| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 50101 | BAA01g28280 | A01 | 17326577 | G | A | upstream_gene_variant | MODIFIER | c.-4222G>A| |
S246 S284 |
| 50102 | BAA01g28280 | A01 | 17327032 | G | A | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S114 |
| 50103 | BAA01g28280 | A01 | 17327110 | C | A | upstream_gene_variant | MODIFIER | c.-3689C>A| |
S37 |
| 50104 | BAA01g28280 | A01 | 17327419 | G | A | upstream_gene_variant | MODIFIER | c.-3380G>A| |
S278 |
| 50105 | BAA01g28280 | A01 | 17328322 | G | A | upstream_gene_variant | MODIFIER | c.-2477G>A| |
S45 |
| 50106 | BAA01g28280 | A01 | 17329488 | C | T | upstream_gene_variant | MODIFIER | c.-1311C>T| |
S179 |
| 50107 | BAA01g28280 | A01 | 17330836 | C | T | missense_variant | MODERATE | c.38C>T|p.Pro13Leu |
S136 |
| 50108 | BAA01g28280 | A01 | 17330980 | G | A | missense_variant | MODERATE | c.182G>A|p.Gly61Asp |
S178 |
| 50109 | BAA01g28280 | A01 | 17331117 | C | T | synonymous_variant | LOW | c.319C>T|p.Leu107Leu |
S78 |
| 50110 | BAA01g28280 | A01 | 17331533 | G | A | intron_variant | MODIFIER | c.649+9G>A| |
S232 |
| 50111 | BAA01g28280 | A01 | 17331586 | G | A | intron_variant | MODIFIER | c.650-44G>A| |
S23 |
| 50112 | BAA01g28280 | A01 | 17332572 | G | A | synonymous_variant | LOW | c.1302G>A|p.Gly434Gly |
S122 |
| 50113 | BAA01g28280 | A01 | 17332637 | C | T | missense_variant | MODERATE | c.1367C>T|p.Ser456Phe |
S286 |
| 50114 | BAA01g28280 | A01 | 17333688 | G | A | downstream_gene_variant | MODIFIER | c.*690G>A| |
S244 |
| 50115 | BAA01g28280 | A01 | 17334076 | C | T | downstream_gene_variant | MODIFIER | c.*1078C>T| |
S103 |
| 50116 | BAA01g28280 | A01 | 17334145 | G | A | downstream_gene_variant | MODIFIER | c.*1147G>A| |
S288 |
| 50117 | BAA01g28290 | A01 | 17343285 | G | A | downstream_gene_variant | MODIFIER | c.*4650C>T| |
S84 S93 |
| 50118 | BAA01g28290 | A01 | 17343327 | C | T | downstream_gene_variant | MODIFIER | c.*4608G>A| |
S77 |
| 50119 | BAA01g28290 | A01 | 17344015 | C | T | downstream_gene_variant | MODIFIER | c.*3920G>A| |
S67 |
| 50120 | BAA01g28290 | A01 | 17344411 | C | T | downstream_gene_variant | MODIFIER | c.*3524G>A| |
S32 |
| 50121 | BAA01g28290 | A01 | 17344673 | G | A | downstream_gene_variant | MODIFIER | c.*3262C>T| |
S178 |
| 50122 | BAA01g28290 | A01 | 17344893 | C | T | downstream_gene_variant | MODIFIER | c.*3042G>A| |
S66 |
| 50123 | BAA01g28290 | A01 | 17346355 | G | A | downstream_gene_variant | MODIFIER | c.*1580C>T| |
S306 S308 |
| 50124 | BAA01g28290 | A01 | 17346705 | C | T | downstream_gene_variant | MODIFIER | c.*1230G>A| |
S10 |
| 50125 | BAA01g28300 | A01 | 17349193 | G | A | downstream_gene_variant | MODIFIER | c.*3012C>T| |
|