Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08200 | A10 | 5897300 | G | A | downstream_gene_variant | MODIFIER | c.*2338C>T| |
S65 |
2 | BAA10g08200 | A10 | 5897459 | C | T | downstream_gene_variant | MODIFIER | c.*2179G>A| |
S275 |
3 | BAA10g08200 | A10 | 5898008 | G | A | downstream_gene_variant | MODIFIER | c.*1630C>T| |
S16 |
4 | BAA10g08200 | A10 | 5898358 | A | T | downstream_gene_variant | MODIFIER | c.*1280T>A| |
S54 |
5 | BAA10g08200 | A10 | 5898642 | C | T | downstream_gene_variant | MODIFIER | c.*996G>A| |
S71 |
6 | BAA10g08200 | A10 | 5899118 | G | A | downstream_gene_variant | MODIFIER | c.*520C>T| |
S36 |
7 | BAA10g08200 | A10 | 5900725 | A | G | synonymous_variant | LOW | c.1098T>C|p.His366His |
S26 |
8 | BAA10g08200 | A10 | 5900742 | C | T | missense_variant | MODERATE | c.1081G>A|p.Glu361Lys |
S32 |
9 | BAA10g08200 | A10 | 5906837 | C | T | upstream_gene_variant | MODIFIER | c.-4394G>A| |
S138 S215 S288 |
10 | BAA10g08200 | A10 | 5906902 | G | A | upstream_gene_variant | MODIFIER | c.-4459C>T| |
S118 |
11 | BAA10g08200 | A10 | 5907420 | G | A | upstream_gene_variant | MODIFIER | c.-4977C>T| |
S99 |