Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03820 | A02 | 1678599 | C | T | synonymous_variant | LOW | c.1689G>A|p.Arg563Arg |
S267 |
2 | BAA02g03820 | A02 | 1678940 | G | T | missense_variant | MODERATE | c.1455C>A|p.Asp485Glu |
S26 |
3 | BAA02g03820 | A02 | 1679230 | G | A | missense_variant | MODERATE | c.1267C>T|p.Arg423Cys |
S282 |
4 | BAA02g03820 | A02 | 1679343 | G | A | missense_variant | MODERATE | c.1244C>T|p.Thr415Ile |
S53 |
5 | BAA02g03820 | A02 | 1679532 | C | T | missense_variant | MODERATE | c.1174G>A|p.Gly392Ser |
S188 |
6 | BAA02g03820 | A02 | 1680282 | C | T | missense_variant | MODERATE | c.698G>A|p.Cys233Tyr |
S268 |
7 | BAA02g03820 | A02 | 1680730 | C | T | synonymous_variant | LOW | c.540G>A|p.Gln180Gln |
S6 |
8 | BAA02g03820 | A02 | 1680794 | C | T | splice_region_variant&intron_variant | LOW | c.482-6G>A| |
S272 |
9 | BAA02g03820 | A02 | 1681540 | G | A | upstream_gene_variant | MODIFIER | c.-66C>T| |
S42 |
10 | BAA02g03820 | A02 | 1681934 | T | C | upstream_gene_variant | MODIFIER | c.-460A>G| |
S290 |
11 | BAA02g03820 | A02 | 1685483 | C | T | upstream_gene_variant | MODIFIER | c.-4009G>A| |
S111 |