Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g05400 | A04 | 3475025 | G | T | upstream_gene_variant | MODIFIER | c.-4766G>T| |
S97 |
2 | BAA04g05400 | A04 | 3475468 | G | A | upstream_gene_variant | MODIFIER | c.-4323G>A| |
S105 S106 |
3 | BAA04g05400 | A04 | 3476892 | G | A | upstream_gene_variant | MODIFIER | c.-2899G>A| |
S199 |
4 | BAA04g05400 | A04 | 3480441 | G | C | missense_variant | MODERATE | c.259G>C|p.Val87Leu |
S155 S211 |
5 | BAA04g05400 | A04 | 3480645 | C | T | missense_variant&splice_region_variant | MODERATE | c.373C>T|p.Pro125Ser |
S221 |
6 | BAA04g05400 | A04 | 3481960 | G | A | synonymous_variant | LOW | c.981G>A|p.Lys327Lys |
S275 |
7 | BAA04g05400 | A04 | 3482132 | C | T | intron_variant | MODIFIER | c.1086+67C>T| |
S293 |
8 | BAA04g05400 | A04 | 3486458 | G | A | stop_gained | HIGH | c.2768G>A|p.Trp923* |
S262 |
9 | BAA04g05400 | A04 | 3489423 | C | T | downstream_gene_variant | MODIFIER | c.*2278C>T| |
S9 |
10 | BAA04g05400 | A04 | 3489426 | C | T | downstream_gene_variant | MODIFIER | c.*2281C>T| |
S136 |
11 | BAA04g05400 | A04 | 3489438 | G | A | downstream_gene_variant | MODIFIER | c.*2293G>A| |
S13 |
12 | BAA04g05400 | A04 | 3489480 | C | T | downstream_gene_variant | MODIFIER | c.*2335C>T| |
S233 |