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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g30920 A01 20007944 G A upstream_gene_variant MODIFIER c.-4529G>A| S284
2 BAA01g30920 A01 20007997 G A upstream_gene_variant MODIFIER c.-4476G>A| S95
3 BAA01g30920 A01 20008113 C T upstream_gene_variant MODIFIER c.-4360C>T| S249
4 BAA01g30920 A01 20008591 G A upstream_gene_variant MODIFIER c.-3882G>A| S32
5 BAA01g30920 A01 20009760 G A upstream_gene_variant MODIFIER c.-2713G>A| S25
6 BAA01g30920 A01 20010970 C T upstream_gene_variant MODIFIER c.-1503C>T| S156
S213
7 BAA01g30920 A01 20010989 C T upstream_gene_variant MODIFIER c.-1484C>T| S192
8 BAA01g30920 A01 20011952 C T upstream_gene_variant MODIFIER c.-521C>T| S155
S211
9 BAA01g30920 A01 20012743 G A missense_variant MODERATE c.271G>A|p.Glu91Lys S37
10 BAA01g30920 A01 20012957 C T missense_variant MODERATE c.485C>T|p.Thr162Ile S10
11 BAA01g30920 A01 20013560 C T intron_variant MODIFIER c.906+182C>T| S168
12 BAA01g30920 A01 20014729 G A downstream_gene_variant MODIFIER c.*463G>A| S284
13 BAA01g30920 A01 20015119 G A downstream_gene_variant MODIFIER c.*853G>A| S236
14 BAA01g30920 A01 20015126 G A downstream_gene_variant MODIFIER c.*860G>A| S193
15 BAA01g30920 A01 20015140 C T downstream_gene_variant MODIFIER c.*874C>T| S277
16 BAA01g30920 A01 20015407 C T downstream_gene_variant MODIFIER c.*1141C>T| S56
17 BAA01g30920 A01 20015564 G A downstream_gene_variant MODIFIER c.*1298G>A| S13
S140
S168
S219
S279
S72
18 BAA01g30920 A01 20015947 G A downstream_gene_variant MODIFIER c.*1681G>A| S287
19 BAA01g30920 A01 20017197 C T downstream_gene_variant MODIFIER c.*2931C>T| S107
20 BAA01g30920 A01 20017757 C T downstream_gene_variant MODIFIER c.*3491C>T| S219
S72
21 BAA01g30920 A01 20018135 C T downstream_gene_variant MODIFIER c.*3869C>T| S87
22 BAA01g30920 A01 20018607 C T downstream_gene_variant MODIFIER c.*4341C>T| S56
23 BAA01g30920 A01 20018810 C T downstream_gene_variant MODIFIER c.*4544C>T| S242