Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08660 | A01 | 3825312 | C | T | downstream_gene_variant | MODIFIER | c.*3219G>A| |
S236 |
2 | BAA01g08660 | A01 | 3828930 | C | T | stop_gained | HIGH | c.1170G>A|p.Trp390* |
S100 |
3 | BAA01g08660 | A01 | 3829193 | G | A | missense_variant | MODERATE | c.907C>T|p.Pro303Ser |
S274 |
4 | BAA01g08660 | A01 | 3829269 | C | T | missense_variant | MODERATE | c.831G>A|p.Met277Ile |
S275 |
5 | BAA01g08660 | A01 | 3829427 | G | A | missense_variant | MODERATE | c.673C>T|p.Arg225Cys |
S190 |
6 | BAA01g08660 | A01 | 3829515 | G | A | synonymous_variant | LOW | c.585C>T|p.Phe195Phe |
S110 |
7 | BAA01g08660 | A01 | 3829537 | G | A | missense_variant | MODERATE | c.563C>T|p.Pro188Leu |
S229 |
8 | BAA01g08660 | A01 | 3829714 | G | A | missense_variant | MODERATE | c.386C>T|p.Pro129Leu |
S293 |
9 | BAA01g08660 | A01 | 3830017 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S207 |
10 | BAA01g08660 | A01 | 3830074 | G | A | missense_variant | MODERATE | c.26C>T|p.Pro9Leu |
S139 |
11 | BAA01g08660 | A01 | 3832671 | C | T | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S218 |
12 | BAA01g08660 | A01 | 3833309 | G | A | upstream_gene_variant | MODIFIER | c.-3210C>T| |
S202 |