Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g58130 | A09 | 57016949 | G | A | synonymous_variant | LOW | c.2400C>T|p.Phe800Phe |
S218 |
2 | BAA09g58130 | A09 | 57017399 | G | A | synonymous_variant | LOW | c.2115C>T|p.Ile705Ile |
S111 |
3 | BAA09g58130 | A09 | 57017452 | C | T | missense_variant | MODERATE | c.2062G>A|p.Val688Ile |
S173 |
4 | BAA09g58130 | A09 | 57018391 | G | A | missense_variant | MODERATE | c.1475C>T|p.Ser492Phe |
S216 |
5 | BAA09g58130 | A09 | 57018899 | C | T | missense_variant | MODERATE | c.1237G>A|p.Ala413Thr |
S20 |
6 | BAA09g58130 | A09 | 57020674 | C | T | synonymous_variant | LOW | c.627G>A|p.Arg209Arg |
S107 |
7 | BAA09g58130 | A09 | 57020755 | C | T | synonymous_variant | LOW | c.546G>A|p.Lys182Lys |
S299 |
8 | BAA09g58130 | A09 | 57021017 | G | A | intron_variant | MODIFIER | c.433-72C>T| |
S295 |
9 | BAA09g58130 | A09 | 57021266 | C | T | synonymous_variant | LOW | c.384G>A|p.Leu128Leu |
S229 |
10 | BAA09g58130 | A09 | 57023442 | G | A | upstream_gene_variant | MODIFIER | c.-1489C>T| |
S130 |
11 | BAA09g58130 | A09 | 57023549 | C | T | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S204 |
12 | BAA09g58130 | A09 | 57023885 | C | T | upstream_gene_variant | MODIFIER | c.-1932G>A| |
S5 |
13 | BAA09g58130 | A09 | 57025094 | G | A | upstream_gene_variant | MODIFIER | c.-3141C>T| |
S34 |
14 | BAA09g58130 | A09 | 57026069 | G | A | upstream_gene_variant | MODIFIER | c.-4116C>T| |
S284 |
15 | BAA09g58130 | A09 | 57026445 | C | T | upstream_gene_variant | MODIFIER | c.-4492G>A| |
S192 |
16 | BAA09g58130 | A09 | 57026517 | G | A | upstream_gene_variant | MODIFIER | c.-4564C>T| |
S225 S73 |