| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 22651 | BAA01g16430 | A01 | 7982612 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.447-1G>A| |
S122 |
| 22652 | BAA01g16420 | A01 | 7983422 | C | T | downstream_gene_variant | MODIFIER | c.*2383C>T| |
S159 S243 |
| 22653 | BAA01g16430 | A01 | 7984570 | C | A | missense_variant | MODERATE | c.1438C>A|p.Pro480Thr |
S182 |
| 22654 | BAA01g16430 | A01 | 7984959 | C | T | missense_variant | MODERATE | c.1651C>T|p.Pro551Ser |
S192 |
| 22655 | BAA01g16420 | A01 | 7985799 | C | T | downstream_gene_variant | MODIFIER | c.*4760C>T| |
S176 |
| 22656 | BAA01g16430 | A01 | 7986090 | C | T | downstream_gene_variant | MODIFIER | c.*394C>T| |
S88 |
| 22657 | BAA01g16440 | A01 | 7986772 | G | A | synonymous_variant | LOW | c.1842C>T|p.Phe614Phe |
S287 |
| 22658 | BAA01g16430 | A01 | 7986852 | C | T | downstream_gene_variant | MODIFIER | c.*1156C>T| |
S243 |
| 22659 | BAA01g16430 | A01 | 7986863 | C | T | downstream_gene_variant | MODIFIER | c.*1167C>T| |
S200 |
| 22660 | BAA01g16450 | A01 | 7991470 | C | T | missense_variant | MODERATE | c.944G>A|p.Gly315Asp |
S136 |
| 22661 | BAA01g16450 | A01 | 7991473 | C | T | missense_variant | MODERATE | c.941G>A|p.Gly314Glu |
S166 |
| 22662 | BAA01g16450 | A01 | 7992059 | G | A | missense_variant | MODERATE | c.533C>T|p.Thr178Met |
S268 |
| 22663 | BAA01g16450 | A01 | 7992127 | G | A | synonymous_variant | LOW | c.465C>T|p.His155His |
S256 |
| 22664 | BAA01g16440 | A01 | 7992372 | C | T | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S8 |
| 22665 | BAA01g16450 | A01 | 7992601 | G | A | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S13 |
| 22666 | BAA01g16440 | A01 | 7992823 | G | A | upstream_gene_variant | MODIFIER | c.-2596C>T| |
S271 |
| 22667 | BAA01g16450 | A01 | 7992929 | G | A | missense_variant | MODERATE | c.88C>T|p.Leu30Phe |
S57 |
| 22668 | BAA01g16450 | A01 | 7992990 | G | A | synonymous_variant | LOW | c.27C>T|p.His9His |
S108 |
| 22669 | BAA01g16440 | A01 | 7993132 | G | A | upstream_gene_variant | MODIFIER | c.-2905C>T| |
S173 |
| 22670 | BAA01g16440 | A01 | 7993778 | G | A | upstream_gene_variant | MODIFIER | c.-3551C>T| |
S109 |
| 22671 | BAA01g16440 | A01 | 7995200 | G | A | upstream_gene_variant | MODIFIER | c.-4973C>T| |
S27 |
| 22672 | BAA01g16450 | A01 | 7996371 | G | A | upstream_gene_variant | MODIFIER | c.-3355C>T| |
S131 |
| 22673 | BAA01g16450 | A01 | 7996479 | C | T | upstream_gene_variant | MODIFIER | c.-3463G>A| |
S265 |
| 22674 | BAA01g16460 | A01 | 7996567 | G | A | missense_variant | MODERATE | c.152C>T|p.Thr51Ile |
S156 |
| 22675 | BAA01g16450 | A01 | 7996906 | G | A | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S251 |