Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01080 | A07 | 746911 | G | A | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S295 |
2 | BAA07g01080 | A07 | 747088 | G | A | missense_variant | MODERATE | c.896C>T|p.Ala299Val |
S239 |
3 | BAA07g01080 | A07 | 747140 | G | A | synonymous_variant | LOW | c.844C>T|p.Leu282Leu |
S177 |
4 | BAA07g01080 | A07 | 747290 | C | T | missense_variant | MODERATE | c.694G>A|p.Glu232Lys |
S28 |
5 | BAA07g01080 | A07 | 747293 | C | T | missense_variant | MODERATE | c.691G>A|p.Val231Ile |
S249 |
6 | BAA07g01080 | A07 | 747419 | G | A | synonymous_variant | LOW | c.565C>T|p.Leu189Leu |
S201 |
7 | BAA07g01080 | A07 | 747440 | G | A | missense_variant | MODERATE | c.544C>T|p.Pro182Ser |
S136 |
8 | BAA07g01080 | A07 | 747614 | C | T | missense_variant | MODERATE | c.370G>A|p.Ala124Thr |
S189 |
9 | BAA07g01080 | A07 | 747632 | G | A | missense_variant | MODERATE | c.352C>T|p.Leu118Phe |
S286 |
10 | BAA07g01080 | A07 | 748330 | C | T | upstream_gene_variant | MODIFIER | c.-347G>A| |
S118 |
11 | BAA07g01080 | A07 | 750715 | C | T | upstream_gene_variant | MODIFIER | c.-2732G>A| |
S281 |
12 | BAA07g01080 | A07 | 751764 | G | A | upstream_gene_variant | MODIFIER | c.-3781C>T| |
S158 |