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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g08520 A02 3669182 G A upstream_gene_variant MODIFIER c.-1247G>A| S199
2 BAA02g08520 A02 3669355 G A upstream_gene_variant MODIFIER c.-1074G>A| S57
3 BAA02g08520 A02 3669432 G A upstream_gene_variant MODIFIER c.-997G>A| S61
4 BAA02g08520 A02 3670722 C T intron_variant MODIFIER c.195+99C>T| S278
5 BAA02g08520 A02 3670923 G A intron_variant MODIFIER c.196-148G>A| S156
6 BAA02g08520 A02 3671174 G A missense_variant MODERATE c.299G>A|p.Gly100Asp S9
7 BAA02g08520 A02 3671477 C T intron_variant MODIFIER c.465-85C>T| S33
8 BAA02g08520 A02 3671508 A T intron_variant MODIFIER c.465-54A>T| S57
9 BAA02g08520 A02 3671642 C T missense_variant&splice_region_variant MODERATE c.545C>T|p.Pro182Leu S123
10 BAA02g08520 A02 3671733 G A intron_variant MODIFIER c.546+90G>A| S165
11 BAA02g08520 A02 3671943 C T intron_variant MODIFIER c.546+300C>T| S78
S83
12 BAA02g08520 A02 3672303 C T intron_variant MODIFIER c.546+660C>T| S270
13 BAA02g08520 A02 3673235 G A intron_variant MODIFIER c.546+1592G>A| S208
14 BAA02g08520 A02 3673286 C T intron_variant MODIFIER c.546+1643C>T| S87
15 BAA02g08520 A02 3673726 C T intron_variant MODIFIER c.546+2083C>T| S200
16 BAA02g08520 A02 3674078 G A intron_variant MODIFIER c.546+2435G>A| S57
17 BAA02g08520 A02 3674569 G A intron_variant MODIFIER c.546+2926G>A| S5
18 BAA02g08520 A02 3675464 C T intron_variant MODIFIER c.547-3222C>T| S25
S264
19 BAA02g08520 A02 3675523 C T intron_variant MODIFIER c.547-3163C>T| S182
20 BAA02g08520 A02 3678760 G A missense_variant MODERATE c.621G>A|p.Met207Ile S107
21 BAA02g08520 A02 3679338 G A downstream_gene_variant MODIFIER c.*500G>A| S265
22 BAA02g08520 A02 3680126 G A downstream_gene_variant MODIFIER c.*1288G>A| S207
S302