Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13580 | A05 | 7046844 | C | T | downstream_gene_variant | MODIFIER | c.*1125G>A| |
S61 |
2 | BAA05g13580 | A05 | 7048333 | G | A | missense_variant | MODERATE | c.2858C>T|p.Ser953Phe |
S149 |
3 | BAA05g13580 | A05 | 7050492 | G | A | synonymous_variant | LOW | c.1866C>T|p.Ile622Ile |
S262 |
4 | BAA05g13580 | A05 | 7050521 | C | T | missense_variant | MODERATE | c.1837G>A|p.Val613Ile |
S164 |
5 | BAA05g13580 | A05 | 7050526 | G | A | missense_variant | MODERATE | c.1832C>T|p.Ala611Val |
S40 S49 |
6 | BAA05g13580 | A05 | 7050577 | C | T | missense_variant | MODERATE | c.1781G>A|p.Cys594Tyr |
S201 |
7 | BAA05g13580 | A05 | 7053204 | G | A | splice_region_variant&intron_variant | LOW | c.468-4C>T| |
S200 |
8 | BAA05g13580 | A05 | 7054225 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.94-1G>A| |
S51 |
9 | BAA05g13580 | A05 | 7055759 | G | A | upstream_gene_variant | MODIFIER | c.-1338C>T| |
S103 |
10 | BAA05g13580 | A05 | 7056786 | C | T | upstream_gene_variant | MODIFIER | c.-2365G>A| |
S139 |
11 | BAA05g13580 | A05 | 7056935 | C | T | upstream_gene_variant | MODIFIER | c.-2514G>A| |
S73 S91 |
12 | BAA05g13580 | A05 | 7057135 | C | T | upstream_gene_variant | MODIFIER | c.-2714G>A| |
S162 |
13 | BAA05g13580 | A05 | 7058501 | C | T | upstream_gene_variant | MODIFIER | c.-4080G>A| |
S270 |