Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
140901	BAA10g26030	A10	20777718	G	A	missense_variant	MODERATE	c.61G>A\|p.Glu21Lys	S273
140902	BAA10g26030	A10	20777983	G	A	missense_variant&splice_region_variant	MODERATE	c.221G>A\|p.Gly74Glu	S303
140903	BAA10g26030	A10	20779122	G	A	splice_acceptor_variant&intron_variant	HIGH	c.613-1G>A\|	S249
140904	BAA10g26030	A10	20779302	C	T	missense_variant	MODERATE	c.662C>T\|p.Thr221Ile	S299
140905	BAA10g26030	A10	20779851	G	A	missense_variant	MODERATE	c.1055G>A\|p.Gly352Glu	S67
140906	BAA10g26030	A10	20780209	C	T	missense_variant	MODERATE	c.1319C>T\|p.Pro440Leu	S292
140907	BAA10g26020	A10	20780546	C	T	upstream_gene_variant	MODIFIER	c.-4910G>A\|	S188
140908	BAA10g26030	A10	20781112	C	T	missense_variant	MODERATE	c.1970C>T\|p.Ser657Phe	S72 S78
140909	BAA10g26040	A10	20782413	C	T	upstream_gene_variant	MODIFIER	c.-750C>T\|	S51
140910	BAA10g26040	A10	20782670	C	T	upstream_gene_variant	MODIFIER	c.-493C>T\|	S148 S30 S31
140911	BAA10g26040	A10	20782914	G	A	upstream_gene_variant	MODIFIER	c.-249G>A\|	S226
140912	BAA10g26040	A10	20783008	C	T	upstream_gene_variant	MODIFIER	c.-155C>T\|	S92
140913	BAA10g26040	A10	20783675	G	A	synonymous_variant	LOW	c.513G>A\|p.Gln171Gln	S207
140914	BAA10g26050	A10	20785033	C	T	splice_region_variant&intron_variant	LOW	c.1497+8G>A\|	S136 S301 S304
140915	BAA10g26060	A10	20785659	G	A	upstream_gene_variant	MODIFIER	c.-2343G>A\|	S279
140916	BAA10g26050	A10	20786365	C	T	missense_variant	MODERATE	c.739G>A\|p.Asp247Asn	S305
140917	BAA10g26060	A10	20786550	C	T	upstream_gene_variant	MODIFIER	c.-1452C>T\|	S45
140918	BAA10g26060	A10	20788182	G	A	missense_variant	MODERATE	c.181G>A\|p.Gly61Arg	S42
140919	BAA10g26060	A10	20788976	C	T	synonymous_variant	LOW	c.975C>T\|p.Leu325Leu	S117
140920	BAA10g26060	A10	20789146	C	T	missense_variant	MODERATE	c.1145C>T\|p.Ser382Leu	S206 S26
140921	BAA10g26060	A10	20789220	C	T	stop_gained	HIGH	c.1219C>T\|p.Gln407*	S210 S225
140922	BAA10g26060	A10	20789260	C	T	missense_variant	MODERATE	c.1259C>T\|p.Ser420Phe	S144
140923	BAA10g26060	A10	20789556	G	A	missense_variant	MODERATE	c.1555G>A\|p.Val519Met	S100
140924	BAA10g26060	A10	20789689	G	A	missense_variant	MODERATE	c.1688G>A\|p.Ser563Asn	S100
140925	BAA10g26060	A10	20789871	C	T	synonymous_variant	LOW	c.1870C>T\|p.Leu624Leu	S129

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