Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g30790 | A01 | 19730326 | C | T | downstream_gene_variant | MODIFIER | c.*4963G>A| |
S182 |
2 | BAA01g30790 | A01 | 19731395 | C | T | downstream_gene_variant | MODIFIER | c.*3894G>A| |
S210 |
3 | BAA01g30790 | A01 | 19731858 | C | T | downstream_gene_variant | MODIFIER | c.*3431G>A| |
S73 |
4 | BAA01g30790 | A01 | 19732277 | G | A | downstream_gene_variant | MODIFIER | c.*3012C>T| |
S268 |
5 | BAA01g30790 | A01 | 19732574 | G | A | downstream_gene_variant | MODIFIER | c.*2715C>T| |
S197 |
6 | BAA01g30790 | A01 | 19733758 | C | T | downstream_gene_variant | MODIFIER | c.*1531G>A| |
S203 |
7 | BAA01g30790 | A01 | 19735341 | A | C | missense_variant | MODERATE | c.1262T>G|p.Leu421Arg |
S109 S37 S89 |
8 | BAA01g30790 | A01 | 19736140 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.931-1G>A| |
S39 |
9 | BAA01g30790 | A01 | 19736663 | G | A | intron_variant | MODIFIER | c.637-158C>T| |
S286 |
10 | BAA01g30790 | A01 | 19738611 | C | T | missense_variant&splice_region_variant | MODERATE | c.253G>A|p.Gly85Arg |
S134 |
11 | BAA01g30790 | A01 | 19739610 | G | A | upstream_gene_variant | MODIFIER | c.-747C>T| |
S294 |
12 | BAA01g30790 | A01 | 19739648 | C | T | upstream_gene_variant | MODIFIER | c.-785G>A| |
S69 |
13 | BAA01g30790 | A01 | 19740496 | C | T | upstream_gene_variant | MODIFIER | c.-1633G>A| |
S139 |
14 | BAA01g30790 | A01 | 19740524 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S158 |
15 | BAA01g30790 | A01 | 19741085 | C | T | upstream_gene_variant | MODIFIER | c.-2222G>A| |
S47 |
16 | BAA01g30790 | A01 | 19741137 | C | T | upstream_gene_variant | MODIFIER | c.-2274G>A| |
S289 S290 |
17 | BAA01g30790 | A01 | 19742684 | C | T | upstream_gene_variant | MODIFIER | c.-3821G>A| |
S162 |
18 | BAA01g30790 | A01 | 19742860 | C | T | upstream_gene_variant | MODIFIER | c.-3997G>A| |
S4 |