Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19040 | A09 | 11510111 | G | A | missense_variant | MODERATE | c.2813C>T|p.Ser938Leu |
S197 |
2 | BAA09g19040 | A09 | 11510420 | C | T | missense_variant | MODERATE | c.2504G>A|p.Gly835Glu |
S242 |
3 | BAA09g19040 | A09 | 11510444 | G | A | missense_variant | MODERATE | c.2480C>T|p.Ser827Phe |
S288 |
4 | BAA09g19040 | A09 | 11510810 | C | T | missense_variant | MODERATE | c.2114G>A|p.Gly705Asp |
S177 |
5 | BAA09g19040 | A09 | 11510995 | C | T | stop_gained | HIGH | c.1929G>A|p.Trp643* |
S296 |
6 | BAA09g19040 | A09 | 11511642 | G | A | synonymous_variant | LOW | c.1356C>T|p.Tyr452Tyr |
S25 |
7 | BAA09g19040 | A09 | 11512382 | C | T | splice_donor_variant&intron_variant | HIGH | c.1004+1G>A| |
S186 |
8 | BAA09g19040 | A09 | 11512620 | G | A | missense_variant | MODERATE | c.767C>T|p.Ser256Phe |
S209 |
9 | BAA09g19040 | A09 | 11512835 | G | A | missense_variant | MODERATE | c.620C>T|p.Ser207Phe |
S301 S304 |
10 | BAA09g19040 | A09 | 11515534 | G | A | upstream_gene_variant | MODIFIER | c.-1750C>T| |
S166 |
11 | BAA09g19040 | A09 | 11516791 | G | A | upstream_gene_variant | MODIFIER | c.-3007C>T| |
S298 S301 |
12 | BAA09g19040 | A09 | 11518338 | C | T | upstream_gene_variant | MODIFIER | c.-4554G>A| |
S295 |