Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g11980 | A05 | 6059236 | G | A | intron_variant | MODIFIER | c.127-123G>A| |
S200 |
2 | BAA05g11980 | A05 | 6059651 | G | A | intron_variant | MODIFIER | c.335-57G>A| |
S296 |
3 | BAA05g11980 | A05 | 6059880 | C | T | synonymous_variant | LOW | c.507C>T|p.Val169Val |
S270 |
4 | BAA05g11980 | A05 | 6061133 | G | A | intron_variant | MODIFIER | c.876+43G>A| |
S75 S81 |
5 | BAA05g11980 | A05 | 6061521 | C | T | missense_variant | MODERATE | c.1097C>T|p.Ser366Phe |
S250 |
6 | BAA05g11980 | A05 | 6062107 | C | T | downstream_gene_variant | MODIFIER | c.*546C>T| |
S116 |
7 | BAA05g11980 | A05 | 6062312 | G | A | downstream_gene_variant | MODIFIER | c.*751G>A| |
S173 |
8 | BAA05g11980 | A05 | 6062688 | G | A | downstream_gene_variant | MODIFIER | c.*1127G>A| |
S37 |
9 | BAA05g11980 | A05 | 6063051 | C | T | downstream_gene_variant | MODIFIER | c.*1490C>T| |
S69 |