| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 79501 | BAA01g41810 | A01 | 27821586 | G | A | upstream_gene_variant | MODIFIER | c.-412C>T| |
S268 |
| 79502 | BAA01g41810 | A01 | 27823619 | C | T | upstream_gene_variant | MODIFIER | c.-2445G>A| |
S273 |
| 79503 | BAA01g41810 | A01 | 27823892 | C | T | upstream_gene_variant | MODIFIER | c.-2718G>A| |
S192 |
| 79504 | BAA01g41840 | A01 | 27829663 | G | A | upstream_gene_variant | MODIFIER | c.-1571G>A| |
S34 |
| 79505 | BAA01g41840 | A01 | 27829710 | G | A | upstream_gene_variant | MODIFIER | c.-1524G>A| |
S70 |
| 79506 | BAA01g41830 | A01 | 27830180 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.558-1G>A| |
S298 |
| 79507 | BAA01g41830 | A01 | 27830253 | G | A | synonymous_variant | LOW | c.630G>A|p.Ala210Ala |
S218 |
| 79508 | BAA01g41840 | A01 | 27831215 | C | T | upstream_gene_variant | MODIFIER | c.-19C>T| |
S103 |
| 79509 | BAA01g41840 | A01 | 27831222 | C | T | upstream_gene_variant | MODIFIER | c.-12C>T| |
S279 |
| 79510 | BAA01g41840 | A01 | 27831530 | G | A | splice_region_variant&synonymous_variant | LOW | c.132G>A|p.Glu44Glu |
S110 |
| 79511 | BAA01g41830 | A01 | 27831976 | G | A | downstream_gene_variant | MODIFIER | c.*1582G>A| |
S283 |
| 79512 | BAA01g41830 | A01 | 27832486 | C | T | downstream_gene_variant | MODIFIER | c.*2092C>T| |
S119 |
| 79513 | BAA01g41830 | A01 | 27832655 | G | A | downstream_gene_variant | MODIFIER | c.*2261G>A| |
S185 |
| 79514 | BAA01g41830 | A01 | 27832923 | C | T | downstream_gene_variant | MODIFIER | c.*2529C>T| |
S128 |
| 79515 | BAA01g41830 | A01 | 27833377 | C | T | downstream_gene_variant | MODIFIER | c.*2983C>T| |
S261 |
| 79516 | BAA01g41830 | A01 | 27833820 | C | T | downstream_gene_variant | MODIFIER | c.*3426C>T| |
S267 |
| 79517 | BAA01g41830 | A01 | 27834457 | G | A | downstream_gene_variant | MODIFIER | c.*4063G>A| |
S105 |
| 79518 | BAA01g41830 | A01 | 27834836 | C | T | downstream_gene_variant | MODIFIER | c.*4442C>T| |
S256 |
| 79519 | BAA01g41850 | A01 | 27835720 | C | T | missense_variant | MODERATE | c.853G>A|p.Asp285Asn |
S12 |
| 79520 | BAA01g41850 | A01 | 27837399 | C | T | synonymous_variant | LOW | c.105G>A|p.Lys35Lys |
S292 |
| 79521 | BAA01g41850 | A01 | 27837470 | C | T | missense_variant | MODERATE | c.34G>A|p.Asp12Asn |
S146 |
| 79522 | BAA01g41850 | A01 | 27838302 | G | A | upstream_gene_variant | MODIFIER | c.-799C>T| |
S185 |
| 79523 | BAA01g41850 | A01 | 27840123 | G | A | upstream_gene_variant | MODIFIER | c.-2620C>T| |
S246 S46 |
| 79524 | BAA01g41850 | A01 | 27841526 | C | T | upstream_gene_variant | MODIFIER | c.-4023G>A| |
S298 |
| 79525 | BAA01g41850 | A01 | 27841556 | C | T | upstream_gene_variant | MODIFIER | c.-4053G>A| |
S277 |