Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41800 | A05 | 39765878 | C | T | synonymous_variant | LOW | c.1440G>A|p.Ala480Ala |
S78 |
2 | BAA05g41800 | A05 | 39766680 | C | T | missense_variant | MODERATE | c.638G>A|p.Gly213Glu |
S185 |
3 | BAA05g41800 | A05 | 39766708 | C | T | missense_variant | MODERATE | c.610G>A|p.Val204Met |
S20 |
4 | BAA05g41800 | A05 | 39766900 | C | T | missense_variant | MODERATE | c.418G>A|p.Glu140Lys |
S203 |
5 | BAA05g41800 | A05 | 39766911 | G | A | missense_variant | MODERATE | c.407C>T|p.Pro136Leu |
S1 S90 |
6 | BAA05g41800 | A05 | 39767033 | G | A | synonymous_variant | LOW | c.285C>T|p.Asn95Asn |
S68 |
7 | BAA05g41800 | A05 | 39767278 | G | A | stop_gained | HIGH | c.40C>T|p.Gln14* |
S298 |
8 | BAA05g41800 | A05 | 39767426 | G | A | upstream_gene_variant | MODIFIER | c.-109C>T| |
S165 |
9 | BAA05g41800 | A05 | 39769449 | C | T | upstream_gene_variant | MODIFIER | c.-2132G>A| |
S217 S248 |
10 | BAA05g41800 | A05 | 39770963 | G | A | upstream_gene_variant | MODIFIER | c.-3646C>T| |
S292 |
11 | BAA05g41800 | A05 | 39771842 | G | A | upstream_gene_variant | MODIFIER | c.-4525C>T| |
S127 |