Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g33060 | A06 | 22357271 | C | A | downstream_gene_variant | MODIFIER | c.*3491G>T| |
S212 |
2 | BAA06g33060 | A06 | 22357393 | G | A | downstream_gene_variant | MODIFIER | c.*3369C>T| |
S263 |
3 | BAA06g33060 | A06 | 22357426 | G | A | downstream_gene_variant | MODIFIER | c.*3336C>T| |
S122 |
4 | BAA06g33060 | A06 | 22357481 | C | T | downstream_gene_variant | MODIFIER | c.*3281G>A| |
S155 |
5 | BAA06g33060 | A06 | 22357514 | C | T | downstream_gene_variant | MODIFIER | c.*3248G>A| |
S178 |
6 | BAA06g33060 | A06 | 22357516 | G | A | downstream_gene_variant | MODIFIER | c.*3246C>T| |
S265 |
7 | BAA06g33060 | A06 | 22357540 | C | T | downstream_gene_variant | MODIFIER | c.*3222G>A| |
S142 |
8 | BAA06g33060 | A06 | 22357722 | G | A | downstream_gene_variant | MODIFIER | c.*3040C>T| |
S67 |
9 | BAA06g33060 | A06 | 22357741 | G | A | downstream_gene_variant | MODIFIER | c.*3021C>T| |
S13 |
10 | BAA06g33060 | A06 | 22358466 | G | A | downstream_gene_variant | MODIFIER | c.*2296C>T| |
S77 |
11 | BAA06g33060 | A06 | 22358932 | T | A | downstream_gene_variant | MODIFIER | c.*1830A>T| |
S274 |
12 | BAA06g33060 | A06 | 22359249 | C | T | downstream_gene_variant | MODIFIER | c.*1513G>A| |
S288 |
13 | BAA06g33060 | A06 | 22361367 | C | T | missense_variant | MODERATE | c.875G>A|p.Ser292Asn |
S236 |
14 | BAA06g33060 | A06 | 22361940 | C | T | splice_region_variant&synonymous_variant | LOW | c.798G>A|p.Glu266Glu |
S155 |
15 | BAA06g33060 | A06 | 22362896 | C | T | missense_variant | MODERATE | c.356G>A|p.Gly119Glu |
S244 |
16 | BAA06g33060 | A06 | 22363614 | G | A | upstream_gene_variant | MODIFIER | c.-143C>T| |
S183 S198 |
17 | BAA06g33060 | A06 | 22365682 | C | T | upstream_gene_variant | MODIFIER | c.-2211G>A| |
S25 |
18 | BAA06g33060 | A06 | 22367687 | C | T | upstream_gene_variant | MODIFIER | c.-4216G>A| |
S7 |
19 | BAA06g33060 | A06 | 22367713 | G | A | upstream_gene_variant | MODIFIER | c.-4242C>T| |
S41 |