| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 179551 | BAA02g19860 | A02 | 10440412 | C | T | missense_variant | MODERATE | c.1663G>A|p.Val555Ile |
S124 |
| 179552 | BAA02g19860 | A02 | 10441592 | T | A | intron_variant | MODIFIER | c.755-92A>T| |
S172 S217 |
| 179553 | BAA02g19860 | A02 | 10445299 | G | A | upstream_gene_variant | MODIFIER | c.-894C>T| |
S298 |
| 179554 | BAA02g19860 | A02 | 10446008 | C | T | upstream_gene_variant | MODIFIER | c.-1603G>A| |
S262 |
| 179555 | BAA02g19860 | A02 | 10448443 | G | A | upstream_gene_variant | MODIFIER | c.-4038C>T| |
S238 |
| 179556 | BAA02g19860 | A02 | 10448567 | G | A | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S189 S226 S250 S41 |
| 179557 | BAA02g19860 | A02 | 10448625 | G | A | upstream_gene_variant | MODIFIER | c.-4220C>T| |
S303 |
| 179558 | BAA02g19890 | A02 | 10449841 | G | A | synonymous_variant | LOW | c.90C>T|p.Val30Val |
S17 |
| 179559 | BAA02g19900 | A02 | 10450194 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.179-1G>A| |
S209 |
| 179560 | BAA02g19880 | A02 | 10450453 | C | T | upstream_gene_variant | MODIFIER | c.-2057G>A| |
S18 |
| 179561 | BAA02g19900 | A02 | 10450692 | G | A | missense_variant | MODERATE | c.97C>T|p.Pro33Ser |
S159 S243 |
| 179562 | BAA02g19880 | A02 | 10451300 | C | T | upstream_gene_variant | MODIFIER | c.-2904G>A| |
S250 |
| 179563 | BAA02g19880 | A02 | 10451396 | G | A | upstream_gene_variant | MODIFIER | c.-3000C>T| |
S57 |
| 179564 | BAA02g19880 | A02 | 10453118 | G | A | upstream_gene_variant | MODIFIER | c.-4722C>T| |
S187 |
| 179565 | BAA02g19890 | A02 | 10454383 | C | T | upstream_gene_variant | MODIFIER | c.-4453G>A| |
S233 |
| 179566 | BAA02g19890 | A02 | 10454385 | T | A | upstream_gene_variant | MODIFIER | c.-4455A>T| |
S138 |
| 179567 | BAA02g19900 | A02 | 10454971 | G | A | upstream_gene_variant | MODIFIER | c.-4183C>T| |
S247 |
| 179568 | BAA02g19900 | A02 | 10455333 | G | A | upstream_gene_variant | MODIFIER | c.-4545C>T| |
S13 |
| 179569 | BAA02g19900 | A02 | 10455353 | G | A | upstream_gene_variant | MODIFIER | c.-4565C>T| |
S166 |
| 179570 | BAA02g19900 | A02 | 10455359 | C | T | upstream_gene_variant | MODIFIER | c.-4571G>A| |
S88 |
| 179571 | BAA02g19910 | A02 | 10456407 | G | A | upstream_gene_variant | MODIFIER | c.-1910G>A| |
S274 |
| 179572 | BAA02g19910 | A02 | 10456755 | G | A | upstream_gene_variant | MODIFIER | c.-1562G>A| |
S187 S61 |
| 179573 | BAA02g19910 | A02 | 10456922 | G | A | upstream_gene_variant | MODIFIER | c.-1395G>A| |
S161 |
| 179574 | BAA02g19910 | A02 | 10456947 | C | T | upstream_gene_variant | MODIFIER | c.-1370C>T| |
S238 |
| 179575 | BAA02g19910 | A02 | 10457031 | C | T | upstream_gene_variant | MODIFIER | c.-1286C>T| |
S292 |