Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g25860 | A06 | 17703955 | G | A | downstream_gene_variant | MODIFIER | c.*4318C>T| |
S23 |
2 | BAA06g25860 | A06 | 17704658 | C | T | downstream_gene_variant | MODIFIER | c.*3615G>A| |
S165 |
3 | BAA06g25860 | A06 | 17705795 | C | T | downstream_gene_variant | MODIFIER | c.*2478G>A| |
S286 |
4 | BAA06g25860 | A06 | 17705939 | G | A | downstream_gene_variant | MODIFIER | c.*2334C>T| |
S103 |
5 | BAA06g25860 | A06 | 17707271 | G | A | downstream_gene_variant | MODIFIER | c.*1002C>T| |
S133 |
6 | BAA06g25860 | A06 | 17707533 | C | T | downstream_gene_variant | MODIFIER | c.*740G>A| |
S10 |
7 | BAA06g25860 | A06 | 17708243 | G | A | downstream_gene_variant | MODIFIER | c.*30C>T| |
S308 S7 |
8 | BAA06g25860 | A06 | 17709108 | G | A | missense_variant | MODERATE | c.1643C>T|p.Pro548Leu |
S281 |
9 | BAA06g25860 | A06 | 17709505 | G | A | synonymous_variant | LOW | c.1326C>T|p.Leu442Leu |
S208 |
10 | BAA06g25860 | A06 | 17710008 | G | A | intron_variant | MODIFIER | c.979-156C>T| |
S233 |
11 | BAA06g25860 | A06 | 17710036 | C | T | intron_variant | MODIFIER | c.979-184G>A| |
S86 |
12 | BAA06g25860 | A06 | 17712595 | C | T | missense_variant | MODERATE | c.5G>A|p.Gly2Glu |
S36 |
13 | BAA06g25860 | A06 | 17712650 | C | T | upstream_gene_variant | MODIFIER | c.-51G>A| |
S107 |
14 | BAA06g25860 | A06 | 17713544 | C | T | upstream_gene_variant | MODIFIER | c.-945G>A| |
S7 |
15 | BAA06g25860 | A06 | 17714448 | G | A | upstream_gene_variant | MODIFIER | c.-1849C>T| |
S133 |
16 | BAA06g25860 | A06 | 17714719 | C | T | upstream_gene_variant | MODIFIER | c.-2120G>A| |
S306 S308 |
17 | BAA06g25860 | A06 | 17716299 | C | T | upstream_gene_variant | MODIFIER | c.-3700G>A| |
S42 |