Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25790 | A02 | 14273391 | C | T | upstream_gene_variant | MODIFIER | c.-4884C>T| |
S75 S81 |
2 | BAA02g25790 | A02 | 14273451 | C | T | upstream_gene_variant | MODIFIER | c.-4824C>T| |
S219 |
3 | BAA02g25790 | A02 | 14273461 | C | T | upstream_gene_variant | MODIFIER | c.-4814C>T| |
S95 |
4 | BAA02g25790 | A02 | 14273487 | G | A | upstream_gene_variant | MODIFIER | c.-4788G>A| |
S119 |
5 | BAA02g25790 | A02 | 14273727 | C | T | upstream_gene_variant | MODIFIER | c.-4548C>T| |
S185 |
6 | BAA02g25790 | A02 | 14273902 | C | T | upstream_gene_variant | MODIFIER | c.-4373C>T| |
S252 |
7 | BAA02g25790 | A02 | 14274019 | C | A | upstream_gene_variant | MODIFIER | c.-4256C>A| |
S234 S256 S265 S271 S299 S50 |
8 | BAA02g25790 | A02 | 14274148 | G | A | upstream_gene_variant | MODIFIER | c.-4127G>A| |
S60 |
9 | BAA02g25790 | A02 | 14274644 | G | C | upstream_gene_variant | MODIFIER | c.-3631G>C| |
S17 |
10 | BAA02g25790 | A02 | 14275308 | G | A | upstream_gene_variant | MODIFIER | c.-2967G>A| |
S302 |
11 | BAA02g25790 | A02 | 14275759 | C | T | upstream_gene_variant | MODIFIER | c.-2516C>T| |
S265 S39 |
12 | BAA02g25790 | A02 | 14275781 | C | T | upstream_gene_variant | MODIFIER | c.-2494C>T| |
S1 S90 |
13 | BAA02g25790 | A02 | 14275838 | G | A | upstream_gene_variant | MODIFIER | c.-2437G>A| |
S202 |
14 | BAA02g25790 | A02 | 14275873 | G | A | upstream_gene_variant | MODIFIER | c.-2402G>A| |
S158 |
15 | BAA02g25790 | A02 | 14275981 | C | T | upstream_gene_variant | MODIFIER | c.-2294C>T| |
S33 |
16 | BAA02g25790 | A02 | 14276228 | G | A | upstream_gene_variant | MODIFIER | c.-2047G>A| |
S44 |
17 | BAA02g25790 | A02 | 14276765 | G | A | upstream_gene_variant | MODIFIER | c.-1510G>A| |
S174 S216 S27 |
18 | BAA02g25790 | A02 | 14277222 | C | T | upstream_gene_variant | MODIFIER | c.-1053C>T| |
S240 |
19 | BAA02g25790 | A02 | 14278288 | G | A | missense_variant | MODERATE | c.14G>A|p.Ser5Asn |
S272 |
20 | BAA02g25790 | A02 | 14278835 | G | A | intron_variant | MODIFIER | c.497+64G>A| |
S189 |
21 | BAA02g25790 | A02 | 14279759 | G | A | missense_variant&splice_region_variant | MODERATE | c.1156G>A|p.Glu386Lys |
S202 |
22 | BAA02g25790 | A02 | 14279833 | G | A | intron_variant | MODIFIER | c.1159-16G>A| |
S143 |
23 | BAA02g25790 | A02 | 14279835 | G | A | intron_variant | MODIFIER | c.1159-14G>A| |
S47 |
24 | BAA02g25790 | A02 | 14279881 | G | A | synonymous_variant | LOW | c.1191G>A|p.Lys397Lys |
S113 |
25 | BAA02g25790 | A02 | 14280304 | C | T | synonymous_variant | LOW | c.1494C>T|p.His498His |
S171 |