Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g24890 | A02 | 13595586 | G | A | downstream_gene_variant | MODIFIER | c.*426C>T| |
S184 |
2 | BAA02g24890 | A02 | 13595706 | G | A | downstream_gene_variant | MODIFIER | c.*306C>T| |
S11 |
3 | BAA02g24890 | A02 | 13596256 | G | A | missense_variant | MODERATE | c.979C>T|p.Leu327Phe |
S80 |
4 | BAA02g24890 | A02 | 13597399 | C | T | synonymous_variant | LOW | c.624G>A|p.Pro208Pro |
S1 S90 |
5 | BAA02g24890 | A02 | 13598374 | C | T | intron_variant | MODIFIER | c.466-520G>A| |
S293 |
6 | BAA02g24890 | A02 | 13598496 | C | T | intron_variant | MODIFIER | c.466-642G>A| |
S296 |
7 | BAA02g24890 | A02 | 13599532 | T | A | intron_variant | MODIFIER | c.465+363A>T| |
S138 |
8 | BAA02g24890 | A02 | 13599575 | C | T | intron_variant | MODIFIER | c.465+320G>A| |
S282 |
9 | BAA02g24890 | A02 | 13600298 | C | T | missense_variant | MODERATE | c.346G>A|p.Glu116Lys |
S32 |
10 | BAA02g24890 | A02 | 13601004 | G | A | intron_variant | MODIFIER | c.176-536C>T| |
S150 |
11 | BAA02g24890 | A02 | 13601241 | C | T | intron_variant | MODIFIER | c.176-773G>A| |
S88 |
12 | BAA02g24890 | A02 | 13601273 | G | A | intron_variant | MODIFIER | c.176-805C>T| |
S293 |
13 | BAA02g24890 | A02 | 13601524 | C | T | intron_variant | MODIFIER | c.176-1056G>A| |
S51 |
14 | BAA02g24890 | A02 | 13602183 | G | A | intron_variant | MODIFIER | c.175+700C>T| |
S44 |
15 | BAA02g24890 | A02 | 13602311 | C | T | intron_variant | MODIFIER | c.175+572G>A| |
S11 |
16 | BAA02g24890 | A02 | 13602333 | C | T | intron_variant | MODIFIER | c.175+550G>A| |
S127 |
17 | BAA02g24890 | A02 | 13604259 | G | A | upstream_gene_variant | MODIFIER | c.-639C>T| |
S208 |
18 | BAA02g24890 | A02 | 13605252 | G | A | upstream_gene_variant | MODIFIER | c.-1632C>T| |
S200 |
19 | BAA02g24890 | A02 | 13607266 | T | A | upstream_gene_variant | MODIFIER | c.-3646A>T| |
S221 |
20 | BAA02g24890 | A02 | 13608038 | C | T | upstream_gene_variant | MODIFIER | c.-4418G>A| |
S280 |
21 | BAA02g24890 | A02 | 13608056 | G | A | upstream_gene_variant | MODIFIER | c.-4436C>T| |
S276 |
22 | BAA02g24890 | A02 | 13608614 | C | T | upstream_gene_variant | MODIFIER | c.-4994G>A| |
S252 |