| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g19830 | A06 | 10346581 | C | T | downstream_gene_variant | MODIFIER | c.*3931G>A| |
S295 |
| 2 | BAA06g19830 | A06 | 10346820 | G | A | downstream_gene_variant | MODIFIER | c.*3692C>T| |
S140 |
| 3 | BAA06g19830 | A06 | 10347817 | G | A | downstream_gene_variant | MODIFIER | c.*2695C>T| |
S118 S53 |
| 4 | BAA06g19830 | A06 | 10347852 | C | T | downstream_gene_variant | MODIFIER | c.*2660G>A| |
S116 |
| 5 | BAA06g19830 | A06 | 10348768 | C | T | downstream_gene_variant | MODIFIER | c.*1744G>A| |
S163 |
| 6 | BAA06g19830 | A06 | 10349795 | T | A | downstream_gene_variant | MODIFIER | c.*717A>T| |
S262 |
| 7 | BAA06g19830 | A06 | 10350510 | G | A | downstream_gene_variant | MODIFIER | c.*2C>T| |
S82 S92 |
| 8 | BAA06g19830 | A06 | 10350616 | C | T | intron_variant | MODIFIER | c.113+21G>A| |
S148 S210 S30 S31 |
| 9 | BAA06g19830 | A06 | 10350645 | G | A | synonymous_variant | LOW | c.105C>T|p.Ile35Ile |
S262 |
| 10 | BAA06g19830 | A06 | 10350680 | C | T | missense_variant | MODERATE | c.70G>A|p.Val24Ile |
S286 |
| 11 | BAA06g19830 | A06 | 10351247 | G | A | upstream_gene_variant | MODIFIER | c.-498C>T| |
S44 |
| 12 | BAA06g19830 | A06 | 10352385 | G | A | upstream_gene_variant | MODIFIER | c.-1636C>T| |
S122 |
| 13 | BAA06g19830 | A06 | 10353004 | C | T | upstream_gene_variant | MODIFIER | c.-2255G>A| |
S105 S106 |
| 14 | BAA06g19830 | A06 | 10353710 | G | A | upstream_gene_variant | MODIFIER | c.-2961C>T| |
S268 |
| 15 | BAA06g19830 | A06 | 10354187 | G | A | upstream_gene_variant | MODIFIER | c.-3438C>T| |
S45 |
| 16 | BAA06g19830 | A06 | 10354197 | C | T | upstream_gene_variant | MODIFIER | c.-3448G>A| |
S232 |
| 17 | BAA06g19830 | A06 | 10355275 | C | T | upstream_gene_variant | MODIFIER | c.-4526G>A| |
S64 |
| 18 | BAA06g19830 | A06 | 10355533 | C | T | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S37 |
| 19 | BAA06g19830 | A06 | 10355700 | T | A | upstream_gene_variant | MODIFIER | c.-4951A>T| |
S2 S3 |