Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g16630 | A04 | 21010052 | C | T | upstream_gene_variant | MODIFIER | c.-2102C>T| |
S92 |
2 | BAA04g16630 | A04 | 21011689 | C | T | upstream_gene_variant | MODIFIER | c.-465C>T| |
S10 |
3 | BAA04g16630 | A04 | 21011868 | C | T | upstream_gene_variant | MODIFIER | c.-286C>T| |
S292 |
4 | BAA04g16630 | A04 | 21012077 | C | T | upstream_gene_variant | MODIFIER | c.-77C>T| |
S210 |
5 | BAA04g16630 | A04 | 21012305 | C | T | missense_variant | MODERATE | c.152C>T|p.Thr51Ile |
S132 S137 S215 |
6 | BAA04g16630 | A04 | 21014359 | C | T | intron_variant | MODIFIER | c.511-65C>T| |
S267 |
7 | BAA04g16630 | A04 | 21014363 | C | T | intron_variant | MODIFIER | c.511-61C>T| |
S18 |
8 | BAA04g16630 | A04 | 21014602 | G | A | missense_variant | MODERATE | c.595G>A|p.Glu199Lys |
S303 |
9 | BAA04g16630 | A04 | 21015508 | C | T | intron_variant | MODIFIER | c.707+794C>T| |
S95 |