Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g54960 | A09 | 55328599 | C | T | upstream_gene_variant | MODIFIER | c.-3607C>T| |
S140 |
2 | BAA09g54960 | A09 | 55329030 | C | T | upstream_gene_variant | MODIFIER | c.-3176C>T| |
S125 |
3 | BAA09g54960 | A09 | 55329107 | G | A | upstream_gene_variant | MODIFIER | c.-3099G>A| |
S79 S91 |
4 | BAA09g54960 | A09 | 55329117 | C | T | upstream_gene_variant | MODIFIER | c.-3089C>T| |
S163 |
5 | BAA09g54960 | A09 | 55329264 | C | T | upstream_gene_variant | MODIFIER | c.-2942C>T| |
S239 |
6 | BAA09g54960 | A09 | 55329367 | G | A | upstream_gene_variant | MODIFIER | c.-2839G>A| |
S177 |
7 | BAA09g54960 | A09 | 55329962 | G | A | upstream_gene_variant | MODIFIER | c.-2244G>A| |
S185 |
8 | BAA09g54960 | A09 | 55330005 | C | T | upstream_gene_variant | MODIFIER | c.-2201C>T| |
S183 |
9 | BAA09g54960 | A09 | 55330179 | G | A | upstream_gene_variant | MODIFIER | c.-2027G>A| |
S39 |
10 | BAA09g54960 | A09 | 55330367 | G | A | upstream_gene_variant | MODIFIER | c.-1839G>A| |
S84 |
11 | BAA09g54960 | A09 | 55330472 | C | T | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S68 |
12 | BAA09g54960 | A09 | 55330496 | C | T | upstream_gene_variant | MODIFIER | c.-1710C>T| |
S20 |
13 | BAA09g54960 | A09 | 55330701 | G | A | upstream_gene_variant | MODIFIER | c.-1505G>A| |
S88 |
14 | BAA09g54960 | A09 | 55331198 | C | T | upstream_gene_variant | MODIFIER | c.-1008C>T| |
S37 |
15 | BAA09g54960 | A09 | 55331254 | G | A | upstream_gene_variant | MODIFIER | c.-952G>A| |
S221 |
16 | BAA09g54960 | A09 | 55332547 | C | T | synonymous_variant | LOW | c.255C>T|p.Pro85Pro |
S134 |
17 | BAA09g54960 | A09 | 55332837 | C | T | missense_variant | MODERATE | c.545C>T|p.Thr182Ile |
S206 S26 |
18 | BAA09g54960 | A09 | 55332927 | C | T | missense_variant | MODERATE | c.635C>T|p.Ser212Phe |
S219 S72 |
19 | BAA09g54960 | A09 | 55334254 | C | T | missense_variant | MODERATE | c.1174C>T|p.His392Tyr |
S146 |
20 | BAA09g54960 | A09 | 55334917 | C | T | downstream_gene_variant | MODIFIER | c.*67C>T| |
S75 S81 |
21 | BAA09g54960 | A09 | 55335162 | C | T | downstream_gene_variant | MODIFIER | c.*312C>T| |
S201 |