Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g41580 | A07 | 36418757 | G | A | missense_variant | MODERATE | c.1669C>T|p.Pro557Ser |
S210 S225 |
2 | BAA07g41580 | A07 | 36419041 | C | T | missense_variant | MODERATE | c.1385G>A|p.Gly462Glu |
S25 S264 |
3 | BAA07g41580 | A07 | 36419495 | G | A | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S170 |
4 | BAA07g41580 | A07 | 36420643 | G | A | synonymous_variant | LOW | c.531C>T|p.Thr177Thr |
S299 |
5 | BAA07g41580 | A07 | 36421270 | G | A | synonymous_variant | LOW | c.294C>T|p.Ile98Ile |
S302 |
6 | BAA07g41580 | A07 | 36421481 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Leu |
S247 |
7 | BAA07g41580 | A07 | 36422053 | C | T | upstream_gene_variant | MODIFIER | c.-490G>A| |
S129 |
8 | BAA07g41580 | A07 | 36422678 | C | T | upstream_gene_variant | MODIFIER | c.-1115G>A| |
S252 |
9 | BAA07g41580 | A07 | 36423208 | G | A | upstream_gene_variant | MODIFIER | c.-1645C>T| |
S186 |