| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 181851 | BAA02g21070 | A02 | 11283807 | C | T | upstream_gene_variant | MODIFIER | c.-3676G>A| |
S132 S215 S89 |
| 181852 | BAA02g21080 | A02 | 11285157 | C | T | upstream_gene_variant | MODIFIER | c.-747C>T| |
S171 |
| 181853 | BAA02g21080 | A02 | 11285787 | G | A | upstream_gene_variant | MODIFIER | c.-117G>A| |
S86 |
| 181854 | BAA02g21080 | A02 | 11286086 | C | T | intron_variant | MODIFIER | c.128+55C>T| |
S261 |
| 181855 | BAA02g21080 | A02 | 11286888 | G | A | missense_variant | MODERATE | c.361G>A|p.Ala121Thr |
S157 |
| 181856 | BAA02g21080 | A02 | 11286894 | C | T | missense_variant | MODERATE | c.367C>T|p.Leu123Phe |
S308 |
| 181857 | BAA02g21090 | A02 | 11288220 | C | T | upstream_gene_variant | MODIFIER | c.-3891C>T| |
S100 |
| 181858 | BAA02g21090 | A02 | 11289957 | C | T | upstream_gene_variant | MODIFIER | c.-2154C>T| |
S75 |
| 181859 | BAA02g21090 | A02 | 11291015 | C | T | upstream_gene_variant | MODIFIER | c.-1096C>T| |
S181 |
| 181860 | BAA02g21090 | A02 | 11291594 | G | A | upstream_gene_variant | MODIFIER | c.-517G>A| |
S264 |
| 181861 | BAA02g21090 | A02 | 11293058 | G | A | missense_variant | MODERATE | c.352G>A|p.Asp118Asn |
S272 |
| 181862 | BAA02g21090 | A02 | 11293436 | G | A | downstream_gene_variant | MODIFIER | c.*337G>A| |
S67 |
| 181863 | BAA02g21110 | A02 | 11295945 | G | A | upstream_gene_variant | MODIFIER | c.-4400G>A| |
S47 |
| 181864 | BAA02g21110 | A02 | 11296450 | G | A | upstream_gene_variant | MODIFIER | c.-3895G>A| |
S58 |
| 181865 | BAA02g21110 | A02 | 11296511 | G | A | upstream_gene_variant | MODIFIER | c.-3834G>A| |
S238 |
| 181866 | BAA02g21110 | A02 | 11296963 | G | A | upstream_gene_variant | MODIFIER | c.-3382G>A| |
S192 |
| 181867 | BAA02g21110 | A02 | 11297533 | C | T | upstream_gene_variant | MODIFIER | c.-2812C>T| |
S226 |
| 181868 | BAA02g21110 | A02 | 11297969 | G | A | upstream_gene_variant | MODIFIER | c.-2376G>A| |
S202 |
| 181869 | BAA02g21110 | A02 | 11298186 | G | A | upstream_gene_variant | MODIFIER | c.-2159G>A| |
S217 S248 |
| 181870 | BAA02g21110 | A02 | 11298227 | G | A | upstream_gene_variant | MODIFIER | c.-2118G>A| |
S7 |
| 181871 | BAA02g21100 | A02 | 11298314 | G | A | missense_variant | MODERATE | c.353C>T|p.Pro118Leu |
S13 |
| 181872 | BAA02g21100 | A02 | 11298825 | C | T | upstream_gene_variant | MODIFIER | c.-159G>A| |
S193 |
| 181873 | BAA02g21100 | A02 | 11298897 | G | A | upstream_gene_variant | MODIFIER | c.-231C>T| |
S4 |
| 181874 | BAA02g21100 | A02 | 11299248 | G | A | upstream_gene_variant | MODIFIER | c.-582C>T| |
S306 S308 |
| 181875 | BAA02g21100 | A02 | 11299450 | C | T | upstream_gene_variant | MODIFIER | c.-784G>A| |
S219 S72 |