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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g18900 A08 15003823 C T downstream_gene_variant MODIFIER c.*173G>A| S130
2 BAA08g18900 A08 15004173 C T synonymous_variant LOW c.1497G>A|p.Lys499Lys S82
S92
3 BAA08g18900 A08 15004477 C T synonymous_variant LOW c.1275G>A|p.Arg425Arg S259
4 BAA08g18900 A08 15005328 C T intron_variant MODIFIER c.916-396G>A| S212
5 BAA08g18900 A08 15005379 C T intron_variant MODIFIER c.916-447G>A| S30
6 BAA08g18900 A08 15005550 C T intron_variant MODIFIER c.916-618G>A| S149
7 BAA08g18900 A08 15005759 G A intron_variant MODIFIER c.916-827C>T| S124
8 BAA08g18900 A08 15005772 C T intron_variant MODIFIER c.916-840G>A| S76
9 BAA08g18900 A08 15006121 G A intron_variant MODIFIER c.916-1189C>T| S87
10 BAA08g18900 A08 15008923 C T synonymous_variant LOW c.414G>A|p.Thr138Thr S278
11 BAA08g18900 A08 15009034 G A synonymous_variant LOW c.303C>T|p.Val101Val S267
12 BAA08g18900 A08 15009223 G A synonymous_variant LOW c.189C>T|p.Leu63Leu S97
13 BAA08g18900 A08 15009243 G A synonymous_variant LOW c.169C>T|p.Leu57Leu S125
14 BAA08g18900 A08 15009340 G A synonymous_variant LOW c.72C>T|p.Leu24Leu S146
15 BAA08g18900 A08 15010834 C T upstream_gene_variant MODIFIER c.-917G>A| S132
S137
16 BAA08g18900 A08 15011509 G A upstream_gene_variant MODIFIER c.-1592C>T| S124
17 BAA08g18900 A08 15013403 C T upstream_gene_variant MODIFIER c.-3486G>A| S168