| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g01710 | A01 | 767589 | C | T | upstream_gene_variant | MODIFIER | c.-2189C>T| |
S71 |
| 2 | BAA01g01710 | A01 | 768977 | G | A | upstream_gene_variant | MODIFIER | c.-801G>A| |
S32 |
| 3 | BAA01g01710 | A01 | 769045 | C | T | upstream_gene_variant | MODIFIER | c.-733C>T| |
S223 |
| 4 | BAA01g01710 | A01 | 770018 | G | A | missense_variant | MODERATE | c.241G>A|p.Val81Met |
S60 |
| 5 | BAA01g01710 | A01 | 770176 | C | T | synonymous_variant | LOW | c.399C>T|p.Arg133Arg |
S164 |
| 6 | BAA01g01710 | A01 | 770864 | G | A | synonymous_variant | LOW | c.717G>A|p.Thr239Thr |
S308 |
| 7 | BAA01g01710 | A01 | 771523 | G | A | missense_variant | MODERATE | c.1261G>A|p.Glu421Lys |
S262 |
| 8 | BAA01g01710 | A01 | 771767 | C | T | missense_variant | MODERATE | c.1505C>T|p.Ser502Phe |
S170 S176 |