Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15010 | A04 | 19889764 | C | T | downstream_gene_variant | MODIFIER | c.*4589G>A| |
S172 |
2 | BAA04g15010 | A04 | 19889799 | C | T | downstream_gene_variant | MODIFIER | c.*4554G>A| |
S110 |
3 | BAA04g15010 | A04 | 19890087 | C | T | downstream_gene_variant | MODIFIER | c.*4266G>A| |
S305 |
4 | BAA04g15010 | A04 | 19890754 | G | A | downstream_gene_variant | MODIFIER | c.*3599C>T| |
S186 |
5 | BAA04g15010 | A04 | 19890777 | G | A | downstream_gene_variant | MODIFIER | c.*3576C>T| |
S99 |
6 | BAA04g15010 | A04 | 19891254 | G | A | downstream_gene_variant | MODIFIER | c.*3099C>T| |
S286 |
7 | BAA04g15010 | A04 | 19891325 | C | T | downstream_gene_variant | MODIFIER | c.*3028G>A| |
S67 |
8 | BAA04g15010 | A04 | 19891441 | G | A | downstream_gene_variant | MODIFIER | c.*2912C>T| |
S62 |
9 | BAA04g15010 | A04 | 19894505 | C | T | missense_variant | MODERATE | c.703G>A|p.Asp235Asn |
S16 |
10 | BAA04g15010 | A04 | 19894574 | C | T | missense_variant | MODERATE | c.634G>A|p.Ala212Thr |
S225 S73 |
11 | BAA04g15010 | A04 | 19894802 | G | A | missense_variant | MODERATE | c.406C>T|p.Leu136Phe |
S56 |
12 | BAA04g15010 | A04 | 19894848 | G | A | synonymous_variant | LOW | c.360C>T|p.Val120Val |
S111 |
13 | BAA04g15010 | A04 | 19898647 | G | A | upstream_gene_variant | MODIFIER | c.-3235C>T| |
S269 |
14 | BAA04g15010 | A04 | 19899580 | C | T | upstream_gene_variant | MODIFIER | c.-4168G>A| |
S25 |
15 | BAA04g15010 | A04 | 19899735 | C | T | upstream_gene_variant | MODIFIER | c.-4323G>A| |
S301 S304 |
16 | BAA04g15010 | A04 | 19899742 | C | T | upstream_gene_variant | MODIFIER | c.-4330G>A| |
S270 |
17 | BAA04g15010 | A04 | 19899822 | C | T | upstream_gene_variant | MODIFIER | c.-4410G>A| |
S255 |
18 | BAA04g15010 | A04 | 19900273 | G | A | upstream_gene_variant | MODIFIER | c.-4861C>T| |
S47 |