Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10100 | A08 | 9223380 | C | T | downstream_gene_variant | MODIFIER | c.*4580G>A| |
S293 |
2 | BAA08g10100 | A08 | 9223859 | T | A | downstream_gene_variant | MODIFIER | c.*4101A>T| |
S63 |
3 | BAA08g10100 | A08 | 9224450 | G | A | downstream_gene_variant | MODIFIER | c.*3510C>T| |
S197 |
4 | BAA08g10100 | A08 | 9224470 | G | A | downstream_gene_variant | MODIFIER | c.*3490C>T| |
S224 |
5 | BAA08g10100 | A08 | 9225244 | C | T | downstream_gene_variant | MODIFIER | c.*2716G>A| |
S56 |
6 | BAA08g10100 | A08 | 9225399 | C | T | downstream_gene_variant | MODIFIER | c.*2561G>A| |
S167 |
7 | BAA08g10100 | A08 | 9225512 | G | A | downstream_gene_variant | MODIFIER | c.*2448C>T| |
S298 |
8 | BAA08g10100 | A08 | 9225913 | G | A | downstream_gene_variant | MODIFIER | c.*2047C>T| |
S301 S304 |
9 | BAA08g10100 | A08 | 9227316 | G | A | downstream_gene_variant | MODIFIER | c.*644C>T| |
S136 |
10 | BAA08g10100 | A08 | 9228272 | C | T | intron_variant | MODIFIER | c.846+54G>A| |
S149 |
11 | BAA08g10100 | A08 | 9228569 | C | T | missense_variant | MODERATE | c.677G>A|p.Cys226Tyr |
S302 |
12 | BAA08g10100 | A08 | 9229770 | G | A | synonymous_variant | LOW | c.96C>T|p.Leu32Leu |
S95 |
13 | BAA08g10100 | A08 | 9229780 | G | A | missense_variant | MODERATE | c.86C>T|p.Ala29Val |
S238 |