Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12120 | A05 | 6152103 | C | T | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S181 |
2 | BAA05g12120 | A05 | 6152177 | C | T | upstream_gene_variant | MODIFIER | c.-4871C>T| |
S188 |
3 | BAA05g12120 | A05 | 6152293 | G | A | upstream_gene_variant | MODIFIER | c.-4755G>A| |
S299 |
4 | BAA05g12120 | A05 | 6152841 | C | T | upstream_gene_variant | MODIFIER | c.-4207C>T| |
S68 |
5 | BAA05g12120 | A05 | 6153477 | G | A | upstream_gene_variant | MODIFIER | c.-3571G>A| |
S62 |
6 | BAA05g12120 | A05 | 6153819 | G | A | upstream_gene_variant | MODIFIER | c.-3229G>A| |
S187 |
7 | BAA05g12120 | A05 | 6155110 | C | T | upstream_gene_variant | MODIFIER | c.-1938C>T| |
S19 |
8 | BAA05g12120 | A05 | 6155159 | C | T | upstream_gene_variant | MODIFIER | c.-1889C>T| |
S229 |
9 | BAA05g12120 | A05 | 6156670 | C | T | upstream_gene_variant | MODIFIER | c.-378C>T| |
S188 |
10 | BAA05g12120 | A05 | 6157213 | C | T | missense_variant | MODERATE | c.166C>T|p.Leu56Phe |
S55 |
11 | BAA05g12120 | A05 | 6157516 | G | A | missense_variant | MODERATE | c.469G>A|p.Glu157Lys |
S149 |
12 | BAA05g12120 | A05 | 6157613 | G | A | missense_variant | MODERATE | c.566G>A|p.Gly189Glu |
S41 |
13 | BAA05g12120 | A05 | 6158339 | G | A | synonymous_variant | LOW | c.954G>A|p.Glu318Glu |
S230 |
14 | BAA05g12120 | A05 | 6158618 | G | A | stop_gained | HIGH | c.1065G>A|p.Trp355* |
S109 |
15 | BAA05g12120 | A05 | 6158654 | G | A | synonymous_variant | LOW | c.1101G>A|p.Thr367Thr |
S40 S49 |
16 | BAA05g12120 | A05 | 6158727 | G | A | missense_variant | MODERATE | c.1174G>A|p.Glu392Lys |
S112 |
17 | BAA05g12120 | A05 | 6162573 | G | A | downstream_gene_variant | MODIFIER | c.*3784G>A| |
S34 |
18 | BAA05g12120 | A05 | 6163152 | G | A | downstream_gene_variant | MODIFIER | c.*4363G>A| |
S11 |
19 | BAA05g12120 | A05 | 6163482 | C | T | downstream_gene_variant | MODIFIER | c.*4693C>T| |
S216 |