Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g21000 | A06 | 11264299 | G | A | synonymous_variant | LOW | c.1584C>T|p.His528His |
S153 |
2 | BAA06g21000 | A06 | 11264328 | G | A | synonymous_variant | LOW | c.1555C>T|p.Leu519Leu |
S176 |
3 | BAA06g21000 | A06 | 11265076 | C | A | synonymous_variant | LOW | c.1053G>T|p.Gly351Gly |
S92 |
4 | BAA06g21000 | A06 | 11265250 | G | A | synonymous_variant | LOW | c.951C>T|p.Leu317Leu |
S246 |
5 | BAA06g21000 | A06 | 11265849 | G | A | synonymous_variant | LOW | c.514C>T|p.Leu172Leu |
S241 |
6 | BAA06g21000 | A06 | 11266172 | G | A | synonymous_variant | LOW | c.330C>T|p.Ser110Ser |
S33 |
7 | BAA06g21000 | A06 | 11266404 | C | T | missense_variant | MODERATE | c.98G>A|p.Arg33His |
S172 |
8 | BAA06g21000 | A06 | 11266443 | G | A | missense_variant | MODERATE | c.59C>T|p.Thr20Ile |
S119 |
9 | BAA06g21000 | A06 | 11268812 | C | T | upstream_gene_variant | MODIFIER | c.-2311G>A| |
S155 S211 |
10 | BAA06g21000 | A06 | 11269448 | C | T | upstream_gene_variant | MODIFIER | c.-2947G>A| |
S247 |
11 | BAA06g21000 | A06 | 11270359 | C | T | upstream_gene_variant | MODIFIER | c.-3858G>A| |
S36 |
12 | BAA06g21000 | A06 | 11271155 | C | T | upstream_gene_variant | MODIFIER | c.-4654G>A| |
S164 |