Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28100 | A10 | 21650389 | C | T | upstream_gene_variant | MODIFIER | c.-3948C>T| |
S157 S163 |
2 | BAA10g28100 | A10 | 21655668 | C | T | missense_variant | MODERATE | c.614C>T|p.Ala205Val |
S195 |
3 | BAA10g28100 | A10 | 21656098 | G | A | missense_variant | MODERATE | c.769G>A|p.Gly257Ser |
S171 |
4 | BAA10g28100 | A10 | 21656310 | G | A | synonymous_variant | LOW | c.861G>A|p.Ser287Ser |
S113 |
5 | BAA10g28100 | A10 | 21656660 | T | A | missense_variant | MODERATE | c.1085T>A|p.Leu362Gln |
S179 |
6 | BAA10g28100 | A10 | 21657388 | C | T | missense_variant | MODERATE | c.1555C>T|p.Pro519Ser |
S18 |
7 | BAA10g28100 | A10 | 21658765 | G | A | downstream_gene_variant | MODIFIER | c.*892G>A| |
S130 |
8 | BAA10g28100 | A10 | 21659516 | C | T | downstream_gene_variant | MODIFIER | c.*1643C>T| |
S40 S49 |
9 | BAA10g28100 | A10 | 21659949 | C | T | downstream_gene_variant | MODIFIER | c.*2076C>T| |
S107 |
10 | BAA10g28100 | A10 | 21660296 | G | A | downstream_gene_variant | MODIFIER | c.*2423G>A| |
S217 |