| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g02330 | A06 | 1418049 | C | T | synonymous_variant | LOW | c.144C>T|p.Ile48Ile |
S225 |
| 2 | BAA06g02330 | A06 | 1418865 | G | A | splice_donor_variant&intron_variant | HIGH | c.657+1G>A| |
S174 |
| 3 | BAA06g02330 | A06 | 1419088 | C | T | missense_variant | MODERATE | c.800C>T|p.Pro267Leu |
S116 |
| 4 | BAA06g02330 | A06 | 1419180 | C | T | missense_variant | MODERATE | c.892C>T|p.Pro298Ser |
S158 |
| 5 | BAA06g02330 | A06 | 1419233 | G | A | synonymous_variant | LOW | c.945G>A|p.Gly315Gly |
S233 |
| 6 | BAA06g02330 | A06 | 1419614 | C | T | stop_gained | HIGH | c.1174C>T|p.Arg392* |
S134 |
| 7 | BAA06g02330 | A06 | 1419726 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1200-1G>A| |
S152 |
| 8 | BAA06g02330 | A06 | 1420756 | C | T | synonymous_variant | LOW | c.1602C>T|p.His534His |
S5 |
| 9 | BAA06g02330 | A06 | 1420996 | C | T | missense_variant | MODERATE | c.1768C>T|p.Leu590Phe |
S133 S301 S304 |
| 10 | BAA06g02330 | A06 | 1421106 | C | T | missense_variant | MODERATE | c.1805C>T|p.Thr602Ile |
S127 |
| 11 | BAA06g02330 | A06 | 1421413 | C | T | synonymous_variant | LOW | c.2112C>T|p.Tyr704Tyr |
S293 |
| 12 | BAA06g02330 | A06 | 1421893 | G | A | synonymous_variant | LOW | c.2433G>A|p.Glu811Glu |
S87 |