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Mutant Information

Variant Information

Single base substitutions: 3

Variant Type	Chromosome	Position	Change	Genotype	Effect	Gene Affected
SBS	Chr11	24783602	C-A	Homo	INTERGENIC
SBS	Chr12	25328532	C-A	Homo	NON_SYNONYMOUS_CODING	LOC_Os12g40910
SBS	Chr9	11330461	C-G	Homo	INTERGENIC

Deletions: 23

Variant Type	Chromosome	Start	End	Size (bp)	Number of Genes
Deletion	Chr2	1911236	1911240	4
Deletion	Chr9	2417064	2417085	21	LOC_Os09g04530
Deletion	Chr9	4396392	4396405	13
Deletion	Chr6	4661424	4661431	7
Deletion	Chr6	5181496	5181508	12
Deletion	Chr6	8142372	8142374	2
Deletion	Chr8	8957952	8957953	1
Deletion	Chr6	11966451	11966453	2
Deletion	Chr10	14120555	14120557	2
Deletion	Chr2	14138255	14138259	4
Deletion	Chr9	15308200	15308201	1	LOC_Os09g25520
Deletion	Chr7	15508261	15508262	1
Deletion	Chr6	15994152	15994155	3	LOC_Os06g28150
Deletion	Chr5	16392001	16412000	20000	3
Deletion	Chr2	19574508	19574513	5
Deletion	Chr2	20905961	20905968	7
Deletion	Chr4	23750631	23750632	1	LOC_Os04g39880
Deletion	Chr6	30957619	30957622	3	LOC_Os06g51180
Deletion	Chr1	32235376	32235377	1	LOC_Os01g55974
Deletion	Chr1	32547716	32547725	9
Deletion	Chr4	33385347	33385348	1
Deletion	Chr2	35005767	35005782	15
Deletion	Chr1	36661509	36661514	5

Insertions: 1

Variant Type	Chromosome	Start	End	Size (bp)	Number of Genes
Insertion	Chr7	21707169	21707169	1

Inversions: 2

Variant Type	Chromosome	Position 1	Position 2	Number of Genes
Inversion	Chr6	5336203	5401042	LOC_Os06g10480
Inversion	Chr12	25153062	25214624	LOC_Os12g40730

No Translocation

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