| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 44651 | BAA01g27010 | A01 | 15316542 | C | T | intron_variant | MODIFIER | c.2959-1125G>A| |
S114 |
| 44652 | BAA01g27010 | A01 | 15316923 | C | T | intron_variant | MODIFIER | c.2959-1506G>A| |
S267 |
| 44653 | BAA01g27010 | A01 | 15316967 | C | T | intron_variant | MODIFIER | c.2959-1550G>A| |
S10 |
| 44654 | BAA01g27010 | A01 | 15317259 | G | A | intron_variant | MODIFIER | c.2958+1418C>T| |
S268 |
| 44655 | BAA01g27010 | A01 | 15317482 | G | A | intron_variant | MODIFIER | c.2958+1195C>T| |
S68 |
| 44656 | BAA01g27010 | A01 | 15317693 | C | T | intron_variant | MODIFIER | c.2958+984G>A| |
S51 |
| 44657 | BAA01g27010 | A01 | 15318157 | C | T | intron_variant | MODIFIER | c.2958+520G>A| |
S213 |
| 44658 | BAA01g27010 | A01 | 15318163 | C | T | intron_variant | MODIFIER | c.2958+514G>A| |
S184 |
| 44659 | BAA01g27010 | A01 | 15318197 | G | A | intron_variant | MODIFIER | c.2958+480C>T| |
S308 |
| 44660 | BAA01g27010 | A01 | 15319558 | C | T | missense_variant | MODERATE | c.2077G>A|p.Asp693Asn |
S231 |
| 44661 | BAA01g27010 | A01 | 15319789 | C | T | missense_variant | MODERATE | c.1846G>A|p.Val616Ile |
S64 |
| 44662 | BAA01g27010 | A01 | 15319900 | C | T | missense_variant | MODERATE | c.1735G>A|p.Glu579Lys |
S255 |
| 44663 | BAA01g27010 | A01 | 15320049 | C | T | missense_variant | MODERATE | c.1696G>A|p.Ala566Thr |
S266 |
| 44664 | BAA01g27010 | A01 | 15320648 | G | A | missense_variant | MODERATE | c.1097C>T|p.Thr366Ile |
S247 |
| 44665 | BAA01g27010 | A01 | 15320672 | G | A | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S37 |
| 44666 | BAA01g27010 | A01 | 15320893 | C | T | synonymous_variant | LOW | c.852G>A|p.Ala284Ala |
S158 |
| 44667 | BAA01g27010 | A01 | 15321050 | C | T | missense_variant | MODERATE | c.695G>A|p.Gly232Asp |
S273 |
| 44668 | BAA01g27010 | A01 | 15321233 | C | T | missense_variant | MODERATE | c.512G>A|p.Gly171Glu |
S221 |
| 44669 | BAA01g27010 | A01 | 15321292 | T | G | missense_variant | MODERATE | c.453A>C|p.Glu151Asp |
S108 S109 S113 S121 S123 S138 S165 S174 S208 S237 S239 S244 S288 S78 S86 |
| 44670 | BAA01g27010 | A01 | 15321294 | C | T | missense_variant | MODERATE | c.451G>A|p.Glu151Lys |
S221 |
| 44671 | BAA01g27010 | A01 | 15321428 | C | T | missense_variant | MODERATE | c.317G>A|p.Arg106His |
S259 |
| 44672 | BAA01g27010 | A01 | 15321793 | C | T | upstream_gene_variant | MODIFIER | c.-49G>A| |
S291 |
| 44673 | BAA01g27010 | A01 | 15322075 | G | A | upstream_gene_variant | MODIFIER | c.-331C>T| |
S180 |
| 44674 | BAA01g27010 | A01 | 15322091 | G | A | upstream_gene_variant | MODIFIER | c.-347C>T| |
S232 |
| 44675 | BAA01g27010 | A01 | 15323543 | G | A | upstream_gene_variant | MODIFIER | c.-1799C>T| |
S142 |