Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42350 | A09 | 48786701 | C | T | downstream_gene_variant | MODIFIER | c.*18G>A| |
S43 |
2 | BAA09g42350 | A09 | 48787072 | C | T | missense_variant | MODERATE | c.1084G>A|p.Ala362Thr |
S77 S82 |
3 | BAA09g42350 | A09 | 48787123 | C | T | missense_variant | MODERATE | c.1033G>A|p.Gly345Arg |
S95 |
4 | BAA09g42350 | A09 | 48787155 | C | T | missense_variant | MODERATE | c.1001G>A|p.Gly334Glu |
S163 |
5 | BAA09g42350 | A09 | 48787512 | G | A | missense_variant | MODERATE | c.644C>T|p.Ala215Val |
S163 |
6 | BAA09g42350 | A09 | 48787516 | G | A | missense_variant | MODERATE | c.640C>T|p.His214Tyr |
S116 |
7 | BAA09g42350 | A09 | 48787672 | G | A | stop_gained | HIGH | c.484C>T|p.Gln162* |
S172 S217 |
8 | BAA09g42350 | A09 | 48788086 | G | A | synonymous_variant | LOW | c.70C>T|p.Leu24Leu |
S165 S227 |
9 | BAA09g42350 | A09 | 48788352 | G | A | upstream_gene_variant | MODIFIER | c.-197C>T| |
S132 S137 S215 S89 |
10 | BAA09g42350 | A09 | 48791065 | C | T | upstream_gene_variant | MODIFIER | c.-2910G>A| |
S278 |
11 | BAA09g42350 | A09 | 48791274 | C | T | upstream_gene_variant | MODIFIER | c.-3119G>A| |
S301 S304 |