| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g18950 | A06 | 9721653 | C | T | upstream_gene_variant | MODIFIER | c.-3312C>T| |
S266 |
| 2 | BAA06g18950 | A06 | 9721667 | G | A | upstream_gene_variant | MODIFIER | c.-3298G>A| |
S213 |
| 3 | BAA06g18950 | A06 | 9721694 | G | A | upstream_gene_variant | MODIFIER | c.-3271G>A| |
S232 |
| 4 | BAA06g18950 | A06 | 9721701 | C | T | upstream_gene_variant | MODIFIER | c.-3264C>T| |
S203 |
| 5 | BAA06g18950 | A06 | 9721730 | T | C | upstream_gene_variant | MODIFIER | c.-3235T>C| |
S18 |
| 6 | BAA06g18950 | A06 | 9722475 | T | A | upstream_gene_variant | MODIFIER | c.-2490T>A| |
S126 |
| 7 | BAA06g18950 | A06 | 9722664 | G | A | upstream_gene_variant | MODIFIER | c.-2301G>A| |
S262 |
| 8 | BAA06g18950 | A06 | 9722703 | G | A | upstream_gene_variant | MODIFIER | c.-2262G>A| |
S15 S3 |
| 9 | BAA06g18950 | A06 | 9722749 | G | A | upstream_gene_variant | MODIFIER | c.-2216G>A| |
S86 |
| 10 | BAA06g18950 | A06 | 9722755 | G | A | upstream_gene_variant | MODIFIER | c.-2210G>A| |
S176 |
| 11 | BAA06g18950 | A06 | 9722898 | G | A | upstream_gene_variant | MODIFIER | c.-2067G>A| |
S270 |
| 12 | BAA06g18950 | A06 | 9722963 | C | T | upstream_gene_variant | MODIFIER | c.-2002C>T| |
S46 |
| 13 | BAA06g18950 | A06 | 9723161 | G | A | upstream_gene_variant | MODIFIER | c.-1804G>A| |
S152 |
| 14 | BAA06g18950 | A06 | 9723310 | G | A | upstream_gene_variant | MODIFIER | c.-1655G>A| |
S292 |
| 15 | BAA06g18950 | A06 | 9723477 | C | T | upstream_gene_variant | MODIFIER | c.-1488C>T| |
S112 |
| 16 | BAA06g18950 | A06 | 9724187 | C | T | upstream_gene_variant | MODIFIER | c.-778C>T| |
S267 |
| 17 | BAA06g18950 | A06 | 9724485 | G | A | upstream_gene_variant | MODIFIER | c.-480G>A| |
S216 |
| 18 | BAA06g18950 | A06 | 9724757 | C | T | upstream_gene_variant | MODIFIER | c.-208C>T| |
S183 S198 |
| 19 | BAA06g18950 | A06 | 9725225 | G | A | splice_region_variant&stop_retained_variant | LOW | c.261G>A|p.Ter87Ter |
S62 |