Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g22120 | A07 | 26581521 | C | T | synonymous_variant | LOW | c.189C>T|p.Leu63Leu |
S284 |
2 | BAA07g22120 | A07 | 26581841 | G | A | missense_variant | MODERATE | c.509G>A|p.Gly170Asp |
S236 |
3 | BAA07g22120 | A07 | 26581980 | G | A | synonymous_variant | LOW | c.648G>A|p.Gly216Gly |
S115 |
4 | BAA07g22120 | A07 | 26582979 | G | A | missense_variant | MODERATE | c.1283G>A|p.Arg428Lys |
S17 S295 |
5 | BAA07g22120 | A07 | 26583302 | G | A | missense_variant | MODERATE | c.1515G>A|p.Met505Ile |
S278 |
6 | BAA07g22120 | A07 | 26583497 | G | A | intron_variant | MODIFIER | c.1593+41G>A| |
S301 |
7 | BAA07g22120 | A07 | 26584100 | C | T | intron_variant | MODIFIER | c.1593+644C>T| |
S232 |
8 | BAA07g22120 | A07 | 26584133 | G | A | intron_variant | MODIFIER | c.1593+677G>A| |
S131 |
9 | BAA07g22120 | A07 | 26584269 | G | A | intron_variant | MODIFIER | c.1593+813G>A| |
S157 S163 |
10 | BAA07g22120 | A07 | 26584365 | G | A | intron_variant | MODIFIER | c.1593+909G>A| |
S71 |
11 | BAA07g22120 | A07 | 26584437 | C | T | intron_variant | MODIFIER | c.1593+981C>T| |
S126 S205 |
12 | BAA07g22120 | A07 | 26584602 | C | T | intron_variant | MODIFIER | c.1593+1146C>T| |
S181 |
13 | BAA07g22120 | A07 | 26584635 | G | A | intron_variant | MODIFIER | c.1593+1179G>A| |
S216 S27 |
14 | BAA07g22120 | A07 | 26588765 | C | T | missense_variant | MODERATE | c.2204C>T|p.Ala735Val |
S162 |