Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44210 | A09 | 49992780 | C | T | downstream_gene_variant | MODIFIER | c.*4754G>A| |
S6 |
2 | BAA09g44210 | A09 | 49995655 | A | T | downstream_gene_variant | MODIFIER | c.*1879T>A| |
S294 |
3 | BAA09g44210 | A09 | 49996085 | C | T | downstream_gene_variant | MODIFIER | c.*1449G>A| |
S302 |
4 | BAA09g44210 | A09 | 49998620 | C | T | missense_variant | MODERATE | c.715G>A|p.Val239Ile |
S212 |
5 | BAA09g44210 | A09 | 49998953 | G | A | synonymous_variant | LOW | c.462C>T|p.Ile154Ile |
S252 |
6 | BAA09g44210 | A09 | 49999137 | T | G | missense_variant | MODERATE | c.278A>C|p.Gln93Pro |
S117 |
7 | BAA09g44210 | A09 | 49999529 | C | T | missense_variant | MODERATE | c.80G>A|p.Gly27Glu |
S136 |
8 | BAA09g44210 | A09 | 50000491 | C | T | upstream_gene_variant | MODIFIER | c.-883G>A| |
S37 |
9 | BAA09g44210 | A09 | 50000792 | A | T | upstream_gene_variant | MODIFIER | c.-1184T>A| |
S298 |
10 | BAA09g44210 | A09 | 50001127 | G | A | upstream_gene_variant | MODIFIER | c.-1519C>T| |
S132 S137 S215 S89 |
11 | BAA09g44210 | A09 | 50001215 | G | A | upstream_gene_variant | MODIFIER | c.-1607C>T| |
S86 |
12 | BAA09g44210 | A09 | 50001354 | G | A | upstream_gene_variant | MODIFIER | c.-1746C>T| |
S87 |
13 | BAA09g44210 | A09 | 50001979 | G | A | upstream_gene_variant | MODIFIER | c.-2371C>T| |
S45 |
14 | BAA09g44210 | A09 | 50003536 | C | T | upstream_gene_variant | MODIFIER | c.-3928G>A| |
S97 |
15 | BAA09g44210 | A09 | 50003589 | C | T | upstream_gene_variant | MODIFIER | c.-3981G>A| |
S58 |
16 | BAA09g44210 | A09 | 50003793 | C | T | upstream_gene_variant | MODIFIER | c.-4185G>A| |
S149 |
17 | BAA09g44210 | A09 | 50003795 | C | T | upstream_gene_variant | MODIFIER | c.-4187G>A| |
S277 |
18 | BAA09g44210 | A09 | 50003909 | C | T | upstream_gene_variant | MODIFIER | c.-4301G>A| |
S225 |