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Mutant Information

Variant Information

Single base substitutions: 25

Variant Type	Chromosome	Position	Change	Genotype	Effect	Gene Affected
SBS	Chr1	2206111	A-T	HET
SBS	Chr1	2877914	C-A	Homo
SBS	Chr1	4570832	C-T	Homo
SBS	Chr1	7805926	C-T	Homo
SBS	Chr1	8484784	C-A	Homo
SBS	Chr1	29199224	G-A	Homo
SBS	Chr2	673522	C-T	HET
SBS	Chr2	4360118	T-G	Homo
SBS	Chr2	4360121	A-G	Homo
SBS	Chr2	5867170	A-T	Homo
SBS	Chr2	11236547	C-G	Homo
SBS	Chr2	18869979	C-T	Homo
SBS	Chr2	21484488	C-A	HET
SBS	Chr2	31095157	T-A	Homo
SBS	Chr3	13294957	A-T	Homo
SBS	Chr3	18894918	A-G	Homo
SBS	Chr3	26975626	C-T	HET
SBS	Chr4	32814069	T-G	HET
SBS	Chr6	12681324	C-A	Homo	NON_SYNONYMOUS_CODING	LOC_Os06g21920
SBS	Chr6	27936692	T-C	HET
SBS	Chr7	23729788	C-T	Homo
SBS	Chr10	18390633	G-C	HET	NON_SYNONYMOUS_CODING	LOC_Os10g34480
SBS	Chr11	10300740	G-A	HET
SBS	Chr11	16754148	T-A	HET
SBS	Chr12	26720704	C-T	Homo

Deletions: 9

Variant Type	Chromosome	Start	End	Size (bp)	Number of Genes
Deletion	Chr2	4360426	4360432	6
Deletion	Chr5	4434021	4434022	1
Deletion	Chr1	4808895	4808897	2
Deletion	Chr3	8002648	8002654	6
Deletion	Chr5	12019469	12019470	1
Deletion	Chr6	14131611	14131613	2
Deletion	Chr5	24623838	24623840	2	LOC_Os05g42100
Deletion	Chr7	27956871	27956892	21
Deletion	Chr2	32622669	32622671	2

Insertions: 1

Variant Type	Chromosome	Start	End	Size (bp)	Number of Genes
Insertion	Chr1	6191452	6191453	2

Inversions: 1

Variant Type	Chromosome	Position 1	Position 2	Number of Genes
Inversion	Chr8	12951525	12972379	LOC_Os08g21695

Translocations: 7

Variant Type	Chromosome	Position 1	Chromosome	Position 2	Number of Genes
Translocation	Chr8	1838976	Chr6	3393331	LOC_Os08g03850
Translocation	Chr10	5484403	Chr2	14658145
Translocation	Chr10	12733183	Chr1	8511348	2
Translocation	Chr8	20159612	Chr6	3357300	LOC_Os08g32540
Translocation	Chr5	20414639	Chr1	43066651
Translocation	Chr6	20501711	Chr1	11600022	LOC_Os01g20820
Translocation	Chr11	25810793	Chr7	12810135

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