Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g37480 | A05 | 36948349 | G | A | upstream_gene_variant | MODIFIER | c.-3601G>A| |
S157 S163 |
2 | BAA05g37480 | A05 | 36948371 | G | A | upstream_gene_variant | MODIFIER | c.-3579G>A| |
S78 S83 |
3 | BAA05g37480 | A05 | 36951610 | C | T | upstream_gene_variant | MODIFIER | c.-340C>T| |
S207 |
4 | BAA05g37480 | A05 | 36952564 | C | T | missense_variant | MODERATE | c.349C>T|p.Pro117Ser |
S146 |
5 | BAA05g37480 | A05 | 36952588 | C | T | stop_gained | HIGH | c.373C>T|p.Gln125* |
S208 S93 |
6 | BAA05g37480 | A05 | 36953339 | G | A | synonymous_variant | LOW | c.723G>A|p.Gly241Gly |
S275 |
7 | BAA05g37480 | A05 | 36954550 | C | T | missense_variant | MODERATE | c.1055C>T|p.Pro352Leu |
S216 |
8 | BAA05g37480 | A05 | 36954986 | G | A | missense_variant | MODERATE | c.1281G>A|p.Met427Ile |
S117 |
9 | BAA05g37480 | A05 | 36956695 | C | T | synonymous_variant | LOW | c.1927C>T|p.Leu643Leu |
S182 |
10 | BAA05g37480 | A05 | 36956762 | C | T | missense_variant | MODERATE | c.1994C>T|p.Ala665Val |
S292 |
11 | BAA05g37480 | A05 | 36958556 | C | T | downstream_gene_variant | MODIFIER | c.*1778C>T| |
S133 |
12 | BAA05g37480 | A05 | 36959655 | G | A | downstream_gene_variant | MODIFIER | c.*2877G>A| |
S61 |