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Mutant Information

Mutant NameFN2666-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN2666-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 98
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr118421985T-AHET
SBSChr11891943C-THET
SBSChr120153958A-THET
SBSChr120697806A-THET
SBSChr120697806A-THETINTERGENIC
SBSChr123159960T-GHET
SBSChr123159960T-GHETINTERGENIC
SBSChr128575834C-THET
SBSChr132138485C-THET
SBSChr132138485C-THETINTRON
SBSChr137566701A-GHET
SBSChr1013053586C-THET
SBSChr1013203684G-AHET
SBSChr1013203684G-AHETSYNONYMOUS_CODING
SBSChr1020419798C-THETINTERGENIC
SBSChr105040174C-AHET
SBSChr105040174C-AHETINTERGENIC
SBSChr108867827C-AHET
SBSChr108867827C-AHETINTERGENIC
SBSChr1115215036C-GHET
SBSChr1120906425A-THET
SBSChr1120906425A-THETINTERGENIC
SBSChr114394509T-CHETNON_SYNONYMOUS_CODINGLOC_Os11g08330
SBSChr1221841571C-THETNON_SYNONYMOUS_CODINGLOC_Os12g35840
SBSChr124215861A-GHET
SBSChr124215861A-GHETINTRON
SBSChr124719648C-AHET
SBSChr124719648C-AHETINTERGENIC
SBSChr220212545G-AHET
SBSChr220212545G-AHETSYNONYMOUS_CODING
SBSChr220696147G-AHET
SBSChr220696147G-AHOMOINTERGENIC
SBSChr22890681G-THomo
SBSChr22890681G-THOMOINTRON
SBSChr313966957C-THET
SBSChr313966957C-THETINTRON
SBSChr321987387G-AHET
SBSChr323651742G-AHET
SBSChr324811687T-GHET
SBSChr324811687T-GHETINTRON
SBSChr332771600A-GHETNON_SYNONYMOUS_CODINGLOC_Os03g57480
SBSChr412905238C-AHETNON_SYNONYMOUS_CODINGLOC_Os04g22790
SBSChr413439346G-AHETSYNONYMOUS_CODING
SBSChr414548274T-AHOMONON_SYNONYMOUS_CODINGLOC_Os04g25170
SBSChr414548274T-AHomoNON_SYNONYMOUS_CODINGLOC_Os04g25170
SBSChr421127408T-AHET
SBSChr421127408T-AHETINTERGENIC
SBSChr424463387G-AHomo
SBSChr424463387G-AHOMOINTRON
SBSChr429084546C-AHETNON_SYNONYMOUS_CODINGLOC_Os04g48760
SBSChr430612116G-AHET
SBSChr431805012C-THET
SBSChr433613056C-THET
SBSChr44508022A-THET
SBSChr45015787C-AHET
SBSChr45015787C-AHETINTERGENIC
SBSChr510166310A-THomo
SBSChr510166310A-THOMOINTERGENIC
SBSChr511988951G-AHOMONON_SYNONYMOUS_CODINGLOC_Os05g20430
SBSChr511988951G-AHomoNON_SYNONYMOUS_CODINGLOC_Os05g20430
SBSChr55559279T-GHET
SBSChr55559279T-GHETINTERGENIC
SBSChr56189526T-AHETNON_SYNONYMOUS_CODINGLOC_Os05g11040
SBSChr624721282T-AHomo
SBSChr624721282T-AHOMOINTERGENIC
SBSChr64048626C-THET
SBSChr64048626C-THETINTERGENIC
SBSChr68495887G-THET
SBSChr69526565G-THET
SBSChr710312621T-AHomo
SBSChr710312621T-AHOMOINTERGENIC
SBSChr710312622G-AHomo
SBSChr710312622G-AHOMOINTERGENIC
SBSChr710480702C-THET
SBSChr711489776G-AHomoNON_SYNONYMOUS_CODINGLOC_Os07g19420
SBSChr722094637C-AHET
SBSChr722094637C-AHETINTERGENIC
SBSChr72458484T-GHomo
SBSChr73231286C-THET
SBSChr73231286C-THETSYNONYMOUS_CODING
SBSChr73366552A-THomo
SBSChr73366552A-THOMOINTRON
SBSChr810904192C-THETINTRON
SBSChr815964272C-GHET
SBSChr815964272C-GHETINTERGENIC
SBSChr82317753T-AHET
SBSChr82317753T-AHETINTERGENIC
SBSChr824089478C-THET
SBSChr916153647C-THETNON_SYNONYMOUS_CODINGLOC_Os09g26620
SBSChr92270314C-AHET
SBSChr92270314C-AHETINTRON
SBSChr94621560A-GHET
SBSChr9641106C-THET
SBSChr9641106C-THETINTERGENIC
SBSChr9644892A-GHET
SBSChr9644892A-GHETINTERGENIC
SBSChr99676857G-THomo
SBSChr99676857G-THOMOINTERGENIC

Deletions: 45
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr760520460521282
DeletionChr51771724177174420
DeletionChr31939037193905821LOC_Os03g04220
DeletionChr4269263026926344LOC_Os04g05380
DeletionChr33699591369959762
DeletionChr85095144509514512
DeletionChr9731696073169611
DeletionChr27956138795613912
DeletionChr88686659868666012
DeletionChr59434136943414482
DeletionChr410755647107556547
DeletionChr310788258107882646
DeletionChr411663448116634513LOC_Os04g20790
DeletionChr12118007021180071082
DeletionChr7118045911180460092
DeletionChr112695248126952546
DeletionChr1014155163141551641
DeletionChr116175671161756721
DeletionChr416656096166561004
DeletionChr1173258861732588712
DeletionChr11180742811807428322
DeletionChr101860700118620000129992
DeletionChr1187014371870144032
DeletionChr12188603661886037711
DeletionChr1019015843190158496
DeletionChr1197619821976198532
DeletionChr120682259206822656
DeletionChr1207373132073731632
DeletionChr320834733208347341
DeletionChr52104123021041247172
DeletionChr321416922214169231
DeletionChr6243543312435433652
DeletionChr624613289246132901
DeletionChr325350185253501894
DeletionChr6258743292587433892
DeletionChr11264705382647055315
DeletionChr3271128922711289972
DeletionChr727702804277028062LOC_Os07g46430
DeletionChr3278498462784986317
DeletionChr8278833102788332010
DeletionChr6282140012822600011999
DeletionChr1284410232844103411
DeletionChr33031715730317177202
DeletionChr4318473933184747986
DeletionChr332522079325220801

Insertions: 13
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr13945123394512422image
InsertionChr13945123394512422image
InsertionChr143000361430003611LOC_Os01g74230image
InsertionChr124269784269825
InsertionChr224310552243105521
InsertionChr3227596062275961712
InsertionChr4105803710580371
InsertionChr43133414313341632image
InsertionChr43133414313341632image
InsertionChr84957394495739962image
InsertionChr84957394495739962image
InsertionChr9130617711306177222image
InsertionChr9130617711306177222image

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1016879281174594312
InversionChr32083126121068189
InversionChr320831273210681922
InversionChr13173029132301893LOC_Os01g55150
InversionChr131730294323019072

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr126457667Chr103607567
TranslocationChr119323569Chr623180839