Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g42390 | A01 | 28166177 | C | T | missense_variant | MODERATE | c.1469G>A|p.Gly490Glu |
S200 |
2 | BAA01g42390 | A01 | 28166680 | G | A | synonymous_variant | LOW | c.1128C>T|p.Pro376Pro |
|
3 | BAA01g42390 | A01 | 28167138 | G | A | missense_variant | MODERATE | c.670C>T|p.His224Tyr |
S267 |
4 | BAA01g42390 | A01 | 28168015 | C | T | missense_variant | MODERATE | c.310G>A|p.Glu104Lys |
S303 |
5 | BAA01g42390 | A01 | 28168235 | G | A | synonymous_variant | LOW | c.90C>T|p.Tyr30Tyr |
S191 |
6 | BAA01g42390 | A01 | 28171216 | C | A | upstream_gene_variant | MODIFIER | c.-2892G>T| |
S121 S154 S160 S161 S163 S180 S193 S194 S20 S221 S297 S6 |
7 | BAA01g42390 | A01 | 28171707 | C | T | upstream_gene_variant | MODIFIER | c.-3383G>A| |
S279 |
8 | BAA01g42390 | A01 | 28172043 | G | A | upstream_gene_variant | MODIFIER | c.-3719C>T| |
S36 |
9 | BAA01g42390 | A01 | 28172068 | G | A | upstream_gene_variant | MODIFIER | c.-3744C>T| |
S306 S308 |
10 | BAA01g42390 | A01 | 28172489 | C | T | upstream_gene_variant | MODIFIER | c.-4165G>A| |
S200 |
11 | BAA01g42390 | A01 | 28172767 | G | A | upstream_gene_variant | MODIFIER | c.-4443C>T| |
S110 |