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Mutant Information

Mutant NameFN4872-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4872-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 50
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr114603420G-CHOMO
SBSChr114611368C-THOMOLOC_Os01g25800
SBSChr114611372G-AHOMOLOC_Os01g25800
SBSChr121120832G-THET
SBSChr124191400C-AHET
SBSChr127337303G-THETLOC_Os01g47770
SBSChr128988811G-AHET
SBSChr131195467C-THET
SBSChr140074637A-GHET
SBSChr14757561G-AHET
SBSChr106606342C-AHET
SBSChr107701842A-THET
SBSChr108313959C-THETLOC_Os10g16670
SBSChr1117721043A-THOMO
SBSChr1127678413G-AHET
SBSChr1213692477T-GHET
SBSChr121912059G-AHOMO
SBSChr1222442640C-THET
SBSChr1225718277C-AHOMO
SBSChr218688409G-AHET
SBSChr235373384A-GHETLOC_Os02g57760
SBSChr27348073G-AHET
SBSChr319191737G-AHET
SBSChr319686782A-THETLOC_Os03g35520
SBSChr36106320A-CHET
SBSChr411984242G-THET
SBSChr413196031G-AHET
SBSChr421828019G-AHET
SBSChr423205530T-AHOMO
SBSChr511434206T-CHETLOC_Os05g19620
SBSChr56710307C-THET
SBSChr6114527T-CHET
SBSChr613673447C-AHET
SBSChr621396519T-CHET
SBSChr626519411C-THET
SBSChr627965814G-AHET
SBSChr715128156A-THET
SBSChr717696653C-AHOMO
SBSChr72372695A-GHET
SBSChr7551222A-THET
SBSChr811309943T-CHET
SBSChr814131266G-AHET
SBSChr81454952G-THOMO
SBSChr816260544G-AHETLOC_Os08g26730
SBSChr819977055G-AHETLOC_Os08g32240
SBSChr84076654C-THETLOC_Os08g07290
SBSChr84685227C-AHET
SBSChr86072687A-CHET
SBSChr913250478C-THET
SBSChr918829377G-THET

Deletions: 70
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr22537722537721
DeletionChr6348267348422156LOC_Os06g01590
DeletionChr877529977534042
DeletionChr6102960710296126
DeletionChr4203463020346312
DeletionChr82103561210358626
DeletionChr92370519237053416
DeletionChr8283161528316195
DeletionChr7363056536305728
DeletionChr4370024037002401
DeletionChr83995432399548251LOC_Os08g07130
DeletionChr115200179520020325
DeletionChr2629479662947961
DeletionChr1163203256320487163
DeletionChr56434802643481211
DeletionChr5676591367659186
DeletionChr11781258278125821
DeletionChr8814270081427023
DeletionChr10855772485577274
DeletionChr10892046289204709
DeletionChr6971129897113014
DeletionChr6100425211004253414
DeletionChr61287900112921000420006
DeletionChr413072467130724682
DeletionChr9139414121394142211
DeletionChr314716160147161601
DeletionChr214856111148561111
DeletionChr41513565215135869218
DeletionChr10160150011615100013600018
DeletionChr816458767164587704
DeletionChr816538787165387882LOC_Os08g27070
DeletionChr216950516169505161
DeletionChr317364983173649853LOC_Os03g30450
DeletionChr11177282971772832933
DeletionChr217832932178329321
DeletionChr418347255183472551
DeletionChr118594891185948922
DeletionChr619551912195519198
DeletionChr419604078196040869
DeletionChr619712055197120628
DeletionChr22001636720016694328
DeletionChr620136156201361583
DeletionChr720725571207255711
DeletionChr720777353207773564
DeletionChr320803562208035632
DeletionChr320886990208869923
DeletionChr3215021972150221620LOC_Os03g38740
DeletionChr1222282382222827639LOC_Os01g39464
DeletionChr522508052225080532
DeletionChr1122751784227517907
DeletionChr5227530012288300013000022
DeletionChr3231293242312934320
DeletionChr2250450012515500011000014
DeletionChr8255521162555214328
DeletionChr1225627668256276769LOC_Os12g41350
DeletionChr725628745256287528
DeletionChr525732012257320121
DeletionChr12261874572618748832
DeletionChr2272899742729001744
DeletionChr827441796274417983
DeletionChr11276207472762084599
DeletionChr628977950289779501LOC_Os06g47900
DeletionChr729320877293208771
DeletionChr6293378012933785252
DeletionChr430820448308204525
DeletionChr231226408312264081
DeletionChr2316191603161917213
DeletionChr333496354334963552
DeletionChr2353453873534540014LOC_Os02g57710
DeletionChr336224916362249172

Insertions: 34
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1176345911763467181
InsertionChr128306762283067621
InsertionChr143149559431495591
InsertionChr1115578672155786721
InsertionChr11227942992279433739
InsertionChr11253860362538611984
InsertionChr1127625718276257192
InsertionChr1211007901110079022
InsertionChr12176803661768040742
InsertionChr1223754643237546442
InsertionChr12262565426256541
InsertionChr2170522617052294
InsertionChr2178912771789132751
InsertionChr223462455234624551
InsertionChr315859880158598812
InsertionChr3253888992538892931
InsertionChr336156175361561806
InsertionChr420974079209740846
InsertionChr4245634042456344643
InsertionChr4761851876185214
InsertionChr5110238101102385445
InsertionChr516070146160701472
InsertionChr5172485101724855445
InsertionChr5178785431787861775
InsertionChr519766461197664611
InsertionChr527403303274033031
InsertionChr5535621753562204
InsertionChr621694693216946931
InsertionChr6777477677747805
InsertionChr711606141116061411
InsertionChr712248590122485934
InsertionChr7232323802323243556
InsertionChr7649042364904231
InsertionChr8143367631433677816

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr417008041700931
InversionChr121312268113789299
InversionChr121312268913789300
InversionChr101567809815998869
InversionChr101568026516150490LOC_Os10g30156

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1114735412Chr715984557
TranslocationChr1114736087Chr715984578