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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g38320 A02 32648995 C T upstream_gene_variant MODIFIER c.-3280C>T| S100
2 BAA02g38320 A02 32649353 C T upstream_gene_variant MODIFIER c.-2922C>T| S64
3 BAA02g38320 A02 32650579 C T upstream_gene_variant MODIFIER c.-1696C>T| S65
4 BAA02g38320 A02 32650611 C T upstream_gene_variant MODIFIER c.-1664C>T| S65
5 BAA02g38320 A02 32650713 T A upstream_gene_variant MODIFIER c.-1562T>A| S186
6 BAA02g38320 A02 32650953 G A upstream_gene_variant MODIFIER c.-1322G>A| S164
7 BAA02g38320 A02 32651812 C T upstream_gene_variant MODIFIER c.-463C>T| S43
8 BAA02g38320 A02 32652887 C T intron_variant MODIFIER c.321+39C>T| S174
9 BAA02g38320 A02 32653206 G A intron_variant MODIFIER c.405+22G>A| S13
10 BAA02g38320 A02 32653547 C T synonymous_variant LOW c.627C>T|p.Phe209Phe S181
11 BAA02g38320 A02 32653658 C T intron_variant MODIFIER c.667-17C>T| S18
12 BAA02g38320 A02 32653754 C T intron_variant MODIFIER c.711+35C>T| S189
S79
S91
13 BAA02g38320 A02 32654988 C T intron_variant MODIFIER c.907-636C>T| S270
14 BAA02g38320 A02 32655005 G A intron_variant MODIFIER c.907-619G>A| S177
15 BAA02g38320 A02 32655383 G A intron_variant MODIFIER c.907-241G>A| S95
16 BAA02g38320 A02 32655533 G A intron_variant MODIFIER c.907-91G>A| S174
S27
17 BAA02g38320 A02 32655930 G A intron_variant MODIFIER c.1077+57G>A| S265
18 BAA02g38320 A02 32656950 C T intron_variant MODIFIER c.1440+24C>T| S255
19 BAA02g38320 A02 32657100 C T synonymous_variant LOW c.1524C>T|p.Ile508Ile S131
20 BAA02g38320 A02 32657117 G A splice_region_variant&intron_variant LOW c.1536+5G>A| S223
21 BAA02g38320 A02 32657169 G A intron_variant MODIFIER c.1537-23G>A| S69
22 BAA02g38320 A02 32659295 C T downstream_gene_variant MODIFIER c.*1759C>T| S277
23 BAA02g38320 A02 32659540 G A downstream_gene_variant MODIFIER c.*2004G>A| S127
24 BAA02g38320 A02 32659926 C T downstream_gene_variant MODIFIER c.*2390C>T| S9
25 BAA02g38320 A02 32660258 G A downstream_gene_variant MODIFIER c.*2722G>A| S158