| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 162101 | BAA02g09060 | A02 | 4000598 | G | A | upstream_gene_variant | MODIFIER | c.-1192G>A| |
S276 |
| 162102 | BAA02g09050 | A02 | 4001235 | G | A | synonymous_variant | LOW | c.123C>T|p.Asp41Asp |
S86 |
| 162103 | BAA02g09050 | A02 | 4001537 | C | T | upstream_gene_variant | MODIFIER | c.-180G>A| |
S135 |
| 162104 | BAA02g09050 | A02 | 4002408 | G | A | upstream_gene_variant | MODIFIER | c.-1051C>T| |
S169 |
| 162105 | BAA02g09070 | A02 | 4005068 | C | T | synonymous_variant | LOW | c.2523G>A|p.Glu841Glu |
S38 |
| 162106 | BAA02g09050 | A02 | 4005721 | C | T | upstream_gene_variant | MODIFIER | c.-4364G>A| |
S255 |
| 162107 | BAA02g09070 | A02 | 4005862 | G | A | synonymous_variant | LOW | c.2158C>T|p.Leu720Leu |
S80 |
| 162108 | BAA02g09060 | A02 | 4006463 | G | A | downstream_gene_variant | MODIFIER | c.*4290G>A| |
S79 S91 |
| 162109 | BAA02g09070 | A02 | 4008159 | G | A | missense_variant | MODERATE | c.707C>T|p.Thr236Ile |
S20 |
| 162110 | BAA02g09070 | A02 | 4008464 | G | A | synonymous_variant | LOW | c.402C>T|p.Leu134Leu |
S232 |
| 162111 | BAA02g09070 | A02 | 4008903 | G | A | upstream_gene_variant | MODIFIER | c.-38C>T| |
S232 |
| 162112 | BAA02g09070 | A02 | 4008911 | C | T | upstream_gene_variant | MODIFIER | c.-46G>A| |
S270 |
| 162113 | BAA02g09070 | A02 | 4009276 | G | A | upstream_gene_variant | MODIFIER | c.-411C>T| |
S69 |
| 162114 | BAA02g09070 | A02 | 4009432 | T | C | upstream_gene_variant | MODIFIER | c.-567A>G| |
S116 |
| 162115 | BAA02g09070 | A02 | 4010226 | G | A | upstream_gene_variant | MODIFIER | c.-1361C>T| |
S223 |
| 162116 | BAA02g09080 | A02 | 4015096 | C | T | upstream_gene_variant | MODIFIER | c.-469G>A| |
S127 |
| 162117 | BAA02g09090 | A02 | 4017842 | C | T | missense_variant | MODERATE | c.10G>A|p.Ala4Thr |
S115 |
| 162118 | BAA02g09080 | A02 | 4018215 | A | T | upstream_gene_variant | MODIFIER | c.-3588T>A| |
S200 |
| 162119 | BAA02g09080 | A02 | 4019103 | G | A | upstream_gene_variant | MODIFIER | c.-4476C>T| |
S76 |
| 162120 | BAA02g09100 | A02 | 4019737 | C | T | missense_variant | MODERATE | c.373G>A|p.Gly125Arg |
S274 |
| 162121 | BAA02g09100 | A02 | 4020038 | G | A | synonymous_variant | LOW | c.72C>T|p.Ser24Ser |
S295 |
| 162122 | BAA02g09090 | A02 | 4020819 | C | T | upstream_gene_variant | MODIFIER | c.-2968G>A| |
S3 |
| 162123 | BAA02g09090 | A02 | 4021937 | G | A | upstream_gene_variant | MODIFIER | c.-4086C>T| |
S188 |
| 162124 | BAA02g09090 | A02 | 4021969 | G | A | upstream_gene_variant | MODIFIER | c.-4118C>T| |
S143 |
| 162125 | BAA02g09100 | A02 | 4023854 | C | T | upstream_gene_variant | MODIFIER | c.-3745G>A| |
S226 |