Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18870 | A09 | 11388503 | C | T | downstream_gene_variant | MODIFIER | c.*1855G>A| |
S67 |
2 | BAA09g18870 | A09 | 11389239 | C | T | downstream_gene_variant | MODIFIER | c.*1119G>A| |
S60 |
3 | BAA09g18870 | A09 | 11389592 | G | A | downstream_gene_variant | MODIFIER | c.*766C>T| |
S198 |
4 | BAA09g18870 | A09 | 11389629 | G | A | downstream_gene_variant | MODIFIER | c.*729C>T| |
S142 |
5 | BAA09g18870 | A09 | 11393832 | G | A | synonymous_variant | LOW | c.8199C>T|p.Ser2733Ser |
S172 S217 |
6 | BAA09g18870 | A09 | 11399355 | C | A | missense_variant | MODERATE | c.2962G>T|p.Gly988Cys |
S255 |
7 | BAA09g18870 | A09 | 11399400 | G | A | missense_variant | MODERATE | c.2917C>T|p.Leu973Phe |
S46 |
8 | BAA09g18870 | A09 | 11399640 | G | A | synonymous_variant | LOW | c.2677C>T|p.Leu893Leu |
S246 |
9 | BAA09g18870 | A09 | 11399744 | G | A | missense_variant | MODERATE | c.2573C>T|p.Ser858Phe |
S149 |
10 | BAA09g18870 | A09 | 11400704 | G | A | missense_variant | MODERATE | c.1613C>T|p.Ser538Phe |
S245 |
11 | BAA09g18870 | A09 | 11400747 | C | T | missense_variant | MODERATE | c.1570G>A|p.Val524Met |
S48 |
12 | BAA09g18870 | A09 | 11402908 | G | A | upstream_gene_variant | MODIFIER | c.-253C>T| |
S152 |
13 | BAA09g18870 | A09 | 11403431 | C | T | upstream_gene_variant | MODIFIER | c.-776G>A| |
S295 |
14 | BAA09g18870 | A09 | 11403434 | C | T | upstream_gene_variant | MODIFIER | c.-779G>A| |
S76 |
15 | BAA09g18870 | A09 | 11404896 | G | A | upstream_gene_variant | MODIFIER | c.-2241C>T| |
S189 |
16 | BAA09g18870 | A09 | 11405815 | C | T | upstream_gene_variant | MODIFIER | c.-3160G>A| |
S249 |
17 | BAA09g18870 | A09 | 11406317 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S293 |
18 | BAA09g18870 | A09 | 11406602 | C | T | upstream_gene_variant | MODIFIER | c.-3947G>A| |
S143 |
19 | BAA09g18870 | A09 | 11407028 | C | T | upstream_gene_variant | MODIFIER | c.-4373G>A| |
S51 |