Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27970 | A08 | 19563071 | G | A | missense_variant | MODERATE | c.476G>A|p.Gly159Glu |
S302 |
2 | BAA08g27970 | A08 | 19566022 | G | A | intron_variant | MODIFIER | c.1072-655G>A| |
S302 |
3 | BAA08g27970 | A08 | 19567537 | C | T | synonymous_variant | LOW | c.1932C>T|p.Val644Val |
S245 |
4 | BAA08g27970 | A08 | 19568471 | G | A | missense_variant | MODERATE | c.2792G>A|p.Gly931Glu |
S65 |
5 | BAA08g27970 | A08 | 19569029 | G | A | missense_variant | MODERATE | c.3350G>A|p.Arg1117Lys |
S117 |
6 | BAA08g27970 | A08 | 19569379 | G | A | missense_variant | MODERATE | c.3700G>A|p.Val1234Ile |
S34 |
7 | BAA08g27970 | A08 | 19569487 | G | A | missense_variant | MODERATE | c.3808G>A|p.Val1270Ile |
S233 |
8 | BAA08g27970 | A08 | 19569855 | G | A | stop_gained | HIGH | c.4176G>A|p.Trp1392* |
S170 |
9 | BAA08g27970 | A08 | 19569974 | C | T | intron_variant | MODIFIER | c.4206+89C>T| |
S133 S171 |
10 | BAA08g27970 | A08 | 19570682 | G | A | missense_variant | MODERATE | c.4319G>A|p.Gly1440Glu |
S292 |
11 | BAA08g27970 | A08 | 19570753 | G | A | missense_variant | MODERATE | c.4390G>A|p.Gly1464Arg |
S37 |
12 | BAA08g27970 | A08 | 19570765 | C | T | synonymous_variant | LOW | c.4402C>T|p.Leu1468Leu |
S167 |
13 | BAA08g27970 | A08 | 19571657 | G | A | missense_variant | MODERATE | c.4982G>A|p.Arg1661Lys |
S72 S78 |