Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
13301	BAA01g10440	A01	4779955	C	T	upstream_gene_variant	MODIFIER	c.-1378G>A\|	S242
13302	BAA01g10440	A01	4780725	C	T	upstream_gene_variant	MODIFIER	c.-2148G>A\|	S296
13303	BAA01g10440	A01	4781100	C	T	upstream_gene_variant	MODIFIER	c.-2523G>A\|	S166
13304	BAA01g10440	A01	4781237	G	A	upstream_gene_variant	MODIFIER	c.-2660C>T\|	S60
13305	BAA01g10440	A01	4782335	G	A	upstream_gene_variant	MODIFIER	c.-3758C>T\|	S263
13306	BAA01g10440	A01	4782402	C	T	upstream_gene_variant	MODIFIER	c.-3825G>A\|	S180 S34 S38
13307	BAA01g10450	A01	4784974	C	T	downstream_gene_variant	MODIFIER	c.*1241G>A\|	S90
13308	BAA01g10450	A01	4786155	C	T	downstream_gene_variant	MODIFIER	c.*60G>A\|	S40 S49
13309	BAA01g10450	A01	4786543	C	T	splice_region_variant&intron_variant	LOW	c.1730+5G>A\|	S38
13310	BAA01g10450	A01	4786599	C	T	missense_variant	MODERATE	c.1679G>A\|p.Arg560His	S182 S46
13311	BAA01g10450	A01	4788211	G	A	synonymous_variant	LOW	c.378C>T\|p.Leu126Leu	S186
13312	BAA01g10450	A01	4789513	G	A	upstream_gene_variant	MODIFIER	c.-494C>T\|	S153
13313	BAA01g10460	A01	4791397	C	T	synonymous_variant	LOW	c.759G>A\|p.Glu253Glu	S202
13314	BAA01g10460	A01	4791399	C	T	missense_variant	MODERATE	c.757G>A\|p.Glu253Lys	S183
13315	BAA01g10460	A01	4791746	G	A	missense_variant	MODERATE	c.410C>T\|p.Ser137Phe	S190
13316	BAA01g10460	A01	4791816	C	T	missense_variant	MODERATE	c.340G>A\|p.Val114Ile	S192
13317	BAA01g10460	A01	4791827	G	A	missense_variant	MODERATE	c.329C>T\|p.Ser110Phe	S84 S93
13318	BAA01g10460	A01	4792184	C	T	synonymous_variant	LOW	c.153G>A\|p.Pro51Pro	S136
13319	BAA01g10460	A01	4792194	C	T	missense_variant	MODERATE	c.143G>A\|p.Cys48Tyr	S44
13320	BAA01g10460	A01	4792212	G	A	missense_variant	MODERATE	c.125C>T\|p.Thr42Ile	S1 S90
13321	BAA01g10450	A01	4792430	G	A	upstream_gene_variant	MODIFIER	c.-3411C>T\|	S45
13322	BAA01g10450	A01	4792449	G	A	upstream_gene_variant	MODIFIER	c.-3430C>T\|	S157
13323	BAA01g10450	A01	4793916	C	T	upstream_gene_variant	MODIFIER	c.-4897G>A\|	S98
13324	BAA01g10460	A01	4794060	C	T	upstream_gene_variant	MODIFIER	c.-1724G>A\|	S198
13325	BAA01g10460	A01	4794077	G	A	upstream_gene_variant	MODIFIER	c.-1741C>T\|	S131

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