Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64000 | A09 | 59586411 | C | T | intron_variant | MODIFIER | c.1860+36G>A| |
S9 |
2 | BAA09g64000 | A09 | 59586609 | G | A | intron_variant | MODIFIER | c.1769+28C>T| |
S221 |
3 | BAA09g64000 | A09 | 59588482 | C | T | missense_variant&splice_region_variant | MODERATE | c.874G>A|p.Val292Met |
S241 |
4 | BAA09g64000 | A09 | 59588540 | C | T | stop_gained | HIGH | c.816G>A|p.Trp272* |
S168 |
5 | BAA09g64000 | A09 | 59588873 | C | T | missense_variant | MODERATE | c.625G>A|p.Ala209Thr |
S303 |
6 | BAA09g64000 | A09 | 59590589 | G | A | missense_variant | MODERATE | c.65C>T|p.Thr22Ile |
S132 S137 S215 S89 |
7 | BAA09g64000 | A09 | 59590679 | C | T | upstream_gene_variant | MODIFIER | c.-26G>A| |
S150 |
8 | BAA09g64000 | A09 | 59590690 | C | T | upstream_gene_variant | MODIFIER | c.-37G>A| |
S90 |
9 | BAA09g64000 | A09 | 59590834 | C | T | upstream_gene_variant | MODIFIER | c.-181G>A| |
S174 |
10 | BAA09g64000 | A09 | 59590861 | T | G | upstream_gene_variant | MODIFIER | c.-208A>C| |
S155 S156 S16 S187 S192 S238 S26 S287 S293 S3 S34 S53 S90 |
11 | BAA09g64000 | A09 | 59590872 | G | A | upstream_gene_variant | MODIFIER | c.-219C>T| |
S161 |
12 | BAA09g64000 | A09 | 59590894 | C | T | upstream_gene_variant | MODIFIER | c.-241G>A| |
S293 |
13 | BAA09g64000 | A09 | 59591176 | C | T | upstream_gene_variant | MODIFIER | c.-523G>A| |
S18 |
14 | BAA09g64000 | A09 | 59591276 | C | T | upstream_gene_variant | MODIFIER | c.-623G>A| |
S117 |
15 | BAA09g64000 | A09 | 59591959 | G | A | upstream_gene_variant | MODIFIER | c.-1306C>T| |
S276 |
16 | BAA09g64000 | A09 | 59592232 | C | T | upstream_gene_variant | MODIFIER | c.-1579G>A| |
S249 |
17 | BAA09g64000 | A09 | 59595210 | G | A | upstream_gene_variant | MODIFIER | c.-4557C>T| |
S187 |