Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20800 | A10 | 18541592 | G | A | downstream_gene_variant | MODIFIER | c.*3217C>T| |
S64 |
2 | BAA10g20800 | A10 | 18542531 | C | T | downstream_gene_variant | MODIFIER | c.*2278G>A| |
S297 |
3 | BAA10g20800 | A10 | 18544888 | G | A | missense_variant&splice_region_variant | MODERATE | c.908C>T|p.Ala303Val |
S32 |
4 | BAA10g20800 | A10 | 18545552 | C | T | synonymous_variant | LOW | c.696G>A|p.Ser232Ser |
S89 |
5 | BAA10g20800 | A10 | 18545581 | C | T | missense_variant | MODERATE | c.667G>A|p.Glu223Lys |
S244 |
6 | BAA10g20800 | A10 | 18546418 | G | A | stop_gained | HIGH | c.76C>T|p.Gln26* |
S1 S90 |
7 | BAA10g20800 | A10 | 18549485 | C | T | upstream_gene_variant | MODIFIER | c.-2992G>A| |
S246 S73 S91 |
8 | BAA10g20800 | A10 | 18549630 | C | T | upstream_gene_variant | MODIFIER | c.-3137G>A| |
S262 |
9 | BAA10g20800 | A10 | 18549992 | C | T | upstream_gene_variant | MODIFIER | c.-3499G>A| |
S208 S219 |
10 | BAA10g20800 | A10 | 18550039 | G | A | upstream_gene_variant | MODIFIER | c.-3546C>T| |
S47 |
11 | BAA10g20800 | A10 | 18551390 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S273 |