Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g37190 | A01 | 24812172 | C | T | upstream_gene_variant | MODIFIER | c.-1376C>T| |
S92 |
2 | BAA01g37190 | A01 | 24813371 | G | A | upstream_gene_variant | MODIFIER | c.-177G>A| |
S294 |
3 | BAA01g37190 | A01 | 24813553 | G | A | missense_variant | MODERATE | c.6G>A|p.Met2Ile |
S259 |
4 | BAA01g37190 | A01 | 24814576 | C | T | missense_variant | MODERATE | c.775C>T|p.Pro259Ser |
S301 S304 |
5 | BAA01g37190 | A01 | 24815469 | C | T | missense_variant | MODERATE | c.953C>T|p.Ala318Val |
S255 |
6 | BAA01g37190 | A01 | 24816115 | C | T | missense_variant | MODERATE | c.1324C>T|p.Pro442Ser |
S239 |
7 | BAA01g37190 | A01 | 24816481 | G | A | missense_variant | MODERATE | c.1528G>A|p.Ala510Thr |
S176 |
8 | BAA01g37190 | A01 | 24817253 | C | T | splice_region_variant&intron_variant | LOW | c.2042-8C>T| |
S72 S78 |
9 | BAA01g37190 | A01 | 24817903 | C | T | synonymous_variant | LOW | c.2448C>T|p.Leu816Leu |
S272 |