Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00820 | A04 | 437089 | G | A | upstream_gene_variant | MODIFIER | c.-4905G>A| |
S277 |
2 | BAA04g00820 | A04 | 437131 | G | A | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S158 |
3 | BAA04g00820 | A04 | 437840 | G | A | upstream_gene_variant | MODIFIER | c.-4154G>A| |
S62 |
4 | BAA04g00820 | A04 | 437880 | G | A | upstream_gene_variant | MODIFIER | c.-4114G>A| |
S127 |
5 | BAA04g00820 | A04 | 438338 | C | T | upstream_gene_variant | MODIFIER | c.-3656C>T| |
S95 |
6 | BAA04g00820 | A04 | 438434 | G | A | upstream_gene_variant | MODIFIER | c.-3560G>A| |
S108 |
7 | BAA04g00820 | A04 | 438497 | C | T | upstream_gene_variant | MODIFIER | c.-3497C>T| |
S76 |
8 | BAA04g00820 | A04 | 439300 | C | T | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S192 S242 |
9 | BAA04g00820 | A04 | 439317 | G | A | upstream_gene_variant | MODIFIER | c.-2677G>A| |
S67 |
10 | BAA04g00820 | A04 | 439641 | C | T | upstream_gene_variant | MODIFIER | c.-2353C>T| |
S293 |
11 | BAA04g00820 | A04 | 439838 | C | T | upstream_gene_variant | MODIFIER | c.-2156C>T| |
S201 |
12 | BAA04g00820 | A04 | 441795 | C | T | upstream_gene_variant | MODIFIER | c.-199C>T| |
S9 |
13 | BAA04g00820 | A04 | 442414 | G | A | missense_variant | MODERATE | c.421G>A|p.Gly141Arg |
S221 |
14 | BAA04g00820 | A04 | 444703 | C | T | downstream_gene_variant | MODIFIER | c.*806C>T| |
S15 S3 |
15 | BAA04g00820 | A04 | 445194 | C | T | downstream_gene_variant | MODIFIER | c.*1297C>T| |
S18 |
16 | BAA04g00820 | A04 | 446721 | C | T | downstream_gene_variant | MODIFIER | c.*2824C>T| |
S16 S56 |
17 | BAA04g00820 | A04 | 447640 | C | T | downstream_gene_variant | MODIFIER | c.*3743C>T| |
S80 |
18 | BAA04g00820 | A04 | 447654 | G | A | downstream_gene_variant | MODIFIER | c.*3757G>A| |
S251 |