Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g19430 | A04 | 22927581 | G | A | missense_variant | MODERATE | c.1762C>T|p.Pro588Ser |
S229 |
2 | BAA04g19430 | A04 | 22927604 | C | T | missense_variant | MODERATE | c.1739G>A|p.Gly580Asp |
S246 |
3 | BAA04g19430 | A04 | 22927710 | C | T | missense_variant | MODERATE | c.1633G>A|p.Ala545Thr |
S156 |
4 | BAA04g19430 | A04 | 22928040 | G | A | stop_gained | HIGH | c.1303C>T|p.Gln435* |
S293 |
5 | BAA04g19430 | A04 | 22928399 | C | T | missense_variant | MODERATE | c.944G>A|p.Gly315Asp |
S132 S137 S215 |
6 | BAA04g19430 | A04 | 22929992 | G | A | missense_variant | MODERATE | c.863C>T|p.Ala288Val |
S186 |
7 | BAA04g19430 | A04 | 22930056 | G | A | missense_variant | MODERATE | c.799C>T|p.Pro267Ser |
S164 |
8 | BAA04g19430 | A04 | 22930317 | C | T | synonymous_variant | LOW | c.690G>A|p.Lys230Lys |
S156 |
9 | BAA04g19430 | A04 | 22930464 | G | A | intron_variant | MODIFIER | c.603+16C>T| |
S206 |
10 | BAA04g19430 | A04 | 22930552 | C | T | synonymous_variant | LOW | c.531G>A|p.Arg177Arg |
S202 |
11 | BAA04g19430 | A04 | 22930553 | C | T | missense_variant | MODERATE | c.530G>A|p.Arg177Lys |
S296 |
12 | BAA04g19430 | A04 | 22935643 | T | A | upstream_gene_variant | MODIFIER | c.-4485A>T| |
S26 |