Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49890 | A09 | 53014208 | C | T | missense_variant | MODERATE | c.2066G>A|p.Gly689Glu |
S225 |
2 | BAA09g49890 | A09 | 53014944 | G | A | missense_variant | MODERATE | c.1646C>T|p.Thr549Ile |
S201 |
3 | BAA09g49890 | A09 | 53015050 | G | A | missense_variant | MODERATE | c.1540C>T|p.Leu514Phe |
S115 |
4 | BAA09g49890 | A09 | 53015444 | G | A | synonymous_variant | LOW | c.1218C>T|p.Ile406Ile |
S190 |
5 | BAA09g49890 | A09 | 53015455 | G | A | missense_variant | MODERATE | c.1207C>T|p.Leu403Phe |
S270 |
6 | BAA09g49890 | A09 | 53015506 | C | T | missense_variant | MODERATE | c.1156G>A|p.Ala386Thr |
S68 |
7 | BAA09g49890 | A09 | 53016206 | G | A | missense_variant | MODERATE | c.620C>T|p.Thr207Ile |
S268 |
8 | BAA09g49890 | A09 | 53017162 | G | A | upstream_gene_variant | MODIFIER | c.-80C>T| |
S167 |
9 | BAA09g49890 | A09 | 53017191 | G | A | upstream_gene_variant | MODIFIER | c.-109C>T| |
S218 |
10 | BAA09g49890 | A09 | 53019584 | C | T | upstream_gene_variant | MODIFIER | c.-2502G>A| |
S297 |
11 | BAA09g49890 | A09 | 53019749 | C | A | upstream_gene_variant | MODIFIER | c.-2667G>T| |
S133 S153 S196 S205 S277 S301 S308 S70 |
12 | BAA09g49890 | A09 | 53020890 | G | A | upstream_gene_variant | MODIFIER | c.-3808C>T| |
S301 S304 |