Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g26800 | A06 | 18443391 | C | T | upstream_gene_variant | MODIFIER | c.-4575C>T| |
S164 |
2 | BAA06g26800 | A06 | 18443638 | G | A | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S103 |
3 | BAA06g26800 | A06 | 18443794 | C | T | upstream_gene_variant | MODIFIER | c.-4172C>T| |
S236 |
4 | BAA06g26800 | A06 | 18444195 | C | T | upstream_gene_variant | MODIFIER | c.-3771C>T| |
S28 |
5 | BAA06g26800 | A06 | 18445011 | A | T | upstream_gene_variant | MODIFIER | c.-2955A>T| |
S229 |
6 | BAA06g26800 | A06 | 18445603 | C | T | upstream_gene_variant | MODIFIER | c.-2363C>T| |
S205 |
7 | BAA06g26800 | A06 | 18446806 | C | T | upstream_gene_variant | MODIFIER | c.-1160C>T| |
S111 |
8 | BAA06g26800 | A06 | 18447046 | C | T | upstream_gene_variant | MODIFIER | c.-920C>T| |
S202 |
9 | BAA06g26800 | A06 | 18447187 | G | A | upstream_gene_variant | MODIFIER | c.-779G>A| |
S122 |
10 | BAA06g26800 | A06 | 18447714 | C | T | upstream_gene_variant | MODIFIER | c.-252C>T| |
S288 |
11 | BAA06g26800 | A06 | 18448131 | C | T | intron_variant | MODIFIER | c.76+90C>T| |
S199 |
12 | BAA06g26800 | A06 | 18448164 | C | T | intron_variant | MODIFIER | c.76+123C>T| |
S298 |
13 | BAA06g26800 | A06 | 18448850 | C | T | missense_variant | MODERATE | c.347C>T|p.Ser116Phe |
S303 |
14 | BAA06g26800 | A06 | 18452212 | A | G | missense_variant | MODERATE | c.1951A>G|p.Ile651Val |
S211 |