Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g39540 | A06 | 25797419 | C | T | upstream_gene_variant | MODIFIER | c.-1872C>T| |
S6 |
2 | BAA06g39540 | A06 | 25797510 | G | A | upstream_gene_variant | MODIFIER | c.-1781G>A| |
S224 |
3 | BAA06g39540 | A06 | 25798794 | G | A | upstream_gene_variant | MODIFIER | c.-497G>A| |
S149 |
4 | BAA06g39540 | A06 | 25799617 | C | T | synonymous_variant | LOW | c.327C>T|p.Leu109Leu |
S135 |
5 | BAA06g39540 | A06 | 25799679 | T | G | missense_variant | MODERATE | c.389T>G|p.Val130Gly |
S140 S15 S151 S155 S188 S197 S287 S298 S47 S58 S83 |
6 | BAA06g39540 | A06 | 25799759 | G | A | missense_variant | MODERATE | c.469G>A|p.Val157Ile |
S219 S72 |
7 | BAA06g39540 | A06 | 25800025 | G | A | synonymous_variant | LOW | c.735G>A|p.Gln245Gln |
S302 |
8 | BAA06g39540 | A06 | 25800387 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1015-1G>A| |
S88 |
9 | BAA06g39540 | A06 | 25800411 | G | A | synonymous_variant | LOW | c.1038G>A|p.Gly346Gly |
S219 S72 |
10 | BAA06g39540 | A06 | 25800491 | C | T | missense_variant | MODERATE | c.1118C>T|p.Ser373Phe |
S153 |