| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g19970 | A04 | 23262817 | G | A | upstream_gene_variant | MODIFIER | c.-4223G>A| |
S162 |
| 2 | BAA04g19970 | A04 | 23262942 | C | T | upstream_gene_variant | MODIFIER | c.-4098C>T| |
S55 |
| 3 | BAA04g19970 | A04 | 23263584 | G | A | upstream_gene_variant | MODIFIER | c.-3456G>A| |
S302 |
| 4 | BAA04g19970 | A04 | 23265391 | C | T | upstream_gene_variant | MODIFIER | c.-1649C>T| |
S139 |
| 5 | BAA04g19970 | A04 | 23265540 | C | T | upstream_gene_variant | MODIFIER | c.-1500C>T| |
S246 |
| 6 | BAA04g19970 | A04 | 23269030 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.739-1G>A| |
S40 S49 |
| 7 | BAA04g19970 | A04 | 23269775 | C | T | missense_variant | MODERATE | c.916C>T|p.Pro306Ser |
S139 |
| 8 | BAA04g19970 | A04 | 23270135 | G | A | missense_variant | MODERATE | c.1276G>A|p.Asp426Asn |
S111 |
| 9 | BAA04g19970 | A04 | 23271872 | G | A | downstream_gene_variant | MODIFIER | c.*1534G>A| |
S70 |
| 10 | BAA04g19970 | A04 | 23271878 | G | A | downstream_gene_variant | MODIFIER | c.*1540G>A| |
S72 S78 |
| 11 | BAA04g19970 | A04 | 23271945 | G | A | downstream_gene_variant | MODIFIER | c.*1607G>A| |
S302 |
| 12 | BAA04g19970 | A04 | 23271951 | G | A | downstream_gene_variant | MODIFIER | c.*1613G>A| |
S35 |
| 13 | BAA04g19970 | A04 | 23271952 | C | T | downstream_gene_variant | MODIFIER | c.*1614C>T| |
S163 |
| 14 | BAA04g19970 | A04 | 23272292 | C | T | downstream_gene_variant | MODIFIER | c.*1954C>T| |
S295 S296 |
| 15 | BAA04g19970 | A04 | 23272948 | C | T | downstream_gene_variant | MODIFIER | c.*2610C>T| |
S1 S90 |
| 16 | BAA04g19970 | A04 | 23273007 | C | T | downstream_gene_variant | MODIFIER | c.*2669C>T| |
S240 |
| 17 | BAA04g19970 | A04 | 23274176 | G | A | downstream_gene_variant | MODIFIER | c.*3838G>A| |
S69 |
| 18 | BAA04g19970 | A04 | 23274395 | G | A | downstream_gene_variant | MODIFIER | c.*4057G>A| |
S126 |