Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02000 | A09 | 1395348 | C | T | missense_variant | MODERATE | c.110G>A|p.Gly37Glu |
S269 |
2 | BAA09g02000 | A09 | 1395402 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Asp |
S291 |
3 | BAA09g02000 | A09 | 1397082 | C | T | upstream_gene_variant | MODIFIER | c.-1535G>A| |
S150 |
4 | BAA09g02000 | A09 | 1397937 | C | T | upstream_gene_variant | MODIFIER | c.-2390G>A| |
S212 |
5 | BAA09g02000 | A09 | 1398870 | C | T | upstream_gene_variant | MODIFIER | c.-3323G>A| |
S71 |
6 | BAA09g02000 | A09 | 1398998 | C | T | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S269 |
7 | BAA09g02000 | A09 | 1399016 | C | T | upstream_gene_variant | MODIFIER | c.-3469G>A| |
S259 |
8 | BAA09g02000 | A09 | 1399346 | C | T | upstream_gene_variant | MODIFIER | c.-3799G>A| |
S134 |
9 | BAA09g02000 | A09 | 1399753 | C | T | upstream_gene_variant | MODIFIER | c.-4206G>A| |
S183 S198 |
10 | BAA09g02000 | A09 | 1399898 | C | T | upstream_gene_variant | MODIFIER | c.-4351G>A| |
S180 |
11 | BAA09g02000 | A09 | 1400138 | G | A | upstream_gene_variant | MODIFIER | c.-4591C>T| |
S308 |