Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
94951	BAA10g03790	A10	1840363	G	A	synonymous_variant	LOW	c.381C>T\|p.Ser127Ser	S245
94952	BAA10g03790	A10	1840552	G	A	synonymous_variant	LOW	c.192C>T\|p.Ile64Ile	S107
94953	BAA10g03790	A10	1840600	C	T	synonymous_variant	LOW	c.144G>A\|p.Glu48Glu	S9
94954	BAA10g03790	A10	1841284	C	T	upstream_gene_variant	MODIFIER	c.-541G>A\|	S233
94955	BAA10g03800	A10	1842228	C	T	missense_variant	MODERATE	c.1403G>A\|p.Gly468Glu	S166
94956	BAA10g03790	A10	1844107	C	T	upstream_gene_variant	MODIFIER	c.-3364G>A\|	S19
94957	BAA10g03790	A10	1844500	C	T	upstream_gene_variant	MODIFIER	c.-3757G>A\|	S121
94958	BAA10g03790	A10	1844620	C	T	upstream_gene_variant	MODIFIER	c.-3877G>A\|	S270
94959	BAA10g03790	A10	1845003	G	A	upstream_gene_variant	MODIFIER	c.-4260C>T\|	S17
94960	BAA10g03790	A10	1845191	G	A	upstream_gene_variant	MODIFIER	c.-4448C>T\|	S242
94961	BAA10g03800	A10	1846836	C	T	upstream_gene_variant	MODIFIER	c.-3206G>A\|	S185
94962	BAA10g03800	A10	1848472	C	T	upstream_gene_variant	MODIFIER	c.-4842G>A\|	S27
94963	BAA10g03800	A10	1848532	C	T	upstream_gene_variant	MODIFIER	c.-4902G>A\|	S197
94964	BAA10g03800-BAA10g03810	A10	1849121	C	T	intergenic_region	MODIFIER	n.1849121C>T\|	S200
94965	BAA10g03800-BAA10g03810	A10	1857521	C	T	intergenic_region	MODIFIER	n.1857521C>T\|	S270
94966	BAA10g03810	A10	1861300	G	A	downstream_gene_variant	MODIFIER	c.*2032C>T\|	S263
94967	BAA10g03810	A10	1862149	G	A	downstream_gene_variant	MODIFIER	c.*1183C>T\|	S157 S163
94968	BAA10g03810	A10	1862205	G	A	downstream_gene_variant	MODIFIER	c.*1127C>T\|	S151
94969	BAA10g03810	A10	1862438	G	A	downstream_gene_variant	MODIFIER	c.*894C>T\|	S273
94970	BAA10g03810	A10	1863159	C	T	downstream_gene_variant	MODIFIER	c.*173G>A\|	S159 S243
94971	BAA10g03810	A10	1863454	G	A	missense_variant	MODERATE	c.2266C>T\|p.His756Tyr	S205
94972	BAA10g03810	A10	1863912	G	A	missense_variant	MODERATE	c.1808C>T\|p.Ser603Leu	S279
94973	BAA10g03810	A10	1864199	C	T	synonymous_variant	LOW	c.1521G>A\|p.Leu507Leu	S117
94974	BAA10g03810	A10	1864550	C	T	synonymous_variant	LOW	c.1170G>A\|p.Glu390Glu	S208 S93
94975	BAA10g03810	A10	1865151	A	C	missense_variant	MODERATE	c.569T>G\|p.Val190Gly	S100 S113 S140 S162 S221 S244 S264 S274 S71 S82

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