Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39830 | A01 | 26450451 | C | T | downstream_gene_variant | MODIFIER | c.*3042G>A| |
S134 |
2 | BAA01g39830 | A01 | 26451153 | G | A | downstream_gene_variant | MODIFIER | c.*2340C>T| |
S218 |
3 | BAA01g39830 | A01 | 26452248 | C | T | downstream_gene_variant | MODIFIER | c.*1245G>A| |
S261 |
4 | BAA01g39830 | A01 | 26453534 | C | T | missense_variant | MODERATE | c.853G>A|p.Glu285Lys |
S64 |
5 | BAA01g39830 | A01 | 26454033 | C | T | intron_variant | MODIFIER | c.823-469G>A| |
S16 |
6 | BAA01g39830 | A01 | 26454166 | G | A | intron_variant | MODIFIER | c.823-602C>T| |
S296 |
7 | BAA01g39830 | A01 | 26454536 | C | T | intron_variant | MODIFIER | c.822+730G>A| |
S192 S286 |
8 | BAA01g39830 | A01 | 26454585 | C | T | intron_variant | MODIFIER | c.822+681G>A| |
S279 |
9 | BAA01g39830 | A01 | 26454672 | C | T | intron_variant | MODIFIER | c.822+594G>A| |
S19 |
10 | BAA01g39830 | A01 | 26454953 | C | T | intron_variant | MODIFIER | c.822+313G>A| |
S275 |
11 | BAA01g39830 | A01 | 26455065 | C | T | intron_variant | MODIFIER | c.822+201G>A| |
S301 S304 |
12 | BAA01g39830 | A01 | 26455464 | G | A | synonymous_variant | LOW | c.624C>T|p.Arg208Arg |
S9 |
13 | BAA01g39830 | A01 | 26455493 | C | T | missense_variant | MODERATE | c.595G>A|p.Glu199Lys |
S11 |
14 | BAA01g39830 | A01 | 26455502 | G | A | missense_variant | MODERATE | c.586C>T|p.Leu196Phe |
S13 |
15 | BAA01g39830 | A01 | 26455599 | G | A | synonymous_variant | LOW | c.489C>T|p.Ala163Ala |
S246 |
16 | BAA01g39830 | A01 | 26455790 | C | T | missense_variant | MODERATE | c.298G>A|p.Glu100Lys |
S200 |
17 | BAA01g39830 | A01 | 26458965 | C | T | upstream_gene_variant | MODIFIER | c.-1177G>A| |
S182 |
18 | BAA01g39830 | A01 | 26459364 | C | T | upstream_gene_variant | MODIFIER | c.-1576G>A| |
S4 |