Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19030 | A09 | 11497760 | C | T | upstream_gene_variant | MODIFIER | c.-4681C>T| |
S295 |
2 | BAA09g19030 | A09 | 11498270 | C | T | upstream_gene_variant | MODIFIER | c.-4171C>T| |
S295 |
3 | BAA09g19030 | A09 | 11500158 | C | T | upstream_gene_variant | MODIFIER | c.-2283C>T| |
S219 |
4 | BAA09g19030 | A09 | 11501454 | C | T | upstream_gene_variant | MODIFIER | c.-987C>T| |
S19 |
5 | BAA09g19030 | A09 | 11503117 | G | A | missense_variant | MODERATE | c.677G>A|p.Arg226Lys |
S202 |
6 | BAA09g19030 | A09 | 11503314 | C | T | intron_variant | MODIFIER | c.838+36C>T| |
S30 S31 |
7 | BAA09g19030 | A09 | 11504004 | G | A | missense_variant | MODERATE | c.1367G>A|p.Gly456Glu |
S201 |
8 | BAA09g19030 | A09 | 11504340 | C | T | missense_variant | MODERATE | c.1703C>T|p.Ser568Phe |
S50 |
9 | BAA09g19030 | A09 | 11504714 | G | A | missense_variant | MODERATE | c.2077G>A|p.Val693Ile |
S236 |
10 | BAA09g19030 | A09 | 11504988 | C | T | missense_variant | MODERATE | c.2351C>T|p.Ser784Phe |
S133 |
11 | BAA09g19030 | A09 | 11505200 | G | A | missense_variant | MODERATE | c.2563G>A|p.Glu855Lys |
S266 |
12 | BAA09g19030 | A09 | 11505246 | C | T | missense_variant | MODERATE | c.2609C>T|p.Ser870Phe |
S153 |
13 | BAA09g19030 | A09 | 11505461 | C | T | downstream_gene_variant | MODIFIER | c.*34C>T| |
S107 |
14 | BAA09g19030 | A09 | 11506050 | G | A | downstream_gene_variant | MODIFIER | c.*623G>A| |
S130 |
15 | BAA09g19030 | A09 | 11506305 | C | T | downstream_gene_variant | MODIFIER | c.*878C>T| |
S303 |
16 | BAA09g19030 | A09 | 11506469 | G | A | downstream_gene_variant | MODIFIER | c.*1042G>A| |
S55 |
17 | BAA09g19030 | A09 | 11507833 | C | T | downstream_gene_variant | MODIFIER | c.*2406C>T| |
S296 |
18 | BAA09g19030 | A09 | 11509128 | C | T | downstream_gene_variant | MODIFIER | c.*3701C>T| |
S37 |