| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g47460 | A09 | 51741071 | C | T | missense_variant | MODERATE | c.1516G>A|p.Asp506Asn |
S228 |
| 2 | BAA09g47460 | A09 | 51741765 | G | A | synonymous_variant | LOW | c.1353C>T|p.Ser451Ser |
S252 |
| 3 | BAA09g47460 | A09 | 51741939 | C | T | splice_donor_variant&intron_variant | HIGH | c.1271+1G>A| |
S279 |
| 4 | BAA09g47460 | A09 | 51742609 | G | A | missense_variant | MODERATE | c.898C>T|p.Leu300Phe |
S11 |
| 5 | BAA09g47460 | A09 | 51745063 | C | T | upstream_gene_variant | MODIFIER | c.-780G>A| |
S272 |
| 6 | BAA09g47460 | A09 | 51745521 | G | A | upstream_gene_variant | MODIFIER | c.-1238C>T| |
S203 |
| 7 | BAA09g47460 | A09 | 51746311 | G | A | upstream_gene_variant | MODIFIER | c.-2028C>T| |
S11 |
| 8 | BAA09g47460 | A09 | 51747012 | C | T | upstream_gene_variant | MODIFIER | c.-2729G>A| |
S25 |