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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g29980	A09	20962091	C	T	intron_variant	MODIFIER	c.2807+144G>A\|	S62
2	BAA09g29980	A09	20962198	C	T	intron_variant	MODIFIER	c.2807+37G>A\|	S127
3	BAA09g29980	A09	20962423	C	T	synonymous_variant	LOW	c.2619G>A\|p.Arg873Arg	S174
4	BAA09g29980	A09	20962579	C	T	synonymous_variant	LOW	c.2463G>A\|p.Lys821Lys	S294
5	BAA09g29980	A09	20962951	C	T	stop_gained	HIGH	c.2091G>A\|p.Trp697*	S168
6	BAA09g29980	A09	20963080	C	T	intron_variant	MODIFIER	c.2020+28G>A\|	S283
7	BAA09g29980	A09	20963380	C	T	intron_variant	MODIFIER	c.1770-22G>A\|	S235
8	BAA09g29980	A09	20964500	C	T	missense_variant	MODERATE	c.904G>A\|p.Glu302Lys	S69
9	BAA09g29980	A09	20964618	G	A	synonymous_variant	LOW	c.786C>T\|p.Leu262Leu	S162
10	BAA09g29980	A09	20964697	C	T	missense_variant	MODERATE	c.707G>A\|p.Arg236His	S87
11	BAA09g29980	A09	20964842	C	T	missense_variant	MODERATE	c.562G>A\|p.Asp188Asn	S287
12	BAA09g29980	A09	20964851	A	C	missense_variant	MODERATE	c.553T>G\|p.Phe185Val	S107 S117 S125 S135 S162 S197 S20 S200 S223 S25 S257 S26 S306 S308 S39 S57
13	BAA09g29980	A09	20964867	G	A	synonymous_variant	LOW	c.537C>T\|p.Asp179Asp	S162
14	BAA09g29980	A09	20965115	G	A	missense_variant	MODERATE	c.289C>T\|p.Pro97Ser	S240
15	BAA09g29980	A09	20965152	G	A	synonymous_variant	LOW	c.252C>T\|p.Ser84Ser	S126
16	BAA09g29980	A09	20965438	G	A	upstream_gene_variant	MODIFIER	c.-35C>T\|	S162
17	BAA09g29980	A09	20965861	G	A	upstream_gene_variant	MODIFIER	c.-458C>T\|	S84 S93
18	BAA09g29980	A09	20965887	C	T	upstream_gene_variant	MODIFIER	c.-484G>A\|	S62
19	BAA09g29980	A09	20966087	G	A	upstream_gene_variant	MODIFIER	c.-684C>T\|	S249
20	BAA09g29980	A09	20966651	C	T	upstream_gene_variant	MODIFIER	c.-1248G>A\|	S277
21	BAA09g29980	A09	20966991	G	A	upstream_gene_variant	MODIFIER	c.-1588C>T\|	S69

Users can query the SNP information according to the gene ID.