Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g29960 | A06 | 20422661 | G | A | upstream_gene_variant | MODIFIER | c.-3303G>A| |
S11 |
2 | BAA06g29960 | A06 | 20422673 | A | T | upstream_gene_variant | MODIFIER | c.-3291A>T| |
S40 S49 |
3 | BAA06g29960 | A06 | 20422724 | C | T | upstream_gene_variant | MODIFIER | c.-3240C>T| |
S111 |
4 | BAA06g29960 | A06 | 20423581 | C | T | upstream_gene_variant | MODIFIER | c.-2383C>T| |
S2 |
5 | BAA06g29960 | A06 | 20423679 | C | T | upstream_gene_variant | MODIFIER | c.-2285C>T| |
S34 |
6 | BAA06g29960 | A06 | 20424017 | C | T | upstream_gene_variant | MODIFIER | c.-1947C>T| |
S83 S88 |
7 | BAA06g29960 | A06 | 20424420 | G | A | upstream_gene_variant | MODIFIER | c.-1544G>A| |
S255 |
8 | BAA06g29960 | A06 | 20424537 | C | T | upstream_gene_variant | MODIFIER | c.-1427C>T| |
S116 |
9 | BAA06g29960 | A06 | 20426426 | C | T | missense_variant | MODERATE | c.463C>T|p.Leu155Phe |
S96 |
10 | BAA06g29960 | A06 | 20426438 | G | A | missense_variant | MODERATE | c.475G>A|p.Val159Met |
S47 |
11 | BAA06g29960 | A06 | 20426542 | G | A | synonymous_variant | LOW | c.579G>A|p.Ala193Ala |
S251 |
12 | BAA06g29960 | A06 | 20426716 | G | A | synonymous_variant | LOW | c.753G>A|p.Arg251Arg |
S206 S26 |
13 | BAA06g29960 | A06 | 20426959 | G | A | downstream_gene_variant | MODIFIER | c.*102G>A| |
S240 |
14 | BAA06g29960 | A06 | 20427751 | G | A | downstream_gene_variant | MODIFIER | c.*894G>A| |
S56 |
15 | BAA06g29960 | A06 | 20429869 | C | T | downstream_gene_variant | MODIFIER | c.*3012C>T| |
S79 S91 |
16 | BAA06g29960 | A06 | 20430369 | G | A | downstream_gene_variant | MODIFIER | c.*3512G>A| |
S241 |
17 | BAA06g29960 | A06 | 20431009 | G | A | downstream_gene_variant | MODIFIER | c.*4152G>A| |
S152 |