Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
113751	BAA10g08970-BAA10g08980	A10	11041416	C	T	intergenic_region	MODIFIER	n.11041416C>T\|	S177
113752	BAA10g08970-BAA10g08980	A10	11043062	G	A	intergenic_region	MODIFIER	n.11043062G>A\|	S217
113753	BAA10g08970-BAA10g08980	A10	11044107	G	A	intergenic_region	MODIFIER	n.11044107G>A\|	S157 S163
113754	BAA10g08970-BAA10g08980	A10	11044344	G	A	intergenic_region	MODIFIER	n.11044344G>A\|	S81 S85
113755	BAA10g08970-BAA10g08980	A10	11044669	C	T	intergenic_region	MODIFIER	n.11044669C>T\|	S193
113756	BAA10g08970-BAA10g08980	A10	11044833	G	A	intergenic_region	MODIFIER	n.11044833G>A\|	S171
113757	BAA10g08970-BAA10g08980	A10	11062014	C	T	intergenic_region	MODIFIER	n.11062014C>T\|	S187
113758	BAA10g08970-BAA10g08980	A10	11062467	C	T	intergenic_region	MODIFIER	n.11062467C>T\|	S173
113759	BAA10g08970-BAA10g08980	A10	11062877	C	T	intergenic_region	MODIFIER	n.11062877C>T\|	S269
113760	BAA10g08970-BAA10g08980	A10	11063613	G	A	intergenic_region	MODIFIER	n.11063613G>A\|	S18
113761	BAA10g08970-BAA10g08980	A10	11066155	G	A	intergenic_region	MODIFIER	n.11066155G>A\|	S139
113762	BAA10g08980	A10	11073937	C	T	downstream_gene_variant	MODIFIER	c.*3557G>A\|	S28
113763	BAA10g08990	A10	11076304	G	A	upstream_gene_variant	MODIFIER	c.-3490G>A\|	S45
113764	BAA10g08990	A10	11076370	G	A	upstream_gene_variant	MODIFIER	c.-3424G>A\|	S184
113765	BAA10g08990	A10	11076572	G	A	upstream_gene_variant	MODIFIER	c.-3222G>A\|	S182
113766	BAA10g08990	A10	11077235	C	T	upstream_gene_variant	MODIFIER	c.-2559C>T\|	S199
113767	BAA10g08990	A10	11077249	G	A	upstream_gene_variant	MODIFIER	c.-2545G>A\|	S105 S106
113768	BAA10g08980	A10	11077505	G	A	missense_variant	MODERATE	c.367C>T\|p.Leu123Phe	S241
113769	BAA10g08980	A10	11077627	G	A	synonymous_variant	LOW	c.315C>T\|p.Val105Val	S107
113770	BAA10g08980	A10	11077886	G	A	missense_variant	MODERATE	c.56C>T\|p.Ser19Leu	S1 S90
113771	BAA10g08980	A10	11077917	G	A	missense_variant	MODERATE	c.25C>T\|p.Leu9Phe	S233
113772	BAA10g08980	A10	11079153	C	T	upstream_gene_variant	MODIFIER	c.-1212G>A\|	S175 S177
113773	BAA10g08980	A10	11079683	G	A	upstream_gene_variant	MODIFIER	c.-1742C>T\|	S77 S82
113774	BAA10g08990	A10	11080141	G	A	splice_region_variant&intron_variant	LOW	c.149+5G>A\|	S32
113775	BAA10g08990	A10	11080442	G	A	missense_variant	MODERATE	c.298G>A\|p.Glu100Lys	S219 S72

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