| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g39080 | A09 | 46792602 | C | T | missense_variant | MODERATE | c.1429G>A|p.Glu477Lys |
S174 |
| 2 | BAA09g39080 | A09 | 46793630 | G | A | synonymous_variant | LOW | c.975C>T|p.Val325Val |
S124 |
| 3 | BAA09g39080 | A09 | 46793740 | C | T | missense_variant | MODERATE | c.865G>A|p.Asp289Asn |
S135 |
| 4 | BAA09g39080 | A09 | 46794580 | G | A | missense_variant | MODERATE | c.25C>T|p.Leu9Phe |
S136 |
| 5 | BAA09g39080 | A09 | 46795138 | G | A | upstream_gene_variant | MODIFIER | c.-534C>T| |
S71 |
| 6 | BAA09g39080 | A09 | 46795414 | C | T | upstream_gene_variant | MODIFIER | c.-810G>A| |
S293 |
| 7 | BAA09g39080 | A09 | 46795856 | G | A | upstream_gene_variant | MODIFIER | c.-1252C>T| |
S116 |
| 8 | BAA09g39080 | A09 | 46796082 | G | A | upstream_gene_variant | MODIFIER | c.-1478C>T| |
S194 |
| 9 | BAA09g39080 | A09 | 46796255 | G | A | upstream_gene_variant | MODIFIER | c.-1651C>T| |
S35 |
| 10 | BAA09g39080 | A09 | 46798258 | G | A | upstream_gene_variant | MODIFIER | c.-3654C>T| |
S265 |
| 11 | BAA09g39080 | A09 | 46798849 | A | T | upstream_gene_variant | MODIFIER | c.-4245T>A| |
S233 |