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Mutant Information

Variant Information

Single base substitutions: 4

Variant Type	Chromosome	Position	Change	Genotype	Effect
SBS	Chr11	24783602	C-A	Homo	INTERGENIC
SBS	Chr2	10846006	G-C	Homo	INTERGENIC
SBS	Chr7	12965712	T-G	Homo	INTERGENIC
SBS	Chr7	14480587	C-T	Homo	SYNONYMOUS_CODING

Deletions: 20

Variant Type	Chromosome	Start	End	Size (bp)	Number of Genes
Deletion	Chr11	3362262	3362263	1
Deletion	Chr6	4661424	4661431	7
Deletion	Chr6	5181496	5181508	12
Deletion	Chr12	7320175	7320179	4
Deletion	Chr5	7675619	7675637	18
Deletion	Chr6	8142372	8142374	2
Deletion	Chr11	11442001	11534000	92000	17
Deletion	Chr11	12716661	12716669	8	LOC_Os11g22160
Deletion	Chr2	12923055	12923056	1
Deletion	Chr12	13152506	13152509	3
Deletion	Chr11	13758186	13758187	1
Deletion	Chr2	14138255	14138259	4
Deletion	Chr6	15994152	15994155	3	LOC_Os06g28150
Deletion	Chr9	16246670	16246684	14
Deletion	Chr2	19574508	19574513	5
Deletion	Chr7	20873841	20873873	32
Deletion	Chr2	20905961	20905968	7
Deletion	Chr1	32235376	32235377	1	LOC_Os01g55974
Deletion	Chr1	32547716	32547725	9
Deletion	Chr1	36661509	36661514	5

Insertions: 2

Variant Type	Chromosome	Start	End	Size (bp)	Number of Genes
Insertion	Chr11	18882115	18882115	1
Insertion	Chr9	8268126	8268126	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

Translocations: 3

Variant Type	Chromosome	Position 1	Chromosome	Position 2	Number of Genes
Translocation	Chr10	19165241	Chr3	10385728	LOC_Os03g18540
Translocation	Chr12	24873904	Chr3	10385730	2
Translocation	Chr12	24874649	Chr10	19168249	2

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