| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 165401 | BAA02g11620 | A02 | 5252447 | G | A | upstream_gene_variant | MODIFIER | c.-1216G>A| |
S192 |
| 165402 | BAA02g11620 | A02 | 5253294 | C | T | upstream_gene_variant | MODIFIER | c.-369C>T| |
S157 S163 |
| 165403 | BAA02g11620 | A02 | 5253992 | C | T | synonymous_variant | LOW | c.330C>T|p.Asn110Asn |
S299 |
| 165404 | BAA02g11620 | A02 | 5254052 | C | T | synonymous_variant | LOW | c.390C>T|p.Phe130Phe |
S51 |
| 165405 | BAA02g11620 | A02 | 5254370 | G | A | synonymous_variant | LOW | c.708G>A|p.Arg236Arg |
S57 |
| 165406 | BAA02g11620 | A02 | 5254875 | G | A | missense_variant | MODERATE | c.1213G>A|p.Glu405Lys |
S107 |
| 165407 | BAA02g11620 | A02 | 5254923 | C | T | missense_variant | MODERATE | c.1261C>T|p.Leu421Phe |
S194 |
| 165408 | BAA02g11620 | A02 | 5255116 | A | C | missense_variant | MODERATE | c.1454A>C|p.Lys485Thr |
S150 S240 S67 |
| 165409 | BAA02g11620 | A02 | 5255190 | G | A | missense_variant | MODERATE | c.1528G>A|p.Glu510Lys |
S52 |
| 165410 | BAA02g11620 | A02 | 5255274 | G | A | missense_variant | MODERATE | c.1612G>A|p.Asp538Asn |
S143 |
| 165411 | BAA02g11620 | A02 | 5255637 | G | A | downstream_gene_variant | MODIFIER | c.*115G>A| |
S158 |
| 165412 | BAA02g11620 | A02 | 5255839 | G | A | downstream_gene_variant | MODIFIER | c.*317G>A| |
S271 |
| 165413 | BAA02g11620 | A02 | 5256259 | A | G | downstream_gene_variant | MODIFIER | c.*737A>G| |
S216 |
| 165414 | BAA02g11620 | A02 | 5256420 | G | A | downstream_gene_variant | MODIFIER | c.*898G>A| |
S20 |
| 165415 | BAA02g11620 | A02 | 5256955 | G | A | downstream_gene_variant | MODIFIER | c.*1433G>A| |
S221 |
| 165416 | BAA02g11630 | A02 | 5258687 | C | T | upstream_gene_variant | MODIFIER | c.-526G>A| |
S208 S219 |
| 165417 | BAA02g11630 | A02 | 5258919 | C | T | upstream_gene_variant | MODIFIER | c.-758G>A| |
S257 |
| 165418 | BAA02g11640 | A02 | 5259127 | C | T | missense_variant | MODERATE | c.1715G>A|p.Gly572Glu |
S299 |
| 165419 | BAA02g11640 | A02 | 5259921 | G | A | missense_variant | MODERATE | c.1187C>T|p.Thr396Ile |
S89 |
| 165420 | BAA02g11640 | A02 | 5260183 | G | A | synonymous_variant | LOW | c.1005C>T|p.Leu335Leu |
S148 S210 S30 S31 |
| 165421 | BAA02g11630 | A02 | 5262054 | C | T | upstream_gene_variant | MODIFIER | c.-3893G>A| |
S13 |
| 165422 | BAA02g11630 | A02 | 5262437 | G | A | upstream_gene_variant | MODIFIER | c.-4276C>T| |
S265 |
| 165423 | BAA02g11630 | A02 | 5262673 | G | A | upstream_gene_variant | MODIFIER | c.-4512C>T| |
S149 |
| 165424 | BAA02g11630 | A02 | 5262951 | G | A | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S155 S211 |
| 165425 | BAA02g11650 | A02 | 5263984 | G | A | synonymous_variant | LOW | c.174C>T|p.Val58Val |
S210 |