Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02440 | A06 | 1485272 | G | A | missense_variant | MODERATE | c.494C>T|p.Thr165Ile |
S122 |
2 | BAA06g02440 | A06 | 1486390 | G | A | upstream_gene_variant | MODIFIER | c.-320C>T| |
S71 |
3 | BAA06g02440 | A06 | 1487362 | C | T | upstream_gene_variant | MODIFIER | c.-1292G>A| |
S170 |
4 | BAA06g02440 | A06 | 1487532 | C | T | upstream_gene_variant | MODIFIER | c.-1462G>A| |
S156 |
5 | BAA06g02440 | A06 | 1488518 | G | A | upstream_gene_variant | MODIFIER | c.-2448C>T| |
S117 |
6 | BAA06g02440 | A06 | 1489297 | C | T | upstream_gene_variant | MODIFIER | c.-3227G>A| |
S277 |
7 | BAA06g02440 | A06 | 1489574 | G | A | upstream_gene_variant | MODIFIER | c.-3504C>T| |
S77 S82 |
8 | BAA06g02440 | A06 | 1489980 | C | T | upstream_gene_variant | MODIFIER | c.-3910G>A| |
S184 |
9 | BAA06g02440 | A06 | 1490885 | G | A | upstream_gene_variant | MODIFIER | c.-4815C>T| |
S217 S248 |
10 | BAA06g02440 | A06 | 1490914 | C | T | upstream_gene_variant | MODIFIER | c.-4844G>A| |
S219 S72 |