Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g24580 | A07 | 27811943 | C | T | downstream_gene_variant | MODIFIER | c.*1333G>A| |
S8 |
2 | BAA07g24580 | A07 | 27813380 | C | T | missense_variant | MODERATE | c.1717G>A|p.Ala573Thr |
S219 S279 |
3 | BAA07g24580 | A07 | 27813910 | G | C | synonymous_variant | LOW | c.1356C>G|p.Ala452Ala |
S125 S178 S234 |
4 | BAA07g24580 | A07 | 27814564 | C | T | missense_variant | MODERATE | c.853G>A|p.Gly285Arg |
S174 |
5 | BAA07g24580 | A07 | 27814672 | G | A | intron_variant | MODIFIER | c.818+19C>T| |
S36 |
6 | BAA07g24580 | A07 | 27814829 | G | A | splice_region_variant&intron_variant | LOW | c.763+4C>T| |
S7 |
7 | BAA07g24580 | A07 | 27814919 | G | A | missense_variant | MODERATE | c.677C>T|p.Thr226Ile |
S209 |
8 | BAA07g24580 | A07 | 27820985 | C | T | upstream_gene_variant | MODIFIER | c.-4885G>A| |
S113 |
9 | BAA07g24580 | A07 | 27820989 | G | A | upstream_gene_variant | MODIFIER | c.-4889C>T| |
S140 |