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


Gene ID

Results: 1 - 38 of 38 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g44920 A02 36885773 C T downstream_gene_variant MODIFIER c.*4031G>A| S176
2 BAA02g44920 A02 36886236 G A downstream_gene_variant MODIFIER c.*3568C>T| S28
3 BAA02g44920 A02 36886867 C T downstream_gene_variant MODIFIER c.*2937G>A| S111
4 BAA02g44920 A02 36887133 G A downstream_gene_variant MODIFIER c.*2671C>T| S41
5 BAA02g44920 A02 36887345 G A downstream_gene_variant MODIFIER c.*2459C>T| S226
6 BAA02g44920 A02 36887446 C T downstream_gene_variant MODIFIER c.*2358G>A| S180
7 BAA02g44920 A02 36887669 G A downstream_gene_variant MODIFIER c.*2135C>T| S20
8 BAA02g44920 A02 36887967 C T downstream_gene_variant MODIFIER c.*1837G>A| S263
9 BAA02g44920 A02 36888105 C T downstream_gene_variant MODIFIER c.*1699G>A| S216
10 BAA02g44920 A02 36888569 C T downstream_gene_variant MODIFIER c.*1235G>A| S103
11 BAA02g44920 A02 36888585 C T downstream_gene_variant MODIFIER c.*1219G>A| S296
12 BAA02g44920 A02 36889161 G A downstream_gene_variant MODIFIER c.*643C>T| S282
13 BAA02g44920 A02 36889327 G A downstream_gene_variant MODIFIER c.*477C>T| S69
14 BAA02g44920 A02 36889943 C T missense_variant MODERATE c.4211G>A|p.Gly1404Glu S237
15 BAA02g44920 A02 36889944 C T missense_variant MODERATE c.4210G>A|p.Gly1404Arg S42
16 BAA02g44920 A02 36891247 G A missense_variant MODERATE c.2990C>T|p.Pro997Leu S226
17 BAA02g44920 A02 36891300 G A synonymous_variant LOW c.2937C>T|p.Pro979Pro S132
S137
S138
S215
S237
S238
S288
S89
18 BAA02g44920 A02 36891508 G A missense_variant MODERATE c.2729C>T|p.Ala910Val S294
19 BAA02g44920 A02 36891553 C T missense_variant MODERATE c.2684G>A|p.Arg895His S52
20 BAA02g44920 A02 36892011 C T intron_variant MODIFIER c.2294+16G>A| S221
21 BAA02g44920 A02 36892271 G A synonymous_variant LOW c.2050C>T|p.Leu684Leu S276
22 BAA02g44920 A02 36892305 G A synonymous_variant LOW c.2016C>T|p.Thr672Thr S209
23 BAA02g44920 A02 36892381 G A missense_variant MODERATE c.1940C>T|p.Ser647Leu S19
24 BAA02g44920 A02 36893112 C T intron_variant MODIFIER c.1458-249G>A| S202
25 BAA02g44920 A02 36893570 G A intron_variant MODIFIER c.1457+117C>T| S143