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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g06930 A08 5682674 C T upstream_gene_variant MODIFIER c.-744C>T| S70
2 BAA08g06930 A08 5683143 C T upstream_gene_variant MODIFIER c.-275C>T| S46
3 BAA08g06930 A08 5683188 G A upstream_gene_variant MODIFIER c.-230G>A| S67
4 BAA08g06930 A08 5683201 G A upstream_gene_variant MODIFIER c.-217G>A| S181
5 BAA08g06930 A08 5683631 G A missense_variant MODERATE c.214G>A|p.Ala72Thr S186
6 BAA08g06930 A08 5683720 C T synonymous_variant LOW c.246C>T|p.Phe82Phe S216
7 BAA08g06930 A08 5683783 G A synonymous_variant LOW c.309G>A|p.Thr103Thr S125
8 BAA08g06930 A08 5684071 G A splice_region_variant&synonymous_variant LOW c.597G>A|p.Glu199Glu S32
9 BAA08g06930 A08 5684517 G A synonymous_variant LOW c.771G>A|p.Arg257Arg S282
10 BAA08g06930 A08 5684531 G A missense_variant MODERATE c.785G>A|p.Gly262Glu S107
11 BAA08g06930 A08 5687217 G A downstream_gene_variant MODIFIER c.*2589G>A| S188
S243
S299
12 BAA08g06930 A08 5687218 G A downstream_gene_variant MODIFIER c.*2590G>A| S37
13 BAA08g06930 A08 5689500 C T downstream_gene_variant MODIFIER c.*4872C>T| S44
14 BAA08g06930 A08 5689546 C T downstream_gene_variant MODIFIER c.*4918C>T| S132
S137
S89