Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g09800 | A04 | 15979939 | G | A | synonymous_variant | LOW | c.1590C>T|p.Tyr530Tyr |
S88 |
2 | BAA04g09800 | A04 | 15980041 | G | A | synonymous_variant | LOW | c.1488C>T|p.Cys496Cys |
S166 |
3 | BAA04g09800 | A04 | 15980376 | C | T | missense_variant | MODERATE | c.1153G>A|p.Asp385Asn |
S268 |
4 | BAA04g09800 | A04 | 15980648 | C | T | missense_variant | MODERATE | c.881G>A|p.Arg294Lys |
S15 S3 |
5 | BAA04g09800 | A04 | 15980918 | G | A | missense_variant | MODERATE | c.611C>T|p.Ala204Val |
S218 |
6 | BAA04g09800 | A04 | 15984036 | C | T | upstream_gene_variant | MODIFIER | c.-2508G>A| |
S167 |
7 | BAA04g09800 | A04 | 15984096 | C | T | upstream_gene_variant | MODIFIER | c.-2568G>A| |
S197 |
8 | BAA04g09800 | A04 | 15984272 | G | A | upstream_gene_variant | MODIFIER | c.-2744C>T| |
S219 |
9 | BAA04g09800 | A04 | 15985010 | C | A | upstream_gene_variant | MODIFIER | c.-3482G>T| |
S107 |