Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02070 | A02 | 919674 | G | A | missense_variant | MODERATE | c.1498C>T|p.Leu500Phe |
S148 S210 S30 S31 |
2 | BAA02g02070 | A02 | 920212 | C | T | missense_variant | MODERATE | c.1114G>A|p.Glu372Lys |
S160 |
3 | BAA02g02070 | A02 | 920868 | G | A | splice_region_variant&intron_variant | LOW | c.795+8C>T| |
S273 |
4 | BAA02g02070 | A02 | 921443 | C | T | splice_region_variant&synonymous_variant | LOW | c.537G>A|p.Arg179Arg |
S80 S85 |
5 | BAA02g02070 | A02 | 921861 | C | T | missense_variant | MODERATE | c.295G>A|p.Glu99Lys |
S267 |
6 | BAA02g02070 | A02 | 924070 | C | T | upstream_gene_variant | MODIFIER | c.-1310G>A| |
S275 |
7 | BAA02g02070 | A02 | 924125 | G | A | upstream_gene_variant | MODIFIER | c.-1365C>T| |
S256 |
8 | BAA02g02070 | A02 | 924185 | C | T | upstream_gene_variant | MODIFIER | c.-1425G>A| |
S200 |
9 | BAA02g02070 | A02 | 926383 | C | T | upstream_gene_variant | MODIFIER | c.-3623G>A| |
S2 |
10 | BAA02g02070 | A02 | 926572 | G | A | upstream_gene_variant | MODIFIER | c.-3812C>T| |
S64 |