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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g23810 A02 12982110 C T downstream_gene_variant MODIFIER c.*3455G>A| S252
2 BAA02g23810 A02 12982471 C T downstream_gene_variant MODIFIER c.*3094G>A| S224
3 BAA02g23810 A02 12985915 G A synonymous_variant LOW c.3309C>T|p.Ile1103Ile S251
4 BAA02g23810 A02 12985919 G A missense_variant MODERATE c.3305C>T|p.Pro1102Leu S153
S213
5 BAA02g23810 A02 12987208 C T missense_variant MODERATE c.2479G>A|p.Glu827Lys S286
6 BAA02g23810 A02 12987649 C T missense_variant MODERATE c.2038G>A|p.Glu680Lys S267
7 BAA02g23810 A02 12987854 G A synonymous_variant LOW c.1833C>T|p.Tyr611Tyr S98
8 BAA02g23810 A02 12987961 C T intron_variant MODIFIER c.1821+91G>A| S1
9 BAA02g23810 A02 12988156 C T missense_variant MODERATE c.1717G>A|p.Ala573Thr S158
10 BAA02g23810 A02 12989719 G A intron_variant MODIFIER c.970-311C>T| S62
11 BAA02g23810 A02 12989844 C T intron_variant MODIFIER c.970-436G>A| S174
12 BAA02g23810 A02 12989958 A C intron_variant MODIFIER c.970-550T>G| S138
13 BAA02g23810 A02 12991044 G A missense_variant MODERATE c.773C>T|p.Thr258Ile S61
14 BAA02g23810 A02 12991829 C T missense_variant MODERATE c.263G>A|p.Gly88Glu S250
15 BAA02g23810 A02 12993200 C T upstream_gene_variant MODIFIER c.-726G>A| S270
16 BAA02g23810 A02 12993312 G A upstream_gene_variant MODIFIER c.-838C>T| S156
17 BAA02g23810 A02 12993828 G A upstream_gene_variant MODIFIER c.-1354C>T| S297
18 BAA02g23810 A02 12993913 G A upstream_gene_variant MODIFIER c.-1439C>T| S223
19 BAA02g23810 A02 12995917 G A upstream_gene_variant MODIFIER c.-3443C>T| S67
S73