Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24600 | A09 | 15775362 | G | A | upstream_gene_variant | MODIFIER | c.-2810G>A| |
S221 |
2 | BAA09g24600 | A09 | 15775485 | C | T | upstream_gene_variant | MODIFIER | c.-2687C>T| |
S32 |
3 | BAA09g24600 | A09 | 15776363 | C | T | upstream_gene_variant | MODIFIER | c.-1809C>T| |
S2 |
4 | BAA09g24600 | A09 | 15776878 | C | T | upstream_gene_variant | MODIFIER | c.-1294C>T| |
S200 |
5 | BAA09g24600 | A09 | 15777556 | C | T | upstream_gene_variant | MODIFIER | c.-616C>T| |
S5 |
6 | BAA09g24600 | A09 | 15779162 | G | A | intron_variant | MODIFIER | c.709+23G>A| |
S100 |
7 | BAA09g24600 | A09 | 15779572 | G | A | missense_variant | MODERATE | c.973G>A|p.Val325Met |
S128 |
8 | BAA09g24600 | A09 | 15780132 | G | A | missense_variant | MODERATE | c.1341G>A|p.Met447Ile |
S185 |
9 | BAA09g24600 | A09 | 15780622 | G | A | missense_variant | MODERATE | c.1657G>A|p.Glu553Lys |
S38 |
10 | BAA09g24600 | A09 | 15780652 | C | T | missense_variant | MODERATE | c.1687C>T|p.His563Tyr |
S95 |