| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 194451 | BAA02g27940 | A02 | 15742232 | C | T | downstream_gene_variant | MODIFIER | c.*2307C>T| |
S100 S82 |
| 194452 | BAA02g27940 | A02 | 15742916 | C | T | downstream_gene_variant | MODIFIER | c.*2991C>T| |
S289 S290 |
| 194453 | BAA02g27940 | A02 | 15743559 | C | T | downstream_gene_variant | MODIFIER | c.*3634C>T| |
S193 |
| 194454 | BAA02g27940 | A02 | 15744353 | G | A | downstream_gene_variant | MODIFIER | c.*4428G>A| |
S298 |
| 194455 | BAA02g27940 | A02 | 15744493 | C | T | downstream_gene_variant | MODIFIER | c.*4568C>T| |
S218 |
| 194456 | BAA02g27950 | A02 | 15745095 | C | T | upstream_gene_variant | MODIFIER | c.-4655C>T| |
S286 |
| 194457 | BAA02g27950 | A02 | 15745750 | C | T | upstream_gene_variant | MODIFIER | c.-4000C>T| |
S51 |
| 194458 | BAA02g27950 | A02 | 15746431 | C | T | upstream_gene_variant | MODIFIER | c.-3319C>T| |
S178 |
| 194459 | BAA02g27950 | A02 | 15747696 | C | T | upstream_gene_variant | MODIFIER | c.-2054C>T| |
S8 |
| 194460 | BAA02g27950 | A02 | 15747756 | C | T | upstream_gene_variant | MODIFIER | c.-1994C>T| |
S219 |
| 194461 | BAA02g27950 | A02 | 15747812 | C | T | upstream_gene_variant | MODIFIER | c.-1938C>T| |
S32 |
| 194462 | BAA02g27950 | A02 | 15748580 | G | A | upstream_gene_variant | MODIFIER | c.-1170G>A| |
S174 S216 S27 |
| 194463 | BAA02g27950 | A02 | 15748642 | A | T | upstream_gene_variant | MODIFIER | c.-1108A>T| |
S272 |
| 194464 | BAA02g27950 | A02 | 15749805 | G | A | missense_variant | MODERATE | c.56G>A|p.Arg19Lys |
S38 |
| 194465 | BAA02g27950 | A02 | 15749864 | C | T | stop_gained | HIGH | c.115C>T|p.Gln39* |
S264 |
| 194466 | BAA02g27950 | A02 | 15750724 | C | T | missense_variant | MODERATE | c.554C>T|p.Ser185Phe |
S181 |
| 194467 | BAA02g27950 | A02 | 15751412 | C | T | synonymous_variant | LOW | c.1242C>T|p.Gly414Gly |
S49 |
| 194468 | BAA02g27950 | A02 | 15751565 | G | A | splice_region_variant&intron_variant | LOW | c.1324-6G>A| |
S148 S30 S31 |
| 194469 | BAA02g27950 | A02 | 15751629 | G | A | missense_variant | MODERATE | c.1382G>A|p.Gly461Glu |
S81 |
| 194470 | BAA02g27960 | A02 | 15753121 | C | T | upstream_gene_variant | MODIFIER | c.-765C>T| |
S164 |
| 194471 | BAA02g27960 | A02 | 15753157 | G | A | upstream_gene_variant | MODIFIER | c.-729G>A| |
S197 |
| 194472 | BAA02g27960 | A02 | 15753272 | C | T | upstream_gene_variant | MODIFIER | c.-614C>T| |
S159 S188 S243 S276 S298 S299 |
| 194473 | BAA02g27960 | A02 | 15753618 | C | T | upstream_gene_variant | MODIFIER | c.-268C>T| |
S14 |
| 194474 | BAA02g27960 | A02 | 15754168 | G | A | missense_variant | MODERATE | c.283G>A|p.Val95Ile |
S38 |
| 194475 | BAA02g27970 | A02 | 15754822 | C | T | upstream_gene_variant | MODIFIER | c.-1475C>T| |
S299 |