| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 165551 | BAA02g11720 | A02 | 5309771 | G | A | synonymous_variant | LOW | c.804C>T|p.Ser268Ser |
S238 |
| 165552 | BAA02g11700 | A02 | 5312377 | G | A | upstream_gene_variant | MODIFIER | c.-4145C>T| |
S82 S92 |
| 165553 | BAA02g11730 | A02 | 5313024 | G | A | synonymous_variant | LOW | c.198C>T|p.Ile66Ile |
S25 |
| 165554 | BAA02g11730 | A02 | 5313095 | C | T | missense_variant | MODERATE | c.127G>A|p.Glu43Lys |
S255 |
| 165555 | BAA02g11730 | A02 | 5313157 | G | A | missense_variant | MODERATE | c.65C>T|p.Pro22Leu |
S4 |
| 165556 | BAA02g11740 | A02 | 5314403 | C | T | synonymous_variant | LOW | c.600G>A|p.Glu200Glu |
S224 |
| 165557 | BAA02g11730 | A02 | 5316665 | G | A | upstream_gene_variant | MODIFIER | c.-3444C>T| |
S206 S26 |
| 165558 | BAA02g11740 | A02 | 5318569 | G | A | upstream_gene_variant | MODIFIER | c.-2762C>T| |
S166 |
| 165559 | BAA02g11760 | A02 | 5319820 | G | A | missense_variant | MODERATE | c.253G>A|p.Ala85Thr |
S229 |
| 165560 | BAA02g11760 | A02 | 5320025 | G | A | missense_variant | MODERATE | c.458G>A|p.Ser153Asn |
S289 S290 |
| 165561 | BAA02g11770 | A02 | 5322626 | C | T | upstream_gene_variant | MODIFIER | c.-435C>T| |
S34 |
| 165562 | BAA02g11770 | A02 | 5322778 | C | T | upstream_gene_variant | MODIFIER | c.-283C>T| |
S277 |
| 165563 | BAA02g11770 | A02 | 5323155 | C | T | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S123 |
| 165564 | BAA02g11770 | A02 | 5323314 | C | T | missense_variant | MODERATE | c.254C>T|p.Pro85Leu |
S135 |
| 165565 | BAA02g11770 | A02 | 5323663 | G | A | stop_gained | HIGH | c.603G>A|p.Trp201* |
S276 |
| 165566 | BAA02g11770 | A02 | 5323852 | G | A | synonymous_variant | LOW | c.792G>A|p.Glu264Glu |
S229 |
| 165567 | BAA02g11780 | A02 | 5325562 | G | A | upstream_gene_variant | MODIFIER | c.-505G>A| |
S198 |
| 165568 | BAA02g11780 | A02 | 5326230 | G | A | missense_variant | MODERATE | c.164G>A|p.Arg55Lys |
S80 |
| 165569 | BAA02g11780 | A02 | 5326563 | G | A | missense_variant | MODERATE | c.497G>A|p.Arg166Lys |
S9 |
| 165570 | BAA02g11780 | A02 | 5326743 | G | A | missense_variant | MODERATE | c.677G>A|p.Arg226Gln |
S206 S26 |
| 165571 | BAA02g11780 | A02 | 5326859 | G | A | missense_variant | MODERATE | c.793G>A|p.Glu265Lys |
S56 |
| 165572 | BAA02g11790 | A02 | 5326955 | C | T | upstream_gene_variant | MODIFIER | c.-982C>T| |
S50 |
| 165573 | BAA02g11790 | A02 | 5328164 | C | T | synonymous_variant | LOW | c.228C>T|p.Ser76Ser |
S308 |
| 165574 | BAA02g11790 | A02 | 5328262 | G | A | missense_variant | MODERATE | c.326G>A|p.Arg109Lys |
S168 |
| 165575 | BAA02g11790 | A02 | 5328350 | G | A | missense_variant | MODERATE | c.414G>A|p.Met138Ile |
S4 |