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 BAA09g17600 A09 10546150 C T downstream_gene_variant MODIFIER c.*2863G>A| S174
2 BAA09g17600 A09 10546657 G A downstream_gene_variant MODIFIER c.*2356C>T| S159
S243
3 BAA09g17600 A09 10546776 G A downstream_gene_variant MODIFIER c.*2237C>T| S286
4 BAA09g17600 A09 10546782 G A downstream_gene_variant MODIFIER c.*2231C>T| S178
5 BAA09g17600 A09 10547679 G A downstream_gene_variant MODIFIER c.*1334C>T| S23
6 BAA09g17600 A09 10549230 C T intron_variant MODIFIER c.976-41G>A| S239
7 BAA09g17600 A09 10549619 G A intron_variant MODIFIER c.975+271C>T| S201
8 BAA09g17600 A09 10549623 G A intron_variant MODIFIER c.975+267C>T| S238
9 BAA09g17600 A09 10550150 C T splice_region_variant&intron_variant LOW c.721-6G>A| S132
S137
S215
S288
10 BAA09g17600 A09 10550486 C T missense_variant MODERATE c.538G>A|p.Glu180Lys S246
11 BAA09g17600 A09 10550634 C T intron_variant MODIFIER c.447+18G>A| S95
12 BAA09g17600 A09 10552637 C T intron_variant MODIFIER c.71-1609G>A| S168
13 BAA09g17600 A09 10552737 G A intron_variant MODIFIER c.71-1709C>T| S184
14 BAA09g17600 A09 10552755 C T intron_variant MODIFIER c.71-1727G>A| S283
15 BAA09g17600 A09 10552912 G A intron_variant MODIFIER c.71-1884C>T| S176
16 BAA09g17600 A09 10553195 C T intron_variant MODIFIER c.71-2167G>A| S71
17 BAA09g17600 A09 10553405 G A intron_variant MODIFIER c.71-2377C>T| S192
18 BAA09g17600 A09 10559162 C T upstream_gene_variant MODIFIER c.-37G>A| S150
19 BAA09g17600 A09 10559367 C T upstream_gene_variant MODIFIER c.-242G>A| S118
20 BAA09g17600 A09 10560142 C T upstream_gene_variant MODIFIER c.-1017G>A| S111
21 BAA09g17600 A09 10560225 C T upstream_gene_variant MODIFIER c.-1100G>A| S123
22 BAA09g17600 A09 10561135 C T upstream_gene_variant MODIFIER c.-2010G>A| S251
23 BAA09g17600 A09 10563400 C T upstream_gene_variant MODIFIER c.-4275G>A| S43