Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05600 | A02 | 2416752 | C | T | synonymous_variant | LOW | c.1983G>A|p.Gln661Gln |
S284 |
2 | BAA02g05600 | A02 | 2416760 | C | T | missense_variant | MODERATE | c.1975G>A|p.Gly659Ser |
S99 |
3 | BAA02g05600 | A02 | 2417049 | C | T | synonymous_variant | LOW | c.1686G>A|p.Arg562Arg |
S88 |
4 | BAA02g05600 | A02 | 2417474 | G | A | missense_variant | MODERATE | c.1261C>T|p.Arg421Cys |
S67 |
5 | BAA02g05600 | A02 | 2417476 | G | A | missense_variant | MODERATE | c.1259C>T|p.Ala420Val |
S286 |
6 | BAA02g05600 | A02 | 2417658 | G | A | synonymous_variant | LOW | c.1077C>T|p.Val359Val |
S190 |
7 | BAA02g05600 | A02 | 2417676 | C | T | synonymous_variant | LOW | c.1059G>A|p.Gly353Gly |
S202 |
8 | BAA02g05600 | A02 | 2418213 | G | A | synonymous_variant | LOW | c.522C>T|p.His174His |
S176 |
9 | BAA02g05600 | A02 | 2418707 | C | T | missense_variant | MODERATE | c.28G>A|p.Asp10Asn |
S243 S299 |
10 | BAA02g05600 | A02 | 2420050 | G | A | upstream_gene_variant | MODIFIER | c.-1316C>T| |
S241 |
11 | BAA02g05600 | A02 | 2421744 | C | T | upstream_gene_variant | MODIFIER | c.-3010G>A| |
S292 |
12 | BAA02g05600 | A02 | 2422392 | C | T | upstream_gene_variant | MODIFIER | c.-3658G>A| |
S130 |
13 | BAA02g05600 | A02 | 2423367 | G | A | upstream_gene_variant | MODIFIER | c.-4633C>T| |
S223 |
14 | BAA02g05600 | A02 | 2423732 | G | A | upstream_gene_variant | MODIFIER | c.-4998C>T| |
S199 |