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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g10030 A04 16238796 G A upstream_gene_variant MODIFIER c.-2315G>A| S75
S81
2 BAA04g10030 A04 16238805 C T upstream_gene_variant MODIFIER c.-2306C>T| S172
S217
3 BAA04g10030 A04 16240773 C T upstream_gene_variant MODIFIER c.-338C>T| S167
4 BAA04g10030 A04 16241372 C T missense_variant MODERATE c.262C>T|p.Pro88Ser S118
5 BAA04g10030 A04 16241506 G A synonymous_variant LOW c.396G>A|p.Arg132Arg S169
6 BAA04g10030 A04 16241555 A G missense_variant MODERATE c.445A>G|p.Thr149Ala S169
7 BAA04g10030 A04 16241737 C T synonymous_variant LOW c.627C>T|p.His209His S184
8 BAA04g10030 A04 16242041 G A missense_variant MODERATE c.931G>A|p.Gly311Arg S158
9 BAA04g10030 A04 16242184 C T synonymous_variant LOW c.1074C>T|p.Ala358Ala S287
10 BAA04g10030 A04 16242395 G A missense_variant MODERATE c.1285G>A|p.Ala429Thr S278
11 BAA04g10030 A04 16242419 C T missense_variant MODERATE c.1309C>T|p.Pro437Ser S28
12 BAA04g10030 A04 16242450 G A missense_variant MODERATE c.1340G>A|p.Arg447Lys S156
13 BAA04g10030 A04 16242455 C T missense_variant MODERATE c.1345C>T|p.Pro449Ser S113
14 BAA04g10030 A04 16242610 G A synonymous_variant LOW c.1500G>A|p.Val500Val S171
15 BAA04g10030 A04 16242737 G A missense_variant MODERATE c.1526G>A|p.Arg509Gln S40
S49
16 BAA04g10030 A04 16243023 C T synonymous_variant LOW c.1812C>T|p.Leu604Leu S32
17 BAA04g10030 A04 16243087 C T synonymous_variant LOW c.1876C>T|p.Leu626Leu S255
18 BAA04g10030 A04 16243276 G A missense_variant MODERATE c.2065G>A|p.Gly689Arg S208
S219
19 BAA04g10030 A04 16243320 G A synonymous_variant LOW c.2109G>A|p.Leu703Leu S190
20 BAA04g10030 A04 16243948 G A missense_variant MODERATE c.2737G>A|p.Glu913Lys S130
21 BAA04g10030 A04 16244329 C T intron_variant MODIFIER c.2901+217C>T| S270
22 BAA04g10030 A04 16244501 C T intron_variant MODIFIER c.2901+389C>T| S136
23 BAA04g10030 A04 16246725 C T synonymous_variant LOW c.3036C>T|p.Leu1012Leu S173
24 BAA04g10030 A04 16247701 G A downstream_gene_variant MODIFIER c.*871G>A| S233
25 BAA04g10030 A04 16247906 C T downstream_gene_variant MODIFIER c.*1076C>T| S140