Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39080 | A01 | 26000416 | C | T | missense_variant | MODERATE | c.2155G>A|p.Val719Ile |
S289 S290 |
2 | BAA01g39080 | A01 | 26000518 | G | A | stop_gained | HIGH | c.2053C>T|p.Gln685* |
S125 |
3 | BAA01g39080 | A01 | 26004207 | C | T | missense_variant | MODERATE | c.791G>A|p.Gly264Glu |
S89 |
4 | BAA01g39080 | A01 | 26005355 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.270-1G>A| |
S43 |
5 | BAA01g39080 | A01 | 26006725 | G | A | intron_variant | MODIFIER | c.269+16C>T| |
S229 |
6 | BAA01g39080 | A01 | 26009023 | G | A | upstream_gene_variant | MODIFIER | c.-1935C>T| |
S117 |
7 | BAA01g39080 | A01 | 26009127 | G | A | upstream_gene_variant | MODIFIER | c.-2039C>T| |
S70 |
8 | BAA01g39080 | A01 | 26009983 | G | A | upstream_gene_variant | MODIFIER | c.-2895C>T| |
S226 |
9 | BAA01g39080 | A01 | 26010115 | C | T | upstream_gene_variant | MODIFIER | c.-3027G>A| |
S11 |
10 | BAA01g39080 | A01 | 26011515 | C | T | upstream_gene_variant | MODIFIER | c.-4427G>A| |
S54 |
11 | BAA01g39080 | A01 | 26011825 | C | T | upstream_gene_variant | MODIFIER | c.-4737G>A| |
S266 |
12 | BAA01g39080 | A01 | 26011833 | C | T | upstream_gene_variant | MODIFIER | c.-4745G>A| |
S221 |