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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g20820 A05 12987579 C T downstream_gene_variant MODIFIER c.*4502G>A| S240
2 BAA05g20820 A05 12987633 C T downstream_gene_variant MODIFIER c.*4448G>A| S280
3 BAA05g20820 A05 12988053 C T downstream_gene_variant MODIFIER c.*4028G>A| S270
4 BAA05g20820 A05 12988532 G A downstream_gene_variant MODIFIER c.*3549C>T| S244
5 BAA05g20820 A05 12990445 C T downstream_gene_variant MODIFIER c.*1636G>A| S67
6 BAA05g20820 A05 12990479 G A downstream_gene_variant MODIFIER c.*1602C>T| S197
7 BAA05g20820 A05 12990965 C T downstream_gene_variant MODIFIER c.*1116G>A| S280
8 BAA05g20820 A05 12992185 G A missense_variant MODERATE c.2377C>T|p.Pro793Ser S150
9 BAA05g20820 A05 12992621 G A intron_variant MODIFIER c.2146+13C>T| S246
10 BAA05g20820 A05 12993266 C T intron_variant MODIFIER c.1845-331G>A| S142
11 BAA05g20820 A05 12993335 C T intron_variant MODIFIER c.1845-400G>A| S25
12 BAA05g20820 A05 12993460 G A intron_variant MODIFIER c.1845-525C>T| S210
13 BAA05g20820 A05 12993863 G A intron_variant MODIFIER c.1845-928C>T| S224
14 BAA05g20820 A05 12993950 C T intron_variant MODIFIER c.1845-1015G>A| S198
15 BAA05g20820 A05 12994082 G A intron_variant MODIFIER c.1845-1147C>T| S293
16 BAA05g20820 A05 12995222 C T intron_variant MODIFIER c.1844+1664G>A| S89
17 BAA05g20820 A05 12995890 C T intron_variant MODIFIER c.1844+996G>A| S267
18 BAA05g20820 A05 12996032 C T intron_variant MODIFIER c.1844+854G>A| S17
19 BAA05g20820 A05 12996040 C T intron_variant MODIFIER c.1844+846G>A| S171
20 BAA05g20820 A05 12996514 C T intron_variant MODIFIER c.1844+372G>A| S280
21 BAA05g20820 A05 12998039 G A intron_variant MODIFIER c.1288-597C>T| S168
22 BAA05g20820 A05 12998864 C T intron_variant MODIFIER c.1287+756G>A| S53
23 BAA05g20820 A05 12998916 G A intron_variant MODIFIER c.1287+704C>T| S37
S73
24 BAA05g20820 A05 13003030 G A synonymous_variant LOW c.247C>T|p.Leu83Leu S186
25 BAA05g20820 A05 13003178 C T synonymous_variant LOW c.183G>A|p.Glu61Glu S202