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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g19660	A02	10220253	G	A	synonymous_variant	LOW	c.1266C>T\|p.Asp422Asp	S187
2	BAA02g19660	A02	10220529	C	T	missense_variant	MODERATE	c.1068G>A\|p.Met356Ile	S165
3	BAA02g19660	A02	10220555	C	T	missense_variant	MODERATE	c.1042G>A\|p.Glu348Lys	S46
4	BAA02g19660	A02	10222328	C	T	synonymous_variant	LOW	c.93G>A\|p.Glu31Glu	S284
5	BAA02g19660	A02	10222478	G	A	upstream_gene_variant	MODIFIER	c.-58C>T\|	S303
6	BAA02g19660	A02	10222698	G	A	upstream_gene_variant	MODIFIER	c.-278C>T\|	S136
7	BAA02g19660	A02	10223055	G	A	upstream_gene_variant	MODIFIER	c.-635C>T\|	S148 S210 S30 S31
8	BAA02g19660	A02	10223731	C	T	upstream_gene_variant	MODIFIER	c.-1311G>A\|	S289 S290
9	BAA02g19660	A02	10224013	G	A	upstream_gene_variant	MODIFIER	c.-1593C>T\|	S174 S27
10	BAA02g19660	A02	10224083	G	A	upstream_gene_variant	MODIFIER	c.-1663C>T\|	S202
11	BAA02g19660	A02	10224869	C	T	upstream_gene_variant	MODIFIER	c.-2449G>A\|	S241
12	BAA02g19660	A02	10225171	G	A	upstream_gene_variant	MODIFIER	c.-2751C>T\|	S247
13	BAA02g19660	A02	10225254	C	T	upstream_gene_variant	MODIFIER	c.-2834G>A\|	S262
14	BAA02g19660	A02	10225283	G	C	upstream_gene_variant	MODIFIER	c.-2863C>G\|	S1 S105 S108 S119 S128 S149 S158 S183 S193 S20 S217 S218 S226 S27 S283 S290 S45 S53 S56
15	BAA02g19660	A02	10225600	A	G	upstream_gene_variant	MODIFIER	c.-3180T>C\|
16	BAA02g19660	A02	10225629	C	T	upstream_gene_variant	MODIFIER	c.-3209G>A\|	S158
17	BAA02g19660	A02	10226197	G	A	upstream_gene_variant	MODIFIER	c.-3777C>T\|	S306 S308
18	BAA02g19660	A02	10226395	G	A	upstream_gene_variant	MODIFIER	c.-3975C>T\|	S256
19	BAA02g19660	A02	10226601	C	T	upstream_gene_variant	MODIFIER	c.-4181G>A\|	S127
20	BAA02g19660	A02	10226804	C	T	upstream_gene_variant	MODIFIER	c.-4384G>A\|	S104 S52
21	BAA02g19660	A02	10227070	G	A	upstream_gene_variant	MODIFIER	c.-4650C>T\|	S288

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