Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17620 | A02 | 8781607 | C | T | missense_variant | MODERATE | c.1162G>A|p.Gly388Arg |
S244 |
2 | BAA02g17620 | A02 | 8781819 | G | A | missense_variant | MODERATE | c.1022C>T|p.Ser341Phe |
S274 |
3 | BAA02g17620 | A02 | 8787380 | G | A | missense_variant&splice_region_variant | MODERATE | c.443C>T|p.Ala148Val |
S140 |
4 | BAA02g17620 | A02 | 8787668 | G | A | missense_variant | MODERATE | c.356C>T|p.Thr119Ile |
S236 |
5 | BAA02g17620 | A02 | 8788232 | T | C | upstream_gene_variant | MODIFIER | c.-209A>G| |
S276 |
6 | BAA02g17620 | A02 | 8788282 | G | A | upstream_gene_variant | MODIFIER | c.-259C>T| |
S182 |
7 | BAA02g17620 | A02 | 8788397 | C | T | upstream_gene_variant | MODIFIER | c.-374G>A| |
S88 |
8 | BAA02g17620 | A02 | 8788698 | C | T | upstream_gene_variant | MODIFIER | c.-675G>A| |
S139 |
9 | BAA02g17620 | A02 | 8788703 | C | T | upstream_gene_variant | MODIFIER | c.-680G>A| |
S13 |
10 | BAA02g17620 | A02 | 8789106 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S179 |
11 | BAA02g17620 | A02 | 8791399 | G | A | upstream_gene_variant | MODIFIER | c.-3376C>T| |
S259 |
12 | BAA02g17620 | A02 | 8791741 | C | T | upstream_gene_variant | MODIFIER | c.-3718G>A| |
S236 |
13 | BAA02g17620 | A02 | 8792447 | G | A | upstream_gene_variant | MODIFIER | c.-4424C>T| |
S159 S243 |
14 | BAA02g17620 | A02 | 8792746 | G | A | upstream_gene_variant | MODIFIER | c.-4723C>T| |
S162 |
15 | BAA02g17620 | A02 | 8792871 | T | A | upstream_gene_variant | MODIFIER | c.-4848A>T| |
S113 S117 S120 S122 S23 S266 S55 S9 |
16 | BAA02g17620 | A02 | 8792883 | C | T | upstream_gene_variant | MODIFIER | c.-4860G>A| |
S186 |
17 | BAA02g17620 | A02 | 8792938 | G | A | upstream_gene_variant | MODIFIER | c.-4915C>T| |
S177 |
18 | BAA02g17620 | A02 | 8793005 | C | T | upstream_gene_variant | MODIFIER | c.-4982G>A| |
S200 |