Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65900 | A09 | 60477102 | G | A | stop_gained | HIGH | c.1681C>T|p.Gln561* |
S161 |
2 | BAA09g65900 | A09 | 60477586 | G | A | missense_variant | MODERATE | c.1271C>T|p.Thr424Ile |
S17 |
3 | BAA09g65900 | A09 | 60477821 | C | T | missense_variant | MODERATE | c.1036G>A|p.Glu346Lys |
S236 |
4 | BAA09g65900 | A09 | 60477824 | C | T | missense_variant | MODERATE | c.1033G>A|p.Glu345Lys |
S67 |
5 | BAA09g65900 | A09 | 60478337 | G | A | intron_variant | MODIFIER | c.857+24C>T| |
S159 S299 |
6 | BAA09g65900 | A09 | 60478436 | G | A | intron_variant | MODIFIER | c.806-24C>T| |
S252 |
7 | BAA09g65900 | A09 | 60478500 | G | A | intron_variant | MODIFIER | c.805+20C>T| |
S295 |
8 | BAA09g65900 | A09 | 60478568 | G | A | missense_variant | MODERATE | c.757C>T|p.Pro253Ser |
S200 |
9 | BAA09g65900 | A09 | 60478637 | G | A | intron_variant | MODIFIER | c.704-16C>T| |
S181 |
10 | BAA09g65900 | A09 | 60480843 | G | A | upstream_gene_variant | MODIFIER | c.-333C>T| |
S187 |
11 | BAA09g65900 | A09 | 60482579 | C | T | upstream_gene_variant | MODIFIER | c.-2069G>A| |
S64 |
12 | BAA09g65900 | A09 | 60484316 | C | T | upstream_gene_variant | MODIFIER | c.-3806G>A| |
S33 |
13 | BAA09g65900 | A09 | 60484353 | C | T | upstream_gene_variant | MODIFIER | c.-3843G>A| |
S61 |