| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 169851 | BAA02g14810 | A02 | 6991507 | G | A | upstream_gene_variant | MODIFIER | c.-1663C>T| |
S11 |
| 169852 | BAA02g14820 | A02 | 6991909 | C | T | synonymous_variant | LOW | c.99C>T|p.Phe33Phe |
S208 |
| 169853 | BAA02g14820 | A02 | 6993247 | G | A | stop_gained | HIGH | c.1091G>A|p.Trp364* |
S278 |
| 169854 | BAA02g14820 | A02 | 6993695 | G | A | synonymous_variant | LOW | c.1449G>A|p.Thr483Thr |
S45 |
| 169855 | BAA02g14820 | A02 | 6994855 | G | A | downstream_gene_variant | MODIFIER | c.*1004G>A| |
S289 S290 |
| 169856 | BAA02g14820 | A02 | 6995837 | G | A | downstream_gene_variant | MODIFIER | c.*1986G>A| |
S35 |
| 169857 | BAA02g14830 | A02 | 6995921 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Glu |
S200 |
| 169858 | BAA02g14830 | A02 | 6996287 | G | A | upstream_gene_variant | MODIFIER | c.-311C>T| |
S11 |
| 169859 | BAA02g14830 | A02 | 6996908 | C | T | upstream_gene_variant | MODIFIER | c.-932G>A| |
S212 |
| 169860 | BAA02g14830 | A02 | 6999541 | C | T | upstream_gene_variant | MODIFIER | c.-3565G>A| |
S249 |
| 169861 | BAA02g14830 | A02 | 6999706 | C | T | upstream_gene_variant | MODIFIER | c.-3730G>A| |
S116 |
| 169862 | BAA02g14830 | A02 | 7000014 | C | T | upstream_gene_variant | MODIFIER | c.-4038G>A| |
S242 |
| 169863 | BAA02g14840 | A02 | 7000108 | C | T | missense_variant | MODERATE | c.2174G>A|p.Arg725Lys |
S84 S93 |
| 169864 | BAA02g14840 | A02 | 7000520 | C | T | missense_variant | MODERATE | c.1928G>A|p.Ser643Asn |
S77 S82 |
| 169865 | BAA02g14840 | A02 | 7000752 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1794-1G>A| |
S47 |
| 169866 | BAA02g14840 | A02 | 7001675 | C | T | intron_variant | MODIFIER | c.1312+34G>A| |
S115 |
| 169867 | BAA02g14840 | A02 | 7002169 | C | T | synonymous_variant | LOW | c.1017G>A|p.Arg339Arg |
S208 S219 |
| 169868 | BAA02g14840 | A02 | 7002943 | C | T | missense_variant | MODERATE | c.683G>A|p.Arg228His |
S115 |
| 169869 | BAA02g14840 | A02 | 7003546 | G | A | missense_variant | MODERATE | c.305C>T|p.Ala102Val |
S48 |
| 169870 | BAA02g14840 | A02 | 7004928 | G | A | upstream_gene_variant | MODIFIER | c.-596C>T| |
S13 S168 S279 S64 |
| 169871 | BAA02g14840 | A02 | 7005049 | G | A | upstream_gene_variant | MODIFIER | c.-717C>T| |
S287 |
| 169872 | BAA02g14840 | A02 | 7005080 | G | A | upstream_gene_variant | MODIFIER | c.-748C>T| |
S246 |
| 169873 | BAA02g14840 | A02 | 7005424 | G | A | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S274 |
| 169874 | BAA02g14840 | A02 | 7006644 | G | A | upstream_gene_variant | MODIFIER | c.-2312C>T| |
S52 |
| 169875 | BAA02g14840 | A02 | 7006856 | C | T | upstream_gene_variant | MODIFIER | c.-2524G>A| |
S77 S82 |