Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00980 | A06 | 667813 | G | A | downstream_gene_variant | MODIFIER | c.*1953C>T| |
S35 |
2 | BAA06g00980 | A06 | 669536 | G | A | downstream_gene_variant | MODIFIER | c.*230C>T| |
S8 |
3 | BAA06g00980 | A06 | 670451 | G | A | synonymous_variant | LOW | c.585C>T|p.Phe195Phe |
S272 |
4 | BAA06g00980 | A06 | 670975 | G | A | intron_variant | MODIFIER | c.355-214C>T| |
S284 |
5 | BAA06g00980 | A06 | 672241 | G | A | intron_variant | MODIFIER | c.239-860C>T| |
S138 |
6 | BAA06g00980 | A06 | 675323 | C | T | upstream_gene_variant | MODIFIER | c.-1392G>A| |
S282 |
7 | BAA06g00980 | A06 | 675533 | G | A | upstream_gene_variant | MODIFIER | c.-1602C>T| |
S35 |
8 | BAA06g00980 | A06 | 677841 | G | A | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S277 |
9 | BAA06g00980 | A06 | 678008 | C | T | upstream_gene_variant | MODIFIER | c.-4077G>A| |
S6 |