSChr229972400G-AHETINTERGENIC
SBSChr2348482G-AHETINTERGENIC
SBSChr2348483A-THETINTERGENIC
SBSChr26376474C-THETINTERGENIC
SBSChr333122697C-THOMOINTERGENIC
SBSChr39704988G-THOMOINTRON
SBSChr426826213A-GHETINTERGENIC
SBSChr511946045C-THOMOINTERGENIC
SBSChr514557293G-AHETINTERGENIC
SBSChr514557294C-AHETINTERGENIC
SBSChr520387783T-CHOMOINTRON
SBSChr520387786G-THOMOINTRON
SBSChr520387787T-AHOMOINTRON
SBSChr610588247G-AHOMOUTR_3_PRIME
SBSChr612981940C-THETINTERGENIC
SBSChr621420894A-THOMOINTRON
SBSChr726752557T-AHETINTERGENIC
SBSChr78475091A-GHOMOINTERGENIC
SBSChr824530469A-CHETINTERGENIC
SBSChr828287040A-GHETINTERGENIC
SBSChr83804896G-AHOMOINTERGENIC
SBSChr922541764C-THETINTERGENIC
SBSChr92569825G-AHETINTRON
SBSChr95679972C-THETINTERGENIC

Deletions: 25
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr1018738187391
DeletionChr9130725013072533
DeletionChr5150971615097204
DeletionChr94672890467290616
DeletionChr661127966141802290066
DeletionChr2700874870087568
DeletionChr7740830074083033
DeletionChr9828488882848957LOC_Os09g14019
DeletionChr79193636919364812
DeletionChr9946817094681711LOC_Os09g15470
DeletionChr1112250011132500010000015
DeletionChr113932640139326488
DeletionChr214060964140609651
DeletionChr1141085171410854225
DeletionChr5145633351456334813
DeletionChr111516911815169809691
DeletionChr515309014153090151
DeletionChr719026030190260322
DeletionChr7199170771991709013LOC_Os07g33320
DeletionChr1021565482215654842
DeletionChr1023024022230240253
DeletionChr825123448251234568
DeletionChr426640872266408742
DeletionChr129039332290393364
DeletionChr429109866291098748

Insertions: 11
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr123798371237983722
InsertionChr140468997404689993
InsertionChr1122634284226342852
InsertionChr11537264953726568LOC_Os11g10040image
InsertionChr217969513179695142
InsertionChr325745703257457053
InsertionChr71274621127464424LOC_Os07g03230image
InsertionChr71455532145554312
InsertionChr724313236243132372
InsertionChr820289288202892903
InsertionChr92166626216665732

Inversions: 4
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1160231836188754LOC_Os11g10910
InversionChr1938390313918587
InversionChr11119028213918447
InversionChr21215356312844308LOC_Os02g21620

Translocations: 7
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr34352543Chr111324341
TranslocationChr115104116Chr6169251732
TranslocationChr116023184Chr1113338912
TranslocationChr116188756Chr111324809
TranslocationChr1110449195Chr617476343LOC_Os11g18540
TranslocationChr1013748729Chr213460116LOC_Os02g22570
TranslocationChr618200621Chr28950278