Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13930 | A09 | 8015377 | G | A | upstream_gene_variant | MODIFIER | c.-4988G>A| |
S219 |
2 | BAA09g13930 | A09 | 8015509 | C | T | upstream_gene_variant | MODIFIER | c.-4856C>T| |
S269 |
3 | BAA09g13930 | A09 | 8016358 | G | A | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S262 |
4 | BAA09g13930 | A09 | 8017063 | G | A | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S181 |
5 | BAA09g13930 | A09 | 8017979 | C | T | upstream_gene_variant | MODIFIER | c.-2386C>T| |
S116 S117 |
6 | BAA09g13930 | A09 | 8018344 | G | A | upstream_gene_variant | MODIFIER | c.-2021G>A| |
S16 |
7 | BAA09g13930 | A09 | 8018839 | G | A | upstream_gene_variant | MODIFIER | c.-1526G>A| |
S299 |
8 | BAA09g13930 | A09 | 8021381 | C | T | intron_variant | MODIFIER | c.587+30C>T| |
S212 |
9 | BAA09g13930 | A09 | 8021756 | G | A | splice_region_variant&intron_variant | LOW | c.776-7G>A| |
S202 |
10 | BAA09g13930 | A09 | 8021870 | C | T | missense_variant | MODERATE | c.883C>T|p.Leu295Phe |
S284 |
11 | BAA09g13930 | A09 | 8022494 | C | T | missense_variant | MODERATE | c.1352C>T|p.Thr451Ile |
S18 |
12 | BAA09g13930 | A09 | 8022714 | C | T | missense_variant | MODERATE | c.1475C>T|p.Thr492Ile |
S148 S210 |
13 | BAA09g13930 | A09 | 8027050 | G | A | downstream_gene_variant | MODIFIER | c.*3634G>A| |
S16 |
14 | BAA09g13930 | A09 | 8027819 | G | A | downstream_gene_variant | MODIFIER | c.*4403G>A| |
S233 |