Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00560 | A06 | 399655 | C | T | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S239 |
2 | BAA06g00560 | A06 | 400450 | C | T | upstream_gene_variant | MODIFIER | c.-233C>T| |
S20 |
3 | BAA06g00560 | A06 | 403953 | C | T | intron_variant | MODIFIER | c.2280+31C>T| |
S305 |
4 | BAA06g00560 | A06 | 404376 | C | T | synonymous_variant | LOW | c.2562C>T|p.Leu854Leu |
S202 |
5 | BAA06g00560 | A06 | 404922 | C | T | synonymous_variant | LOW | c.2931C>T|p.Cys977Cys |
S98 |
6 | BAA06g00560 | A06 | 405126 | G | A | missense_variant | MODERATE | c.3046G>A|p.Ala1016Thr |
S294 |
7 | BAA06g00560 | A06 | 407249 | G | A | missense_variant | MODERATE | c.4387G>A|p.Gly1463Arg |
S159 S299 |
8 | BAA06g00560 | A06 | 408958 | G | A | missense_variant | MODERATE | c.5588G>A|p.Gly1863Glu |
S149 |
9 | BAA06g00560 | A06 | 410653 | C | T | downstream_gene_variant | MODIFIER | c.*571C>T| |
S230 |
10 | BAA06g00560 | A06 | 411908 | G | A | downstream_gene_variant | MODIFIER | c.*1826G>A| |
S244 |
11 | BAA06g00560 | A06 | 412773 | C | T | downstream_gene_variant | MODIFIER | c.*2691C>T| |
S240 |
12 | BAA06g00560 | A06 | 412813 | C | T | downstream_gene_variant | MODIFIER | c.*2731C>T| |
S242 |
13 | BAA06g00560 | A06 | 413186 | C | T | downstream_gene_variant | MODIFIER | c.*3104C>T| |
S274 |
14 | BAA06g00560 | A06 | 413554 | G | A | downstream_gene_variant | MODIFIER | c.*3472G>A| |
S161 |
15 | BAA06g00560 | A06 | 414704 | G | A | downstream_gene_variant | MODIFIER | c.*4622G>A| |
S105 S106 |