Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39070 | A05 | 38233349 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.49-1G>A| |
S286 |
2 | BAA05g39070 | A05 | 38234020 | G | A | missense_variant&splice_region_variant | MODERATE | c.367G>A|p.Glu123Lys |
S240 |
3 | BAA05g39070 | A05 | 38235505 | C | T | synonymous_variant | LOW | c.778C>T|p.Leu260Leu |
S149 |
4 | BAA05g39070 | A05 | 38236140 | G | A | missense_variant | MODERATE | c.1009G>A|p.Glu337Lys |
S90 |
5 | BAA05g39070 | A05 | 38237195 | C | T | missense_variant | MODERATE | c.1378C>T|p.Pro460Ser |
S171 |
6 | BAA05g39070 | A05 | 38238564 | G | A | missense_variant | MODERATE | c.2101G>A|p.Ala701Thr |
S150 S246 |
7 | BAA05g39070 | A05 | 38238885 | C | T | missense_variant | MODERATE | c.2330C>T|p.Thr777Met |
S177 |
8 | BAA05g39070 | A05 | 38241696 | G | A | downstream_gene_variant | MODIFIER | c.*2549G>A| |
S243 S299 |