| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 27951 | BAA01g19740 | A01 | 9730281 | C | T | downstream_gene_variant | MODIFIER | c.*394G>A| |
S128 |
| 27952 | BAA01g19740 | A01 | 9731189 | C | T | upstream_gene_variant | MODIFIER | c.-101G>A| |
S41 |
| 27953 | BAA01g19740 | A01 | 9731228 | G | A | upstream_gene_variant | MODIFIER | c.-140C>T| |
S291 |
| 27954 | BAA01g19740 | A01 | 9731513 | G | A | upstream_gene_variant | MODIFIER | c.-425C>T| |
S58 |
| 27955 | BAA01g19740 | A01 | 9731645 | G | A | upstream_gene_variant | MODIFIER | c.-557C>T| |
S43 |
| 27956 | BAA01g19740 | A01 | 9732683 | G | A | upstream_gene_variant | MODIFIER | c.-1595C>T| |
S57 |
| 27957 | BAA01g19740 | A01 | 9733692 | G | A | upstream_gene_variant | MODIFIER | c.-2604C>T| |
S71 |
| 27958 | BAA01g19740 | A01 | 9735475 | C | T | upstream_gene_variant | MODIFIER | c.-4387G>A| |
S170 |
| 27959 | BAA01g19740 | A01 | 9735570 | C | T | upstream_gene_variant | MODIFIER | c.-4482G>A| |
S79 |
| 27960 | BAA01g19740 | A01 | 9735919 | G | A | upstream_gene_variant | MODIFIER | c.-4831C>T| |
S287 |
| 27961 | BAA01g19740 | A01 | 9736074 | G | A | upstream_gene_variant | MODIFIER | c.-4986C>T| |
S95 |
| 27962 | BAA01g19750 | A01 | 9737230 | G | A | downstream_gene_variant | MODIFIER | c.*338C>T| |
S131 |
| 27963 | BAA01g19750 | A01 | 9737920 | C | T | intron_variant | MODIFIER | c.274-10G>A| |
S260 |
| 27964 | BAA01g19750 | A01 | 9738669 | C | T | upstream_gene_variant | MODIFIER | c.-368G>A| |
S153 |
| 27965 | BAA01g19750 | A01 | 9739315 | C | T | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S179 |
| 27966 | BAA01g19750 | A01 | 9739577 | C | T | upstream_gene_variant | MODIFIER | c.-1276G>A| |
S135 |
| 27967 | BAA01g19750 | A01 | 9739586 | C | T | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S198 |
| 27968 | BAA01g19750 | A01 | 9740101 | G | A | upstream_gene_variant | MODIFIER | c.-1800C>T| |
S180 |
| 27969 | BAA01g19750 | A01 | 9740922 | C | T | upstream_gene_variant | MODIFIER | c.-2621G>A| |
S213 |
| 27970 | BAA01g19750 | A01 | 9741813 | G | A | upstream_gene_variant | MODIFIER | c.-3512C>T| |
S281 |
| 27971 | BAA01g19760 | A01 | 9744342 | C | T | upstream_gene_variant | MODIFIER | c.-103C>T| |
S134 |
| 27972 | BAA01g19760 | A01 | 9744602 | C | T | missense_variant | MODERATE | c.158C>T|p.Pro53Leu |
S33 |
| 27973 | BAA01g19760 | A01 | 9744688 | G | A | intron_variant | MODIFIER | c.220+24G>A| |
S98 |
| 27974 | BAA01g19760 | A01 | 9745697 | C | T | downstream_gene_variant | MODIFIER | c.*683C>T| |
S289 S290 |
| 27975 | BAA01g19760 | A01 | 9745785 | C | T | downstream_gene_variant | MODIFIER | c.*771C>T| |
S111 |