| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g07960 | A07 | 17135694 | C | T | downstream_gene_variant | MODIFIER | c.*4202G>A| |
S42 |
| 2 | BAA07g07960 | A07 | 17136005 | G | A | downstream_gene_variant | MODIFIER | c.*3891C>T| |
S115 |
| 3 | BAA07g07960 | A07 | 17136128 | G | A | downstream_gene_variant | MODIFIER | c.*3768C>T| |
S10 |
| 4 | BAA07g07960 | A07 | 17136739 | G | A | downstream_gene_variant | MODIFIER | c.*3157C>T| |
S33 |
| 5 | BAA07g07960 | A07 | 17136873 | G | A | downstream_gene_variant | MODIFIER | c.*3023C>T| |
S87 |
| 6 | BAA07g07960 | A07 | 17138421 | G | A | downstream_gene_variant | MODIFIER | c.*1475C>T| |
S134 |
| 7 | BAA07g07960 | A07 | 17138594 | C | T | downstream_gene_variant | MODIFIER | c.*1302G>A| |
S148 S210 S30 S31 |
| 8 | BAA07g07960 | A07 | 17138826 | G | A | downstream_gene_variant | MODIFIER | c.*1070C>T| |
S65 |
| 9 | BAA07g07960 | A07 | 17139054 | C | A | downstream_gene_variant | MODIFIER | c.*842G>T| |
S304 |
| 10 | BAA07g07960 | A07 | 17139505 | C | T | downstream_gene_variant | MODIFIER | c.*391G>A| |
S192 |
| 11 | BAA07g07960 | A07 | 17139521 | G | A | downstream_gene_variant | MODIFIER | c.*375C>T| |
S274 |
| 12 | BAA07g07960 | A07 | 17139982 | G | A | stop_gained&splice_region_variant | HIGH | c.1369C>T|p.Arg457* |
S245 |
| 13 | BAA07g07960 | A07 | 17140162 | G | T | intron_variant | MODIFIER | c.1367-178C>A| |
S266 |
| 14 | BAA07g07960 | A07 | 17140180 | G | A | intron_variant | MODIFIER | c.1367-196C>T| |
S185 |
| 15 | BAA07g07960 | A07 | 17140723 | C | T | intron_variant | MODIFIER | c.1367-739G>A| |
S42 |
| 16 | BAA07g07960 | A07 | 17141242 | G | A | intron_variant | MODIFIER | c.1367-1258C>T| |
S46 |
| 17 | BAA07g07960 | A07 | 17141855 | C | T | intron_variant | MODIFIER | c.1366+1662G>A| |
S195 S262 |
| 18 | BAA07g07960 | A07 | 17144316 | C | T | stop_gained | HIGH | c.567G>A|p.Trp189* |
S47 |
| 19 | BAA07g07960 | A07 | 17144582 | G | A | missense_variant | MODERATE | c.301C>T|p.Pro101Ser |
S172 |
| 20 | BAA07g07960 | A07 | 17147013 | G | A | upstream_gene_variant | MODIFIER | c.-456C>T| |
S233 |
| 21 | BAA07g07960 | A07 | 17147091 | C | T | upstream_gene_variant | MODIFIER | c.-534G>A| |
S96 |
| 22 | BAA07g07960 | A07 | 17147123 | C | T | upstream_gene_variant | MODIFIER | c.-566G>A| |
S197 |
| 23 | BAA07g07960 | A07 | 17147375 | C | T | upstream_gene_variant | MODIFIER | c.-818G>A| |
S216 |
| 24 | BAA07g07960 | A07 | 17148780 | C | T | upstream_gene_variant | MODIFIER | c.-2223G>A| |
S126 |
| 25 | BAA07g07960 | A07 | 17149921 | C | T | upstream_gene_variant | MODIFIER | c.-3364G>A| |
S95 |