Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15590 | A10 | 15910029 | G | A | intron_variant | MODIFIER | c.722-36C>T| |
S80 |
2 | BAA10g15590 | A10 | 15910092 | G | A | synonymous_variant | LOW | c.708C>T|p.Ala236Ala |
S233 |
3 | BAA10g15590 | A10 | 15912557 | C | T | upstream_gene_variant | MODIFIER | c.-1301G>A| |
S104 S52 |
4 | BAA10g15590 | A10 | 15913640 | G | A | upstream_gene_variant | MODIFIER | c.-2384C>T| |
S288 |
5 | BAA10g15590 | A10 | 15913667 | G | A | upstream_gene_variant | MODIFIER | c.-2411C>T| |
S270 |
6 | BAA10g15590 | A10 | 15914276 | C | T | upstream_gene_variant | MODIFIER | c.-3020G>A| |
S229 |
7 | BAA10g15590 | A10 | 15914524 | G | A | upstream_gene_variant | MODIFIER | c.-3268C>T| |
S63 |
8 | BAA10g15590 | A10 | 15914896 | G | A | upstream_gene_variant | MODIFIER | c.-3640C>T| |
S9 |
9 | BAA10g15590 | A10 | 15914980 | G | A | upstream_gene_variant | MODIFIER | c.-3724C>T| |
S55 |
10 | BAA10g15590 | A10 | 15915170 | C | T | upstream_gene_variant | MODIFIER | c.-3914G>A| |
S298 |