| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g02000 | A07 | 1479382 | G | A | synonymous_variant | LOW | c.474C>T|p.Phe158Phe |
S135 |
| 2 | BAA07g02000 | A07 | 1479686 | C | T | synonymous_variant | LOW | c.396G>A|p.Gln132Gln |
S189 |
| 3 | BAA07g02000 | A07 | 1480026 | G | A | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S72 S78 |
| 4 | BAA07g02000 | A07 | 1480093 | G | A | synonymous_variant | LOW | c.78C>T|p.Asn26Asn |
S171 |
| 5 | BAA07g02000 | A07 | 1480351 | G | A | upstream_gene_variant | MODIFIER | c.-181C>T| |
S158 S278 |
| 6 | BAA07g02000 | A07 | 1481749 | C | T | upstream_gene_variant | MODIFIER | c.-1579G>A| |
S130 |
| 7 | BAA07g02000 | A07 | 1481778 | G | A | upstream_gene_variant | MODIFIER | c.-1608C>T| |
S262 |
| 8 | BAA07g02000 | A07 | 1482165 | C | T | upstream_gene_variant | MODIFIER | c.-1995G>A| |
S274 |
| 9 | BAA07g02000 | A07 | 1485096 | C | T | upstream_gene_variant | MODIFIER | c.-4926G>A| |
S183 S198 |