| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 22551 | BAA01g16360 | A01 | 7945985 | G | A | upstream_gene_variant | MODIFIER | c.-1772G>A| |
S256 |
| 22552 | BAA01g16360 | A01 | 7947100 | C | T | upstream_gene_variant | MODIFIER | c.-657C>T| |
S278 |
| 22553 | BAA01g16360 | A01 | 7947445 | G | A | upstream_gene_variant | MODIFIER | c.-312G>A| |
S129 |
| 22554 | BAA01g16350 | A01 | 7948333 | C | T | downstream_gene_variant | MODIFIER | c.*1497C>T| |
S10 |
| 22555 | BAA01g16360 | A01 | 7948904 | G | A | missense_variant | MODERATE | c.709G>A|p.Glu237Lys |
S157 |
| 22556 | BAA01g16360 | A01 | 7948980 | C | T | missense_variant&splice_region_variant | MODERATE | c.785C>T|p.Ala262Val |
S38 |
| 22557 | BAA01g16350 | A01 | 7949031 | C | T | downstream_gene_variant | MODIFIER | c.*2195C>T| |
S39 |
| 22558 | BAA01g16360 | A01 | 7950332 | G | A | missense_variant | MODERATE | c.1588G>A|p.Asp530Asn |
S245 |
| 22559 | BAA01g16370 | A01 | 7952187 | C | T | upstream_gene_variant | MODIFIER | c.-2912C>T| |
S100 |
| 22560 | BAA01g16370 | A01 | 7952937 | G | A | upstream_gene_variant | MODIFIER | c.-2162G>A| |
S279 |
| 22561 | BAA01g16360 | A01 | 7953982 | G | A | synonymous_variant | LOW | c.3549G>A|p.Arg1183Arg |
S245 |
| 22562 | BAA01g16360 | A01 | 7954062 | G | A | missense_variant | MODERATE | c.3629G>A|p.Gly1210Glu |
S23 |
| 22563 | BAA01g16370 | A01 | 7954100 | C | T | upstream_gene_variant | MODIFIER | c.-999C>T| |
S171 |
| 22564 | BAA01g16380 | A01 | 7957131 | C | T | upstream_gene_variant | MODIFIER | c.-3279C>T| |
S62 |
| 22565 | BAA01g16380 | A01 | 7958247 | C | T | upstream_gene_variant | MODIFIER | c.-2163C>T| |
S18 |
| 22566 | BAA01g16380 | A01 | 7958868 | C | T | upstream_gene_variant | MODIFIER | c.-1542C>T| |
S198 |
| 22567 | BAA01g16380 | A01 | 7959026 | C | T | upstream_gene_variant | MODIFIER | c.-1384C>T| |
S167 |
| 22568 | BAA01g16380 | A01 | 7959092 | C | T | upstream_gene_variant | MODIFIER | c.-1318C>T| |
S88 |
| 22569 | BAA01g16380 | A01 | 7960521 | C | T | missense_variant | MODERATE | c.112C>T|p.Pro38Ser |
S291 |
| 22570 | BAA01g16380 | A01 | 7960639 | C | T | missense_variant | MODERATE | c.230C>T|p.Ser77Phe |
S265 |
| 22571 | BAA01g16370 | A01 | 7961476 | G | A | downstream_gene_variant | MODIFIER | c.*3906G>A| |
S173 |
| 22572 | BAA01g16380 | A01 | 7962199 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.811-1G>A| |
S58 |
| 22573 | BAA01g16390 | A01 | 7962479 | G | A | upstream_gene_variant | MODIFIER | c.-4064G>A| |
S28 |
| 22574 | BAA01g16390 | A01 | 7962537 | C | T | upstream_gene_variant | MODIFIER | c.-4006C>T| |
S33 |
| 22575 | BAA01g16390 | A01 | 7962933 | C | T | upstream_gene_variant | MODIFIER | c.-3610C>T| |
S20 |