Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01120 | A04 | 649255 | C | G | synonymous_variant | LOW | c.690G>C|p.Gly230Gly |
S238 S257 S267 |
2 | BAA04g01120 | A04 | 649267 | A | G | synonymous_variant | LOW | c.678T>C|p.His226His |
S238 S257 S267 |
3 | BAA04g01120 | A04 | 649324 | T | C | synonymous_variant | LOW | c.621A>G|p.Lys207Lys |
S213 S257 S267 |
4 | BAA04g01120 | A04 | 649327 | A | G | synonymous_variant | LOW | c.618T>C|p.Thr206Thr |
S213 S257 S267 |
5 | BAA04g01120 | A04 | 649335 | G | A | synonymous_variant | LOW | c.610C>T|p.Leu204Leu |
S213 S257 S267 |
6 | BAA04g01120 | A04 | 649344 | T | G | missense_variant | MODERATE | c.601A>C|p.Ile201Leu |
S213 S257 S267 |
7 | BAA04g01120 | A04 | 649396 | C | T | synonymous_variant | LOW | c.549G>A|p.Pro183Pro |
S257 S267 |
8 | BAA04g01120 | A04 | 649402 | T | A | synonymous_variant | LOW | c.543A>T|p.Gly181Gly |
S257 S267 |
9 | BAA04g01120 | A04 | 649440 | T | C | missense_variant | MODERATE | c.505A>G|p.Ile169Val |
S220 S257 S267 |
10 | BAA04g01120 | A04 | 649468 | A | G | synonymous_variant | LOW | c.477T>C|p.Ile159Ile |
S220 S257 |
11 | BAA04g01120 | A04 | 649492 | C | T | synonymous_variant | LOW | c.453G>A|p.Glu151Glu |
S220 S257 |
12 | BAA04g01120 | A04 | 649495 | G | T | synonymous_variant | LOW | c.450C>A|p.Ala150Ala |
S220 S257 |
13 | BAA04g01120 | A04 | 649504 | T | G | synonymous_variant | LOW | c.441A>C|p.Ile147Ile |
S220 S257 |
14 | BAA04g01120 | A04 | 649507 | T | C | synonymous_variant | LOW | c.438A>G|p.Leu146Leu |
S220 S257 |
15 | BAA04g01120 | A04 | 649510 | G | A | synonymous_variant | LOW | c.435C>T|p.Ile145Ile |
S220 S257 |
16 | BAA04g01120 | A04 | 649535 | G | A | missense_variant | MODERATE | c.410C>T|p.Thr137Ile |
S112 |
17 | BAA04g01120 | A04 | 650485 | C | T | upstream_gene_variant | MODIFIER | c.-186G>A| |
S20 |