Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41700 | A09 | 48342164 | A | T | missense_variant | MODERATE | c.1284T>A|p.Asp428Glu |
S87 |
2 | BAA09g41700 | A09 | 48342202 | G | A | stop_gained | HIGH | c.1246C>T|p.Gln416* |
S150 |
3 | BAA09g41700 | A09 | 48342476 | C | T | synonymous_variant | LOW | c.972G>A|p.Glu324Glu |
S223 |
4 | BAA09g41700 | A09 | 48342566 | C | T | synonymous_variant | LOW | c.882G>A|p.Ser294Ser |
S208 S93 |
5 | BAA09g41700 | A09 | 48344962 | G | A | missense_variant | MODERATE | c.311C>T|p.Thr104Ile |
S305 |
6 | BAA09g41700 | A09 | 48345062 | G | A | stop_gained | HIGH | c.211C>T|p.Gln71* |
S167 |
7 | BAA09g41700 | A09 | 48345248 | C | T | missense_variant | MODERATE | c.25G>A|p.Glu9Lys |
S135 |
8 | BAA09g41700 | A09 | 48349985 | C | T | upstream_gene_variant | MODIFIER | c.-4713G>A| |
S18 |
9 | BAA09g41700 | A09 | 48350100 | C | T | upstream_gene_variant | MODIFIER | c.-4828G>A| |
S40 S49 |