Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09570 | A01 | 4253284 | C | T | missense_variant&splice_region_variant | MODERATE | c.1882G>A|p.Glu628Lys |
S81 S85 |
2 | BAA01g09570 | A01 | 4253787 | C | T | missense_variant | MODERATE | c.1462G>A|p.Ala488Thr |
S247 |
3 | BAA01g09570 | A01 | 4257865 | C | T | intron_variant | MODIFIER | c.1086+2042G>A| |
S16 S270 |
4 | BAA01g09570 | A01 | 4258300 | C | T | intron_variant | MODIFIER | c.1086+1607G>A| |
S200 |
5 | BAA01g09570 | A01 | 4259282 | G | A | intron_variant | MODIFIER | c.1086+625C>T| |
S95 |
6 | BAA01g09570 | A01 | 4259915 | G | A | stop_gained | HIGH | c.1078C>T|p.Gln360* |
S40 S49 |
7 | BAA01g09570 | A01 | 4260403 | C | T | intron_variant | MODIFIER | c.736-146G>A| |
S148 S30 S31 |
8 | BAA01g09570 | A01 | 4260440 | C | T | intron_variant | MODIFIER | c.736-183G>A| |
S247 |
9 | BAA01g09570 | A01 | 4260562 | G | A | intron_variant | MODIFIER | c.735+94C>T| |
S181 |
10 | BAA01g09570 | A01 | 4260819 | G | A | missense_variant | MODERATE | c.649C>T|p.Leu217Phe |
S96 |
11 | BAA01g09570 | A01 | 4261635 | G | A | missense_variant | MODERATE | c.25C>T|p.Pro9Ser |
S207 |
12 | BAA01g09570 | A01 | 4261892 | C | T | upstream_gene_variant | MODIFIER | c.-233G>A| |
S109 |
13 | BAA01g09570 | A01 | 4262964 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S97 |
14 | BAA01g09570 | A01 | 4263550 | G | A | upstream_gene_variant | MODIFIER | c.-1891C>T| |
S280 |
15 | BAA01g09570 | A01 | 4263807 | C | T | upstream_gene_variant | MODIFIER | c.-2148G>A| |
S155 S211 |
16 | BAA01g09570 | A01 | 4264167 | C | T | upstream_gene_variant | MODIFIER | c.-2508G>A| |
S192 |
17 | BAA01g09570 | A01 | 4266569 | C | T | upstream_gene_variant | MODIFIER | c.-4910G>A| |
S246 |