Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27690 | A09 | 18137899 | G | A | missense_variant | MODERATE | c.632C>T|p.Thr211Ile |
S245 |
2 | BAA09g27690 | A09 | 18138085 | G | A | missense_variant | MODERATE | c.446C>T|p.Ala149Val |
S207 |
3 | BAA09g27690 | A09 | 18138440 | C | T | synonymous_variant | LOW | c.195G>A|p.Leu65Leu |
S103 |
4 | BAA09g27690 | A09 | 18138582 | C | T | missense_variant | MODERATE | c.53G>A|p.Gly18Glu |
S116 |
5 | BAA09g27690 | A09 | 18139233 | G | A | upstream_gene_variant | MODIFIER | c.-599C>T| |
S53 |
6 | BAA09g27690 | A09 | 18139677 | C | A | upstream_gene_variant | MODIFIER | c.-1043G>T| |
S12 |
7 | BAA09g27690 | A09 | 18140100 | G | A | upstream_gene_variant | MODIFIER | c.-1466C>T| |
S12 |
8 | BAA09g27690 | A09 | 18140352 | C | T | upstream_gene_variant | MODIFIER | c.-1718G>A| |
S234 |
9 | BAA09g27690 | A09 | 18140418 | C | T | upstream_gene_variant | MODIFIER | c.-1784G>A| |
S275 |
10 | BAA09g27690 | A09 | 18140797 | C | T | upstream_gene_variant | MODIFIER | c.-2163G>A| |
S164 |
11 | BAA09g27690 | A09 | 18141353 | G | A | upstream_gene_variant | MODIFIER | c.-2719C>T| |
S183 S198 |
12 | BAA09g27690 | A09 | 18141436 | C | T | upstream_gene_variant | MODIFIER | c.-2802G>A| |
S186 |
13 | BAA09g27690 | A09 | 18141650 | C | T | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S6 |
14 | BAA09g27690 | A09 | 18142019 | G | A | upstream_gene_variant | MODIFIER | c.-3385C>T| |
S167 |
15 | BAA09g27690 | A09 | 18143175 | G | A | upstream_gene_variant | MODIFIER | c.-4541C>T| |
S59 |
16 | BAA09g27690 | A09 | 18143302 | C | T | upstream_gene_variant | MODIFIER | c.-4668G>A| |
S132 S137 S215 S288 S89 |
17 | BAA09g27690 | A09 | 18143424 | C | T | upstream_gene_variant | MODIFIER | c.-4790G>A| |
S188 |
18 | BAA09g27690 | A09 | 18143530 | T | C | upstream_gene_variant | MODIFIER | c.-4896A>G| |
S42 |