| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 43501 | BAA01g26650 | A01 | 14957361 | C | T | upstream_gene_variant | MODIFIER | c.-3481C>T| |
S125 |
| 43502 | BAA01g26650 | A01 | 14958085 | G | A | upstream_gene_variant | MODIFIER | c.-2757G>A| |
S172 |
| 43503 | BAA01g26640 | A01 | 14959043 | C | T | upstream_gene_variant | MODIFIER | c.-294G>A| |
S53 |
| 43504 | BAA01g26640 | A01 | 14960625 | C | T | upstream_gene_variant | MODIFIER | c.-1876G>A| |
S18 |
| 43505 | BAA01g26650 | A01 | 14960962 | C | T | missense_variant | MODERATE | c.121C>T|p.Pro41Ser |
S136 |
| 43506 | BAA01g26650 | A01 | 14961240 | C | T | synonymous_variant | LOW | c.399C>T|p.Leu133Leu |
S231 |
| 43507 | BAA01g26640 | A01 | 14961750 | G | A | upstream_gene_variant | MODIFIER | c.-3001C>T| |
S284 |
| 43508 | BAA01g26640 | A01 | 14962157 | C | T | upstream_gene_variant | MODIFIER | c.-3408G>A| |
S134 S179 S193 |
| 43509 | BAA01g26640 | A01 | 14962888 | C | T | upstream_gene_variant | MODIFIER | c.-4139G>A| |
S184 |
| 43510 | BAA01g26640 | A01 | 14962889 | G | A | upstream_gene_variant | MODIFIER | c.-4140C>T| |
S238 |
| 43511 | BAA01g26640 | A01 | 14963121 | G | A | upstream_gene_variant | MODIFIER | c.-4372C>T| |
S174 S27 |
| 43512 | BAA01g26640 | A01 | 14963179 | C | T | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S176 |
| 43513 | BAA01g26640 | A01 | 14963350 | G | A | upstream_gene_variant | MODIFIER | c.-4601C>T| |
S210 S225 |
| 43514 | BAA01g26640 | A01 | 14963738 | C | T | upstream_gene_variant | MODIFIER | c.-4989G>A| |
S54 |
| 43515 | BAA01g26670 | A01 | 14963805 | C | T | upstream_gene_variant | MODIFIER | c.-3340C>T| |
S134 |
| 43516 | BAA01g26670 | A01 | 14964383 | G | A | upstream_gene_variant | MODIFIER | c.-2762G>A| |
S149 |
| 43517 | BAA01g26670 | A01 | 14964897 | C | T | upstream_gene_variant | MODIFIER | c.-2248C>T| |
S277 |
| 43518 | BAA01g26670 | A01 | 14965179 | G | A | upstream_gene_variant | MODIFIER | c.-1966G>A| |
S14 |
| 43519 | BAA01g26670 | A01 | 14965806 | C | T | upstream_gene_variant | MODIFIER | c.-1339C>T| |
S75 |
| 43520 | BAA01g26660 | A01 | 14966198 | C | T | missense_variant | MODERATE | c.215G>A|p.Arg72Lys |
S170 |
| 43521 | BAA01g26670 | A01 | 14966383 | G | A | upstream_gene_variant | MODIFIER | c.-762G>A| |
S68 |
| 43522 | BAA01g26660 | A01 | 14966427 | G | A | missense_variant | MODERATE | c.80C>T|p.Ala27Val |
S33 |
| 43523 | BAA01g26660 | A01 | 14966756 | G | A | upstream_gene_variant | MODIFIER | c.-250C>T| |
S5 |
| 43524 | BAA01g26660 | A01 | 14967125 | C | T | upstream_gene_variant | MODIFIER | c.-619G>A| |
S42 |
| 43525 | BAA01g26660 | A01 | 14967794 | G | A | upstream_gene_variant | MODIFIER | c.-1288C>T| |
S110 S13 S219 S279 S72 |