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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g17000 A02 8435825 G A upstream_gene_variant MODIFIER c.-2485G>A| S67
2 BAA02g17000 A02 8435926 G A upstream_gene_variant MODIFIER c.-2384G>A| S162
3 BAA02g17000 A02 8436243 C T upstream_gene_variant MODIFIER c.-2067C>T| S250
4 BAA02g17000 A02 8437404 G A upstream_gene_variant MODIFIER c.-906G>A| S98
5 BAA02g17000 A02 8438316 G A missense_variant MODERATE c.7G>A|p.Asp3Asn S286
6 BAA02g17000 A02 8438482 G A missense_variant MODERATE c.173G>A|p.Gly58Glu S246
7 BAA02g17000 A02 8438569 G A missense_variant MODERATE c.260G>A|p.Gly87Glu S176
8 BAA02g17000 A02 8438687 G A missense_variant MODERATE c.286G>A|p.Glu96Lys S168
9 BAA02g17000 A02 8438793 G A intron_variant MODIFIER c.372+20G>A| S199
10 BAA02g17000 A02 8439133 C T missense_variant MODERATE c.443C>T|p.Ala148Val S182
11 BAA02g17000 A02 8439780 G A intron_variant MODIFIER c.875+61G>A| S23
12 BAA02g17000 A02 8440943 G A synonymous_variant LOW c.1458G>A|p.Leu486Leu S259
13 BAA02g17000 A02 8441455 C T missense_variant MODERATE c.1885C>T|p.Pro629Ser S100
14 BAA02g17000 A02 8441456 C T missense_variant MODERATE c.1886C>T|p.Pro629Leu S42
15 BAA02g17000 A02 8441617 C T missense_variant MODERATE c.2047C>T|p.Pro683Ser S64
16 BAA02g17000 A02 8442458 G A downstream_gene_variant MODIFIER c.*324G>A| S239
17 BAA02g17000 A02 8442995 G A downstream_gene_variant MODIFIER c.*861G>A| S190
18 BAA02g17000 A02 8443410 G A downstream_gene_variant MODIFIER c.*1276G>A| S305
19 BAA02g17000 A02 8444106 G A downstream_gene_variant MODIFIER c.*1972G>A| S188
20 BAA02g17000 A02 8444123 G A downstream_gene_variant MODIFIER c.*1989G>A| S150
21 BAA02g17000 A02 8446170 G A downstream_gene_variant MODIFIER c.*4036G>A| S23
22 BAA02g17000 A02 8446255 C T downstream_gene_variant MODIFIER c.*4121C>T| S202
23 BAA02g17000 A02 8446515 G A downstream_gene_variant MODIFIER c.*4381G>A| S296
24 BAA02g17000 A02 8446840 C T downstream_gene_variant MODIFIER c.*4706C>T| S82