Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18690 | A10 | 17420929 | C | T | missense_variant | MODERATE | c.1282G>A|p.Ala428Thr |
S45 |
2 | BAA10g18690 | A10 | 17421243 | C | T | synonymous_variant | LOW | c.1065G>A|p.Gly355Gly |
S194 |
3 | BAA10g18690 | A10 | 17421297 | G | A | synonymous_variant | LOW | c.1011C>T|p.Thr337Thr |
S293 |
4 | BAA10g18690 | A10 | 17421726 | C | T | synonymous_variant | LOW | c.582G>A|p.Arg194Arg |
S173 |
5 | BAA10g18690 | A10 | 17421785 | C | T | missense_variant | MODERATE | c.523G>A|p.Glu175Lys |
S177 |
6 | BAA10g18690 | A10 | 17421992 | G | A | missense_variant | MODERATE | c.424C>T|p.Pro142Ser |
S16 |
7 | BAA10g18690 | A10 | 17422002 | C | T | synonymous_variant | LOW | c.414G>A|p.Arg138Arg |
S148 S30 S31 |
8 | BAA10g18690 | A10 | 17422339 | C | T | synonymous_variant | LOW | c.195G>A|p.Arg65Arg |
S11 |
9 | BAA10g18690 | A10 | 17422672 | G | A | upstream_gene_variant | MODIFIER | c.-139C>T| |
S205 |
10 | BAA10g18690 | A10 | 17425182 | C | T | upstream_gene_variant | MODIFIER | c.-2649G>A| |
S51 |
11 | BAA10g18690 | A10 | 17426855 | C | T | upstream_gene_variant | MODIFIER | c.-4322G>A| |
S269 |
12 | BAA10g18690 | A10 | 17427262 | C | T | upstream_gene_variant | MODIFIER | c.-4729G>A| |
S203 |