Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10630 | A10 | 12392263 | C | T | upstream_gene_variant | MODIFIER | c.-3487C>T| |
S92 |
2 | BAA10g10630 | A10 | 12392402 | C | T | upstream_gene_variant | MODIFIER | c.-3348C>T| |
S110 |
3 | BAA10g10630 | A10 | 12395490 | G | A | upstream_gene_variant | MODIFIER | c.-260G>A| |
S251 |
4 | BAA10g10630 | A10 | 12396761 | C | T | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S131 |
5 | BAA10g10630 | A10 | 12397604 | C | T | missense_variant | MODERATE | c.1628C>T|p.Ser543Phe |
S56 |
6 | BAA10g10630 | A10 | 12397957 | C | T | missense_variant | MODERATE | c.1981C>T|p.Arg661Trp |
S12 |
7 | BAA10g10630 | A10 | 12399134 | A | T | downstream_gene_variant | MODIFIER | c.*1067A>T| |
S251 |
8 | BAA10g10630 | A10 | 12400474 | G | A | downstream_gene_variant | MODIFIER | c.*2407G>A| |
S186 |
9 | BAA10g10630 | A10 | 12400792 | G | A | downstream_gene_variant | MODIFIER | c.*2725G>A| |
S35 |
10 | BAA10g10630 | A10 | 12402447 | G | A | downstream_gene_variant | MODIFIER | c.*4380G>A| |
S32 |
11 | BAA10g10630 | A10 | 12402578 | C | T | downstream_gene_variant | MODIFIER | c.*4511C>T| |
S200 |
12 | BAA10g10630 | A10 | 12403029 | C | T | downstream_gene_variant | MODIFIER | c.*4962C>T| |
S294 |