| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g21020 | A05 | 13206342 | C | T | upstream_gene_variant | MODIFIER | c.-4591C>T| |
S202 |
| 2 | BAA05g21020 | A05 | 13207141 | C | T | upstream_gene_variant | MODIFIER | c.-3792C>T| |
S176 |
| 3 | BAA05g21020 | A05 | 13207219 | G | A | upstream_gene_variant | MODIFIER | c.-3714G>A| |
S176 |
| 4 | BAA05g21020 | A05 | 13207541 | G | A | upstream_gene_variant | MODIFIER | c.-3392G>A| |
S192 |
| 5 | BAA05g21020 | A05 | 13207674 | C | T | upstream_gene_variant | MODIFIER | c.-3259C>T| |
S239 S33 |
| 6 | BAA05g21020 | A05 | 13208186 | C | T | upstream_gene_variant | MODIFIER | c.-2747C>T| |
S57 |
| 7 | BAA05g21020 | A05 | 13211573 | G | A | missense_variant | MODERATE | c.454G>A|p.Asp152Asn |
S122 |
| 8 | BAA05g21020 | A05 | 13212100 | G | A | splice_region_variant&intron_variant | LOW | c.718-4G>A| |
S262 |
| 9 | BAA05g21020 | A05 | 13212248 | C | T | missense_variant | MODERATE | c.862C>T|p.Pro288Ser |
S262 |