| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g04600 | A07 | 3802263 | G | A | upstream_gene_variant | MODIFIER | c.-3314G>A| |
S110 |
| 2 | BAA07g04600 | A07 | 3802506 | C | T | upstream_gene_variant | MODIFIER | c.-3071C>T| |
|
| 3 | BAA07g04600 | A07 | 3805677 | C | T | missense_variant | MODERATE | c.101C>T|p.Ser34Phe |
S13 |
| 4 | BAA07g04600 | A07 | 3805993 | C | T | synonymous_variant | LOW | c.417C>T|p.Ser139Ser |
S95 |
| 5 | BAA07g04600 | A07 | 3806733 | A | C | missense_variant | MODERATE | c.1049A>C|p.Lys350Thr |
S138 S173 S271 S275 S42 S48 |
| 6 | BAA07g04600 | A07 | 3807674 | C | T | missense_variant | MODERATE | c.1990C>T|p.His664Tyr |
S4 |
| 7 | BAA07g04600 | A07 | 3807972 | C | T | missense_variant | MODERATE | c.2288C>T|p.Pro763Leu |
S156 |
| 8 | BAA07g04600 | A07 | 3807979 | C | T | synonymous_variant | LOW | c.2295C>T|p.Val765Val |
S118 |