| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g18720 | A07 | 24674370 | C | T | downstream_gene_variant | MODIFIER | c.*2673G>A| |
S192 |
| 2 | BAA07g18720 | A07 | 24675043 | G | A | downstream_gene_variant | MODIFIER | c.*2000C>T| |
S178 |
| 3 | BAA07g18720 | A07 | 24675176 | C | T | downstream_gene_variant | MODIFIER | c.*1867G>A| |
S302 |
| 4 | BAA07g18720 | A07 | 24675682 | C | T | downstream_gene_variant | MODIFIER | c.*1361G>A| |
S302 |
| 5 | BAA07g18720 | A07 | 24676319 | G | A | downstream_gene_variant | MODIFIER | c.*724C>T| |
S117 |
| 6 | BAA07g18720 | A07 | 24678667 | G | A | intron_variant | MODIFIER | c.1440-57C>T| |
S38 |
| 7 | BAA07g18720 | A07 | 24678981 | C | T | missense_variant | MODERATE | c.1307G>A|p.Gly436Asp |
S284 |
| 8 | BAA07g18720 | A07 | 24679033 | G | A | missense_variant | MODERATE | c.1255C>T|p.Arg419Cys |
S118 |
| 9 | BAA07g18720 | A07 | 24679116 | C | T | missense_variant | MODERATE | c.1172G>A|p.Gly391Asp |
S233 |
| 10 | BAA07g18720 | A07 | 24680110 | G | A | intron_variant | MODIFIER | c.581+20C>T| |
S118 |
| 11 | BAA07g18720 | A07 | 24680332 | G | A | synonymous_variant | LOW | c.493C>T|p.Leu165Leu |
S112 |
| 12 | BAA07g18720 | A07 | 24680583 | C | T | missense_variant | MODERATE | c.325G>A|p.Val109Met |
S114 |
| 13 | BAA07g18720 | A07 | 24680595 | C | T | splice_region_variant&intron_variant | LOW | c.317-4G>A| |
S303 |
| 14 | BAA07g18720 | A07 | 24681692 | G | A | upstream_gene_variant | MODIFIER | c.-700C>T| |
S183 |
| 15 | BAA07g18720 | A07 | 24683468 | T | C | upstream_gene_variant | MODIFIER | c.-2476A>G| |
S290 |
| 16 | BAA07g18720 | A07 | 24684221 | G | A | upstream_gene_variant | MODIFIER | c.-3229C>T| |
S39 |
| 17 | BAA07g18720 | A07 | 24684377 | C | T | upstream_gene_variant | MODIFIER | c.-3385G>A| |
S162 |
| 18 | BAA07g18720 | A07 | 24684934 | C | T | upstream_gene_variant | MODIFIER | c.-3942G>A| |
S32 |