| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 197451 | BAA02g29300 | A02 | 16753832 | C | T | upstream_gene_variant | MODIFIER | c.-1710G>A| |
S100 |
| 197452 | BAA02g29300 | A02 | 16753989 | G | A | upstream_gene_variant | MODIFIER | c.-1867C>T| |
S7 |
| 197453 | BAA02g29300 | A02 | 16754079 | C | T | upstream_gene_variant | MODIFIER | c.-1957G>A| |
S11 |
| 197454 | BAA02g29310 | A02 | 16757053 | G | A | missense_variant&splice_region_variant | MODERATE | c.2239C>T|p.Pro747Ser |
S69 |
| 197455 | BAA02g29310 | A02 | 16758069 | G | A | missense_variant | MODERATE | c.1646C>T|p.Ser549Phe |
S186 |
| 197456 | BAA02g29310 | A02 | 16758204 | G | A | missense_variant | MODERATE | c.1511C>T|p.Ser504Phe |
S268 |
| 197457 | BAA02g29310 | A02 | 16758822 | C | T | intron_variant | MODIFIER | c.1268+25G>A| |
S39 |
| 197458 | BAA02g29310 | A02 | 16759550 | G | A | intron_variant | MODIFIER | c.642+39C>T| |
S111 |
| 197459 | BAA02g29310 | A02 | 16760644 | C | T | upstream_gene_variant | MODIFIER | c.-28G>A| |
S276 |
| 197460 | BAA02g29310 | A02 | 16760687 | G | A | upstream_gene_variant | MODIFIER | c.-71C>T| |
S69 |
| 197461 | BAA02g29310 | A02 | 16761237 | C | T | upstream_gene_variant | MODIFIER | c.-621G>A| |
S245 |
| 197462 | BAA02g29310 | A02 | 16765085 | C | T | upstream_gene_variant | MODIFIER | c.-4469G>A| |
S296 |
| 197463 | BAA02g29310 | A02 | 16765446 | G | A | upstream_gene_variant | MODIFIER | c.-4830C>T| |
S41 |
| 197464 | BAA02g29320 | A02 | 16766447 | C | T | upstream_gene_variant | MODIFIER | c.-202G>A| |
S221 |
| 197465 | BAA02g29330 | A02 | 16767301 | C | T | missense_variant | MODERATE | c.1619G>A|p.Cys540Tyr |
S77 |
| 197466 | BAA02g29330 | A02 | 16767447 | C | T | synonymous_variant | LOW | c.1473G>A|p.Ser491Ser |
S293 |
| 197467 | BAA02g29330 | A02 | 16768378 | C | T | missense_variant | MODERATE | c.664G>A|p.Val222Met |
S240 |
| 197468 | BAA02g29320 | A02 | 16768671 | C | T | upstream_gene_variant | MODIFIER | c.-2426G>A| |
S303 |
| 197469 | BAA02g29320 | A02 | 16769072 | G | A | upstream_gene_variant | MODIFIER | c.-2827C>T| |
S295 |
| 197470 | BAA02g29320 | A02 | 16769664 | C | T | upstream_gene_variant | MODIFIER | c.-3419G>A| |
S171 |
| 197471 | BAA02g29320 | A02 | 16770323 | G | A | upstream_gene_variant | MODIFIER | c.-4078C>T| |
S33 |
| 197472 | BAA02g29330 | A02 | 16771412 | C | T | intron_variant | MODIFIER | c.545-965G>A| |
S78 |
| 197473 | BAA02g29330 | A02 | 16771420 | G | T | intron_variant | MODIFIER | c.545-973C>A| |
S129 |
| 197474 | BAA02g29330 | A02 | 16772180 | C | T | intron_variant | MODIFIER | c.545-1733G>A| |
S53 |
| 197475 | BAA02g29330 | A02 | 16772539 | G | A | intron_variant | MODIFIER | c.545-2092C>T| |
S125 |