Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
129201	BAA10g17110-BAA10g17120	A10	16631286	G	A	intergenic_region	MODIFIER	n.16631286G>A\|	S238
129202	BAA10g17110-BAA10g17120	A10	16631708	G	A	intergenic_region	MODIFIER	n.16631708G>A\|	S280
129203	BAA10g17120	A10	16633680	G	A	upstream_gene_variant	MODIFIER	c.-3033G>A\|	S157 S163
129204	BAA10g17120	A10	16633882	G	A	upstream_gene_variant	MODIFIER	c.-2831G>A\|	S57
129205	BAA10g17120	A10	16634676	G	A	upstream_gene_variant	MODIFIER	c.-2037G>A\|	S293
129206	BAA10g17120	A10	16635519	C	T	upstream_gene_variant	MODIFIER	c.-1194C>T\|	S242
129207	BAA10g17120	A10	16636481	C	T	upstream_gene_variant	MODIFIER	c.-232C>T\|	S161
129208	BAA10g17120	A10	16636609	G	A	upstream_gene_variant	MODIFIER	c.-104G>A\|	S53
129209	BAA10g17120	A10	16636693	G	A	upstream_gene_variant	MODIFIER	c.-20G>A\|	S219 S72
129210	BAA10g17120	A10	16636941	G	A	missense_variant	MODERATE	c.229G>A\|p.Glu77Lys	S81
129211	BAA10g17120	A10	16637140	C	T	missense_variant	MODERATE	c.428C>T\|p.Pro143Leu	S95
129212	BAA10g17130	A10	16643804	G	A	downstream_gene_variant	MODIFIER	c.*741C>T\|	S132 S137 S215
129213	BAA10g17130	A10	16644382	C	T	downstream_gene_variant	MODIFIER	c.*163G>A\|	S116
129214	BAA10g17130	A10	16644678	G	A	missense_variant	MODERATE	c.344C>T\|p.Pro115Leu	S10
129215	BAA10g17130	A10	16645205	G	A	upstream_gene_variant	MODIFIER	c.-184C>T\|	S128
129216	BAA10g17130	A10	16646209	C	T	upstream_gene_variant	MODIFIER	c.-1188G>A\|	S282
129217	BAA10g17130	A10	16647367	C	T	upstream_gene_variant	MODIFIER	c.-2346G>A\|	S115
129218	BAA10g17130	A10	16647870	C	T	upstream_gene_variant	MODIFIER	c.-2849G>A\|	S197
129219	BAA10g17130	A10	16648352	G	A	upstream_gene_variant	MODIFIER	c.-3331C>T\|	S71
129220	BAA10g17130	A10	16649984	C	T	upstream_gene_variant	MODIFIER	c.-4963G>A\|	S174 S27 S39
129221	BAA10g17140	A10	16650983	G	A	upstream_gene_variant	MODIFIER	c.-1193G>A\|	S203
129222	BAA10g17140	A10	16652468	G	A	missense_variant	MODERATE	c.220G>A\|p.Glu74Lys	S1 S90
129223	BAA10g17140	A10	16652506	G	A	synonymous_variant	LOW	c.258G>A\|p.Lys86Lys	S223
129224	BAA10g17140	A10	16653313	G	A	missense_variant	MODERATE	c.646G>A\|p.Glu216Lys	S14
129225	BAA10g17140	A10	16653675	G	A	synonymous_variant	LOW	c.1008G>A\|p.Glu336Glu	S151 S263

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