Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67950 | A09 | 61336471 | G | A | upstream_gene_variant | MODIFIER | c.-1197G>A| |
S209 |
2 | BAA09g67950 | A09 | 61337927 | G | A | missense_variant | MODERATE | c.260G>A|p.Gly87Asp |
S17 |
3 | BAA09g67950 | A09 | 61338322 | C | T | missense_variant | MODERATE | c.655C>T|p.Leu219Phe |
S306 S308 |
4 | BAA09g67950 | A09 | 61338331 | G | A | missense_variant | MODERATE | c.664G>A|p.Gly222Arg |
S197 |
5 | BAA09g67950 | A09 | 61338651 | G | A | synonymous_variant | LOW | c.984G>A|p.Leu328Leu |
S247 |
6 | BAA09g67950 | A09 | 61338818 | C | T | missense_variant | MODERATE | c.1151C>T|p.Ser384Phe |
S153 S213 |
7 | BAA09g67950 | A09 | 61339357 | C | T | missense_variant | MODERATE | c.1690C>T|p.Pro564Ser |
S75 S81 |
8 | BAA09g67950 | A09 | 61339708 | C | T | missense_variant | MODERATE | c.2041C>T|p.Leu681Phe |
S20 |
9 | BAA09g67950 | A09 | 61341552 | G | A | downstream_gene_variant | MODIFIER | c.*1449G>A| |
S69 |
10 | BAA09g67950 | A09 | 61342189 | C | T | downstream_gene_variant | MODIFIER | c.*2086C>T| |
S37 |
11 | BAA09g67950 | A09 | 61342222 | G | A | downstream_gene_variant | MODIFIER | c.*2119G>A| |
S107 |
12 | BAA09g67950 | A09 | 61343024 | C | T | downstream_gene_variant | MODIFIER | c.*2921C>T| |
S236 |
13 | BAA09g67950 | A09 | 61344296 | G | A | downstream_gene_variant | MODIFIER | c.*4193G>A| |
S273 |