| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g27510 | A09 | 18009009 | G | A | upstream_gene_variant | MODIFIER | c.-4987G>A| |
S33 |
| 2 | BAA09g27510 | A09 | 18009147 | G | A | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S69 |
| 3 | BAA09g27510 | A09 | 18009939 | C | T | upstream_gene_variant | MODIFIER | c.-4057C>T| |
S277 |
| 4 | BAA09g27510 | A09 | 18011967 | G | A | upstream_gene_variant | MODIFIER | c.-2029G>A| |
S223 |
| 5 | BAA09g27510 | A09 | 18012342 | C | T | upstream_gene_variant | MODIFIER | c.-1654C>T| |
S241 |
| 6 | BAA09g27510 | A09 | 18012488 | C | T | upstream_gene_variant | MODIFIER | c.-1508C>T| |
S179 |
| 7 | BAA09g27510 | A09 | 18012867 | C | T | upstream_gene_variant | MODIFIER | c.-1129C>T| |
S306 S308 |
| 8 | BAA09g27510 | A09 | 18013112 | C | T | upstream_gene_variant | MODIFIER | c.-884C>T| |
S188 |
| 9 | BAA09g27510 | A09 | 18013137 | C | T | upstream_gene_variant | MODIFIER | c.-859C>T| |
S148 S210 |
| 10 | BAA09g27510 | A09 | 18013578 | G | A | upstream_gene_variant | MODIFIER | c.-418G>A| |
S183 S198 |
| 11 | BAA09g27510 | A09 | 18013940 | G | A | upstream_gene_variant | MODIFIER | c.-56G>A| |
S266 |
| 12 | BAA09g27510 | A09 | 18014398 | G | A | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S209 |
| 13 | BAA09g27510 | A09 | 18014614 | G | A | missense_variant | MODERATE | c.619G>A|p.Gly207Arg |
S210 S225 |
| 14 | BAA09g27510 | A09 | 18014655 | G | A | synonymous_variant | LOW | c.660G>A|p.Arg220Arg |
S65 |
| 15 | BAA09g27510 | A09 | 18015407 | G | A | synonymous_variant | LOW | c.1158G>A|p.Lys386Lys |
S157 S163 |
| 16 | BAA09g27510 | A09 | 18016061 | G | A | missense_variant | MODERATE | c.1632G>A|p.Met544Ile |
S149 |
| 17 | BAA09g27510 | A09 | 18016577 | C | T | synonymous_variant | LOW | c.1992C>T|p.Phe664Phe |
S30 S31 |
| 18 | BAA09g27510 | A09 | 18016696 | G | A | intron_variant | MODIFIER | c.2088+23G>A| |
S79 S91 |
| 19 | BAA09g27510 | A09 | 18016705 | C | T | intron_variant | MODIFIER | c.2088+32C>T| |
S144 |
| 20 | BAA09g27510 | A09 | 18016896 | G | A | missense_variant | MODERATE | c.2230G>A|p.Gly744Arg |
S44 |
| 21 | BAA09g27510 | A09 | 18017298 | C | T | missense_variant | MODERATE | c.2551C>T|p.Leu851Phe |
S257 |
| 22 | BAA09g27510 | A09 | 18017964 | T | C | downstream_gene_variant | MODIFIER | c.*637T>C| |
S303 |
| 23 | BAA09g27510 | A09 | 18018390 | G | A | downstream_gene_variant | MODIFIER | c.*1063G>A| |
S183 S198 |
| 24 | BAA09g27510 | A09 | 18019060 | G | A | downstream_gene_variant | MODIFIER | c.*1733G>A| |
S134 |
| 25 | BAA09g27510 | A09 | 18021065 | G | A | downstream_gene_variant | MODIFIER | c.*3738G>A| |
S181 |