| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178851 | BAA02g19610 | A02 | 10193731 | G | A | downstream_gene_variant | MODIFIER | c.*4996C>T| |
S19 |
| 178852 | BAA02g19610 | A02 | 10193884 | C | T | downstream_gene_variant | MODIFIER | c.*4843G>A| |
S163 |
| 178853 | BAA02g19610 | A02 | 10195084 | G | A | downstream_gene_variant | MODIFIER | c.*3643C>T| |
S187 |
| 178854 | BAA02g19610 | A02 | 10197593 | C | T | downstream_gene_variant | MODIFIER | c.*1134G>A| |
S52 |
| 178855 | BAA02g19610 | A02 | 10197937 | C | T | downstream_gene_variant | MODIFIER | c.*790G>A| |
S67 |
| 178856 | BAA02g19610 | A02 | 10198157 | C | T | downstream_gene_variant | MODIFIER | c.*570G>A| |
S249 |
| 178857 | BAA02g19610 | A02 | 10198723 | G | A | downstream_gene_variant | MODIFIER | c.*4C>T| |
S155 |
| 178858 | BAA02g19610 | A02 | 10199229 | C | T | synonymous_variant | LOW | c.900G>A|p.Gln300Gln |
S185 |
| 178859 | BAA02g19610 | A02 | 10199338 | G | A | intron_variant | MODIFIER | c.803-12C>T| |
S13 |
| 178860 | BAA02g19610 | A02 | 10199819 | G | A | intron_variant | MODIFIER | c.553-10C>T| |
S134 |
| 178861 | BAA02g19610 | A02 | 10200011 | G | A | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S288 |
| 178862 | BAA02g19610 | A02 | 10200567 | C | T | upstream_gene_variant | MODIFIER | c.-55G>A| |
S88 |
| 178863 | BAA02g19610 | A02 | 10204680 | G | A | upstream_gene_variant | MODIFIER | c.-4168C>T| |
S168 |
| 178864 | BAA02g19610 | A02 | 10204993 | C | T | upstream_gene_variant | MODIFIER | c.-4481G>A| |
S233 |
| 178865 | BAA02g19620 | A02 | 10205971 | G | A | upstream_gene_variant | MODIFIER | c.-254G>A| |
S207 |
| 178866 | BAA02g19620 | A02 | 10206454 | C | T | missense_variant | MODERATE | c.230C>T|p.Pro77Leu |
S281 |
| 178867 | BAA02g19630 | A02 | 10206916 | C | T | downstream_gene_variant | MODIFIER | c.*3021G>A| |
S171 |
| 178868 | BAA02g19620 | A02 | 10208445 | G | A | synonymous_variant | LOW | c.1173G>A|p.Lys391Lys |
S161 |
| 178869 | BAA02g19630 | A02 | 10210296 | C | T | missense_variant | MODERATE | c.1648G>A|p.Glu550Lys |
S219 S72 |
| 178870 | BAA02g19630 | A02 | 10210328 | G | A | missense_variant | MODERATE | c.1616C>T|p.Ser539Phe |
S167 S236 S262 S263 |
| 178871 | BAA02g19630 | A02 | 10210570 | C | T | stop_gained | HIGH | c.1374G>A|p.Trp458* |
S105 |
| 178872 | BAA02g19640 | A02 | 10211116 | G | A | upstream_gene_variant | MODIFIER | c.-3737G>A| |
S111 |
| 178873 | BAA02g19640 | A02 | 10211402 | G | A | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S257 |
| 178874 | BAA02g19640 | A02 | 10211509 | C | T | upstream_gene_variant | MODIFIER | c.-3344C>T| |
S216 S241 S265 S39 |
| 178875 | BAA02g19640 | A02 | 10211544 | C | T | upstream_gene_variant | MODIFIER | c.-3309C>T| |
S233 |