Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00940 | A04 | 546582 | G | A | upstream_gene_variant | MODIFIER | c.-4564G>A| |
S136 |
2 | BAA04g00940 | A04 | 548958 | A | T | upstream_gene_variant | MODIFIER | c.-2188A>T| |
S69 |
3 | BAA04g00940 | A04 | 551056 | C | T | upstream_gene_variant | MODIFIER | c.-90C>T| |
S74 |
4 | BAA04g00940 | A04 | 551255 | C | T | missense_variant | MODERATE | c.110C>T|p.Ser37Leu |
S148 |
5 | BAA04g00940 | A04 | 551545 | C | T | missense_variant | MODERATE | c.400C>T|p.Arg134Cys |
S308 |
6 | BAA04g00940 | A04 | 551676 | C | T | synonymous_variant | LOW | c.531C>T|p.Arg177Arg |
S172 |
7 | BAA04g00940 | A04 | 551929 | C | T | synonymous_variant | LOW | c.784C>T|p.Leu262Leu |
S124 |
8 | BAA04g00940 | A04 | 552103 | G | A | missense_variant | MODERATE | c.958G>A|p.Asp320Asn |
S188 |
9 | BAA04g00940 | A04 | 552454 | G | A | missense_variant | MODERATE | c.1165G>A|p.Val389Ile |
S77 S82 |
10 | BAA04g00940 | A04 | 552788 | C | T | missense_variant | MODERATE | c.1499C>T|p.Ala500Val |
S296 |
11 | BAA04g00940 | A04 | 553151 | C | T | downstream_gene_variant | MODIFIER | c.*251C>T| |
S249 |
12 | BAA04g00940 | A04 | 553714 | C | T | downstream_gene_variant | MODIFIER | c.*814C>T| |
S122 |
13 | BAA04g00940 | A04 | 554451 | G | A | downstream_gene_variant | MODIFIER | c.*1551G>A| |
S188 |
14 | BAA04g00940 | A04 | 555017 | G | A | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S171 |
15 | BAA04g00940 | A04 | 556080 | G | A | downstream_gene_variant | MODIFIER | c.*3180G>A| |
S211 S227 |
16 | BAA04g00940 | A04 | 556464 | G | A | downstream_gene_variant | MODIFIER | c.*3564G>A| |
S133 |
17 | BAA04g00940 | A04 | 556486 | G | A | downstream_gene_variant | MODIFIER | c.*3586G>A| |
S221 |