Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
140351	BAA10g25520	A10	20590330	G	A	missense_variant	MODERATE	c.2282G>A\|p.Gly761Asp	S63
140352	BAA10g25530	A10	20591940	C	T	missense_variant	MODERATE	c.715G>A\|p.Glu239Lys	S84
140353	BAA10g25530	A10	20592013	G	A	synonymous_variant	LOW	c.642C>T\|p.Leu214Leu	S18
140354	BAA10g25530	A10	20592950	C	T	upstream_gene_variant	MODIFIER	c.-221G>A\|	S68
140355	BAA10g25530	A10	20594703	C	T	upstream_gene_variant	MODIFIER	c.-1974G>A\|	S72 S78
140356	BAA10g25530	A10	20595172	T	A	upstream_gene_variant	MODIFIER	c.-2443A>T\|	S157 S166 S257 S70
140357	BAA10g25530	A10	20595293	C	T	upstream_gene_variant	MODIFIER	c.-2564G>A\|	S37
140358	BAA10g25530	A10	20596094	C	T	upstream_gene_variant	MODIFIER	c.-3365G>A\|	S301 S304
140359	BAA10g25540	A10	20598462	G	A	missense_variant	MODERATE	c.62G>A\|p.Gly21Glu	S182
140360	BAA10g25540	A10	20598483	G	A	missense_variant	MODERATE	c.83G>A\|p.Gly28Glu	S71
140361	BAA10g25550	A10	20599583	G	A	upstream_gene_variant	MODIFIER	c.-1097G>A\|	S205
140362	BAA10g25550	A10	20600798	C	T	missense_variant	MODERATE	c.119C>T\|p.Pro40Leu	S211 S227
140363	BAA10g25550	A10	20600822	C	T	missense_variant	MODERATE	c.143C>T\|p.Ser48Phe	S209
140364	BAA10g25550	A10	20601163	G	A	missense_variant	MODERATE	c.484G>A\|p.Asp162Asn	S105
140365	BAA10g25560	A10	20602087	C	T	upstream_gene_variant	MODIFIER	c.-1608C>T\|	S162
140366	BAA10g25560	A10	20602923	C	T	upstream_gene_variant	MODIFIER	c.-772C>T\|	S162
140367	BAA10g25560	A10	20602985	C	T	upstream_gene_variant	MODIFIER	c.-710C>T\|	S5
140368	BAA10g25560	A10	20603425	C	T	upstream_gene_variant	MODIFIER	c.-270C>T\|	S187 S188 S299
140369	BAA10g25560	A10	20603437	G	A	upstream_gene_variant	MODIFIER	c.-258G>A\|	S177
140370	BAA10g25560	A10	20604139	G	A	missense_variant	MODERATE	c.445G>A\|p.Asp149Asn	S184
140371	BAA10g25570	A10	20605434	C	T	upstream_gene_variant	MODIFIER	c.-331C>T\|	S185
140372	BAA10g25550	A10	20605990	G	A	downstream_gene_variant	MODIFIER	c.*4387G>A\|	S15 S3
140373	BAA10g25550	A10	20606166	C	T	downstream_gene_variant	MODIFIER	c.*4563C>T\|	S78
140374	BAA10g25570	A10	20606812	G	A	missense_variant	MODERATE	c.662G>A\|p.Arg221Lys	S127
140375	BAA10g25570	A10	20606858	C	T	synonymous_variant	LOW	c.708C>T\|p.Phe236Phe	S295

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