| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g20960 | A07 | 25937043 | G | A | synonymous_variant | LOW | c.2130C>T|p.Phe710Phe |
S134 |
| 2 | BAA07g20960 | A07 | 25937687 | G | A | missense_variant | MODERATE | c.1486C>T|p.Leu496Phe |
S128 |
| 3 | BAA07g20960 | A07 | 25941610 | C | T | intron_variant | MODIFIER | c.1215+928G>A| |
S86 |
| 4 | BAA07g20960 | A07 | 25942461 | G | A | intron_variant | MODIFIER | c.1215+77C>T| |
S53 |
| 5 | BAA07g20960 | A07 | 25943111 | C | T | synonymous_variant | LOW | c.642G>A|p.Ala214Ala |
S279 |
| 6 | BAA07g20960 | A07 | 25943141 | C | T | stop_gained | HIGH | c.612G>A|p.Trp204* |
S42 |
| 7 | BAA07g20960 | A07 | 25944749 | G | A | upstream_gene_variant | MODIFIER | c.-777C>T| |
S74 |
| 8 | BAA07g20960 | A07 | 25944897 | C | T | upstream_gene_variant | MODIFIER | c.-925G>A| |
S168 |
| 9 | BAA07g20960 | A07 | 25948200 | C | T | upstream_gene_variant | MODIFIER | c.-4228G>A| |
S37 |