Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g21660 | A05 | 19839029 | G | A | downstream_gene_variant | MODIFIER | c.*1878C>T| |
S292 |
2 | BAA05g21660 | A05 | 19839060 | C | T | downstream_gene_variant | MODIFIER | c.*1847G>A| |
S255 |
3 | BAA05g21660 | A05 | 19840093 | C | T | downstream_gene_variant | MODIFIER | c.*814G>A| |
S8 |
4 | BAA05g21660 | A05 | 19840293 | C | T | downstream_gene_variant | MODIFIER | c.*614G>A| |
S142 |
5 | BAA05g21660 | A05 | 19840865 | G | A | downstream_gene_variant | MODIFIER | c.*42C>T| |
S301 S304 |
6 | BAA05g21660 | A05 | 19841133 | C | T | missense_variant | MODERATE | c.398G>A|p.Arg133Lys |
S12 |
7 | BAA05g21660 | A05 | 19841167 | C | T | missense_variant | MODERATE | c.364G>A|p.Val122Ile |
S240 |
8 | BAA05g21660 | A05 | 19841574 | C | T | upstream_gene_variant | MODIFIER | c.-44G>A| |
S64 |
9 | BAA05g21660 | A05 | 19843723 | G | A | upstream_gene_variant | MODIFIER | c.-2193C>T| |
S166 |
10 | BAA05g21660 | A05 | 19843742 | C | T | upstream_gene_variant | MODIFIER | c.-2212G>A| |
S232 |
11 | BAA05g21660 | A05 | 19843838 | C | T | upstream_gene_variant | MODIFIER | c.-2308G>A| |
S42 |
12 | BAA05g21660 | A05 | 19843915 | G | A | upstream_gene_variant | MODIFIER | c.-2385C>T| |
S296 |
13 | BAA05g21660 | A05 | 19843989 | G | A | upstream_gene_variant | MODIFIER | c.-2459C>T| |
S123 |
14 | BAA05g21660 | A05 | 19844195 | C | T | upstream_gene_variant | MODIFIER | c.-2665G>A| |
S295 |
15 | BAA05g21660 | A05 | 19844290 | G | A | upstream_gene_variant | MODIFIER | c.-2760C>T| |
S134 |
16 | BAA05g21660 | A05 | 19844482 | G | A | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S151 S263 |
17 | BAA05g21660 | A05 | 19845175 | C | T | upstream_gene_variant | MODIFIER | c.-3645G>A| |
S84 S93 |
18 | BAA05g21660 | A05 | 19845675 | G | A | upstream_gene_variant | MODIFIER | c.-4145C>T| |
S293 |
19 | BAA05g21660 | A05 | 19846012 | G | A | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S97 |