Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11120 | A08 | 9975027 | G | A | downstream_gene_variant | MODIFIER | c.*4338C>T| |
S16 |
2 | BAA08g11120 | A08 | 9975814 | C | T | downstream_gene_variant | MODIFIER | c.*3551G>A| |
S177 |
3 | BAA08g11120 | A08 | 9975905 | C | T | downstream_gene_variant | MODIFIER | c.*3460G>A| |
S6 |
4 | BAA08g11120 | A08 | 9977406 | T | C | downstream_gene_variant | MODIFIER | c.*1959A>G| |
S264 |
5 | BAA08g11120 | A08 | 9977851 | G | A | downstream_gene_variant | MODIFIER | c.*1514C>T| |
S64 |
6 | BAA08g11120 | A08 | 9978029 | C | T | downstream_gene_variant | MODIFIER | c.*1336G>A| |
S247 |
7 | BAA08g11120 | A08 | 9978370 | G | A | downstream_gene_variant | MODIFIER | c.*995C>T| |
S39 |
8 | BAA08g11120 | A08 | 9978414 | G | A | downstream_gene_variant | MODIFIER | c.*951C>T| |
S281 |
9 | BAA08g11120 | A08 | 9981043 | G | A | missense_variant | MODERATE | c.278C>T|p.Thr93Met |
S221 |
10 | BAA08g11120 | A08 | 9981248 | G | A | stop_gained | HIGH | c.73C>T|p.Arg25* |
S192 |
11 | BAA08g11120 | A08 | 9981404 | G | A | upstream_gene_variant | MODIFIER | c.-84C>T| |
S81 S85 |
12 | BAA08g11120 | A08 | 9982691 | G | A | upstream_gene_variant | MODIFIER | c.-1371C>T| |
S298 |
13 | BAA08g11120 | A08 | 9983013 | G | A | upstream_gene_variant | MODIFIER | c.-1693C>T| |
S242 |
14 | BAA08g11120 | A08 | 9985207 | C | T | upstream_gene_variant | MODIFIER | c.-3887G>A| |
S60 |
15 | BAA08g11120 | A08 | 9985236 | C | T | upstream_gene_variant | MODIFIER | c.-3916G>A| |
S114 |