Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g31770 | A09 | 40014294 | C | T | upstream_gene_variant | MODIFIER | c.-4992C>T| |
S1 S90 |
2 | BAA09g31770 | A09 | 40015054 | G | A | upstream_gene_variant | MODIFIER | c.-4232G>A| |
S25 |
3 | BAA09g31770 | A09 | 40015400 | C | T | upstream_gene_variant | MODIFIER | c.-3886C>T| |
S115 |
4 | BAA09g31770 | A09 | 40015687 | C | T | upstream_gene_variant | MODIFIER | c.-3599C>T| |
S37 |
5 | BAA09g31770 | A09 | 40015941 | G | A | upstream_gene_variant | MODIFIER | c.-3345G>A| |
S155 S211 |
6 | BAA09g31770 | A09 | 40016046 | G | A | upstream_gene_variant | MODIFIER | c.-3240G>A| |
S270 |
7 | BAA09g31770 | A09 | 40016080 | C | T | upstream_gene_variant | MODIFIER | c.-3206C>T| |
S70 |
8 | BAA09g31770 | A09 | 40016595 | C | T | upstream_gene_variant | MODIFIER | c.-2691C>T| |
S213 |
9 | BAA09g31770 | A09 | 40016811 | C | T | upstream_gene_variant | MODIFIER | c.-2475C>T| |
S278 |
10 | BAA09g31770 | A09 | 40017634 | C | T | upstream_gene_variant | MODIFIER | c.-1652C>T| |
S97 |
11 | BAA09g31770 | A09 | 40017877 | G | A | upstream_gene_variant | MODIFIER | c.-1409G>A| |
S217 |
12 | BAA09g31770 | A09 | 40018126 | G | A | upstream_gene_variant | MODIFIER | c.-1160G>A| |
S136 |
13 | BAA09g31770 | A09 | 40018246 | C | T | upstream_gene_variant | MODIFIER | c.-1040C>T| |
S81 S85 |
14 | BAA09g31770 | A09 | 40018256 | G | A | upstream_gene_variant | MODIFIER | c.-1030G>A| |
S79 S84 |
15 | BAA09g31770 | A09 | 40018367 | G | A | upstream_gene_variant | MODIFIER | c.-919G>A| |
S133 |
16 | BAA09g31770 | A09 | 40018372 | C | T | upstream_gene_variant | MODIFIER | c.-914C>T| |
S193 |
17 | BAA09g31770 | A09 | 40018642 | G | A | upstream_gene_variant | MODIFIER | c.-644G>A| |
S210 S225 |
18 | BAA09g31770 | A09 | 40019036 | G | A | upstream_gene_variant | MODIFIER | c.-250G>A| |
S107 |
19 | BAA09g31770 | A09 | 40019179 | C | T | upstream_gene_variant | MODIFIER | c.-107C>T| |
S293 |
20 | BAA09g31770 | A09 | 40019987 | C | T | missense_variant | MODERATE | c.575C>T|p.Ala192Val |
S1 |
21 | BAA09g31770 | A09 | 40022499 | G | A | downstream_gene_variant | MODIFIER | c.*1987G>A| |
S221 |
22 | BAA09g31770 | A09 | 40023538 | C | T | downstream_gene_variant | MODIFIER | c.*3026C>T| |
S159 S243 S299 |
23 | BAA09g31770 | A09 | 40023745 | G | A | downstream_gene_variant | MODIFIER | c.*3233G>A| |
S45 |
24 | BAA09g31770 | A09 | 40023813 | C | T | downstream_gene_variant | MODIFIER | c.*3301C>T| |
S123 |
25 | BAA09g31770 | A09 | 40023875 | G | A | downstream_gene_variant | MODIFIER | c.*3363G>A| |
S287 |