Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g29230 | A03 | 13601011 | G | A | downstream_gene_variant | MODIFIER | c.*4979C>T| |
S283 |
2 | BAA03g29230 | A03 | 13601866 | C | T | downstream_gene_variant | MODIFIER | c.*4124G>A| |
S256 |
3 | BAA03g29230 | A03 | 13603061 | G | A | downstream_gene_variant | MODIFIER | c.*2929C>T| |
S303 S31 |
4 | BAA03g29230 | A03 | 13603377 | T | C | downstream_gene_variant | MODIFIER | c.*2613A>G| |
S28 |
5 | BAA03g29230 | A03 | 13604304 | G | A | downstream_gene_variant | MODIFIER | c.*1686C>T| |
S305 |
6 | BAA03g29230 | A03 | 13604517 | T | A | downstream_gene_variant | MODIFIER | c.*1473A>T| |
S117 |
7 | BAA03g29230 | A03 | 13606184 | G | A | missense_variant | MODERATE | c.1646C>T|p.Ala549Val |
S303 |
8 | BAA03g29230 | A03 | 13606359 | G | A | missense_variant | MODERATE | c.1471C>T|p.Pro491Ser |
S246 |
9 | BAA03g29230 | A03 | 13606837 | C | T | missense_variant | MODERATE | c.1160G>A|p.Gly387Asp |
S123 |
10 | BAA03g29230 | A03 | 13607303 | T | C | missense_variant | MODERATE | c.694A>G|p.Thr232Ala |
S51 |
11 | BAA03g29230 | A03 | 13607539 | C | T | missense_variant | MODERATE | c.555G>A|p.Met185Ile |
S247 |
12 | BAA03g29230 | A03 | 13607765 | G | A | synonymous_variant | LOW | c.399C>T|p.Ser133Ser |
S54 |
13 | BAA03g29230 | A03 | 13607875 | C | T | missense_variant | MODERATE | c.289G>A|p.Gly97Arg |
S152 |
14 | BAA03g29230 | A03 | 13608282 | C | T | intron_variant | MODIFIER | c.133-181G>A| |
S304 |
15 | BAA03g29230 | A03 | 13610946 | C | T | upstream_gene_variant | MODIFIER | c.-2067G>A| |
S264 |
16 | BAA03g29230 | A03 | 13612991 | C | A | upstream_gene_variant | MODIFIER | c.-4112G>T| |
S304 |
17 | BAA03g29230 | A03 | 13613041 | G | A | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S305 |
18 | BAA03g29230 | A03 | 13613105 | G | A | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S284 |
19 | BAA03g29230 | A03 | 13613875 | G | A | upstream_gene_variant | MODIFIER | c.-4996C>T| |
S89 |