Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22500 | A09 | 14080463 | C | T | downstream_gene_variant | MODIFIER | c.*2107G>A| |
S263 |
2 | BAA09g22500 | A09 | 14080808 | C | T | downstream_gene_variant | MODIFIER | c.*1762G>A| |
S293 |
3 | BAA09g22500 | A09 | 14082237 | C | T | downstream_gene_variant | MODIFIER | c.*333G>A| |
S174 S27 |
4 | BAA09g22500 | A09 | 14083118 | C | T | missense_variant | MODERATE | c.2890G>A|p.Ala964Thr |
S302 |
5 | BAA09g22500 | A09 | 14084368 | G | A | intron_variant | MODIFIER | c.2437-39C>T| |
S308 |
6 | BAA09g22500 | A09 | 14085291 | G | A | missense_variant | MODERATE | c.1867C>T|p.Leu623Phe |
S42 |
7 | BAA09g22500 | A09 | 14085609 | C | T | intron_variant | MODIFIER | c.1702+65G>A| |
S111 |
8 | BAA09g22500 | A09 | 14091061 | C | T | upstream_gene_variant | MODIFIER | c.-725G>A| |
S96 |
9 | BAA09g22500 | A09 | 14091063 | G | A | upstream_gene_variant | MODIFIER | c.-727C>T| |
S284 |
10 | BAA09g22500 | A09 | 14091305 | G | A | upstream_gene_variant | MODIFIER | c.-969C>T| |
S298 |
11 | BAA09g22500 | A09 | 14092261 | G | A | upstream_gene_variant | MODIFIER | c.-1925C>T| |
S98 |
12 | BAA09g22500 | A09 | 14092639 | G | A | upstream_gene_variant | MODIFIER | c.-2303C>T| |
S208 S219 |
13 | BAA09g22500 | A09 | 14092706 | C | T | upstream_gene_variant | MODIFIER | c.-2370G>A| |
S18 |
14 | BAA09g22500 | A09 | 14092901 | G | A | upstream_gene_variant | MODIFIER | c.-2565C>T| |
S70 |
15 | BAA09g22500 | A09 | 14093657 | G | A | upstream_gene_variant | MODIFIER | c.-3321C>T| |
S175 S189 |
16 | BAA09g22500 | A09 | 14093702 | G | A | upstream_gene_variant | MODIFIER | c.-3366C>T| |
S56 |
17 | BAA09g22500 | A09 | 14094210 | C | T | upstream_gene_variant | MODIFIER | c.-3874G>A| |
S156 |
18 | BAA09g22500 | A09 | 14095012 | G | A | upstream_gene_variant | MODIFIER | c.-4676C>T| |
S166 |
19 | BAA09g22500 | A09 | 14095093 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S176 |