| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g26450 | A09 | 17185526 | G | A | upstream_gene_variant | MODIFIER | c.-269G>A| |
S245 S265 S298 |
| 2 | BAA09g26450 | A09 | 17185911 | G | A | synonymous_variant | LOW | c.117G>A|p.Leu39Leu |
S57 |
| 3 | BAA09g26450 | A09 | 17186045 | G | A | intron_variant | MODIFIER | c.175-11G>A| |
S251 |
| 4 | BAA09g26450 | A09 | 17186112 | C | T | synonymous_variant | LOW | c.231C>T|p.His77His |
S99 |
| 5 | BAA09g26450 | A09 | 17186926 | C | T | missense_variant | MODERATE | c.1045C>T|p.His349Tyr |
S171 |
| 6 | BAA09g26450 | A09 | 17187231 | T | A | synonymous_variant | LOW | c.1350T>A|p.Pro450Pro |
S9 |
| 7 | BAA09g26450 | A09 | 17187569 | A | G | intron_variant | MODIFIER | c.1559-65A>G| |
S130 S182 |
| 8 | BAA09g26450 | A09 | 17187620 | C | T | intron_variant | MODIFIER | c.1559-14C>T| |
S58 |
| 9 | BAA09g26450 | A09 | 17187637 | G | A | missense_variant | MODERATE | c.1562G>A|p.Gly521Glu |
S192 |
| 10 | BAA09g26450 | A09 | 17187689 | G | A | synonymous_variant | LOW | c.1614G>A|p.Pro538Pro |
S87 |
| 11 | BAA09g26450 | A09 | 17188241 | C | T | synonymous_variant | LOW | c.2166C>T|p.Asp722Asp |
S212 |
| 12 | BAA09g26450 | A09 | 17188367 | C | T | synonymous_variant | LOW | c.2292C>T|p.Ser764Ser |
S148 S210 |
| 13 | BAA09g26450 | A09 | 17188805 | G | A | synonymous_variant | LOW | c.2730G>A|p.Arg910Arg |
S126 |
| 14 | BAA09g26450 | A09 | 17196864 | C | T | downstream_gene_variant | MODIFIER | c.*4450C>T| |
S43 |