Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44220 | A06 | 28357291 | C | T | synonymous_variant | LOW | c.2502G>A|p.Gln834Gln |
S282 |
2 | BAA06g44220 | A06 | 28357591 | C | T | synonymous_variant | LOW | c.2202G>A|p.Glu734Glu |
S269 |
3 | BAA06g44220 | A06 | 28357803 | C | T | missense_variant | MODERATE | c.1990G>A|p.Asp664Asn |
S62 |
4 | BAA06g44220 | A06 | 28358087 | C | T | missense_variant | MODERATE | c.1706G>A|p.Arg569Lys |
S196 |
5 | BAA06g44220 | A06 | 28359174 | C | T | missense_variant | MODERATE | c.619G>A|p.Asp207Asn |
S132 S137 S215 S89 |
6 | BAA06g44220 | A06 | 28359329 | G | A | missense_variant | MODERATE | c.464C>T|p.Ser155Leu |
S295 |
7 | BAA06g44220 | A06 | 28362409 | G | A | upstream_gene_variant | MODIFIER | c.-2617C>T| |
S262 |
8 | BAA06g44220 | A06 | 28363971 | G | A | upstream_gene_variant | MODIFIER | c.-4179C>T| |
S289 S290 |