Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10290 | A10 | 12045035 | G | A | synonymous_variant | LOW | c.969C>T|p.Ala323Ala |
S293 |
2 | BAA10g10290 | A10 | 12045295 | G | A | intron_variant | MODIFIER | c.725-16C>T| |
S288 |
3 | BAA10g10290 | A10 | 12046945 | G | A | missense_variant | MODERATE | c.719C>T|p.Thr240Ile |
S202 |
4 | BAA10g10290 | A10 | 12047416 | G | A | missense_variant | MODERATE | c.248C>T|p.Pro83Leu |
S126 S61 |
5 | BAA10g10290 | A10 | 12047443 | T | A | missense_variant | MODERATE | c.221A>T|p.Glu74Val |
S299 |
6 | BAA10g10290 | A10 | 12048757 | C | T | upstream_gene_variant | MODIFIER | c.-988G>A| |
S203 |
7 | BAA10g10290 | A10 | 12049943 | G | A | upstream_gene_variant | MODIFIER | c.-2174C>T| |
S62 |
8 | BAA10g10290 | A10 | 12050339 | C | T | upstream_gene_variant | MODIFIER | c.-2570G>A| |
S199 |
9 | BAA10g10290 | A10 | 12051466 | C | T | upstream_gene_variant | MODIFIER | c.-3697G>A| |
S259 |
10 | BAA10g10290 | A10 | 12051598 | G | A | upstream_gene_variant | MODIFIER | c.-3829C>T| |
S157 S163 |
11 | BAA10g10290 | A10 | 12052144 | C | T | upstream_gene_variant | MODIFIER | c.-4375G>A| |
S169 |